Developmental Timing of mRNA Translation-Integration of Distinct Regulatory Elements

被引:33
作者
Macnicol, Melanie C. [1 ]
Macnicol, Angus M. [1 ]
机构
[1] Univ Arkansas Med Sci, Dept Neurobiol & Dev Sci, Little Rock, AR 72205 USA
基金
美国国家卫生研究院;
关键词
XENOPUS OOCYTE MATURATION; BINDING PROTEIN MUSASHI-1; CYTOPLASMIC POLYADENYLATION; CELL-CYCLE; C-MOS; MEIOTIC MATURATION; MAP KINASE; IN-VITRO; CPEB ACTIVATION; GERM-CELLS;
D O I
10.1002/mrd.21191
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
Targeted mRNA translation is emerging as a critical mechanism to control gene expression during developmental processes. Exciting new findings have revealed a critical role for regulatory elements within the mRNA untranslated regions to direct the timing of mRNA translation. Regulatory elements can be targeted by sequence-specific binding proteins to direct either repression or activation of mRNA translation in response to developmental signals. As new regulatory elements continue to be identified it has become clear that targeted mRNAs can contain multiple regulatory elements, directing apparently contradictory translational patterns. How is this complex regulatory input integrated? In this review, we focus on a new challenge area how sequence-specific RNA binding proteins respond to developmental signals and functionally integrate to regulate the extent and timing of target mRNA translation. We discuss current understanding with a particular emphasis on the control of cell cycle progression that is mediated through a complex interplay of distinct mRNA regulatory elements during Xenopus oocyte maturation.
引用
收藏
页码:662 / 669
页数:8
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