<!DOCTYPE article
PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.4 20190208//EN"
       "JATS-journalpublishing1.dtd">
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" article-type="research-article" dtd-version="1.4" xml:lang="en">
 <front>
  <journal-meta>
   <journal-id journal-id-type="publisher-id">Food Processing: Techniques and Technology</journal-id>
   <journal-title-group>
    <journal-title xml:lang="en">Food Processing: Techniques and Technology</journal-title>
    <trans-title-group xml:lang="ru">
     <trans-title>Техника и технология пищевых производств</trans-title>
    </trans-title-group>
   </journal-title-group>
   <issn publication-format="print">2074-9414</issn>
   <issn publication-format="online">2313-1748</issn>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="publisher-id">110807</article-id>
   <article-id pub-id-type="doi">10.21603/2074-9414-2025-4-2601</article-id>
   <article-id pub-id-type="edn">PRHCIY</article-id>
   <article-categories>
    <subj-group subj-group-type="toc-heading" xml:lang="ru">
     <subject>ОРИГИНАЛЬНАЯ СТАТЬЯ</subject>
    </subj-group>
    <subj-group subj-group-type="toc-heading" xml:lang="en">
     <subject>ORIGINAL ARTICLE</subject>
    </subj-group>
    <subj-group>
     <subject>ОРИГИНАЛЬНАЯ СТАТЬЯ</subject>
    </subj-group>
   </article-categories>
   <title-group>
    <article-title xml:lang="en">Dispersed and Tandem Repeats in Genomes and Genes of Some Mammalian Species</article-title>
    <trans-title-group xml:lang="ru">
     <trans-title>Диспергированные и тандемные повторы в геномах и генах некоторых видов млекопитающих</trans-title>
    </trans-title-group>
   </title-group>
   <contrib-group content-type="authors">
    <contrib contrib-type="author">
     <contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3808-3086</contrib-id>
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Косовский</surname>
       <given-names>Глеб Юрьевич</given-names>
      </name>
      <name xml:lang="en">
       <surname>Kosovsky</surname>
       <given-names>Gleb Yu.</given-names>
      </name>
     </name-alternatives>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
    <contrib contrib-type="author">
     <contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3879-6935</contrib-id>
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Глазко</surname>
       <given-names>Татьяна Теодоровна</given-names>
      </name>
      <name xml:lang="en">
       <surname>Glazko</surname>
       <given-names>Tatiana T.</given-names>
      </name>
     </name-alternatives>
     <email>tglazko@rambler.ru</email>
     <xref ref-type="aff" rid="aff-2"/>
    </contrib>
   </contrib-group>
   <aff-alternatives id="aff-1">
    <aff>
     <institution xml:lang="ru">Научно-исследовательский институт пушного звероводства и кролиководства имени В. А. Афанасьева</institution>
     <city>пос. Родники</city>
     <country>Россия</country>
    </aff>
    <aff>
     <institution xml:lang="en">Scientific Research Institute of Fur-Bearing Animal Breeding and Rabbit Breeding n.a. V.A. Afanas'ev</institution>
     <city>Rodniki</city>
     <country>Russian Federation</country>
    </aff>
   </aff-alternatives>
   <aff-alternatives id="aff-2">
    <aff>
     <institution xml:lang="ru">Научно-исследовательский институт пушного звероводства и кролиководства имени В. А. Афанасьева</institution>
     <city>пос. Родники</city>
     <country>Россия</country>
    </aff>
    <aff>
     <institution xml:lang="en">Scientific Research Institute of Fur-Bearing Animal Breeding and Rabbit Breeding n.a. V.A. Afanas'ev</institution>
     <city>Rodniki</city>
     <country>Russian Federation</country>
    </aff>
   </aff-alternatives>
   <pub-date publication-format="print" date-type="pub" iso-8601-date="2025-12-25T00:00:00+03:00">
    <day>25</day>
    <month>12</month>
    <year>2025</year>
   </pub-date>
   <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2025-12-25T00:00:00+03:00">
    <day>25</day>
    <month>12</month>
    <year>2025</year>
   </pub-date>
   <volume>55</volume>
   <issue>4</issue>
   <fpage>687</fpage>
   <lpage>709</lpage>
   <history>
    <date date-type="received" iso-8601-date="2025-08-12T00:00:00+03:00">
     <day>12</day>
     <month>08</month>
     <year>2025</year>
    </date>
    <date date-type="accepted" iso-8601-date="2025-10-07T00:00:00+03:00">
     <day>07</day>
     <month>10</month>
     <year>2025</year>
    </date>
   </history>
   <self-uri xlink:href="https://fptt.ru/en/issues/24078/24080/">https://fptt.ru/en/issues/24078/24080/</self-uri>
   <abstract xml:lang="ru">
    <p>Развитие методов генного и геномного редактирования повышает актуальность прогноза и уменьшения вероятности нецелевых, плейотропных последствий. Одним из таких направлений может быть оценка структурно-функциональных особенностей геномных мишеней редактирования по наиболее полиморфным геномным элементам, таким как транспозоны. Цель исследования – выявить распределения транспозонов в генах, наиболее часто выбираемых в качестве мишеней генного редактирования, и на их флангах у разных видов млекопитающих. &#13;
Исследование выполнялось на геномных последовательностях человека (Homo sapiens), крупного рогатого скота (Bos taurus), домашнего кролика (Oryctolagus cuniculus) и домовой мыши (Mus musculus) белок-кодирующих генов миостатина (mstn), меланофилина (mlph), рецептора лептина (lepr), белка ремоделинга хроматина (хромосома Х, atrx), генов эволюционно консервативной петли хроматина (фактор регуляции транскрипции – auts2, N-ацетилгалактозаминилтрансфераза – galnt17, кальций связывающий белок 1 – caln1), а также их флангов. Распределение транспозонов оценивали с использованием программы RepeatMasker, статистическую обработку выполняли с применением программы Jamovi. Рассматривались следующие генные и геномные особенности: частота встречаемости разных типов диспергированных повторов, доминирующих у предковых видов млекопитающих и затем вытесненных молодыми вариантами; зависимость частоты встречаемости разных повторов от локализации в аутосомах и хромосоме Х, функциональной принадлежности групп генов, их локализации в общей и разных хромосомах, перекрывания генов. Выявлены отличия по частотам встречаемости «древних» и «молодых» транспозонов между человеком, крупным рогатым скотом и грызунами, по-видимому, связанные с разной скоростью смены поколений; обнаружены ассоциации между функциями белков и консервативностью генетического сцепления между кодирующими их генами; генетически сцепленные гены у разных видов отличались по обогащенности «древними» транспозонами, что, предположительно, ассоциировано с видоспецифичными различиями в защищенности от транспозиций соответствующих геномных районов.&#13;
