To localize or not to localize: mRNA fate is in 3′UTR ends

被引:304
作者
Andreassi, Catia [1 ,2 ]
Riccio, Antonella [1 ,2 ]
机构
[1] UCL, MRC Lab Mol & Cell Biol, London WC1E 6BT, England
[2] UCL, Dept Neurosci Physiol & Pharmacol, London WC1E 6BT, England
基金
英国医学研究理事会;
关键词
DENDRITIC TARGETING ELEMENT; ACTIVITY-DEPENDENT POLYADENYLATION; CIS-ACTING ELEMENTS; CYTOPLASMIC POLYADENYLATION; BINDING PROTEIN; TRANSLATIONAL CONTROL; GENE-EXPRESSION; ALTERNATIVE POLYADENYLATION; TRANSCRIPTION FACTORS; UNTRANSLATED REGIONS;
D O I
10.1016/j.tcb.2009.06.001
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Translation of localized mRNA is a fast and efficient way of reacting to extracellular stimuli with the added benefit of providing spatial resolution to the cellular response. The efficacy of this adaptive response ultimately relies on the ability to express a particular protein at the right time and in the right place. Although mRNA localization is a mechanism shared by most organisms, it is especially relevant in highly polarized cells, such as differentiated neurons. T-Untranslated regions (3'UTRs) of mRNAs are critical both for the targeting of transcripts to specific subcellular compartments and for translational control. Here we review recent studies that indicate how, in response to extracellular cues, nuclear and cytoplasmic remodeling of the 3'UTR contributes to mRNA localization and local protein synthesis.
引用
收藏
页码:465 / 474
页数:10
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