首页> 外文期刊>Biology of Reproduction: Offical Journal of the Society for the Study of Reproduction >Dramatic Changes in 67 miRNAs During Initiation of First Wave of Spermatogenesis in Mus musculus Testis: Global Regulatory Insights Generated by miRNA-mRNA Network Analysis
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Dramatic Changes in 67 miRNAs During Initiation of First Wave of Spermatogenesis in Mus musculus Testis: Global Regulatory Insights Generated by miRNA-mRNA Network Analysis

机译:在Mus Musculus Testis中第一波精子发生期间发生的67 miRNA的显着变化:MiRNA-mRNA网络分析产生的全球监管见解

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We mapped global changes in miRNA and mRNA profiles spanning the first wave of spermatogenesis using prepubertal (Postnatal Day 8 [P8]), pubertai (P16), and adolescent (P24) Mus musculus testes and identified the differential expression of 67 miRNAs and 8226 mRNAs. These two data sets were integrated into miRNA-deperident regulatory networks based on miRWalk predictions. In a network representing the P8 to P16 transition, downregulation of four miRNAs and upregulation of 19 miRNAs were linked with 81 upregulated target mRNAs and 228 downregulated target mRNAs, respectively. Furthermore, during the P16 to P24 transition, two miRNAs were downregulated, and eight miRNAs were upregulated, which linked with 64 upregulated mRNAs and 389 downregulated mRNAs, respectively. Only three of the miRNAs present in the network (miR-34b-5p, miR-34c, and miR-449a) showed a progressive increase from P8 through P16 to P24, while the remaining miRNAs in the network showed statistically significant changes in their levels either during the P8 to P16 transition or during the P16 to P24 transition. Analysis of the chromosomal location of these differentially expressed miRNAs showed that 14 out of 25 miRNAs upregulated from P8 to P16, and 18 out of 40 miRNAs upregulated from P8 to P24 were X-linked. This is suggestive of their escape from meiotic sex chromosome inactivation and postmeiotic sex chromatin. This integrated network of miRNA-level and mRNA-level changes in mouse testis during the first wave of spermatogenesis is expected to build a base for evaluating the role of miRNA-mediated gene expression regulation in maturing mammalian testis.
机译:我们使用Prepubertal(第8天[P8]),青少年(P16)和青少年(P24)Mus Musculus睾丸映射了MiRNA和mRNA谱的全局变化,并鉴定了67 miRNA和8226 mRNA的差异表达。这两个数据集基于miRWALK预测集成到MiRNA-Deperient Indoctionation网络中。在代表P8至P16过渡的网络中,四个miRNA的下调和19 miRNA的上调分别与81个上调的靶MRNA和228个下调的靶MRNA连接。此外,在P16至P24过渡期间,下调两种miRNA,上调了八个miRNA,其分别与64个上调的MRNA和389个下调的MRNA连接。网络中存在的MIRNA中只有三个(MIR-34B-5P,MIR-34C和MIR-449A)显示从P8到P16到P24的逐步增加,而网络中的剩余MIRNA在其水平上显示出统计上显着的变化在P8到P16期间或在P16期间转换到P24转变。这些差异表达MIRNA的染色体位置的分析表明,从P8至P16上调的25个miRNA中的14个,其中40个miRNA中的18个从P8到P24上调是X键。这促进了他们逃避的减少人性染色体灭活和后生育染色质。这种综合网络在第一波精子发生期间小鼠睾丸的MiRNA级和mRNA水平变化的变化是为了评估miRNA介导的基因表达调节在成熟哺乳动物睾丸中的作用的基础。

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