The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men

被引:473
|
作者
Kawaguchi, TK
Skaletsky, H
Brown, LG
Minx, PJ
Cordum, HS
Waterston, RH
Wilson, RK
Silber, S
Oates, R
Rozen, S
Page, DC
机构
[1] MIT, Howard Hughes Med Inst, Whitehead Inst, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02142 USA
[3] Washington Univ, Sch Med, Genome Sequencing Ctr, St Louis, MO 63108 USA
[4] St Lukes Hosp, Infertil Ctr St Louis, St Louis, MO 63107 USA
[5] Boston Univ, Sch Med, Dept Urol, Boston, MA 02228 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/ng757
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Deletions of the AZFc (azoospermia factor c) region of the Y chromosome are the most common known cause of spermatogenic failure. We determined the complete nucleotide sequence of AZFc by identifying and distinguishing between near-identical amplicons (massive repeat units) using an iterative mapping-sequencing process. A complex of three palindromes, the largest spanning 3 Mb with 99.97% identity between its arms, encompasses the AZFc region. The palindromes are constructed from six distinct families of amplicons, with unit lengths of 115-678 kb, and may have resulted from tandem duplication and inversion during primate evolution. The palindromic complex contains 11 families of transcription units, all expressed in testis. Deletions of AZFc that cause infertility are remarkably uniform, spanning a 3.5-Mb segment and bounded by 229-kb direct repeats that probably served as substrates for homologous recombination.
引用
收藏
页码:279 / 286
页数:8
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