Literature DB >> 29487178

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

Masatoshi Takagi1, Takao Ono2, Toyoaki Natsume3, Chiyomi Sakamoto4, Mitsuyoshi Nakao4, Noriko Saitoh4,5, Masato T Kanemaki3, Tatsuya Hirano2, Naoko Imamoto6.   

Abstract

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.
© 2018. Published by The Company of Biologists Ltd.

Entities:  

Keywords:  AID; Auxin-inducible degron; Condensin; Ki-67; Mitotic chromosome

Mesh:

Substances:

Year:  2018        PMID: 29487178     DOI: 10.1242/jcs.212092

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  16 in total

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9.  Common Fragile Sites Are Characterized by Faulty Condensin Loading after Replication Stress.

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