Полученные данные о видо- и ген-специфичных особенностях распределения транспозонов необходимо учитывать в целях предупреждения нежелательных эффектов редактирования соответствующих геномных районов.</p>
   </abstract>
   <trans-abstract xml:lang="en">
    <p>Gene and genome editing improves the prognosis by preventing non-target or pleiotropic consequences. Genomic editing targets can be assessed by localizing their structural and functional traits on the most polymorphic genomic elements, e.g., by transposons. This research clarified the distribution of transposons in the most popular gene editing targets and on their flanks in different mammalian species.&#13;
The study covered the genomic sequences of humans (Homo sapiens), cattle (Bos taurus), domestic rabbits (Oryctolagus cuniculus), and house mice (Mus musculus). It involved the protein-coding genes of myostatin (mstn), melanophilin (mlph), leptin receptor (lepr), X-localized chromatin remodeling protein (atrx), and three genes in the evolutionarily conserved chromatin loop (transcrip-tion regulation factor – auts2, N-acetylgalactosaminyl transferase – galnt17, calcium binding protein 1 – caln1), as well as at least four genes on their flanks. The distribution of transposons was estimated using RepeatMasker; the statistical processing relied on the Jamovi software. The analysis was conducted for the following gene and genomic traits: 1) the frequency of dispersed repeats that were dominant in ancestral species to be displaced by later varieties; 2) the correlation between the frequency and the localization in autosomes and chromosome X, the functional affiliation of gene groups, their localization in the same and different chromosomes, and gene overlap.&#13;
The differences in the frequencies of ancient and young transposons between humans, cattle, and rodents were associated with different rates of generational exchange. The research also revealed some links between the protein functions and the conservatism of genetic linkage. The blocks of genetically linked genes across the species differed in ancient transposons, which depended on the species-specific differences in the protection of the corresponding genomic regions from transpositions.&#13;
The data on species- and gene-specific traits of transposons distribution may help to prevent undesirable pleiotropic effects of genetic modifications.</p>
   </trans-abstract>
   <kwd-group xml:lang="ru">
    <kwd>Генное редактирование</kwd>
    <kwd>генетическое сцепление</kwd>
    <kwd>хроматиновая петля</kwd>
    <kwd>эволюционная консервативность</kwd>
    <kwd>«древние» и «молодые» транспозоны</kwd>
    <kwd>человек</kwd>
    <kwd>крупный рогатый скот</kwd>
    <kwd>домашний кролик</kwd>
    <kwd>домовая мышь</kwd>
   </kwd-group>
   <kwd-group xml:lang="en">
    <kwd>Gene editing</kwd>
    <kwd>genetic linkage</kwd>
    <kwd>chromatin loop</kwd>
    <kwd>evolutionary conservatism</kwd>
    <kwd>ancient and young transposons</kwd>
    <kwd>Homo sapiens</kwd>
    <kwd>Bos taurus</kwd>
    <kwd>Oryctolagus cuniculus</kwd>
    <kwd>Mus musculus</kwd>
   </kwd-group>
   <funding-group>
    <funding-statement xml:lang="ru">Исследование поддержано Министерством науки и высшего образования Российской Федерации (государственное задание № 075-00503-25-02).</funding-statement>
    <funding-statement xml:lang="en">The study is supported by the Ministry of Science and Higher Education of the Russian Federation (state agreement No. 075-00503-25-02).</funding-statement>
   </funding-group>
  </article-meta>
 </front>
 <body>
  <p></p>
 </body>
 <back>
  <ref-list>
   <ref id="B1">
    <label>1.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Alariqi M, Ramadan M, Yu L, Hui F, Hussain A, et al. Enhancing specificity, precision, accessibility, flexibility, and safety to overcome traditional CRISPR/Cas editing challenges and shape future innovations. Advanced Science. 2025;12(28):e2416331. https://doi.org/10.1002/advs.202416331</mixed-citation>
     <mixed-citation xml:lang="en">Alariqi M, Ramadan M, Yu L, Hui F, Hussain A, et al. Enhancing specificity, precision, accessibility, flexibility, and safety to overcome traditional CRISPR/Cas editing challenges and shape future innovations. Advanced Science. 2025;12(28):e2416331. https://doi.org/10.1002/advs.202416331</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B2">
    <label>2.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Pandey S, Choudhari JK, Tripathi A, Singh A, Antony A, et al. Artificial intelligence-based genome editing in CRISPR/Cas9. Artificial Intelligence (AI) in Cell and Genetic Engineering. 2025;2952:273–282. https://doi.org/10.1007/978-1-0716-4690-8_16</mixed-citation>
     <mixed-citation xml:lang="en">Pandey S, Choudhari JK, Tripathi A, Singh A, Antony A, et al. Artificial intelligence-based genome editing in CRISPR/Cas9. Artificial Intelligence (AI) in Cell and Genetic Engineering. 2025;2952:273–282. https://doi.org/10.1007/978-1-0716-4690-8_16</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B3">
    <label>3.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Косовский Г. Ю., Скобель О. И., Глазко Т. Т. Потенциальные источники негативных эффектов генного редактирования у животных. Сельскохозяйственная биология. 2024. Т. 59. № 6. С. 1118–1130. https://doi.org/10.15389/agrobiology.2024.6.1118eng</mixed-citation>
     <mixed-citation xml:lang="en">Kosovsky GYu, Skobel OI, Glazko TT. Potential sources of negative effects of gene editing in animals. Agricultural Biology. 2024;59(6):1118–1130. (In Russ.) https://doi.org/10.15389/agrobiology.2024.6.1118eng</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B4">
    <label>4.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Глазко В. И., Косовский Г. Ю., Глазко Т. Т. Геномное редактирование животных сельскохозяйственных видов. Рязань: Book Jet; 2024. 164 c.</mixed-citation>
     <mixed-citation xml:lang="en">Glazko VI, Kosovskiy GYu, Glazko TT. Genomic editing of livestock animals. Ryazan: Book Jet; 2024. 164 p. (In Russ.)]</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B5">
    <label>5.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Kwon D-H, Gim G-M, Yum S-Y, Jang G. Current status and future of gene engineering in livestock. BMB Reports. 2024;57(1):50–59. https://doi.org/10.5483/BMBRep.2023-0208</mixed-citation>
