<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<article article-type="research-article" dtd-version="1.3" 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" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">ssmu</journal-id><journal-title-group><journal-title xml:lang="ru">Бюллетень сибирской медицины</journal-title><trans-title-group xml:lang="en"><trans-title>Bulletin of Siberian Medicine</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1682-0363</issn><issn pub-type="epub">1819-3684</issn><publisher><publisher-name>Siberian State Medical University, the Ministry of Healthcare of the Russian Federation</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.20538/1682-0363-2012-3-18-21</article-id><article-id custom-type="elpub" pub-id-type="custom">ssmu-472</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ЭКСПЕРИМЕНТАЛЬНЫЕ И КЛИНИЧЕСКИЕ ИССЛЕДОВАНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>EXPERIMENTAL AND CLINICAL INVESTIGATIONS</subject></subj-group></article-categories><title-group><article-title>Полиморфный локус rs3088232 гена BRDT ассоциирован с риском идиопатического мужского бесплодия в выборке жителей Западно-Сибирского региона России</article-title><trans-title-group xml:lang="en"><trans-title>Polymorphism rs3088232 in the BRDT gene is associated with idiopathic male infertility in the West Siberian Region of Russia</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Вайнер</surname><given-names>А. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Wainer</surname><given-names>A. S.</given-names></name></name-alternatives><email xlink:type="simple">max@niboch.nsc.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Нагайцев</surname><given-names>В. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Nagaitsev</surname><given-names>V. M.</given-names></name></name-alternatives><email xlink:type="simple">max@niboch.nsc.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Королькова</surname><given-names>О. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Korolkova</surname><given-names>O. V.</given-names></name></name-alternatives><email xlink:type="simple">max@niboch.nsc.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Востриков</surname><given-names>В. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Vostrikov</surname><given-names>V. V.</given-names></name></name-alternatives><email xlink:type="simple">max@niboch.nsc.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Осадчук</surname><given-names>Л. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Osadchuk</surname><given-names>L. V.</given-names></name></name-alternatives><email xlink:type="simple">max@niboch.nsc.ru</email><xref ref-type="aff" rid="aff-4"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Печковский</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Pechkovsky</surname><given-names>Ye. V.</given-names></name></name-alternatives><email xlink:type="simple">max@niboch.nsc.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Малиновская</surname><given-names>И. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Malinovskaya</surname><given-names>I. S.</given-names></name></name-alternatives><email xlink:type="simple">max@niboch.nsc.ru</email><xref ref-type="aff" rid="aff-5"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Филипенко</surname><given-names>М. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Filipenko</surname><given-names>M. L.</given-names></name></name-alternatives><email xlink:type="simple">max@niboch.nsc.ru</email><xref ref-type="aff" rid="aff-3"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>Институт химической биологии и фундаментальной медицины СО РАН, Новосибирский государственный университет, г. Новосибирск</institution><country>Russian Federation</country></aff><aff xml:lang="ru" id="aff-2"><institution>Алтайский государственный медицинский университет, г. Барнаул</institution><country>Russian Federation</country></aff><aff xml:lang="ru" id="aff-3"><institution>Институт химической биологии и фундаментальной медицины СО РАН, г. Новосибирск</institution><country>Russian Federation</country></aff><aff xml:lang="ru" id="aff-4"><institution>Институт цитологии и генетики СО РАН, г. Новосибирск</institution><country>Russian Federation</country></aff><aff xml:lang="ru" id="aff-5"><institution>Сибирский государственный медицинский университет, г. Томск</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2012</year></pub-date><pub-date pub-type="epub"><day>28</day><month>06</month><year>2012</year></pub-date><volume>11</volume><issue>3</issue><fpage>18</fpage><lpage>21</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Вайнер А.С., Нагайцев В.М., Королькова О.В., Востриков В.В., Осадчук Л.В., Печковский Е.В., Малиновская И.С., Филипенко М.Л., 2012</copyright-statement><copyright-year>2012</copyright-year><copyright-holder xml:lang="ru">Вайнер А.С., Нагайцев В.М., Королькова О.В., Востриков В.В., Осадчук Л.В., Печковский Е.В., Малиновская И.С., Филипенко М.Л.</copyright-holder><copyright-holder xml:lang="en">Wainer A.S., Nagaitsev V.M., Korolkova O.V., Vostrikov V.V., Osadchuk L.V., Pechkovsky Y.V., Malinovskaya I.S., Filipenko M.L.