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Dev Cell. 2008 Feb;14(2):263-74. doi: 10.1016/j.devcel.2007.11.016.

HTP-3 links DSB formation with homolog pairing and crossing over during C. elegans meiosis.

Author information

1
Department of Biology, McGill University, Montreal, Quebec H3A 1B1, Canada.

Abstract

Repair of the programmed meiotic double-strand breaks (DSBs) that initiate recombination must be coordinated with homolog pairing to generate crossovers capable of directing chromosome segregation. Chromosome pairing and synapsis proceed independently of recombination in worms and flies, suggesting a paradoxical lack of coregulation. Here, we find that the meiotic axis component HTP-3 links DSB formation with homolog pairing and synapsis. HTP-3 forms complexes with the DSB repair components MRE-11/RAD-50 and the meiosis-specific axis component HIM-3. Loss of htp-3 or mre-11 recapitulates meiotic phenotypes consistent with a failure to generate DSBs, suggesting that HTP-3 associates with MRE-11/RAD-50 in a complex required for meiotic DSB formation. Loss of HTP-3 eliminates HIM-3 localization to axes and HIM-3-dependent homolog alignment, synapsis, and crossing over. Our study reveals a mechanism for coupling meiotic DSB formation with homolog pairing through the essential participation of an axis component with complexes mediating both processes.

PMID:
18267094
DOI:
10.1016/j.devcel.2007.11.016
[Indexed for MEDLINE]
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