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

被引:479
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
相关论文
共 49 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]   Complete sequence and gene map of a human major histocompatibility complex [J].
Beck, S ;
Geraghty, D ;
Inoko, H ;
Rowen, L ;
Aguado, B ;
Bahram, S ;
Campbell, RD ;
Forbes, SA ;
Guillaudeux, T ;
Hood, L ;
Horton, R ;
Janer, M ;
Jasoni, C ;
Madan, A ;
Milne, S ;
Neville, M ;
Oka, A ;
Qin, S ;
Ribas-Despuig, G ;
Rogers, J ;
Shiina, T ;
Spies, T ;
Tamiya, G ;
Tashiro, H ;
Trowsdale, J ;
Vu, Q ;
Williams, L ;
Yamazaki, M .
NATURE, 1999, 401 (6756) :921-923
[3]   Divergent outcomes of intrachromosomal recombination on the human Y chromosome: male infertility and recurrent polymorphism [J].
Blanco, P ;
Shlumukova, M ;
Sargent, CA ;
Jobling, MA ;
Affara, N ;
Hurles, ME .
JOURNAL OF MEDICAL GENETICS, 2000, 37 (10) :752-758
[4]   Prediction of complete gene structures in human genomic DNA [J].
Burge, C ;
Karlin, S .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 268 (01) :78-94
[5]   Structure and organization of the RBMY genes on the human Y chromosome:: Transposition and amplification of an ancestral autosomal hnRNPG gene [J].
Chai, NN ;
Zhou, HY ;
Hernandez, J ;
Najmabadi, H ;
Bhasin, S ;
Yen, PH .
GENOMICS, 1998, 49 (02) :283-289
[6]   The candidate spermatogenesis gene RBMY has a homologue on the human X chromosome [J].
Delbridge, ML ;
Lingenfelter, PA ;
Disteche, CM ;
Graves, JAM .
NATURE GENETICS, 1999, 22 (03) :223-224
[7]   NIGMS HUMAN RODENT SOMATIC-CELL HYBRID MAPPING PANEL-1 AND PANEL-2 [J].
DRWINGA, HL ;
TOJI, LH ;
KIM, CH ;
GREENE, AE ;
MULIVOR, RA .
GENOMICS, 1993, 16 (02) :311-314
[8]   Expression of RBM in the nuclei of human germ cells is dependent on a critical region of the Y chromosome long arm [J].
Elliott, DJ ;
Millar, MR ;
Oghene, K ;
Ross, A ;
Kiesewetter, F ;
Pryor, J ;
McIntyre, M ;
Hargreave, TB ;
Saunders, PTK ;
Vogt, PH ;
Chandley, AC ;
Cooke, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (08) :3848-3853
[9]   THE HUMAN Y-CHROMOSOME - OVERLAPPING DNA CLONES SPANNING THE EUCHROMATIC REGION [J].
FOOTE, S ;
VOLLRATH, D ;
HILTON, A ;
PAGE, DC .
SCIENCE, 1992, 258 (5079) :60-66
[10]   Submicroscopic deletions in the Y chromosome of infertile men [J].
Girardi, SK ;
Mielnik, A ;
Schlegel, PN .
HUMAN REPRODUCTION, 1997, 12 (08) :1635-1641