Skip Navigation



Mol. Hum. Reprod. Advance Access published online on February 25, 2005

Molecular Human Reproduction, doi:10.1093/molehr/gah153
This Article
Right arrow Advance Access manuscript (PDF) Freely available
Right arrow All Versions of this Article:
11/4/295    most recent
gah153v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Vinci, G.
Right arrow Articles by McElreavey, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Vinci, G.
Right arrow Articles by McElreavey, K.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Molecular Human Reproduction © European Society of Human Reproduction and Embryology 2005; all rights reserved
Received October 18, 2004
Accepted January 7, 2005

Article

A deletion of a novel heat shock gene on the Y chromosome associated with azoospermia

Giovanna Vinci 1, Florina Raicu 2, Luis Popa 2, Olivia Popa 2, Relu Cocos 3, and Ken McElreavey 1*

1 Reproduction, Fertility and Populations, Institut Pasteur, 25 rue du Dr Roux, 75724 Paris Cedex 15, France
2 Institute of Genetics, University of Bucharest, Aleea Portocalelor, nr 1-3, Bucharest, Romania
3 Genetics Department, University of Medicine and Pharmacy "Carol Davila", Bucharest, Romania


   Abstract

Deletions of the Y chromosome are a significant cause of spermatogenic failure. Three major deletion intervals have been defined and termed AZFa, AZFb and AZFc. Here, we report an unusual case of a proximal AZFb deletion that includes the Y chromosome palindromic sequence P4 and a novel heat shock factor (HSFY). This deletion neither include the genes EIF1AY, RPS4Y2 nor copies of the RBMY1 genes. The individual presented with idiopathic azoospermia. We propose that deletions of the testis-specific HSFY gene family may be a cause of unexplained cases of idiopathic male infertility. This deletion would not have been detected using current protocols for Y chromosome microdeletion screens, therefore we recommend that current screening protocols be extended to include this region and other palindrome sequences that contain genes expressed specifically in the testis.

Keywords: AZFb; heat shock gene; male infertility; Y chromosome.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.