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小 RNA 谱分析及普通狨猴(一种模式灵长类动物)成年睾丸中 piRNA 簇的特征。

Small RNA profiling and characterization of piRNA clusters in the adult testes of the common marmoset, a model primate.

机构信息

Department of Molecular Biology, Keio University School of Medicine, Shinjuku-ku, Tokyo 160-8582, Japan.

Department of Physiology, Keio University School of Medicine, Shinjuku-ku, Tokyo 160-8582, Japan.

出版信息

RNA. 2014 Aug;20(8):1223-37. doi: 10.1261/rna.045310.114. Epub 2014 Jun 9.

DOI:10.1261/rna.045310.114
PMID:24914035
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4105748/
Abstract

Small RNAs mediate gene silencing by binding Argonaute/Piwi proteins to regulate target RNAs. Here, we describe small RNA profiling of the adult testes of Callithrix jacchus, the common marmoset. The most abundant class of small RNAs in the adult testis was piRNAs, although 353 novel miRNAs but few endo-siRNAs were also identified. MARWI, a marmoset homolog of mouse MIWI and a very abundant PIWI in adult testes, associates with piRNAs that show characteristics of mouse pachytene piRNAs. As in other mammals, most marmoset piRNAs are derived from conserved clustered regions in the genome, which are annotated as intergenic regions. However, unlike in mice, marmoset piRNA clusters are also found on the X chromosome, suggesting escape from meiotic sex chromosome inactivation by the X-linked clusters. Some of the piRNA clusters identified contain antisense-orientated pseudogenes, suggesting the possibility that pseudogene-derived piRNAs may regulate parental functional protein-coding genes. More piRNAs map to transposable element (TE) subfamilies when they have copies in piRNA clusters. In addition, the strand bias observed for piRNAs mapped to each TE subfamily correlates with the polarity of copies inserted in clusters. These findings suggest that pachytene piRNA clusters determine the abundance and strand-bias of TE-derived piRNAs, may regulate protein-coding genes via pseudogene-derived piRNAs, and may even play roles in meiosis in the adult marmoset testis.

摘要

小 RNA 通过结合 Argonaute/ Piwi 蛋白来介导基因沉默,从而调节靶 RNA。在这里,我们描述了食蟹猴(Callithrix jacchus)成年睾丸的小 RNA 图谱。成年睾丸中最丰富的小 RNA 类别是 piRNA,但也鉴定到了 353 个新的 miRNA 和少量的内源性 siRNA。MARWI 是食蟹猴的 MIWI 同源物,也是成年睾丸中非常丰富的 PIWI,它与表现出与小鼠减数前期 piRNA 特征的 piRNA 相关联。与其他哺乳动物一样,大多数食蟹猴 piRNA 来源于基因组中保守的簇状区域,这些区域被注释为基因间区。然而,与小鼠不同的是,食蟹猴 piRNA 簇也存在于 X 染色体上,这表明 X 连锁簇逃避了减数分裂性染色体失活。鉴定出的一些 piRNA 簇包含反义取向的假基因,这表明假基因衍生的 piRNA 可能调节亲本功能蛋白编码基因。当 piRNA 簇中存在拷贝时,更多的 piRNA 映射到转座元件(TE)亚家族。此外,映射到每个 TE 亚家族的 piRNA 的链偏倚与插入簇中的拷贝的极性相关。这些发现表明减数前期 piRNA 簇决定了 TE 衍生的 piRNA 的丰度和链偏倚,可能通过假基因衍生的 piRNA 调节蛋白编码基因,甚至可能在成年食蟹猴睾丸的减数分裂中发挥作用。

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