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银叶猴中由 Y 染色体/常染色体易位引发的独立“染色体谱系”的快速出现。

Rapid emergence of independent "chromosomal lineages" in silvered-leaf monkey triggered by Y/autosome translocation.

机构信息

Department of Biology, University of Bari, Bari, Italy.

Department of Biology, University of Florence, 50122, Florence, Italy.

出版信息

Sci Rep. 2018 Feb 19;8(1):3250. doi: 10.1038/s41598-018-21509-4.

Abstract

Sex/autosome translocations are rare events. The only known example in catarrhines is in the silvered-leaf monkey. Here the Y chromosome was reciprocally translocated with chromosome 1. The rearrangement produced an XXYY sex chromosome system. At least three chromosomal variants of the intact chromosome 1 are known to exist. We characterized in high resolution the translocation products (Y and Y) and the polymorphic forms of the intact chromosome 1 with a panel of more than 150 human BAC clones. We showed that the translocation products were extremely rearranged, in contrast to the high level of marker order conservation of the other silvered-leaf monkey chromosomes. Surprisingly, each translocation product appeared to form independent "chromosome lineages"; each having a myriad of distinct rearrangements. We reconstructed the evolutionary history of the translocation products by comparing the homologous chromosomes of two other colobine species: the African mantled guereza and the Indian langur. The results showed a massive reuse of breakpoints: only 12, out of the 40 breaks occurred in domains never reused in other rearrangements, while, strikingly, some domains were used up to four times. Such frequent breakpoint reuse if proved to be a general phenomenon has profound implications for mechanisms of chromosome evolution.

摘要

性染色体/常染色体易位是罕见的事件。在灵长类动物中,唯一已知的例子是银叶猴。在这里,Y 染色体与 1 号染色体发生了相互易位。这种重排产生了一个 XXYY 性染色体系统。至少有三种完整的 1 号染色体的染色体变体已知存在。我们使用超过 150 个人类 BAC 克隆的小组,以高分辨率对易位产物(Y 和 Y)和完整的 1 号染色体的多态形式进行了表征。我们表明,易位产物发生了极其严重的重排,与其他银叶猴染色体的标记顺序高度保守形成鲜明对比。令人惊讶的是,每个易位产物似乎都形成了独立的“染色体谱系”;每个都有无数独特的重排。我们通过比较另外两种疣猴物种(非洲长尾猴和印度叶猴)的同源染色体,重建了易位产物的进化历史。结果表明,大量重复使用了断点:在其他重排中从未重复使用的区域中,只有 40 个断点中的 12 个发生了断点,而引人注目的是,一些区域被重复使用了多达四次。如果这种频繁的断点重复使用被证明是一种普遍现象,那么它将对染色体进化的机制产生深远的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63b2/5818525/5aa94f0a60eb/41598_2018_21509_Fig1_HTML.jpg

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