<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Genes &amp; Cells</journal-id><journal-title-group><journal-title xml:lang="en">Genes &amp; Cells</journal-title><trans-title-group xml:lang="ru"><trans-title>Гены и Клетки</trans-title></trans-title-group><trans-title-group xml:lang="zh"><trans-title>Genes and Cells</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2313-1829</issn><issn publication-format="electronic">2500-2562</issn><publisher><publisher-name xml:lang="en">Human Stem Cells Institute</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">120589</article-id><article-id pub-id-type="doi">10.23868/gc120589</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Long noncoding RNA expression pattern in the X inactivation center of rodents</article-title><trans-title-group xml:lang="ru"><trans-title>ПРОФИЛИ ЭКСПРЕССИИ НЕТРАНСЛИРУЕМЫХ РНК В ЦЕНТРЕ ИНАКТИВАЦИИ У МЫШЕВИДНЫХ ГРЫЗУНОВ</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Elisaphenko</surname><given-names>E. A</given-names></name><name xml:lang="ru"><surname>Елисафенко</surname><given-names>Е. А</given-names></name></name-alternatives><email>antares@bionet.nsc.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Shevchenko</surname><given-names>A. I</given-names></name><name xml:lang="ru"><surname>Шевченко</surname><given-names>А. И</given-names></name></name-alternatives><email>antares@bionet.nsc.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Zakian</surname><given-names>S. M</given-names></name><name xml:lang="ru"><surname>Закиян</surname><given-names>С. М</given-names></name></name-alternatives><email>antares@bionet.nsc.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff3"/><xref ref-type="aff" rid="aff4"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Federal Research Center Institute of Cytology and Genetics, the Siberian Branch of the Russian Academy of Sciences</institution></aff><aff><institution xml:lang="ru">ФГБНУ «Федеральный исследовательский центр Институт цитологии и генетики СО РАН»</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Institute of Chemical Biology and Fundamental Medicine, the Siberian Branch of the Russian Academy of Sciences</institution></aff><aff><institution xml:lang="ru">ФГБНУ «Институтхимической биологии и фундаментальной медицины СО РАН»</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">State Research Institute of Circulation Pathology, Ministry of Healthcare of the Russian Federation</institution></aff><aff><institution xml:lang="ru">ФГБУ «Новосибирский научно-исследовательский институт патологии кровообращения имени академика Е.Н. Мешалкина» Министерства здравоохранения РФ</institution></aff></aff-alternatives><aff-alternatives id="aff4"><aff><institution xml:lang="en">National Research University Novosibirsk State University</institution></aff><aff><institution xml:lang="ru">Новосибирский национальный исследовательский государственный университет</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2016-06-15" publication-format="electronic"><day>15</day><month>06</month><year>2016</year></pub-date><volume>11</volume><issue>2</issue><issue-title xml:lang="en">VOL 11, NO2 (2016)</issue-title><issue-title xml:lang="ru">ТОМ 11, №2 (2016)</issue-title><fpage>82</fpage><lpage>86</lpage><history><date date-type="received" iso-8601-date="2023-01-05"><day>05</day><month>01</month><year>2023</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2016, Eco-Vector</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2016, Эко-Вектор</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="en">Eco-Vector</copyright-holder><copyright-holder xml:lang="ru">Эко-Вектор</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://genescells.ru/2313-1829/article/view/120589">https://genescells.ru/2313-1829/article/view/120589</self-uri><abstract xml:lang="en"><p>Transcriptome analysis of several cell lines with different differentiation degree has been carried out in three rodent species - voles, rats, and mice. As a result, expression profiles of X-inactivation center genes have been generated. In mice, new data on how expression of key genes of X-inactivation center, Xist and Tsix, changes during ontogenesis have been obtained. New types of transcripts have been revealed. In voles, Xist expression was observed in all 8 cell lines examined. Interestingly, main vole Xist transcript had 7 exons as those of rats and mice. In addition, Xist antisense transcript, Tsix, was expressed in 4 vole cell lines and was presented by both spliced and unspliced variants. Expression between the Enox (Jpx) and Xist genes has been revealed in three vole cell lines. Additional variants of Tsix transcripts were observed when studied expression profiles of several rat cell lines. The variants were not present in mice and voles. Compared to mice and voles, Tsix expression level in rats was several times higher than that of Xist.</p></abstract><trans-abstract xml:lang="ru"><p>Для трех видов грызунов полевок, крысы и мыши проведен анализ транскриптомов нескольких клеточных линий, различающихся степенью дифференцировки, по результатам которого построены профили экспрессии генов в центре инактивации Х-хромосомы. Для мыши получены новые данные о том, как изменяется экспрессия ключевых генов центра инактивации Xist и Tsix в онтогенезе. Выявлены новые формы транскриптов. У полевок во всех 8 исследованных линиях клеток наблюдается экспрессия гена Xist. Интересно отметить, что преобладающий транскрипт гена Xist полевок, также как Xist крысы и мыши, имеет 7 экзонов. Кроме того, в четырех линиях клеток полевок, экспрессируется антисмысловой транскрипт - Tsix, который представлен как сплайсированными, так и несплайсированными вариантами. В трех линиях клеток у полевок выявляется экспрессия между генами Enox (Jpx) и Xist. При исследовании профиля экспрессии нескольких клеточных линий крысы были выявлены дополнительные варианты транскриптов гена Tsix, которых нет у мыши и полевки. Уровень экспрессии гена Tsix у крысы, в отличие от мыши и полевки, в разы превышает экспрессию Xist.