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://bulletin.ssmu.ru/jour/article/view/472">https://bulletin.ssmu.ru/jour/article/view/472</self-uri><abstract><p>Носительство аллельных вариантов генов, приводящих к нарушениям сперматогенеза, может быть причиной идиопатического мужского бесплодия. В настоящем исследовании был проведен анализ ассоциации локуса rs3088232 гена BRDT с риском данной патологии на выборке из 105 бесплодных пациентов и 230 здоровых мужчин. В результате работы была выявлена ассоциация аллеля G (OR = 1,80; CI 1,16—2,80; p = 0,008) и генотипа GG (OR = 6,47; CI 1,23—34,15; p = 0,01) с идиопатическим мужским бесплодием.</p></abstract><trans-abstract xml:lang="en"><p>Allelic variants of genes involved in spermatogenesis can contribute to the genetic predisposition to idiopathic male infertility. In the present study we investigated the association of polymorphism rs3088232 in the BRDT gene with the risk of this pathology on the sample of 105 infertile patients and 230 healthy controls. We revealed the association of allele G (OR = 1.80; CI 1.16—2.80; p = 0.008) and genotype GG (OR = 6.47; CI 1.23—34.15; p = 0.01) with idiopathic male infertility.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>идиопатическое мужское бесплодие</kwd><kwd>ген BRDT</kwd><kwd>аллельные варианты генов</kwd></kwd-group><kwd-group xml:lang="en"><kwd>idiopathic male infertility</kwd><kwd>BRDT gene</kwd><kwd>allelic variants</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Интеграционный грант СО РАН № 84 и 17,  Федеральная целевая программа «Научные и научно-педагогические кадры инновационной России» на 2009—2013 гг., ГК № 16.740.11.0633 от 02.06.2011 г.</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Aston K.I., Carrell D.T. Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and</mixed-citation><mixed-citation xml:lang="en">Aston K.I., Carrell D.T. Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">severe oligozoospermia // J. Androl. 2009. V. 30, № 6. P. 711—725.</mixed-citation><mixed-citation xml:lang="en">severe oligozoospermia // J. Androl. 2009. V. 30, № 6. P. 711—725.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Aston K.I., Krausz C., Laface I. et al. Evaluation of 172 can-didate polymorphisms for association with oligozoospermia or azoospermia in a large cohort of men of European descent // Hum Reprod. 2010. V. 25. № 6. P. 1383—1397.</mixed-citation><mixed-citation xml:lang="en">Aston K.I., Krausz C., Laface I. et al. Evaluation of 172 can-didate polymorphisms for association with oligozoospermia or azoospermia in a large cohort of men of European descent // Hum Reprod. 2010. V. 25. № 6. P. 1383—1397.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Berkovits B.D., Wolgemuth D.J. The first bromodomain of the testis-specific double bromodomain protein Brdt is required for chromocenter organization that is modulated by genetic background // Dev. Biol. 2011. [published ahead of print].</mixed-citation><mixed-citation xml:lang="en">Berkovits B.D., Wolgemuth D.J. The first bromodomain of the testis-specific double bromodomain protein Brdt is required for chromocenter organization that is modulated by genetic background // Dev. Biol. 2011. [published ahead of print].</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Ferlin A., Arredi B., Foresta C. Genetic causes of male in-fertility // Reprod Toxicol. 2006. V. 22, № 2. P. 133—141.</mixed-citation><mixed-citation xml:lang="en">Ferlin A., Arredi B., Foresta C. Genetic causes of male in-fertility // Reprod Toxicol. 2006. V. 22, № 2. P. 133—141.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Moriniere J., Rousseaux S., Steuerwald U. et al. Coopera-tive binding of two acetylation marks on a histone tail by a single bromodomain // Nature. 2009. V. 461, № 7264. P. 664—668.</mixed-citation><mixed-citation xml:lang="en">Moriniere J., Rousseaux S., Steuerwald U. et al. Coopera-tive binding of two acetylation marks on a histone tail by a single bromodomain // Nature. 2009. V. 461, № 7264. P. 664—668.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Plaseski T., Noveski P., Popeska Z. et al. Association Study of Single Nucleotide Polymorphisms in FASLG, JMJDIA, LOC203413, TEX15, BRDT, OR2W3, INSR and TAS2R38 Genes with Male Infertility // J. Androl. 2011. [published ahead of print].</mixed-citation><mixed-citation xml:lang="en">Plaseski T., Noveski P., Popeska Z. et al. Association Study of Single Nucleotide Polymorphisms in FASLG, JMJDIA, LOC203413, TEX15, BRDT, OR2W3, INSR and TAS2R38 Genes with Male Infertility // J. Androl. 2011. [published ahead of print].</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Pivot-Pajot C., Caron C., Govin J. et al. Acetylation-dependent chromatin reorganization by BRDT, a testis-specific bromodomain-containing protein // Mol. Cell. Biol. 2003. V. 23, № 15. P. 5354—5365.</mixed-citation><mixed-citation xml:lang="en">Pivot-Pajot C., Caron C., Govin J. et al. Acetylation-dependent chromatin reorganization by BRDT, a testis-specific bromodomain-containing protein // Mol. Cell. Biol. 2003. V. 23, № 15. P. 5354—5365.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Shang E., Nickerson H.D., Wen D. et al. The first bromo-domain of Brdt, a testis-specific member of the BET sub-family of double-bromodomain-containing proteins, is essential for male germ cell differentiation // Development. 2007. V. 134, № 19. P. 3507—3515.</mixed-citation><mixed-citation xml:lang="en">Shang E., Nickerson H.D., Wen D. et al. The first bromo-domain of Brdt, a testis-specific member of the BET sub-family of double-bromodomain-containing proteins, is essential for male germ cell differentiation // Development. 2007. V. 134, № 19. P. 3507—3515.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
