Identification of piRNAs in the central nervous system

被引:235
作者
Lee, Eun Joo [1 ,2 ]
Banerjee, Sourav [1 ,2 ]
Zhou, Hongjun [1 ,2 ]
Jammalamadaka, Aruna [3 ]
Arcila, Mary [1 ,2 ]
Manjunath, B. S. [3 ]
Kosik, Kenneth S. [1 ,2 ]
机构
[1] Univ Calif Santa Barbara, Neurosci Res Inst, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Dept Mol Cellular & Dev Biol, Santa Barbara, CA 93106 USA
[3] Univ Calif Santa Barbara, Dept Elect & Comp Engn, Santa Barbara, CA 93106 USA
基金
美国国家科学基金会;
关键词
piRNA; deep sequencing; dendrite; spine development; CYCLIN-DEPENDENT KINASE-5; TRANSFER-RNA GENES; DNA METHYLATION; STEM-CELLS; PIWI; PROTEIN; GERMLINE; PATHWAY; HOMOLOG; COMPLEX;
D O I
10.1261/rna.2565011
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
Piwi-interacting RNAs (piRNAs) are small noncoding RNAs generated by a conserved pathway. Their most widely studied function involves restricting transposable elements, particularly in the germline, where piRNAs are highly abundant. Increasingly, another set of piRNAs derived from intergenic regions appears to have a role in the regulation of mRNA from early embryos and gonads. We report a more widespread expression of a limited set of piRNAs and particularly focus on their expression in the hippocampus. Deep sequencing of extracted RNA from the mouse hippocampus revealed a set of small RNAs in the size range of piRNAs. These were confirmed by their presence in the piRNA database as well as coimmunoprecipitation with MIWI. Their expression was validated by Northern blot and in situ hybridization in cultured hippocampal neurons, where signal from one piRNA extended to the dendritic compartment. Antisense suppression of this piRNA suggested a role in spine morphogenesis. Possible targets include genes, which control spine shape by a distinctive mechanism in comparison to microRNAs.
引用
收藏
页码:1090 / 1099
页数:10
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