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在灵长类动物进化过程中,端粒重复序列在染色体内部断裂位点的插入。

Insertion of telomeric repeats at intrachromosomal break sites during primate evolution.

作者信息

Nergadze Solomon G, Rocchi Mariano, Azzalin Claus M, Mondello Chiara, Giulotto Elena

机构信息

Dipartimento di Genetica e Microbiologia, Università degli Studi di Pavia, 27100 Pavia, Italy.

出版信息

Genome Res. 2004 Sep;14(9):1704-10. doi: 10.1101/gr.2778904. Epub 2004 Aug 12.

DOI:10.1101/gr.2778904
PMID:15310657
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC515315/
Abstract

Short blocks of telomeric-like DNA (Interstitial Telomeric Sequences, ITSs) are found far from chromosome ends. We addressed the question as to how such sequences arise by comparing the loci of 10 human ITSs with their genomic orthologs in 12 primate species. The ITSs did not derive from expansion of pre-existing TTAGGG units, as described for other microsatellites, but appeared suddenly during evolution. Nine insertion events were dated along the primate evolutionary tree, the dates ranging between 40 and 6 million years ago. Sequence comparisons suggest that in each case the block of (TTAGGG)n DNA arose as a result of double-strand break repair. In fact, ancestral sequences were either interrupted precisely by the tract of telomeric-like repeats or showed the typical modifications observed at double-strand break repair sites such as short deletions, addition of random sequences, or duplications. Similar conclusions were drawn from the analysis of a chimpanzee-specific ITS. We propose that telomeric sequences were inserted by the capture of a telomeric DNA fragment at the break site or by the telomerase enzyme. Our conclusions indicate that human ITSs are relics of ancient breakage rather than fragile sites themselves, as previously suggested.

摘要

短片段的端粒样DNA(间质端粒序列,ITSs)在远离染色体末端的位置被发现。我们通过比较10个人类ITSs与其在12种灵长类动物中的基因组直系同源序列,探讨了这些序列是如何产生的问题。ITSs并非如其他微卫星那样源自预先存在的TTAGGG单元的扩增,而是在进化过程中突然出现。沿着灵长类进化树确定了9次插入事件的时间,时间范围在4000万至600万年前之间。序列比较表明,在每种情况下,(TTAGGG)n DNA片段都是双链断裂修复的结果。事实上,祖先序列要么被端粒样重复序列精确打断,要么显示出在双链断裂修复位点观察到的典型修饰,如短缺失、随机序列添加或重复。对一个黑猩猩特异性ITS的分析也得出了类似的结论。我们提出,端粒序列是通过在断裂位点捕获端粒DNA片段或通过端粒酶插入的。我们的结论表明,人类ITSs是古代断裂的遗迹,而不是如先前所认为的那样本身就是脆弱位点。

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本文引用的文献

1
Evolutionary breakpoints are co-localized with fragile sites and intrachromosomal telomeric sequences in primates.在灵长类动物中,进化断点与脆性位点和染色体内端粒序列共定位。
Cytogenet Genome Res. 2005;108(1-3):234-47. doi: 10.1159/000080822.
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Beginning to understand the end of the chromosome.开始理解染色体的末端。
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Nucleic Acids Res. 2002 Jul 1;30(13):2862-70. doi: 10.1093/nar/gkf396.
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New ways not to make ends meet: telomerase, DNA damage proteins and heterochromatin.入不敷出的新方式:端粒酶、DNA损伤蛋白与异染色质。
Oncogene. 2002 Jan 21;21(4):553-63. doi: 10.1038/sj.onc.1205082.
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Protection of mammalian telomeres.哺乳动物端粒的保护
Oncogene. 2002 Jan 21;21(4):532-40. doi: 10.1038/sj.onc.1205080.
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The influence of DNA double-strand break structure on end-joining in human cells.DNA双链断裂结构对人类细胞中末端连接的影响。
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