     <mixed-citation xml:lang="en">Kwon D-H, Gim G-M, Yum S-Y, Jang G. Current status and future of gene engineering in livestock. BMB Reports. 2024;57(1):50–59. https://doi.org/10.5483/BMBRep.2023-0208</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B6">
    <label>6.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Tahsin A, Tasnim Z, Chowdhury M, Hassin K, Meraz GH, et al. CRISPR-Embedding: CRISPR/Cas9 off-target activity prediction using DNA k-mer embedding. Computational and Structural Biotechnology Reports. 2025;2:100043. https://doi.org/10.1016/j.csbr.2025.100043</mixed-citation>
     <mixed-citation xml:lang="en">Tahsin A, Tasnim Z, Chowdhury M, Hassin K, Meraz GH, et al. CRISPR-Embedding: CRISPR/Cas9 off-target activity prediction using DNA k-mer embedding. Computational and Structural Biotechnology Reports. 2025;2:100043. https://doi.org/10.1016/j.csbr.2025.100043</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B7">
    <label>7.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Groza T, Gomez FL, Mashhadi HH, Muñoz-Fuentes V, Gunes O, et al. The international mouse phenotyping consortium: Comprehensive knockout phenotyping underpinning the study of human disease. Nucleic Acids Research. 2023;51(D1):D1038–D1045. https://doi.org/10.1093/nar/gkac972</mixed-citation>
     <mixed-citation xml:lang="en">Groza T, Gomez FL, Mashhadi HH, Muñoz-Fuentes V, Gunes O, et al. The international mouse phenotyping consortium: Comprehensive knockout phenotyping underpinning the study of human disease. Nucleic Acids Research. 2023;51(D1):D1038–D1045. https://doi.org/10.1093/nar/gkac972</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B8">
    <label>8.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Buckley RM, Kortschak RD, Adelson DL. Divergent genome evolution caused by regional variation in DNA gain and loss between human and mouse. PLOS Computational Biology. 2018;14(4):e1006091. https://doi.org/10.1371/journal.pcbi.1006091</mixed-citation>
     <mixed-citation xml:lang="en">Buckley RM, Kortschak RD, Adelson DL. Divergent genome evolution caused by regional variation in DNA gain and loss between human and mouse. PLOS Computational Biology. 2018;14(4):e1006091. https://doi.org/10.1371/journal.pcbi.1006091</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B9">
    <label>9.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Ali A, Han K, Liang P. Role of transposable elements in gene regulation in the human genome. Life. 2021;11(2):118. https://doi.org/10.3390/life11020118</mixed-citation>
     <mixed-citation xml:lang="en">Ali A, Han K, Liang P. Role of transposable elements in gene regulation in the human genome. Life. 2021;11(2):118. https://doi.org/10.3390/life11020118</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B10">
    <label>10.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Modzelewski AJ, Gan Chong J, Wang T, He L. Mammalian genome innovation through transposon domestication. Nature Cell Biology. 2022;24(9):1332–1340. https://doi.org/10.1038/s41556-022-00970-4</mixed-citation>
     <mixed-citation xml:lang="en">Modzelewski AJ, Gan Chong J, Wang T, He L. Mammalian genome innovation through transposon domestication. Nature Cell Biology. 2022;24(9):1332–1340. https://doi.org/10.1038/s41556-022-00970-4</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B11">
    <label>11.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Zeng L, Pederson SM, Kortschak RD, Adelson DL. Transposable elements and gene expression during the evolution of amniotes. Mobile DNA. 2018;9:17. https://doi.org/10.1186/s13100-018-0124-5</mixed-citation>
     <mixed-citation xml:lang="en">Zeng L, Pederson SM, Kortschak RD, Adelson DL. Transposable elements and gene expression during the evolution of amniotes. Mobile DNA. 2018;9:17. https://doi.org/10.1186/s13100-018-0124-5</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B12">
    <label>12.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Gebrie A. Transposable elements as essential elements in the control of gene expression. Mobile DNA. 2023;14(1):9. https://doi.org/10.1186/s13100-023-00297-3</mixed-citation>
     <mixed-citation xml:lang="en">Gebrie A. Transposable elements as essential elements in the control of gene expression. Mobile DNA. 2023;14(1):9. https://doi.org/10.1186/s13100-023-00297-3</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B13">
    <label>13.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Monsen Ø, Grønvold L, Datsomor A, Harvey T, Kijas J, et al. The role of transposon activity in shaping cisregulatory element evolution after whole-genome duplication. Genome Research. 2025;35(3):475–488. https://doi.org/10.1101/gr.278931.124</mixed-citation>
     <mixed-citation xml:lang="en">Monsen Ø, Grønvold L, Datsomor A, Harvey T, Kijas J, et al. The role of transposon activity in shaping cisregulatory element evolution after whole-genome duplication. Genome Research. 2025;35(3):475–488. https://doi.org/10.1101/gr.278931.124</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B14">
    <label>14.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Silaeva YY, Safonova PD, Popov DV, Filatov MA, Okulova YuD, et al. Generation of LEPR knockout rabbits with CRISPR/CAS9 system. Doklady Biological Sciences. 2024;518:248–255. https://doi.org/10.1134/S0012496624600234</mixed-citation>
     <mixed-citation xml:lang="en">Silaeva YY, Safonova PD, Popov DV, Filatov MA, Okulova YuD, et al. Generation of LEPR knockout rabbits with CRISPR/CAS9 system. Doklady Biological Sciences. 2024;518:248–255. https://doi.org/10.1134/S0012496624600234</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B15">
    <label>15.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Andrade P, Alves JM, Pereira P, Rubin CJ, Silva E, et al. Selection against domestication alleles in introduced rabbit populations. Nature Ecology &amp; Evolution. 2024;8(8):1543–1555. https://doi.org/10.1038/s41559-024-02443-3</mixed-citation>
     <mixed-citation xml:lang="en">Andrade P, Alves JM, Pereira P, Rubin CJ, Silva E, et al. Selection against domestication alleles in introduced rabbit populations. Nature Ecology &amp; Evolution. 2024;8(8):1543–1555. https://doi.org/10.1038/s41559-024-02443-3</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B16">
    <label>16.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Farré M, Kim J, Proskuryakova AA, Zhang Y, Kulemzina AI, et al. Evolution of gene regulation in ruminants differs between evolutionary breakpoint regions and homologous synteny blocks. Genome Research. 2019;29(4):576–589. https://doi.org/10.1101/gr.239863.118</mixed-citation>
