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Centromere/kinetochore is assembled through CENP-C oligomerization

Authors :
1000030565099
0000-0001-8433-1111
Hara, Masatoshi
1000080437243
0000-0002-1361-2642
Ariyoshi, Mariko
Sano, Tomoki
1000070868710
Nozawa, Ryu-Suke
1000060547058
Shinkai, Soya
1000050348843
Onami, Shuichi
Jansen, Isabelle
1000050421368
Hirota, Toru
1000060321600
Fukagawa, Tatsuo
1000030565099
0000-0001-8433-1111
Hara, Masatoshi
1000080437243
0000-0002-1361-2642
Ariyoshi, Mariko
Sano, Tomoki
1000070868710
Nozawa, Ryu-Suke
1000060547058
Shinkai, Soya
1000050348843
Onami, Shuichi
Jansen, Isabelle
1000050421368
Hirota, Toru
1000060321600
Fukagawa, Tatsuo
Publication Year :
2023

Abstract

Hara M., Ariyoshi M., Sano T., et al. Centromere/kinetochore is assembled through CENP-C oligomerization. Molecular Cell 83, 2188 (2023); https://doi.org/10.1016/j.molcel.2023.05.023.<br />Kinetochore is an essential protein complex required for accurate chromosome segregation. The constitutive centromere-associated network (CCAN), a subcomplex of the kinetochore, associates with centromeric chromatin and provides a platform for the kinetochore assembly. The CCAN protein CENP-C is thought to be a central hub for the centromere/kinetochore organization. However, the role of CENP-C in CCAN assembly needs to be elucidated. Here, we demonstrate that both the CCAN-binding domain and the C-terminal region that includes the Cupin domain of CENP-C are necessary and sufficient for chicken CENP-C function. Structural and biochemical analyses reveal self-oligomerization of the Cupin domains of chicken and human CENP-C. We find that the CENP-C Cupin domain oligomerization is vital for CENP-C function, centromeric localization of CCAN, and centromeric chromatin organization. These results suggest that CENP-C facilitates the centromere/kinetochore assembly through its oligomerization.

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1409766579
Document Type :
Electronic Resource