CDK1-Cyclin B1 Activates RNMT, Coordinating mRNA Cap Methylation with G1 Phase Transcription

被引:55
作者
Aregger, Michael [1 ,3 ]
Kaskar, Aneesa [1 ]
Varshney, Dhaval [1 ]
Fernandez-Sanchez, Maria Elena [1 ,4 ]
Inesta-Vaquera, Francisco A. [1 ]
Weidlich, Simone [2 ]
Cowling, Victoria H. [1 ]
机构
[1] Univ Dundee, Sch Life Sci, Ctr Gene Regulat & Express, MRC Phosphorylat & Ubiquitylat, Dundee DD1 5EH, Scotland
[2] Univ Dundee, Div Signal Transduct Therapy, Dundee DD1 5EH, Scotland
[3] Univ Toronto, Donnelly Ctr Cellular & Biomol Res, Toronto, ON M5S 3E1, Canada
[4] Inst Curie, Ctr Rech, Unite Physicochim Curie, Unites Mixtes Rech 168, F-75005 Paris, France
基金
英国医学研究理事会; 英国惠康基金;
关键词
CELL-CYCLE; STRUCTURAL INSIGHTS; POLYMERASE-II; METHYLTRANSFERASE; MECHANISM; BINDING; PROTEINS; COMPLEX; CODE;
D O I
10.1016/j.molcel.2016.02.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The creation of translation-competent mRNA is dependent on RNA polymerase II transcripts being modified by addition of the 7-methylguanosine (m7G) cap. The factors that mediate splicing, nuclear export, and translation initiation are recruited to the transcript via the cap. The cap structure is formed by several activities and completed by RNMT (RNA guanine-7 methyltransferase), which catalyzes N7 methylation of the cap guanosine. We report that CDK1-cyclin B1 phosphorylates the RNMT regulatory domain on T77 during G2/M phase of the cell cycle. RNMT T77 phosphorylation activates the enzyme both directly and indirectly by inhibiting interaction with KPNA2, an RNMT inhibitor. RNMT T77 phosphorylation results in elevated m7G cap methyltransferase activity at the beginning of G1 phase, coordinating mRNA capping with the burst of transcription that occurs following nuclear envelope reformation. RNMT T77 phosphorylation is required for the production of cohort of proteins, and inhibiting T77 phosphorylation reduces the cell proliferation rate.
引用
收藏
页码:734 / 746
页数:13
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