spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

First published online 8 July 2008
doi: 10.1242/jcs.033233


Journal of Cell Science 121, 2445-2451 (2008)
Published by The Company of Biologists 2008
This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplementary Material
Right arrow All Versions of this Article:
jcs.033233v1
121/15/2445    most recent
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 Related articles in JCS
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 Download to citation manager
Right arrow reprints & permissions
Google Scholar
Right arrow Articles by Hamer, G.
Right arrow Articles by Höög, C.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hamer, G.
Right arrow Articles by Höög, C.

Research Article

Progression of meiotic recombination requires structural maturation of the central element of the synaptonemal complex

Geert Hamer1, Hong Wang1, Ewelina Bolcun-Filas2, Howard J. Cooke2, Ricardo Benavente3 and Christer Höög1,*

1 Department of Cell and Molecular Biology, Karolinska Institute, Berzelius väg 35, Stockholm, SE-171 77, Sweden
2 Medical Research Council Human Genetics Unit, Western General Hospital, Edinburgh EH4 2XU, Scotland, UK
3 Department of Cell and Developmental Biology, Biocenter of the University of Würzburg, Am Hubland, Würzburg 97074, Germany

* Author for correspondence (e-mail: Christer.Hoog{at}ki.se)

Accepted 8 May 2008

The synaptonemal complex is an elaborate meiosis-specific supramolecular protein assembly that promotes chromosome synapsis and meiotic recombination. We inactivated the meiosis-specific gene Tex12 and found that TEX12 is essential for progression of meiosis in both male and female germ cells. Structural analysis of the synaptonemal complex in Tex12–/– meiocytes revealed a disrupted central element structure, a dense structure residing between the synapsed homologous chromosomes. Chromosome synapsis is initiated at multiple positions along the paired homologous chromosomes in Tex12–/– meiotic cells, but fails to propagate along the chromosomes. Furthermore, although meiotic recombination is initiated in Tex12–/– meiotic cells, these early recombination events do not develop into meiotic crossovers. Hence, the mere initiation of synapsis is not sufficient to support meiotic crossing-over. Our results show that TEX12 is a component of the central element structure of the synaptonemal complex required for propagation of synapsis along the paired homologous chromosomes and maturation of early recombination events into crossovers.

Key words: Chromosome synapsis, Meiosis, Meiotic recombination, Synaptonemal complex, TEX12


Related articles in JCS:

TEX12: zipping chromosomes up

JCS 2008 121: 1502. [Full Text]  






© The Company of Biologists Ltd 2008