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Transcriptome profiling of the developing male germ line identifies the miR-29 family as a global regulator during meiosis

机译:发育雄性细胞的转录组分析鉴定了MiR-29家族作为MeIosis期间的全球调节剂

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摘要

MicroRNAs are essential for spermatogenesis. However, the stage-specific requirements for particular miRNAs in the male mammalian germ line remain largely uncharacterized. The miR-34 family is, to date, the only miRNA proven to be necessary for the production of sperm in mammals, though its germline roles are poorly understood. Here, we generate and analyze paired small RNA and mRNA profiles across different stages of germline development in male mice, focusing on time points shortly before and during meiotic prophase I. We show that in addition to miR-34, miR-29 also mediates widespread repression of mRNA targets during meiotic prophase I in the male mouse germline. Furthermore, we demonstrate that predicted miR-29 target mRNAs in meiotic cells are largely distinct from those of miR-34, indicating that miR-29 performs a regulatory function independent of miR-34. Prior to this work, no germline role has been attributed to miR-29. To begin to understand roles for miR-29 in the germ line, we identify targets of miR-29 undergoing post transcriptional downregulation during meiotic prophase I, which likely correspond to the direct targets of miR-29. Interestingly, candidate direct targets of miR-29 are enriched in transcripts encoding extracellular matrix components. Our results implicate the miR-29 family as an important regulatory factor during male meiosis.
机译:microRNA对于精子发生至关重要。然而,雄性哺乳动物种系中特定miRNA的特定阶段特异性要求仍然很大程度上是无表的。迄今为止,MiR-34家族是唯一一项被证明的MiRNA在哺乳动物中产生精子,尽管其种系的角色知之甚少。在这里,我们在雄性小鼠中产生和分析不同阶段的配对的小型RNA和mRNA型材,在发光PRAPHase I之前不久和期间的时间点聚焦。除了MIR-34之外,MIR-29还介导广泛介绍在雄性小鼠芽髓中减少人性预防酶I的mRNA靶标。此外,我们证明预测的MIR-29在减数分裂细胞中的靶MRNA在很大程度上不同于miR-34的靶标mRNA,表明MiR-29独立于miR-34的调节功能。在这项工作之前,没有任何种子作用归因于miR-29。为了开始了解生殖器中miR-29的角色,我们识别在减少人类预言型IIOR-29的直接目标中经历转录后下调的MiR-29的目标。有趣的是,MiR-29的候选直程靶向编码细胞外基质组分的转录物中。我们的结果将MIR-29家族归因于雄性十分病期间的重要监管因素。

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