Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
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 ISI Web of Science
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 arrow Search for citing articles in:
ISI Web of Science (16)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Kerr, S. M.
Right arrow Articles by Cooke, H. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kerr, S. M.
Right arrow Articles by Cooke, H. J.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Molecular Genetics, Vol 5, 1139-1148, Copyright © 1996 by Oxford University Press


ARTICLES

Ott, a mouse X-linked multigene family expressed specifically during meiosis

SM Kerr, MH Taggart, M Lee and HJ Cooke
Medical Research Council Human Genetics Unit, Western General Hospital, Edinburgh, UK.

The tissue expression patterns of 10 mouse testis cDNAs were analysed by RT-PCR to search for new mammalian meiotic genes. The homologue of the rat synaptonemal complex protein gene SCP1 is expressed in embryonic ovary, adult brain and testis. One novel gene is stringently testis specific and another is expressed exclusively in testis and embryonic ovary. The latter clone is not expressed in the testes of adult sex-reversed mice which lack germ cells, and therefore represents a meiosis-specific gene. It is part of a mouse multigene family, members of which are clustered and map genetically and physically to a single region of the X chromosome. We have named this family Ott (ovary testis transcribed). Steady-state levels of a 2.3 kb polyadenylated Ott mRNA are high throughout meiotic prophase in the testis when the X chromosome is generally transcriptionally inactive. A second transcript of 1 kb is also detectable from 4 weeks of age onwards. The two mRNAs have different 3' ends and contain different protein coding information. At least seven Ott genes are transcribed specifically during meiosis and are predicted to encode "pioneer' proteins with an unusual structure, containing tandem arrays of a degenerate eight amino acid repeat. This work could lead to the identification of a human Ott homologue, which is likely to be X-linked and would provide a candidate locus for some cases of male infertility.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Hum Reprod UpdateHome page
K. Stouffs, H. Tournaye, I. Liebaers, and W. Lissens
Male infertility and the involvement of the X chromosome
Hum. Reprod. Update, November 1, 2009; 15(6): 623 - 637.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
P. J. Wang, D. C. Page, and J. R. McCarrey
Differential expression of sex-linked and autosomal germ-cell-specific genes during spermatogenesis in the mouse
Hum. Mol. Genet., October 1, 2005; 14(19): 2911 - 2918.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
S. J. Armstrong, A. P. Caryl, G. H. Jones, and F. C. H. Franklin
Asy1, a protein required for meiotic chromosome synapsis, localizes to axis-associated chromatin in Arabidopsis and Brassica
J. Cell Sci., September 15, 2002; 115(18): 3645 - 3655.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. A. Cook, T. Matsui, L. Li, and A. Rosenzweig
Transcriptional Effects of Chronic Akt Activation in the Heart
J. Biol. Chem., June 14, 2002; 277(25): 22528 - 22533.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
O. Tureci, U. Sahin, C. Zwick, M. Koslowski, G. Seitz, and M. Pfreundschuh
Identification of a meiosis-specific protein as a member of the class of cancer/testis antigens
PNAS, April 28, 1998; 95(9): 5211 - 5216.
[Abstract] [Full Text] [PDF]



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.