Cloning and expression profiling of testis-expressed microRNAs

被引:216
作者
Ro, Seungil
Park, Chanjae
Sanders, Kenton M.
McCarrey, John R.
Yan, Wei
机构
[1] Univ Nevada, Sch Med, Dept Physiol & Cell Biol, Reno, NV 89557 USA
[2] Univ Texas San Antonio, Dept Biol, San Antonio, TX 78249 USA
关键词
microRNAs; small RNAs; non-coding RNAs; germ cells; spermatogenesis; testis;
D O I
10.1016/j.ydbio.2007.09.009
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:592 / 602
页数:11
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