Radford Sarah J, Hoang Tranchau L, Głuszek A Agata, Ohkura Hiroyuki, McKim Kim S
Waksman Institute of Microbiology, Rutgers, The State University of New Jersey, Piscataway, New Jersey, United States of America.
Waksman Institute of Microbiology, Rutgers, The State University of New Jersey, Piscataway, New Jersey, United States of America; Department of Genetics, Rutgers, The State University of New Jersey, Piscataway, New Jersey, United States of America.
PLoS Genet. 2015 Oct 16;11(10):e1005605. doi: 10.1371/journal.pgen.1005605. eCollection 2015 Oct.
In oocytes, where centrosomes are absent, the chromosomes direct the assembly of a bipolar spindle. Interactions between chromosomes and microtubules are essential for both spindle formation and chromosome segregation, but the nature and function of these interactions is not clear. We have examined oocytes lacking two kinetochore proteins, NDC80 and SPC105R, and a centromere-associated motor protein, CENP-E, to characterize the impact of kinetochore-microtubule attachments on spindle assembly and chromosome segregation in Drosophila oocytes. We found that the initiation of spindle assembly results from chromosome-microtubule interactions that are kinetochore-independent. Stabilization of the spindle, however, depends on both central spindle and kinetochore components. This stabilization coincides with changes in kinetochore-microtubule attachments and bi-orientation of homologs. We propose that the bi-orientation process begins with the kinetochores moving laterally along central spindle microtubules towards their minus ends. This movement depends on SPC105R, can occur in the absence of NDC80, and is antagonized by plus-end directed forces from the CENP-E motor. End-on kinetochore-microtubule attachments that depend on NDC80 are required to stabilize bi-orientation of homologs. A surprising finding was that SPC105R but not NDC80 is required for co-orientation of sister centromeres at meiosis I. Together, these results demonstrate that, in oocytes, kinetochore-dependent and -independent chromosome-microtubule attachments work together to promote the accurate segregation of chromosomes.
在没有中心体的卵母细胞中,染色体指导双极纺锤体的组装。染色体与微管之间的相互作用对于纺锤体形成和染色体分离都至关重要,但这些相互作用的性质和功能尚不清楚。我们研究了缺乏两种动粒蛋白NDC80和SPC105R以及一种着丝粒相关运动蛋白CENP-E的卵母细胞,以表征动粒-微管附着对果蝇卵母细胞纺锤体组装和染色体分离的影响。我们发现纺锤体组装的起始源于不依赖动粒的染色体-微管相互作用。然而,纺锤体的稳定依赖于中央纺锤体和动粒成分。这种稳定与动粒-微管附着的变化以及同源物的双定向一致。我们提出双定向过程始于动粒沿着中央纺锤体微管向其负端横向移动。这种移动依赖于SPC105R,在没有NDC80的情况下也能发生,并且受到来自CENP-E运动蛋白的正端定向力的拮抗。依赖于NDC80的端对端动粒-微管附着是稳定同源物双定向所必需的。一个惊人的发现是,在减数分裂I时,姐妹着丝粒的共定向需要SPC105R而不是NDC80。总之,这些结果表明,在卵母细胞中,依赖动粒和不依赖动粒的染色体-微管附着共同作用以促进染色体的准确分离。