首页> 外文期刊>Journal of Biophysical and Biochemical Cytology >Regulating chromosomal movement by the cochaperone FKB-6 ensures timely pairing and synapsis
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Regulating chromosomal movement by the cochaperone FKB-6 ensures timely pairing and synapsis

机译:通过伴侣蛋白FKB-6调节染色体运动可确保及时配对和突触

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In meiotic prophase I, homologous chromosome pairing is promoted through chromosome movement mediated by nuclear envelope proteins, microtubules, and dynein. After proper homologue pairing has been established, the synaptonemal complex (SC) assembles along the paired homologues, stabilizing their interaction and allowing for crossing over to occur. Previous studies have shown that perturbing chromosome movement leads to pairing defects and SC polycomplex formation. We show that FKB-6 plays a role in SC assembly and is required for timely pairing and proper double-strand break repair kinetics. FKB-6 localizes outside the nucleus, and in its absence, the microtubule network is altered. FKB-6 is required for proper movement of dynein, increasing resting time between movements. Attenuating chromosomal movement in fkb-6 mutants partially restores the defects in synapsis, in agreement with FKB-6 acting by decreasing chromosomal movement. Therefore, we suggest that FKB-6 plays a role in regulating dynein movement by preventing excess chromosome movement, which is essential for proper SC assembly and homologous chromosome pairing.
机译:在减数分裂前期I中,通过核被膜蛋白,微管和动力蛋白介导的染色体运动促进同源染色体配对。建立正确的同源物配对后,突触复合物(SC)沿配对的同源物组装,稳定它们之间的相互作用并允许交叉发生。先前的研究表明,干扰染色体运动会导致配对缺陷和SC多复合物的形成。我们表明,FKB-6在SC组装中起作用,对于及时配对和正确的双链断裂修复动力学是必需的。 FKB-6定位在细胞核之外,并且在不存在的情况下,微管网络也会发生变化。动力蛋白的正常运动需要FKB-6,这增加了运动之间的休息时间。减弱fkb-6突变体中的染色体运动,可以部分恢复突触中的缺陷,这与FKB-6通过降低染色体运动来发挥作用是一致的。因此,我们建议FKB-6通过阻止过多的染色体移动来调节动力蛋白的运动,这对于正确的SC组装和同源染色体配对是必不可少的。

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