Gene copy number reduction in the azoospermia factor c (AZFc) region and its effect on total motile sperm count

被引:46
作者
Noordam, Michiel J. [1 ]
Westerveld, G. Henrike [1 ]
Hovingh, Suzanne E. [1 ]
van Daalen, Saskia K. M. [1 ]
Korver, Cindy M. [1 ]
van der Veen, Fulco [1 ]
van Pelt, Ans M. M. [1 ]
Repping, Sjoerd [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Ctr Reprod Med, Dept Obstet & Gynecol, NL-1105 AZ Amsterdam, Netherlands
关键词
HUMAN Y-CHROMOSOME; REPEAT LENGTH VARIATION; SPERMATOGENIC FAILURE; SEMEN QUALITY; DELETIONS; MUTATION; POLYMORPHISM; MEN;
D O I
10.1093/hmg/ddr119
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The azoospermia factor c (AZFc) region harbors multi-copy genes that are expressed in the testis. Deletions of the AZFc region lead to reduced copy numbers of these genes. Four (partial) AZFc deletions have been described of which the b2/b4 and gr/gr deletions affect semen quality. In most studies, (partial) AZFc deletions are identified and characterized using plus/minus sequence site tag (STS) polymerase chain reaction (PCR). However, secondary duplications increase the gene copy number without re-introducing the STS boundary marker. Consequently, the actual copy number of AZFc genes cannot be determined via STS PCR. In the current study, we first set out to determine by quantitative real-time PCR the actual copy number of all AZFc genes in men with (partial) AZFc deletions based on STS PCR. We then analyzed whether reduced gene copy numbers of each AZFc gene family were associated with reduced total motile sperm count (TMC), regardless of the type of deletion. We screened 840 men and identified 31 unrelated men with (partial) deletions of AZFc based on STS PCR. Of these 31 men, 6 men (19%) had one or more secondary duplications. For all AZFc genes, we found an association between a reduction in the copy number of each individual AZFc gene and reduced TMC. In gr/gr-deleted men, restoration of reduced gene copy numbers restored their TMC to normal values. Our findings suggest that the gene content of the AZFc region has been preserved throughout evolution through a dosage effect of the AZFc genes on TMC safeguarding male fertility.
引用
收藏
页码:2457 / 2463
页数:7
相关论文
共 21 条
[11]   Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure [J].
Repping, S ;
Skaletsky, H ;
Lange, J ;
Silber, S ;
van der Veen, F ;
Oates, RD ;
Page, DC ;
Rozen, S .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) :906-922
[12]   High mutation rates have driven extensive structural polymorphism among human Y chromosomes [J].
Repping, S ;
van Daalen, SKM ;
Brown, LG ;
Korver, CM ;
Lange, J ;
Marszalek, JD ;
Pyntikova, T ;
van der Veen, F ;
Skaletsky, H ;
Page, DC ;
Rozen, S .
NATURE GENETICS, 2006, 38 (04) :463-467
[13]   Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection [J].
Repping, S ;
Skaletsky, H ;
Brown, L ;
van Daalen, SKM ;
Korver, CM ;
Pyntikova, T ;
Kuroda-Kawaguchi, T ;
de Vries, JWA ;
Oates, RD ;
Silber, S ;
van der Veen, F ;
Page, DC ;
Rozen, S .
NATURE GENETICS, 2003, 35 (03) :247-251
[14]   A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region [J].
Repping, S ;
van Daalen, SKM ;
Korver, CM ;
Brown, LG ;
Marszalek, JD ;
Gianotten, J ;
Oates, RD ;
Silber, S ;
van der Veen, F ;
Page, DC ;
Rozen, S .
GENOMICS, 2004, 83 (06) :1046-1052
[15]   Four DAZ genes in two clusters found in the AZFc region of the human Y chromosome [J].
Saxena, R ;
de Vries, JWA ;
Repping, S ;
Alagappan, RK ;
Skaletsky, H ;
Brown, LG ;
Ma, P ;
Chen, ES ;
Hoovers, JMN ;
Page, DC .
GENOMICS, 2000, 67 (03) :256-267
[16]   EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art 2004 [J].
Simoni, M ;
Bakker, E ;
Krausz, C .
INTERNATIONAL JOURNAL OF ANDROLOGY, 2004, 27 (04) :240-249
[17]   The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes [J].
Skaletsky, H ;
Kuroda-Kawaguchi, T ;
Minx, PJ ;
Cordum, HS ;
Hillier, L ;
Brown, LG ;
Repping, S ;
Pyntikova, T ;
Ali, J ;
Bieri, T ;
Chinwalla, A ;
Delehaunty, A ;
Delehaunty, K ;
Du, H ;
Fewell, G ;
Fulton, L ;
Fulton, R ;
Graves, T ;
Hou, SF ;
Latrielle, P ;
Leonard, S ;
Mardis, E ;
Maupin, R ;
McPherson, J ;
Miner, T ;
Nash, W ;
Nguyen, C ;
Ozersky, P ;
Pepin, K ;
Rock, S ;
Rohlfing, T ;
Scott, K ;
Schultz, B ;
Strong, C ;
Tin-Wollam, A ;
Yang, SP ;
Waterston, RH ;
Wilson, RK ;
Rozen, S ;
Page, DC .
NATURE, 2003, 423 (6942) :825-U2
[18]   Y chromosome gr/gr deletions are a risk factor for low semen quality [J].
Visser, L. ;
Westerveld, G. H. ;
Korver, C. M. ;
van Daalen, S. K. M. ;
Hovingh, S. E. ;
Rozen, S. ;
van der Veen, F. ;
Repping, S. .
HUMAN REPRODUCTION, 2009, 24 (10) :2667-2673
[19]   Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11 [J].
Vogt, PH ;
Edelmann, A ;
Kirsch, S ;
Henegariu, O ;
Hirschmann, P ;
Kiesewetter, F ;
Kohn, FM ;
Schill, WB ;
Farah, S ;
Ramos, C ;
Hartmann, M ;
Hartschuh, W ;
Meschede, D ;
Behre, HM ;
Castel, A ;
Nieschlag, E ;
Weidner, W ;
Grone, HJ ;
Jung, A ;
Engel, W ;
Haidl, G .
HUMAN MOLECULAR GENETICS, 1996, 5 (07) :933-943
[20]   CAG repeat length variation in the polymerase gamma (POLG) gene: effect on semen quality [J].
Westerveld, G. H. ;
Kaaij-Visser, L. ;
Tanck, M. ;
van der Veen, F. ;
Repping, S. .
MOLECULAR HUMAN REPRODUCTION, 2008, 14 (04) :245-249