AZFc Deletions and Spermatogenic Failure: A Population-Based Survey of 20,000 Y Chromosomes

Deletions involving the Y chromosome's AZFc region are the most common known genetic cause of severe spermatogenic failure (SSF). Six recurrent interstitial deletions affecting the region have been reported, but their population genetics are largely unexplored. We assessed the deletions' p...

Full description

Bibliographic Details
Main Authors: Rozen, Steven G (Author), Marszalek, Janet D. (Author), Irenze, Kathryn (Author), Skaletsky, Helen (Author), Brown, Laura G. (Author), Oates, Robert D. (Author), Silber, Sherman J (Author), Ardlie, Kristin (Author), Page, David C (Author)
Other Authors: Massachusetts Institute of Technology. Department of Biology (Contributor), Whitehead Institute for Biomedical Research (Contributor), Page, David C. (Contributor)
Format: Article
Language:English
Published: Elsevier, 2014-11-12T13:35:10Z.
Subjects:
Online Access:Get fulltext
LEADER 02643 am a22003253u 4500
001 91523
042 |a dc 
100 1 0 |a Rozen, Steven G.  |e author 
100 1 0 |a Massachusetts Institute of Technology. Department of Biology  |e contributor 
100 1 0 |a Whitehead Institute for Biomedical Research  |e contributor 
100 1 0 |a Page, David C.  |e contributor 
700 1 0 |a Marszalek, Janet D.  |e author 
700 1 0 |a Irenze, Kathryn  |e author 
700 1 0 |a Skaletsky, Helen  |e author 
700 1 0 |a Brown, Laura G.  |e author 
700 1 0 |a Oates, Robert D.  |e author 
700 1 0 |a Silber, Sherman J.  |e author 
700 1 0 |a Ardlie, Kristin  |e author 
700 1 0 |a Page, David C  |e author 
245 0 0 |a AZFc Deletions and Spermatogenic Failure: A Population-Based Survey of 20,000 Y Chromosomes 
260 |b Elsevier,   |c 2014-11-12T13:35:10Z. 
856 |z Get fulltext  |u http://hdl.handle.net/1721.1/91523 
520 |a Deletions involving the Y chromosome's AZFc region are the most common known genetic cause of severe spermatogenic failure (SSF). Six recurrent interstitial deletions affecting the region have been reported, but their population genetics are largely unexplored. We assessed the deletions' prevalence in 20,884 men in five populations and found four of the six deletions (presented here in descending order of prevalence): gr/gr, b2/b3, b1/b3, and b2/b4. One of every 27 men carried one of these four deletions. The 1.6 Mb gr/gr deletion, found in one of every 41 men, almost doubles the risk of SSF and accounts for ~2% of SSF, although <2% of men with the deletion are affected. The 1.8 Mb b2/b3 deletion, found in one of every 90 men, does not appear to be a risk factor for SSF. The 1.6 Mb b1/b3 deletion, found in one of every 994 men, appears to increase the risk of SSF by a factor of 2.5, although <2% of men with the deletion are affected, and it accounts for only 0.15% of SSF. The 3.5 Mb b2/b4 deletion, found in one of every 2,320 men, increases the risk of SSF 145 times and accounts for ~6% of SSF; the observed prevalence should approximate the rate at which the deletion arises anew in each generation. We conclude that a single rare variant of major effect (the b2/b4 deletion) and a single common variant of modest effect (the gr/gr deletion) are largely responsible for the AZFc region's contribution to SSF in the population. 
520 |a National Institutes of Health (U.S.) 
520 |a Howard Hughes Medical Institute 
520 |a Singapore. Agency for Science, Technology and Research 
520 |a Singapore. Ministry of Health 
546 |a en_US 
655 7 |a Article 
773 |t The American Journal of Human Genetics