     <mixed-citation xml:lang="en">Farré M, Kim J, Proskuryakova AA, Zhang Y, Kulemzina AI, et al. Evolution of gene regulation in ruminants differs between evolutionary breakpoint regions and homologous synteny blocks. Genome Research. 2019;29(4):576–589. https://doi.org/10.1101/gr.239863.118</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B17">
    <label>17.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Damas J, Corbo M, Kim J, Turner-Maier J, Farré M, et al. Evolution of the ancestral mammalian karyotype and syntenic regions. Proceedings of the National Academy of Sciences. 2022;119(40):e2209139119. https://doi.org/10.1073/pnas.2209139119</mixed-citation>
     <mixed-citation xml:lang="en">Damas J, Corbo M, Kim J, Turner-Maier J, Farré M, et al. Evolution of the ancestral mammalian karyotype and syntenic regions. Proceedings of the National Academy of Sciences. 2022;119(40):e2209139119. https://doi.org/10.1073/pnas.2209139119</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B18">
    <label>18.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Li L, Zhang T, Farhab M, Xia XX, Reza AMMT, et al. Comprehensive analysis of circRNAs and lncRNAs involvement in the development of skeletal muscle in myostatin-deficient rabbits. Animal Biotechnology. 2025;36(1):2465624. https://doi.org/10.1080/10495398.2025.2465624</mixed-citation>
     <mixed-citation xml:lang="en">Li L, Zhang T, Farhab M, Xia XX, Reza AMMT, et al. Comprehensive analysis of circRNAs and lncRNAs involvement in the development of skeletal muscle in myostatin-deficient rabbits. Animal Biotechnology. 2025;36(1):2465624. https://doi.org/10.1080/10495398.2025.2465624</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B19">
    <label>19.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Lee J, Kim D-H, Lee K. Research note: Injection of adenoviral CRISPR/Cas9 system targeting melanophilin gene into different sites of embryos induced regional feather color changes in posthatch quail. Poultry Science. 2023;102(11):103087. https://doi.org/10.1016/j.psj.2023.103087</mixed-citation>
     <mixed-citation xml:lang="en">Lee J, Kim D-H, Lee K. Research note: Injection of adenoviral CRISPR/Cas9 system targeting melanophilin gene into different sites of embryos induced regional feather color changes in posthatch quail. Poultry Science. 2023;102(11):103087. https://doi.org/10.1016/j.psj.2023.103087</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B20">
    <label>20.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Chen CY, Seward CH, Song Y, Inamdar M, Leddy AM, et al. Galnt17 loss-of-function leads to developmental delay and abnormal coordination, activity, and social interactions with cerebellar vermis pathology. Developmental Biology. 2022;490:155–171. https://doi.org/10.1016/j.ydbio.2022.08.002</mixed-citation>
     <mixed-citation xml:lang="en">Chen CY, Seward CH, Song Y, Inamdar M, Leddy AM, et al. Galnt17 loss-of-function leads to developmental delay and abnormal coordination, activity, and social interactions with cerebellar vermis pathology. Developmental Biology. 2022;490:155–171. https://doi.org/10.1016/j.ydbio.2022.08.002</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B21">
    <label>21.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Hubley R, Finn RD, Clements J, Eddy SR, Jones TA, et al. The Dfam database of repetitive DNA families. Nucleic Acids Research. 2016;44(D1):D81–D89. https://doi.org/10.1093/nar/gkv1272</mixed-citation>
     <mixed-citation xml:lang="en">Hubley R, Finn RD, Clements J, Eddy SR, Jones TA, et al. The Dfam database of repetitive DNA families. Nucleic Acids Research. 2016;44(D1):D81–D89. https://doi.org/10.1093/nar/gkv1272</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B22">
    <label>22.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Sriwastva MK, Deng ZB, Wang B, Teng Y, Kumar A, et al. Exosome-like nanoparticles from Mulberry bark prevent DSS-induced colitis via the AhR/COPS8 pathway. EMBO Reports. 2022;23(3):e53365. https://doi.org/10.15252/embr.202153365</mixed-citation>
     <mixed-citation xml:lang="en">Sriwastva MK, Deng ZB, Wang B, Teng Y, Kumar A, et al. Exosome-like nanoparticles from Mulberry bark prevent DSS-induced colitis via the AhR/COPS8 pathway. EMBO Reports. 2022;23(3):e53365. https://doi.org/10.15252/embr.202153365</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B23">
    <label>23.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Liu Y, Shah SV, Xiang X, Wang J, Deng ZB, et al. COP9-associated CSN5 regulates exosomal protein deubiquitination and sorting. The American Journal of Pathology. 2009;174(4):1415–1425. https://doi.org/10.2353/ajpath.2009.080861</mixed-citation>
     <mixed-citation xml:lang="en">Liu Y, Shah SV, Xiang X, Wang J, Deng ZB, et al. COP9-associated CSN5 regulates exosomal protein deubiquitination and sorting. The American Journal of Pathology. 2009;174(4):1415–1425. https://doi.org/10.2353/ajpath.2009.080861</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B24">
    <label>24.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Wang H, Mizuno K, Takahashi N, Kobayashi E, Shirakawa J, et al. Melanophilin accelerates insulin granule fusion without predocking to the plasma membrane. Diabetes. 2020;69(12):2655–2666. https://doi.org/10.2337/db20-0069</mixed-citation>
     <mixed-citation xml:lang="en">Wang H, Mizuno K, Takahashi N, Kobayashi E, Shirakawa J, et al. Melanophilin accelerates insulin granule fusion without predocking to the plasma membrane. Diabetes. 2020;69(12):2655–2666. https://doi.org/10.2337/db20-0069</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B25">
    <label>25.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Chon NL, Tran S, Miller CS, Lin H, Knight JD. A conserved electrostatic membrane-binding surface in synaptotagminlike proteins revealed using molecular phylogenetic analysis and homology modeling. Protein Science. 2024;33(1):e4850. https://doi.org/10.1002/pro.4850</mixed-citation>
     <mixed-citation xml:lang="en">Chon NL, Tran S, Miller CS, Lin H, Knight JD. A conserved electrostatic membrane-binding surface in synaptotagminlike proteins revealed using molecular phylogenetic analysis and homology modeling. Protein Science. 2024;33(1):e4850. https://doi.org/10.1002/pro.4850</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B26">
    <label>26.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Babina M, Franke K, Bal G. How “neuronal” are human skin mast cells? International Journal of Molecular Sciences. 2022;23(18):10871. https://doi.org/10.3390/ijms231810871</mixed-citation>
