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

Abstract:

: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.

journal_name

J Cell Sci

journal_title

Journal of cell science

authors

Hamer G,Wang H,Bolcun-Filas E,Cooke HJ,Benavente R,Höög C

doi

10.1242/jcs.033233

subject

Has Abstract

pub_date

2008-08-01 00:00:00

pages

2445-51

issue

Pt 15

eissn

0021-9533

issn

1477-9137

pii

jcs.033233

journal_volume

121

pub_type

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