The Ecm11-Gmc2 Complex Promotes Synaptonemal Complex Formation through Assembly of Transverse Filaments in Budding Yeast

被引:70
作者
Humphryes, Neil [1 ]
Leung, Wing-Kit [1 ]
Argunhan, Bilge [1 ]
Terentyev, Yaroslav [1 ]
Dvorackova, Martina [1 ]
Tsubouchi, Hideo [1 ]
机构
[1] Univ Sussex, MRC, Genome Damage & Stabil Ctr, Brighton, E Sussex, England
基金
英国生物技术与生命科学研究理事会;
关键词
MEIOTIC CHROMOSOME SYNAPSIS; MEIOSIS-SPECIFIC PROTEIN; DOUBLE-STRAND BREAK; SACCHAROMYCES-CEREVISIAE; ELEMENT PROTEIN; RECOMBINATION; SUMO; SEGREGATION; INITIATION; RED1;
D O I
10.1371/journal.pgen.1003194
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
During meiosis, homologous chromosomes pair at close proximity to form the synaptonemal complex (SC). This association is mediated by transverse filament proteins that hold the axes of homologous chromosomes together along their entire length. Transverse filament proteins are highly aggregative and can form an aberrant aggregate called the polycomplex that is unassociated with chromosomes. Here, we show that the Ecm11-Gmc2 complex is a novel SC component, functioning to facilitate assembly of the yeast transverse filament protein, Zip1. Ecm11 and Gmc2 initially localize to the synapsis initiation sites, then throughout the synapsed regions of paired homologous chromosomes. The absence of either Ecm11 or Gmc2 substantially compromises the chromosomal assembly of Zip1 as well as polycomplex formation, indicating that the complex is required for extensive Zip1 polymerization. We also show that Ecm11 is SUMOylated in a Gmc2-dependent manner. Remarkably, in the unSUMOylatable ecm11 mutant, assembly of chromosomal Zip1 remained compromised while polycomplex formation became frequent. We propose that the Ecm11-Gmc2 complex facilitates the assembly of Zip1 and that SUMOylation of Ecm11 is critical for ensuring chromosomal assembly of Zip1, thus suppressing polycomplex formation.
引用
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页数:14
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