     <mixed-citation xml:lang="en">Babina M, Franke K, Bal G. How “neuronal” are human skin mast cells? International Journal of Molecular Sciences. 2022;23(18):10871. https://doi.org/10.3390/ijms231810871</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B27">
    <label>27.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Bed’hom B, Vaez M, Coville JL, Gourichon D, Chastel O, et al. The lavender plumage colour in Japanese quail is associated with a complex mutation in the region of MLPH that is related to differences in growth, feed consumption and body temperature. BMC Genomics. 2012;13:442. https://doi.org/10.1186/1471-2164-13-442</mixed-citation>
     <mixed-citation xml:lang="en">Bed’hom B, Vaez M, Coville JL, Gourichon D, Chastel O, et al. The lavender plumage colour in Japanese quail is associated with a complex mutation in the region of MLPH that is related to differences in growth, feed consumption and body temperature. BMC Genomics. 2012;13:442. https://doi.org/10.1186/1471-2164-13-442</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B28">
    <label>28.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Ly T, Oh JY, Sivakumar N, Shehata S, La Santa Medina N, et al. Sequential appetite suppression by oral and visceral feedback to the brainstem. Nature. 2023;624:130–137. https://doi.org/10.1038/s41586-023-06758-2</mixed-citation>
     <mixed-citation xml:lang="en">Ly T, Oh JY, Sivakumar N, Shehata S, La Santa Medina N, et al. Sequential appetite suppression by oral and visceral feedback to the brainstem. Nature. 2023;624:130–137. https://doi.org/10.1038/s41586-023-06758-2</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B29">
    <label>29.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Beaumont KA, Hamilton NA, Moores MT, Brown DL, Ohbayashi N, et al. The recycling endosome protein Rab17 regulates melanocytic filopodia formation and melanosome trafficking. Traffic. 2011;12(5):627–643. https://doi.org/10.1111/j.1600-0854.2011.01172.x</mixed-citation>
     <mixed-citation xml:lang="en">Beaumont KA, Hamilton NA, Moores MT, Brown DL, Ohbayashi N, et al. The recycling endosome protein Rab17 regulates melanocytic filopodia formation and melanosome trafficking. Traffic. 2011;12(5):627–643. https://doi.org/10.1111/j.1600-0854.2011.01172.x</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B30">
    <label>30.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Li P, Zhang Q, Tang H. INPP1 up-regulation by miR-27a contributes to the growth, migration and invasion of human cervical cancer. Journal of Cellular and Molecular Medicine. 2019;23(11):7709–7716. https://doi.org/10.1111/jcmm.14644</mixed-citation>
     <mixed-citation xml:lang="en">Li P, Zhang Q, Tang H. INPP1 up-regulation by miR-27a contributes to the growth, migration and invasion of human cervical cancer. Journal of Cellular and Molecular Medicine. 2019;23(11):7709–7716. https://doi.org/10.1111/jcmm.14644</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B31">
    <label>31.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Molloy AM, Pangilinan F, Mills JL, Shane B, O’Neill MB, et al. A common polymorphism in HIBCH influences methylmalonic acid concentrations in blood independently of cobalamin. The American Journal of Human Genetics. 2016;98(5):869–882. https://doi.org/10.1016/j.ajhg.2016.03.005</mixed-citation>
     <mixed-citation xml:lang="en">Molloy AM, Pangilinan F, Mills JL, Shane B, O’Neill MB, et al. A common polymorphism in HIBCH influences methylmalonic acid concentrations in blood independently of cobalamin. The American Journal of Human Genetics. 2016;98(5):869–882. https://doi.org/10.1016/j.ajhg.2016.03.005</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B32">
    <label>32.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Dias AP, Rehmani T, Salih M, Tuana B. Tail-anchored membrane protein SLMAP3 is essential for targeting centrosomal proteins to the nuclear envelope in skeletal myogenesis. Open Biology. 2024;14(10):240094. https://doi.org/10.1098/rsob.240094</mixed-citation>
     <mixed-citation xml:lang="en">Dias AP, Rehmani T, Salih M, Tuana B. Tail-anchored membrane protein SLMAP3 is essential for targeting centrosomal proteins to the nuclear envelope in skeletal myogenesis. Open Biology. 2024;14(10):240094. https://doi.org/10.1098/rsob.240094</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B33">
    <label>33.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Grobet L, Martin LJR, Poncelet D, Pirottin D, Brouwers B, et al. A deletion in the bovine myostatin gene causes the double-muscled phenotype in cattle. Nature Genetics. 1997;17:71–74. https://doi.org/10.1038/ng0997-71</mixed-citation>
     <mixed-citation xml:lang="en">Grobet L, Martin LJR, Poncelet D, Pirottin D, Brouwers B, et al. A deletion in the bovine myostatin gene causes the double-muscled phenotype in cattle. Nature Genetics. 1997;17:71–74. https://doi.org/10.1038/ng0997-71</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B34">
    <label>34.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Kambadur R, Sharma M, Smith TP, Bass JJ. Mutations in myostatin (GDF8) in double-muscled Belgian Blue and Piedmontese cattle. Genome Research. 1997;7:910–915. https://doi.org/10.1101/gr.7.9.910</mixed-citation>
     <mixed-citation xml:lang="en">Kambadur R, Sharma M, Smith TP, Bass JJ. Mutations in myostatin (GDF8) in double-muscled Belgian Blue and Piedmontese cattle. Genome Research. 1997;7:910–915. https://doi.org/10.1101/gr.7.9.910</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B35">
    <label>35.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Mosher DS, Quignon P, Bustamante CD, Sutter NB, Mellersh CS, et al. A mutation in the myostatin gene increases muscle mass and enhances racing performance in heterozygote dogs. PLOS Genetics. 2007;3(5):e79. https://doi.org/10.1371/journal.pgen.0030079</mixed-citation>
     <mixed-citation xml:lang="en">Mosher DS, Quignon P, Bustamante CD, Sutter NB, Mellersh CS, et al. A mutation in the myostatin gene increases muscle mass and enhances racing performance in heterozygote dogs. PLOS Genetics. 2007;3(5):e79. https://doi.org/10.1371/journal.pgen.0030079</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B36">
    <label>36.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Boman IA, Våge DI. An insertion in the coding region of the myostatin (MSTN) gene affects carcass conformation and fatness in the Norwegian Spælsau (Ovis aries). BMC Research Notes. 2009;2:98. https://doi.org/10.1186/1756-0500-2-98</mixed-citation>