</p></trans-abstract><kwd-group xml:lang="en"><kwd>X-inactivation center</kwd><kwd>long non-coging RNA</kwd><kwd>rodents</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>центр инативации Х-хромосомы</kwd><kwd>длинные нетранслируемы РНК</kwd><kwd>грызуны</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Brockdorff N., Ashworth A., Kay G.F. et al. Conservation of position and exclusive expression of mouse Xist from the inactive X chromosome. Nature 1991; 351(6324): 329-31.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Lee J.T., Davidow L.S., Warshawsky D. Tsix, a gene antisense to Xist at the X-inactivation centre. Nat. Genet. 1999; 21: 400-4.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Chureau C., Prissette M., Bourdet A. et al. Comparative sequence analysis of the X-inactivation center region in mouse, human, and bovine. Genome Res. 2002; 12t6): 894-908.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Penny G.D., Kay G.F., Sheardown S. et al. Requirement for Xist in X chromosome inactivation. Nature 1996; 379(6561): 131-7.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Tian D., Sun S., Lee J.T. The long noncoding RNA, jpx, is a molecular switch for x chromosome inactivation. Cell 2010; 143(3): 390-403.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Lee J.T., Lu N. Targeted mutagenesis of Tsix leads to nonrandom X inactivation. Cell. 1999; 99: 47-57.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Shevchenko A.I., Malakhova A., Elisaphenko E. et al. Variability of sequence surrounding the Xist gene in rodents suggests taxon-specific regulation of X chromosome inactivation. PLoS One 2011; 6(8): e22771.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Migeon B.R., Chowdhury A.K., Dunston J., McIntosh I. Identification of TSIX, encoding an RNA antisense to human XIST, reveals differences from its murine counterpart: implications for X inactivation. Am. J. Hum. Genet. 2001; 69(5): 951-60.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Sado T., Wang Z., Sasaki H., Li E. Regulation of imprinted X-chromosome inactivation in mice by Tsix. Dev. 2001; 128: 1275-86.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Cohen H.R., Panning B. XIST RNA exhibits nuclear retention and exhibits reduced association with the export factor TAP/NXF1. Chromosoma 2007; 116(4): 373-83.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Ogawa Y., Lee J.T. Xite, X-inactivation intergenic transcription elements that regulate the probability of choice. Mol. Cell. 2003; 11(3): 731-43.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Ohhata T., Hoki Y., Sasaki H., Sado T. Crucial role of antisense transcription across the Xist promoter in Tsix-mediated Xist chromatin modification. Dev. 2008; 135(2): 227-35.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Lee J.T., Lu N., Han Y. Genetic analysis of the mouse X inactivation center defines an 80-kb multifunction domain. PNAS USA 1999; 96(7): 3836-41.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Migeon B.R., Winter H., Kazi E. et al. Low-copy-number human transgene is recognized as an X inactivation center in mouse ES cells, but fails to induce cis-inactivation in chimeric mice. Genomics 2001; 71(2): 156-62.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Lee J.T. Homozygous Tsix mutant mice reveal a sex-ratio distortion and revert to random X-inactivation. Nat. Genet. 2002; 32(1): 195-200.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Migeon B.R., Lee C.H., Chowdhury A.K., Carpenter H. Species differences in TSIX/Tsix reveal the roles of these genes in X-chromosome inactivation. Am. J. Hum. Genet. 2002; 71(2): 286-93.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Brown C.J., Chow J.C. Beyond sense: The role of antisense RNA in controlling Xist expression. Semin. Cell Dev. Biol. 2003; 14(6): 341-7.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Vaskova E.A., Medvedev S.P., Sorokina A.E. et al. Transcriptome Characteristics and X-Chromosome Inactivation Status in Cultured Rat Pluripotent Stem Cells. Stem Cells Dev. 2015; 24(24): 2912-24.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Langmead B., Salzberg S.L. Fast gapped-read alignment with Bowtie 2. Nat. Methods 2012, 9(4): 357-59.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Kearse M., Moir R., Wilson A. et al. Geneious. Bioinformatics. 2012; 28(12): 1647-9.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Elisaphenko E.A., Kolesnikov N.N., Shevchenko A.I. et al. A dual origin of the Xist gene from a protein-coding gene and a set of transposable elements. PLoS One. 2008; 3(6): e2521.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Nesterova T.B., Slobodyanyuk S.Y., Elisaphenko E.A. et al. Characterization of the genomic Xist locus in rodents reveals conservation of overall gene structure and tandem repeats but rapid evolution of unique sequence. Genome Res. 2001, 11: 833-49.</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Lee J.T. Disruption of imprinted X inactivation by parent-of-origin effects at Tsix. Cell 2000, 103(1): 17-27.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Marahrens Y., Panning B., Dausman J. et al. Xist-deficient mice are defective in dosage compensation but not spermatogenesis. Genes Dev. 1997, 11(2): 156-66.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Sarkar M.K., Gayen S., Kumar S. et al. An Xist-activating antisense RNA required for X-chromosome inactivation. Nat. Commun. 2015, 6: 8564.</mixed-citation></ref></ref-list></back></article>
