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联会复合体的中心元件蛋白 ZEP1 调控水稻减数分裂过程中的交叉数。

The central element protein ZEP1 of the synaptonemal complex regulates the number of crossovers during meiosis in rice.

机构信息

State Key Laboratory of Plant Genomics and Center for Plant Gene Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.

出版信息

Plant Cell. 2010 Feb;22(2):417-30. doi: 10.1105/tpc.109.070789. Epub 2010 Feb 12.

Abstract

ZEP1, a transverse filament (TF) protein, is the rice (Oryza sativa) homolog of Arabidopsis thaliana ZYP1. In the Tos17-insertional zep1 mutants, homologous chromosomes align along the entire length of the chromosome, but the synaptonemal complex is not assembled in early prophase I. Crossovers are well formed, and 12 bivalents could be detected from diakinesis to metaphase I, which leads to equal chromosomal segregation in anaphase I. Moreover, the number of crossovers has a tendency to be increased compared with that in the wild type. These phenomena are different from the TF mutants identified so far in other organisms. Chiasma terminalization of the bivalent, which occurs frequently in the wild type, seldom occurred in zep1. Transmission electron micrographs and immunodetection using an antibody against ZEP1 showed that ZEP1 is the central element of the synaptonemal complex. Although PAIR2 and MER3 were loaded normally in zep1, their dissociation was delayed severely compared with the wild type. In addition, ZEP1 is reloaded onto chromosomes in early microspores as the chromosome decondense, suggesting that ZEP1 might have other biological functions during this process.

摘要

ZEP1 是一种横向细丝(TF)蛋白,是拟南芥 ZYP1 的水稻(Oryza sativa)同源物。在 Tos17 插入的 zep1 突变体中,同源染色体沿着染色体的全长排列,但联会复合体在早期前期 I 中未组装。交叉形成良好,在减数分裂到中期 I 期间可以检测到 12 个二价体,这导致后期 I 中染色体的均等分离。此外,与野生型相比,交叉的数量有增加的趋势。这些现象与迄今为止在其他生物体中鉴定的 TF 突变体不同。在野生型中经常发生的二价体交叉终化很少发生在 zep1 中。电镜照片和用针对 ZEP1 的抗体进行的免疫检测表明,ZEP1 是联会复合体的中心元件。尽管 PAIR2 和 MER3 在 zep1 中正常加载,但与野生型相比,它们的解离严重延迟。此外,ZEP1 在染色体解压缩时重新加载到早期小孢子上,表明 ZEP1 在这个过程中可能具有其他生物学功能。

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