| Literature DB >> 25320077 |
Nicole Ortogero1, Andrew S Schuster1, Daniel K Oliver1, Connor R Riordan1, Annie S Hong1, Grant W Hennig1, Dickson Luong1, Jianqiang Bao1, Bhupal P Bhetwal1, Seungil Ro1, John R McCarrey2, Wei Yan3.
Abstract
PIWI-interacting RNAs (piRNAs) are small noncoding RNAs that bind PIWI family proteins exclusively expressed in the germ cells of mammalian gonads. MIWI2-associated piRNAs are essential for silencing transposons during primordial germ cell development, and MIWI-bound piRNAs are required for normal spermatogenesis during adulthood in mice. Although piRNAs have long been regarded as germ cell-specific, increasing lines of evidence suggest that somatic cells also express piRNA-like RNAs (pilRNAs). Here, we report the detection of abundant pilRNAs in somatic cells, which are similar to MIWI-associated piRNAs mainly expressed in pachytene spermatocytes and round spermatids in the testis. Based on small RNA deep sequencing and quantitative PCR analyses, pilRNA expression is dynamic and displays tissue specificity. Although pilRNAs are similar to pachytene piRNAs in both size and genomic origins, they have a distinct ping-pong signature. Furthermore, pilRNA biogenesis appears to utilize a yet to be identified pathway, which is different from all currently known small RNA biogenetic pathways. In addition, pilRNAs appear to preferentially target the 3'-UTRs of mRNAs in a partially complementary manner. Our data suggest that pilRNAs, as an integral component of the small RNA transcriptome in somatic cell lineages, represent a distinct population of small RNAs that may have functions similar to germ cell piRNAs.Entities:
Keywords: Gene Regulation; RNA; RNA Interference (RNAi); Somatic Cell Genetics; Transposable Element (TE)
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Year: 2014 PMID: 25320077 PMCID: PMC4239631 DOI: 10.1074/jbc.M114.613232
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157