4.4 Article

Cloning and expression profiling of testis-expressed microRNAs

期刊

DEVELOPMENTAL BIOLOGY
卷 311, 期 2, 页码 592-602

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ydbio.2007.09.009

关键词

microRNAs; small RNAs; non-coding RNAs; germ cells; spermatogenesis; testis

资金

  1. NICHD NIH HHS [HD050281, R03 HD048855, R03 HD048855-01, R03 HD048855-02, HD048855, R01 HD050281] Funding Source: Medline

向作者/读者索取更多资源

Using a new small RNA cloning method, we identified 141 miRNAs from the mouse testis, of which 29 were novel. The 141 miRNAs were mapped onto all chromosomes except the Y chromosome and 2/3 of these miRNA genes exist as clusters. similar to 70% of these miRNA genes were located in intronic or intergenic regions, whereas the remaining miRNAs were derived from exonic sequences. We further validated these cloned miRNAs by examining their expression in multiple mouse organs including developing testes and also in purified spermatogenic cells using semi-quantitative PCR analyses. Our expression profiling assays revealed that 60% of the testis-expressed miRNAs were ubiquitously expressed and the remaining are either preferentially (35%) or exclusively (5%) expressed in the testis. We also observed a lack of strand selection during testicular miRNA biogenesis, characterized by paired expression of both the 5' strands and 3' strands derived from the same precursor miRNAs. The present work identified numerous miRNAs preferentially or exclusively expressed in the testis, which would be interesting targets for further functional studies. (C) 2007 Elsevier Inc. All rights reserved.

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