Posttranscriptional Crossregulation between Drosha and DGCR8

被引:327
作者
Han, Jinju [1 ]
Pedersen, Jakob S. [2 ]
Kwon, S. Chul [1 ]
Belair, Cassandra D. [3 ,4 ]
Kim, Young-Kook [1 ]
Yeom, Kyu-Hyeon [1 ]
Yang, Woo-Young [1 ]
Haussler, David [5 ]
Blelloch, Robert [3 ,4 ]
Kim, V. Narry [1 ]
机构
[1] Seoul Natl Univ, Sch Biol Sci, Seoul 151742, South Korea
[2] Univ Copenhagen, Dept Biol, Bioinformat Ctr, DK-2200 Copenhagen, Denmark
[3] Univ Calif San Francisco, Inst Regenerat Med, Ctr Reprod Sci, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Urol, San Francisco, CA 94143 USA
[5] Univ Calif Santa Cruz, Ctr Biomol Sci & Engn, Santa Cruz, CA 95064 USA
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
MICROPROCESSOR COMPLEX; MICRORNA BIOGENESIS; ALZHEIMERS-DISEASE; RNA INTERFERENCE; EXPRESSION; PROLIFERATION; DROSOPHILA; MIR-222; PATHWAY; CELLS;
D O I
10.1016/j.cell.2008.10.053
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 Drosha-DGCR8 complex, also known as Microprocessor, is essential for microRNA (miRNA) maturation. Drosha functions as the catalytic subunit, while DGCR8 (also known as Pasha) recognizes the RNA substrate. Although the action mechanism of this complex has been intensively studied, it remains unclear how Drosha and DGCR8 are regulated and if these proteins have any additional role(s) apart from miRNA processing. Here, we report that Drosha and DGCR8 regulate each other posttranscriptionally. The Drosha-DGCR8 complex cleaves the hairpin structures embedded in the DGCR8 mRNA and thereby destabilizes the mRNA. We further find that DGCR8 stabilizes the Drosha protein via protein-protein interaction. This crossregulation between Drosha and DGCR8 may contribute to the homeostatic control of miRNA biogenesis. Furthermore, microarray analyses suggest that a number of mRNAs may be downregulated in a Microprocessor-dependent, miRNA-independent manner. Our study reveals a previously unsuspected function of Microprocessor in mRNA stability control.
引用
收藏
页码:75 / 84
页数:10
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