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SETDB2 interacts with BUBR1 to induce accurate chromosome segregation independently of its histone methyltransferase activity.
Tu, Yanhong; Zhang, Haomiao; Xia, Jialin; Zhao, Yu; Yang, Ruifang; Feng, Jing; Ma, Xueyun; Li, Jing.
Afiliação
  • Tu Y; School of Laboratory Medicine and Biotechnology, Southern Medical University, Guangzhou, China.
  • Zhang H; The Second Affiliated Hospital, The Chinese University of Hong Kong, Shenzhen, China.
  • Xia J; The Third School of Clinical Medicine, Southern Medical University, Guangzhou, China.
  • Zhao Y; School of Laboratory Medicine and Biotechnology, Southern Medical University, Guangzhou, China.
  • Yang R; Anhui University of Science and Technology Affiliated Fengxian Hospital, Shanghai, China.
  • Feng J; Anhui University of Science and Technology Affiliated Fengxian Hospital, Shanghai, China.
  • Ma X; School of Laboratory Medicine and Biotechnology, Southern Medical University, Guangzhou, China.
  • Li J; The Second Affiliated Hospital, The Chinese University of Hong Kong, Shenzhen, China.
FEBS Open Bio ; 14(3): 444-454, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38151757
ABSTRACT
SETDB2 is a H3K9 histone methyltransferase required for accurate chromosome segregation. Its H3K9 histone methyltransferase activity was reported to be associated with chromosomes during metaphase. Here, we confirm that SETDB2 is required for mitosis and accurate chromosome segregation. However, these functions are independent of its histone methyltransferase activity. Further analysis showed that SETDB2 can interact with BUBR1, and is required for CDC20 binding to BUBR1 and APC/C complex and CYCLIN B1 degradation. The ability of SETDB2 to regulate the binding of CDC20 to BUBR1 or APC/C complex, and stabilization of CYCLIN B1 are also independent of its histone methyltransferase activity. These results suggest that SETDB2 interacts with BUBR1 to promote binding of CDC20 to BUBR1 and APC3, then degrades CYCLIN B1 to ensure accurate chromosome segregation and mitosis, independently of its histone methyltransferase activity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Serina-Treonina Quinases / Segregação de Cromossomos Idioma: En Revista: FEBS Open Bio Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Serina-Treonina Quinases / Segregação de Cromossomos Idioma: En Revista: FEBS Open Bio Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido