Department of Biological Sciences, University of North Texas, Denton, TX, USA.
Cell Div. 2008 Feb 4;3:6. doi: 10.1186/1747-1028-3-6.
The spindle checkpoint delays the onset of anaphase until all sister chromatids are aligned properly at the metaphase plate. To investigate the role san-1, the MAD3 homologue, has in Caenorhabditis elegans embryos we used RNA interference (RNAi) to identify genes synthetic lethal with the viable san-1(ok1580) deletion mutant.
The san-1(ok1580) animal has low penetrating phenotypes including an increased incidence of males, larvae arrest, slow growth, protruding vulva, and defects in vulva morphogenesis. We found that the viability of san-1(ok1580) embryos is significantly reduced when HCP-1 (CENP-F homologue), MDF-1 (MAD-1 homologue), MDF-2 (MAD-2 homologue) or BUB-3 (predicted BUB-3 homologue) are reduced by RNAi. Interestingly, the viability of san-1(ok1580) embryos is not significantly reduced when the paralog of HCP-1, HCP-2, is reduced. The phenotype of san-1(ok1580);hcp-1(RNAi) embryos includes embryonic and larval lethality, abnormal organ development, and an increase in abnormal chromosome segregation (aberrant mitotic nuclei, anaphase bridging). Several of the san-1(ok1580);hcp-1(RNAi) animals displayed abnormal kinetochore (detected by MPM-2) and microtubule structure. The survival of mdf-2(RNAi);hcp-1(RNAi) embryos but not bub-3(RNAi);hcp-1(RNAi) embryos was also compromised. Finally, we found that san-1(ok1580) and bub-3(RNAi), but not hcp-1(RNAi) embryos, were sensitive to anoxia, suggesting that like SAN-1, BUB-3 has a functional role as a spindle checkpoint protein.
Together, these data suggest that in the C. elegans embryo, HCP-1 interacts with a subset of the spindle checkpoint pathway. Furthermore, the fact that san-1(ok1580);hcp-1(RNAi) animals had a severe viability defect whereas in the san-1(ok1580);hcp-2(RNAi) and san-1(ok1580);hcp-2(ok1757) animals the viability defect was not as severe suggesting that hcp-1 and hcp-2 are not completely redundant.
纺锤体检查点延迟了后期的开始,直到所有的姐妹染色单体在中期板上正确对齐。为了研究 MAD3 同源物 san-1 在秀丽隐杆线虫胚胎中的作用,我们使用 RNA 干扰 (RNAi) 来鉴定与存活的 san-1(ok1580)缺失突变体具有合成致死性的基因。
san-1(ok1580)动物具有低穿透表型,包括雄性发生率增加、幼虫停滞、生长缓慢、突出的阴道和阴道形态发生缺陷。我们发现,当 HCP-1(CENP-F 同源物)、MDF-1(MAD-1 同源物)、MDF-2(MAD-2 同源物)或 BUB-3(预测的 BUB-3 同源物)的 RNAi 降低时,san-1(ok1580)胚胎的存活率显著降低。有趣的是,当 HCP-1 的旁系同源物 HCP-2 减少时,san-1(ok1580)胚胎的存活率并没有显著降低。san-1(ok1580);hcp-1(RNAi)胚胎的表型包括胚胎和幼虫致死、器官发育异常和异常染色体分离增加(异常有丝分裂核、后期桥接)。一些 san-1(ok1580);hcp-1(RNAi)动物显示出异常的动粒(通过 MPM-2 检测到)和微管结构。mdf-2(RNAi);hcp-1(RNAi)胚胎的存活但 bub-3(RNAi);hcp-1(RNAi)胚胎的存活不受影响。最后,我们发现 san-1(ok1580)和 bub-3(RNAi),但不是 hcp-1(RNAi)胚胎,对缺氧敏感,这表明像 SAN-1 一样,BUB-3 作为纺锤体检查点蛋白具有功能作用。
总之,这些数据表明,在秀丽隐杆线虫胚胎中,HCP-1 与纺锤体检查点途径的一部分相互作用。此外,san-1(ok1580);hcp-1(RNAi)动物的严重生存缺陷,而在 san-1(ok1580);hcp-2(RNAi)和 san-1(ok1580);hcp-2(ok1757)动物的生存缺陷并不那么严重,这表明 hcp-1 和 hcp-2 并不完全冗余。