Identification of many microRNAs that copurify with polyribosomes in mammalian neurons

被引:446
作者
Kim, J
Krichevsky, A
Grad, Y
Hayes, GD
Kosik, KS
Church, GM
Ruvkun, G
机构
[1] Massachusetts Gen Hosp, Dept Mol Biol, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02114 USA
[3] Brigham & Womens Hosp, Dept Neurol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Lipper Ctr Computat Genet, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
关键词
translational control; noncoding RNA; messenger ribonucleoprotein complex (mRNP);
D O I
10.1073/pnas.2333854100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Localized translation in mammalian dendrites may play a role in synaptic plasticity and contribute to the molecular basis for learning and memory. The regulatory mechanisms that control localized translation in neurons are not well understood. We propose a role for microRNAs (miRNAs), a class of noncoding RNAs, as mediators of neuronal translational regulation. We have identified 86 miRNAs expressed in mammalian neurons, of which 40 have not previously been reported. A subset of these miRNAs exhibits temporally regulated expression in cortical cultures. Moreover, all of the miRNAs that were tested cofractionate with polyribosomes, the sites of active translation. These findings indicate that a large, diverse population of miRNAs may function to regulate translation in mammalian neurons.
引用
收藏
页码:360 / 365
页数:6
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