     <mixed-citation xml:lang="en">Boman IA, Våge DI. An insertion in the coding region of the myostatin (MSTN) gene affects carcass conformation and fatness in the Norwegian Spælsau (Ovis aries). BMC Research Notes. 2009;2:98. https://doi.org/10.1186/1756-0500-2-98</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B37">
    <label>37.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Sahu AR, Jeichitra V, Rajendran R, Raja A. Novel report on mutation in exon 3 of myostatin (MSTN) gene in Nilagiri sheep: An endangered breed of South India. Tropical Animal Health and Production. 2019;51:1817–1822. https://doi.org/10.1007/s11250-019-01873-7</mixed-citation>
     <mixed-citation xml:lang="en">Sahu AR, Jeichitra V, Rajendran R, Raja A. Novel report on mutation in exon 3 of myostatin (MSTN) gene in Nilagiri sheep: An endangered breed of South India. Tropical Animal Health and Production. 2019;51:1817–1822. https://doi.org/10.1007/s11250-019-01873-7</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B38">
    <label>38.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Stinckens A, Luyten T, Bijttebier J, Van den Maagdenberg K, Dieltiens D, et al. Characterization of the complete porcine MSTN gene and expression levels in pig breeds differing in muscularity. Animal Genetics. 2008;39(6):586–596. https://doi.org/10.1111/j.1365-2052.2008.01774.x</mixed-citation>
     <mixed-citation xml:lang="en">Stinckens A, Luyten T, Bijttebier J, Van den Maagdenberg K, Dieltiens D, et al. Characterization of the complete porcine MSTN gene and expression levels in pig breeds differing in muscularity. Animal Genetics. 2008;39(6):586–596. https://doi.org/10.1111/j.1365-2052.2008.01774.x</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B39">
    <label>39.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Schuelke M, Wagner KR, Stolz LE, Hübner C, Riebel T, et al. Myostatin mutation associated with gross muscle hypertrophy in a child. The New England Journal of Medicine. 2004;350(26):2682–2688. https://doi.org/10.1056/NEJMoa040933</mixed-citation>
     <mixed-citation xml:lang="en">Schuelke M, Wagner KR, Stolz LE, Hübner C, Riebel T, et al. Myostatin mutation associated with gross muscle hypertrophy in a child. The New England Journal of Medicine. 2004;350(26):2682–2688. https://doi.org/10.1056/NEJMoa040933</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B40">
    <label>40.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Saunders MA, Good JM, Lawrence EC, Ferrell RE, Li W-H, et al. Human adaptive evolution at myostatin (GDF8), a regulator of muscle growth. The American Journal of Human Genetics. 2006;79(6):1089–1097. https://doi.org/10.1086/509707</mixed-citation>
     <mixed-citation xml:lang="en">Saunders MA, Good JM, Lawrence EC, Ferrell RE, Li W-H, et al. Human adaptive evolution at myostatin (GDF8), a regulator of muscle growth. The American Journal of Human Genetics. 2006;79(6):1089–1097. https://doi.org/10.1086/509707</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B41">
    <label>41.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Marzec P, Richer M, Lahue RS. Therapeutic targeting of mismatch repair proteins in triplet repeat expansion diseases. DNA Repair. 2025;147:103817. https://doi.org/10.1016/j.dnarep.2025.103817</mixed-citation>
     <mixed-citation xml:lang="en">Marzec P, Richer M, Lahue RS. Therapeutic targeting of mismatch repair proteins in triplet repeat expansion diseases. DNA Repair. 2025;147:103817. https://doi.org/10.1016/j.dnarep.2025.103817</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B42">
    <label>42.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Edvardson S, Cinnamon Y, Ta-Shma A, Shaag A, Yim YI, et al. A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonism. PLOS One. 2012;7(5):e36458. https://doi.org/10.1371/journal.pone.0036458</mixed-citation>
     <mixed-citation xml:lang="en">Edvardson S, Cinnamon Y, Ta-Shma A, Shaag A, Yim YI, et al. A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonism. PLOS One. 2012;7(5):e36458. https://doi.org/10.1371/journal.pone.0036458</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B43">
    <label>43.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Han Y-C, Ma B, Guo S, Yang M, Li L-J, et al. Leptin regulates disc cartilage endplate degeneration and ossification through activation of the MAPK-ERK signalling pathway in vivo and in vitro. Journal of Cellular and Molecular Medicine. 2018;22(4):2098–2109. https://doi.org/10.1111/jcmm.13398</mixed-citation>
     <mixed-citation xml:lang="en">Han Y-C, Ma B, Guo S, Yang M, Li L-J, et al. Leptin regulates disc cartilage endplate degeneration and ossification through activation of the MAPK-ERK signalling pathway in vivo and in vitro. Journal of Cellular and Molecular Medicine. 2018;22(4):2098–2109. https://doi.org/10.1111/jcmm.13398</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B44">
    <label>44.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Xiao H, Li W, Qin Y, Lin Z, Qian C, et al. Crosstalk between lipid metabolism and bone homeostasis: Exploring intricate signaling relationships. Research. 2024;7:0447. https://doi.org/10.34133/research.0447</mixed-citation>
     <mixed-citation xml:lang="en">Xiao H, Li W, Qin Y, Lin Z, Qian C, et al. Crosstalk between lipid metabolism and bone homeostasis: Exploring intricate signaling relationships. Research. 2024;7:0447. https://doi.org/10.34133/research.0447</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B45">
    <label>45.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Londraville RL, Tuttle M, Liu Q, Andronowski JM. Endospanin is a candidate for regulating leptin sensitivity. Frontiers in Physiology. 2022;12:786299. https://doi.org/10.3389/fphys.2021.786299</mixed-citation>
     <mixed-citation xml:lang="en">Londraville RL, Tuttle M, Liu Q, Andronowski JM. Endospanin is a candidate for regulating leptin sensitivity. Frontiers in Physiology. 2022;12:786299. https://doi.org/10.3389/fphys.2021.786299</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B46">
    <label>46.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Su Y, Ding J, Yang F, He C, Xu Y, et al. The regulatory role of PDE4B in the progression of inflammatory function study. Frontiers in Pharmacology. 2022;13:982130. https://doi.org/10.3389/fphar.2022.982130</mixed-citation>
     <mixed-citation xml:lang="en">Su Y, Ding J, Yang F, He C, Xu Y, et al. The regulatory role of PDE4B in the progression of inflammatory function study. Frontiers in Pharmacology. 2022;13:982130. https://doi.org/10.3389/fphar.2022.982130</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B47">
