Ki-67 and condensins support the integrity of mitotic chromosomes through distinct mechanisms

被引:37
作者
Takagi, Masatoshi [1 ]
Ono, Takao [2 ]
Natsume, Toyoaki [3 ]
Sakamoto, Chiyomi [4 ]
Nakao, Mitsuyoshi [4 ]
Saitoh, Noriko [4 ,5 ]
Kanemaki, Masato T. [3 ]
Hirano, Tatsuya [2 ]
Imamoto, Naoko [1 ]
机构
[1] RIKEN, Cellular Dynam Lab, Wako, Saitama 3510198, Japan
[2] RIKEN, Chromosome Dynam Lab, Wako, Saitama 3510198, Japan
[3] NIG, Div Mol Cell Engn, Mishima, Shizuoka 4118540, Japan
[4] Kumamoto Univ, Dept Med Cell Biol, IMEG, Kumamoto 8600811, Japan
[5] JFCR, Dept Canc Biol, Canc Inst, Tokyo 1358550, Japan
基金
日本学术振兴会;
关键词
Ki-67; Condensin; Mitotic chromosome; Auxin-inducible degron; AID; HUMAN-CELLS; PROTEIN; ARCHITECTURE; SEGREGATION;
D O I
10.1242/jcs.212092
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Although condensins play essential roles in mitotic chromosome assembly, Ki-67 (also known as MKI67), a protein localizing to the periphery of mitotic chromosomes, had also been shown to make a contribution to the process. To examine their respective roles, we generated a set of HCT116-based cell lines expressing Ki-67 and/or condensin subunits that were fused with an auxin-inducible degron for their conditional degradation. Both the localization and the dynamic behavior of Ki-67 on mitotic chromosomes were not largely affected upon depletion of condensin subunits, and vice versa. When both Ki-67 and SMC2 (a core subunit of condensins) were depleted, ball-like chromosome clusters with no sign of discernible thread-like structures were observed. This severe defective phenotype was distinct from that observed in cells depleted of either Ki-67 or SMC2 alone. Our results show that Ki-67 and condensins, which localize to the external surface and the central axis of mitotic chromosomes, respectively, have independent yet cooperative functions in supporting the structural integrity of mitotic chromosomes.
引用
收藏
页数:13
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