The BRCA1/BARD1-Interacting Protein OLA1 Functions in Centrosome Regulation

被引:62
作者
Matsuzawa, Ayako [1 ]
Kanno, Shin-ichiro [2 ]
Nakayama, Masahiro [1 ]
Mochiduki, Hironori [1 ]
Wei, Leizhen [1 ]
Shimaoka, Tatsuro [4 ]
Furukawa, Yumiko [1 ]
Kato, Kei [1 ]
Shibata, Shun [1 ]
Yasui, Akira [2 ]
Ishioka, Chikashi [3 ]
Chiba, Natsuko [1 ]
机构
[1] Tohoku Univ, IDAC, Dept Mol Immunol, Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Tohoku Univ, IDAC, Div Dynam Proteome Canc & Aging, Aoba Ku, Sendai, Miyagi 9808575, Japan
[3] Tohoku Univ, IDAC, Dept Clin Oncol, Aoba Ku, Sendai, Miyagi 9808575, Japan
[4] Saitama Canc Ctr, Res Inst Clin Oncol, Ina, Saitama 3620806, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
OXIDATIVE STRESS-RESPONSE; NUCLEAR-EXPORT-SIGNAL; OBG-LIKE ATPASE; GAMMA-TUBULIN; BRCA1-DEPENDENT UBIQUITINATION; MICROTUBULE NUCLEATION; CELL-CYCLE; BRCA1; IDENTIFICATION; BREAST;
D O I
10.1016/j.molcel.2013.10.028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The breast and ovarian cancer-specific tumor suppressor BRCA1, along with its heterodimer partner BRCA1-associated RING domain protein (BARD1), plays important roles in DNA repair, centrosome regulation, and transcription. To explore further functions of BRCA1/BARD1, we performed mass spectrometry analysis and identified Obg-like ATPase 1 (OLA1) as a protein that interacts with the carboxy-terminal region of BARD1. OLA1 directly bound to the amino-terminal region of BRCA1 and g-tubulin. OLA1 localized to centrosomes in interphase and to the spindle pole in mitotic phase, and its knockdown resulted in centrosome amplification and the activation of microtubule aster formation. OLA1 with a mutation observed in breast cancer cell line, E168Q, failed to bind BRCA1 and rescue the OLA1 knockdown-induced centrosome amplification. BRCA1 variant I42V also abrogated the binding of BRCA1 to OLA1. These findings suggest that OLA1 plays an important role in centrosome regulation together with BRCA1.
引用
收藏
页码:101 / 114
页数:14
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