    <label>47.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Decet M, Scott P, Kuenen S, Meftah D, Swerts J, et al. A candidate loss-of-function variant in SGIP1 causes synaptic dysfunction and recessive parkinsonism. Cell Reports Medicine. 2024;5(10):101749. https://doi.org/10.1016/j.xcrm.2024.101749</mixed-citation>
     <mixed-citation xml:lang="en">Decet M, Scott P, Kuenen S, Meftah D, Swerts J, et al. A candidate loss-of-function variant in SGIP1 causes synaptic dysfunction and recessive parkinsonism. Cell Reports Medicine. 2024;5(10):101749. https://doi.org/10.1016/j.xcrm.2024.101749</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B48">
    <label>48.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Fang Y, Barrows D, Dabas Y, Carroll TS, Singer S, et al. ATRX guards against aberrant differentiation in mesenchymal progenitor cells. Nucleic Acids Research. 2024;52(9):4950–4968. https://doi.org/10.1093/nar/gkae160</mixed-citation>
     <mixed-citation xml:lang="en">Fang Y, Barrows D, Dabas Y, Carroll TS, Singer S, et al. ATRX guards against aberrant differentiation in mesenchymal progenitor cells. Nucleic Acids Research. 2024;52(9):4950–4968. https://doi.org/10.1093/nar/gkae160</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B49">
    <label>49.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Rigueur D. A primer for fibroblast growth factor 16 (FGF16). Differentiation. 2024;140:100817. https://doi.org/10.1016/j.diff.2024.100817</mixed-citation>
     <mixed-citation xml:lang="en">Rigueur D. A primer for fibroblast growth factor 16 (FGF16). Differentiation. 2024;140:100817. https://doi.org/10.1016/j.diff.2024.100817</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B50">
    <label>50.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Del Pino Molina L, Monzón Manzano E, Gianelli C, Bravo Gallego LY, Bujalance Fernández J, et al. Effects of two different variants in the MAGT1 gene on B cell subsets, platelet function, and cell glycome composition. Frontiers in Immunology. 2025;16:1547808. https://doi.org/10.3389/fimmu.2025.1547808</mixed-citation>
     <mixed-citation xml:lang="en">Del Pino Molina L, Monzón Manzano E, Gianelli C, Bravo Gallego LY, Bujalance Fernández J, et al. Effects of two different variants in the MAGT1 gene on B cell subsets, platelet function, and cell glycome composition. Frontiers in Immunology. 2025;16:1547808. https://doi.org/10.3389/fimmu.2025.1547808</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B51">
    <label>51.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Liu X, Li W, Yang C, Luo J, Tang B. Cuproptosis-related genes signature could predict prognosis and the response of immunotherapy in cervical cancer. Translational Cancer Research. 2025;14(1):129–140. https://doi.org/10.21037/tcr-24-641</mixed-citation>
     <mixed-citation xml:lang="en">Liu X, Li W, Yang C, Luo J, Tang B. Cuproptosis-related genes signature could predict prognosis and the response of immunotherapy in cervical cancer. Translational Cancer Research. 2025;14(1):129–140. https://doi.org/10.21037/tcr-24-641</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B52">
    <label>52.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Bai T, Wang L, Qiao Z, Wang Z. Cuproptosis, a potential target for the therapy of diabetic critical limb ischemia. Free Radical Biology and Medicine. 2025;234:131–140. https://doi.org/10.1016/j.freeradbiomed.2025.04.022</mixed-citation>
     <mixed-citation xml:lang="en">Bai T, Wang L, Qiao Z, Wang Z. Cuproptosis, a potential target for the therapy of diabetic critical limb ischemia. Free Radical Biology and Medicine. 2025;234:131–140. https://doi.org/10.1016/j.freeradbiomed.2025.04.022</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B53">
    <label>53.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Lu B, Nie X-H, Yin R, Ding P, Su Z-Z, et al. PGAM4 silencing inhibited glycolysis and chemoresistance to temozolomide in glioma cells. Cell Biology International. 2023;47(4):776–786. https://doi.org/10.1002/cbin.11983</mixed-citation>
     <mixed-citation xml:lang="en">Lu B, Nie X-H, Yin R, Ding P, Su Z-Z, et al. PGAM4 silencing inhibited glycolysis and chemoresistance to temozolomide in glioma cells. Cell Biology International. 2023;47(4):776–786. https://doi.org/10.1002/cbin.11983</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B54">
    <label>54.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Hori K, Shimaoka K, Hoshino M. AUTS2 gene: Keys to understanding the pathogenesis of neurodevelopmental disorders. Cells. 2021;11(1):11. https://doi.org/10.3390/cells11010011</mixed-citation>
     <mixed-citation xml:lang="en">Hori K, Shimaoka K, Hoshino M. AUTS2 gene: Keys to understanding the pathogenesis of neurodevelopmental disorders. Cells. 2021;11(1):11. https://doi.org/10.3390/cells11010011</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B55">
    <label>55.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Weisner PA, Chen CY, Sun Y, Yoo J, Kao WC, et al. A mouse mutation that dysregulates neighboring Galnt17 and Auts2 genes is associated with phenotypes related to the human AUTS2 syndrome. G3 Genes. 2019;9(11):3891–3906. https://doi.org/10.1534/g3.119.400723</mixed-citation>
     <mixed-citation xml:lang="en">Weisner PA, Chen CY, Sun Y, Yoo J, Kao WC, et al. A mouse mutation that dysregulates neighboring Galnt17 and Auts2 genes is associated with phenotypes related to the human AUTS2 syndrome. G3 Genes. 2019;9(11):3891–3906. https://doi.org/10.1534/g3.119.400723</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B56">
    <label>56.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Raman J, Guan Y, Perrine CL, Gerken TA, Tabak LA. UDP-N-acetyl-α-D-galactosamine: polypeptide N-acetylgalactosaminyltransferases: Completion of the family tree. Glycobiology. 2012;22(6):768–777. https://doi.org/10.1093/glycob/cwr183</mixed-citation>
     <mixed-citation xml:lang="en">Raman J, Guan Y, Perrine CL, Gerken TA, Tabak LA. UDP-N-acetyl-α-D-galactosamine: polypeptide N-acetylgalactosaminyltransferases: Completion of the family tree. Glycobiology. 2012;22(6):768–777. https://doi.org/10.1093/glycob/cwr183</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B57">
    <label>57.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Narimatsu Y, Büll C, Chen Y-H, Wandall HH, Yang Z, et al. Genetic glycoengineering in mammalian cells. Journal of Biological Chemistry. 2021;296:100448. https://doi.org/10.1016/j.jbc.2021.100448</mixed-citation>
