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本文引用的文献

1
INO80 chromatin remodeling complex promotes the removal of UV lesions by the nucleotide excision repair pathway.INO80 染色质重塑复合物促进核苷酸切除修复途径去除 UV 损伤。
Proc Natl Acad Sci U S A. 2010 Oct 5;107(40):17274-9. doi: 10.1073/pnas.1008388107. Epub 2010 Sep 20.
2
PMS2 endonuclease activity has distinct biological functions and is essential for genome maintenance.PMS2 内切酶活性具有独特的生物学功能,对于基因组的维持是必不可少的。
Proc Natl Acad Sci U S A. 2010 Jul 27;107(30):13384-9. doi: 10.1073/pnas.1008589107. Epub 2010 Jul 12.
3
Mouse MOV10L1 associates with Piwi proteins and is an essential component of the Piwi-interacting RNA (piRNA) pathway.鼠 MOV10L1 与 Piwi 蛋白结合,是 Piwi 相互作用 RNA (piRNA) 途径的必需组成部分。
Proc Natl Acad Sci U S A. 2010 Jun 29;107(26):11841-6. doi: 10.1073/pnas.1003953107. Epub 2010 Jun 1.
4
BLM has early and late functions in homologous recombination repair in mouse embryonic stem cells.BLM 在小鼠胚胎干细胞的同源重组修复中有早期和晚期的功能。
Oncogene. 2010 Aug 19;29(33):4705-14. doi: 10.1038/onc.2010.214. Epub 2010 Jun 7.
5
Small RNA class transition from siRNA/piRNA to miRNA during pre-implantation mouse development.在小鼠胚胎植入前发育过程中,小 RNA 从 siRNA/piRNA 向 miRNA 的类别转变。
Nucleic Acids Res. 2010 Aug;38(15):5141-51. doi: 10.1093/nar/gkq229. Epub 2010 Apr 12.
6
Mechanisms of recombination between diverged sequences in wild-type and BLM-deficient mouse and human cells.野生型和 BLM 缺陷型小鼠和人细胞中分化序列间重组的机制。
Mol Cell Biol. 2010 Apr;30(8):1887-97. doi: 10.1128/MCB.01553-09. Epub 2010 Feb 12.
7
The TDRD9-MIWI2 complex is essential for piRNA-mediated retrotransposon silencing in the mouse male germline.TDRD9-MIWI2 复合物对于小鼠雄性生殖细胞中 piRNA 介导的逆转录转座子沉默是必需的。
Dev Cell. 2009 Dec;17(6):775-87. doi: 10.1016/j.devcel.2009.10.012.
8
A broadly conserved pathway generates 3'UTR-directed primary piRNAs.广泛保守的通路产生 3'UTR 导向的初级 piRNAs。
Curr Biol. 2009 Dec 29;19(24):2066-76. doi: 10.1016/j.cub.2009.11.064.
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Newly identified CHO ERCC3/XPB mutations and phenotype characterization.新鉴定的 CHO ERCC3/XPB 突变及表型特征。
Mutagenesis. 2010 Mar;25(2):179-85. doi: 10.1093/mutage/gep059. Epub 2009 Nov 25.
10
A regulatory circuit for piwi by the large Maf gene traffic jam in Drosophila.果蝇中大型Maf基因traffic jam对piwi的调控回路
Nature. 2009 Oct 29;461(7268):1296-9. doi: 10.1038/nature08501. Epub 2009 Oct 7.

piRNA 谱在小鼠精子发生特定阶段的分析。

piRNA profiling during specific stages of mouse spermatogenesis.

机构信息

State Key Laboratory of Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100080, China.

出版信息

RNA. 2011 Jul;17(7):1191-203. doi: 10.1261/rna.2648411. Epub 2011 May 20.

DOI:10.1261/rna.2648411
PMID:21602304
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3138557/
Abstract

PIWI-interacting RNAs (piRNAs) are a class of small RNAs abundantly expressed in animal gonads. piRNAs that map to retrotransposons are generated by a "ping-pong" amplification loop to suppress the activity of retrotransposons. However, the biogenesis and function of other categories of piRNAs have yet to be investigated. In this study, we first profiled the expression of small RNAs in type A spermatogonia, pachytene spermatocytes, and round spermatids by deep sequencing. We then focused on the computational analysis of the potential piRNAs generated in the present study as well as other published sets. piRNAs mapping to retrotransposons, mRNAs, and intergenic regions had different length distributions and were differentially regulated in spermatogenesis. piRNA-generating mRNAs (PRMRs), whose expression positively correlated with their piRNA products, constituted one-third of the protein-coding genes and were evolutionarily conserved and enriched with splicing isoforms and antisense transcripts. PRMRs with piRNAs preferentially mapped to CDSs and 3' UTRs partitioned into three clusters differentially expressed during spermatogenesis and enriched with unique sets of functional annotation terms related to housekeeping activities as well as spermatogenesis-specific processes. Intergenic piRNAs were divided into 2992 clusters probably representing novel transcriptional units that have not been reported. The transcripts of a large number of genes involved in spermatogenesis are the precursors of piRNAs, and these genes are intricately regulated by alternative splicing and antisense transcripts. piRNAs, whose regulatory role in gene expression awaits to be identified, are clearly products of a novel regulatory process that needs to be defined.

摘要

PIWI 相互作用 RNA(piRNAs)是一类在动物生殖腺中大量表达的小 RNA。映射到逆转录转座子的 piRNAs 通过“乒乓”扩增环产生,以抑制逆转录转座子的活性。然而,其他类别的 piRNAs 的生物发生和功能尚未得到研究。在这项研究中,我们首先通过深度测序对 A 型精原细胞、粗线期精母细胞和圆形精子中小 RNA 的表达进行了分析。然后,我们专注于对本研究中生成的潜在 piRNAs 以及其他已发表的数据集进行计算分析。映射到逆转录转座子、mRNA 和基因间区的 piRNAs 具有不同的长度分布,并在精子发生过程中受到不同的调控。piRNA 生成的 mRNA(PRMRs),其表达与其 piRNA 产物呈正相关,构成三分之一的蛋白质编码基因,具有进化保守性,并富含剪接异构体和反义转录本。具有 piRNA 的 PRMR 优先映射到 CDS 和 3'UTR,这些区域分为三个簇,在精子发生过程中表达差异,并富集了与管家活动以及精子发生特异性过程相关的独特功能注释术语集。基因间 piRNAs 分为 2992 个簇,可能代表尚未报道的新转录单元。大量参与精子发生的基因的转录本是 piRNAs 的前体,这些基因的表达受到选择性剪接和反义转录本的复杂调控。piRNAs 的基因表达调控作用有待确定,它们显然是一种新的调控过程的产物,需要进一步定义。