首页> 美国卫生研究院文献>Genetics >Evidence That Intergenic Spacer Repeats of Drosophila Melanogaster Rrna Genes Function as X-Y Pairing Sites in Male Meiosis and a General Model for Achiasmatic Pairing
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Evidence That Intergenic Spacer Repeats of Drosophila Melanogaster Rrna Genes Function as X-Y Pairing Sites in Male Meiosis and a General Model for Achiasmatic Pairing

机译:的果蝇黑变种Rrna基因的基因间隔物重复作为男性减数分裂中X-Y配对位点的证据以及一个全向性配对模型。

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摘要

In Drosophila melanogaster males, X-Y meiotic chromosome pairing is mediated by the nucleolus organizers (NOs) which are located in the X heterochromatin (Xh) and near the Y centromere. Deficiencies for Xh disrupt X-Y meiotic pairing and cause high frequencies of X-Y nondisjunction. Insertion of cloned rRNA genes on an Xh(-) chromosome partially restores normal X-Y pairing and disjunction. To map the sequences within an inserted, X-linked rRNA gene responsible for stimulating X-Y pairing, partial deletions were generated by P element-mediated destabilization of the insert. Complete deletions of the rRNA transcription unit did not interfere with the ability to stimulate X-Y pairing as long as most of the intergenic spacer (IGS) remained. Within groups of deletions that lacked the entire transcription unit and differed only in length of residual IGS material, pairing ability was proportional to the dose of 240-bp intergenic spacer repeats. Deletions of the complete rRNA transcription unit or of the 28S sequences alone blocked nucleolus formation, as determined by binding of an antinucleolar antibody, yet did not interfere with pairing ability, suggesting that X-Y pairing may not be mechanistically related to nucleolus formation. A model for achiasmatic pairing in Drosophila males based upon the combined action of topoisomerase I and a strand transferase is proposed.
机译:在果蝇黑腹果蝇雄性中,X-Y减数分裂染色体配对由位于X异染色质(Xh)和Y着丝粒附近的核仁组织者(NOs)介导。 Xh的缺乏会破坏X-Y减数分裂配对,并导致X-Y不分离的高频率。 Xh(-)染色体上的克隆的rRNA基因插入部分恢复正常的X-Y配对和分离。为了在负责刺激X-Y配对的插入的,X连接的rRNA基因中定位序列,通过P元件介导的插入物的不稳定产生了部分缺失。只要保留大多数基因间间隔子(IGS),rRNA转录单位的完全缺失就不会干扰刺激X-Y配对的能力。在缺少整个转录单位的缺失组中,仅残留IGS物质的长度不同,配对能力与240 bp基因间隔子重复序列的剂量成正比。完整的rRNA转录单位或28S序列的缺失仅阻断了核仁的形成,这是通过抗核仁抗体的结合确定的,但并未干扰配对能力,这表明X-Y配对可能与核仁的形成在机理上不相关。提出了一种基于拓扑异构酶I和链转移酶的联合作用的果蝇雄性无性配对的模型。

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