     <mixed-citation xml:lang="en">Narimatsu Y, Büll C, Chen Y-H, Wandall HH, Yang Z, et al. Genetic glycoengineering in mammalian cells. Journal of Biological Chemistry. 2021;296:100448. https://doi.org/10.1016/j.jbc.2021.100448</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B58">
    <label>58.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Engmann O, Labonté B, Mitchell A, Bashtrykov P, Calipari ES, et al. Cocaine-induced chromatin modifications associate with increased expression and three-dimensional looping of Auts2. Biological Psychiatry. 2017;82(11):794–805. https://doi.org/10.1016/j.biopsych.2017.04.013</mixed-citation>
     <mixed-citation xml:lang="en">Engmann O, Labonté B, Mitchell A, Bashtrykov P, Calipari ES, et al. Cocaine-induced chromatin modifications associate with increased expression and three-dimensional looping of Auts2. Biological Psychiatry. 2017;82(11):794–805. https://doi.org/10.1016/j.biopsych.2017.04.013</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B59">
    <label>59.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Courchesne E, Karns CM, Davis HR, Ziccardi R, Carper RA, et al. Unusual brain growth patterns in early life in patients with autistic disorder: An MRI study. Neurology. 2011;76(24):2111. https://doi.org/10.1212/01.wnl.0000399191.79091.28</mixed-citation>
     <mixed-citation xml:lang="en">Courchesne E, Karns CM, Davis HR, Ziccardi R, Carper RA, et al. Unusual brain growth patterns in early life in patients with autistic disorder: An MRI study. Neurology. 2011;76(24):2111. https://doi.org/10.1212/01.wnl.0000399191.79091.28</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B60">
    <label>60.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Kelly E, Meng F, Fujita H, Morgado F, Kazemi Y, et al. Regulation of autism-relevant behaviors by cerebellarprefrontal cortical circuits. Nature Neuroscience. 2020;23:1102–1110. https://doi.org/10.1038/s41593-020-0665-z</mixed-citation>
     <mixed-citation xml:lang="en">Kelly E, Meng F, Fujita H, Morgado F, Kazemi Y, et al. Regulation of autism-relevant behaviors by cerebellarprefrontal cortical circuits. Nature Neuroscience. 2020;23:1102–1110. https://doi.org/10.1038/s41593-020-0665-z</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B61">
    <label>61.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Gilbert J, Man H-Y. Fundamental elements in autism: From neurogenesis and neurite growth to synaptic plasticity. Frontiers in Cellular Neuroscience. 2017;11:359. https://doi.org/10.3389/fncel.2017.00359</mixed-citation>
     <mixed-citation xml:lang="en">Gilbert J, Man H-Y. Fundamental elements in autism: From neurogenesis and neurite growth to synaptic plasticity. Frontiers in Cellular Neuroscience. 2017;11:359. https://doi.org/10.3389/fncel.2017.00359</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B62">
    <label>62.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Warren WC, Hillier LW, Marshall Graves JA, Birney E, Ponting CP, et al. Genome analysis of the platypus reveals unique signatures of evolution. Nature. 2008;453:175–183. https://doi.org/10.1038/nature06936</mixed-citation>
     <mixed-citation xml:lang="en">Warren WC, Hillier LW, Marshall Graves JA, Birney E, Ponting CP, et al. Genome analysis of the platypus reveals unique signatures of evolution. Nature. 2008;453:175–183. https://doi.org/10.1038/nature06936</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B63">
    <label>63.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Adelson DL, Raison JM, Edgar RC. Characterization and distribution of retrotransposons and simple sequence repeats in the bovine genome. Proceedings of the National Academy of Sciences. 2009;106(31):12855–12860. https://doi.org/10.1073/pnas.0901282106</mixed-citation>
     <mixed-citation xml:lang="en">Adelson DL, Raison JM, Edgar RC. Characterization and distribution of retrotransposons and simple sequence repeats in the bovine genome. Proceedings of the National Academy of Sciences. 2009;106(31):12855–12860. https://doi.org/10.1073/pnas.0901282106</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B64">
    <label>64.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Glazko VI, Kosovsky GYu, Glazko TT. The sources of genome variability as domestication drivers (review). Agricultural Biology. 2022;57(5):832–851. https://doi.org/10.15389/agrobiology.2022.5.832eng</mixed-citation>
     <mixed-citation xml:lang="en">Glazko VI, Kosovsky GYu, Glazko TT. The sources of genome variability as domestication drivers (review). Agricultural Biology. 2022;57(5):832–851. https://doi.org/10.15389/agrobiology.2022.5.832eng</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B65">
    <label>65.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Zattera ML, Bruschi DP. Transposable elements as a source of novel repetitive DNA in the eukaryote genome. Cells. 2022;11(21):3373. https://doi.org/10.3390/cells11213373</mixed-citation>
     <mixed-citation xml:lang="en">Zattera ML, Bruschi DP. Transposable elements as a source of novel repetitive DNA in the eukaryote genome. Cells. 2022;11(21):3373. https://doi.org/10.3390/cells11213373</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B66">
    <label>66.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Zhao P, Peng C, Fang L, Wang Z, Liu GE. Taming transposable elements in livestock and poultry: A review of their roles and applications. Genetics Selection Evolution. 2023;55(1):50. https://doi.org/10.1186/s12711-023-00821-2</mixed-citation>
     <mixed-citation xml:lang="en">Zhao P, Peng C, Fang L, Wang Z, Liu GE. Taming transposable elements in livestock and poultry: A review of their roles and applications. Genetics Selection Evolution. 2023;55(1):50. https://doi.org/10.1186/s12711-023-00821-2</mixed-citation>
    </citation-alternatives>
   </ref>
   <ref id="B67">
    <label>67.</label>
    <citation-alternatives>
     <mixed-citation xml:lang="ru">Mikina W, Hałakuc P, Milanowski R. Transposon-derived introns as an element shaping the structure of eukaryotic genomes. Mobile DNA. 2024;15(1):15. https://doi.org/10.1186/s13100-024-00325-w</mixed-citation>
     <mixed-citation xml:lang="en">Mikina W, Hałakuc P, Milanowski R. Transposon-derived introns as an element shaping the structure of eukaryotic genomes. Mobile DNA. 2024;15(1):15. https://doi.org/10.1186/s13100-024-00325-w</mixed-citation>
    </citation-alternatives>
   </ref>
  </ref-list>
 </back>
</article>
