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本文引用的文献

1
Genome-Scale Analysis of Programmed DNA Elimination Sites in Tetrahymena thermophila.《嗜热四膜虫中程序化 DNA 消除位点的全基因组分析》
G3 (Bethesda). 2011 Nov;1(6):515-22. doi: 10.1534/g3.111.000927. Epub 2011 Nov 1.
2
Keeping the soma free of transposons: programmed DNA elimination in ciliates.保持体细胞内无转座子:纤毛虫中的程序性 DNA 消除。
J Biol Chem. 2011 Oct 28;286(43):37045-52. doi: 10.1074/jbc.R111.276964. Epub 2011 Sep 13.
3
RNA-directed epigenetic regulation of DNA rearrangements.RNA 指导的 DNA 重排的表观遗传调控。
Essays Biochem. 2010 Sep 20;48(1):89-100. doi: 10.1042/bse0480089.
4
Purification of Tetrahymena nuclei by sedimentation at unit gravity.通过单位重力沉降法纯化四膜虫细胞核。
Cold Spring Harb Protoc. 2010 Apr;2010(4):pdb.prot4501. doi: 10.1101/pdb.prot4501.
5
A domesticated piggyBac transposase plays key roles in heterochromatin dynamics and DNA cleavage during programmed DNA deletion in Tetrahymena thermophila.家猪转座酶在嗜热四膜虫程序性 DNA 缺失过程中异染色质动态和 DNA 切割中发挥关键作用。
Mol Biol Cell. 2010 May 15;21(10):1753-62. doi: 10.1091/mbc.e09-12-1079. Epub 2010 Mar 31.
6
The Tetrahymena argonaute-binding protein Giw1p directs a mature argonaute-siRNA complex to the nucleus.四膜虫 Argonaute 结合蛋白 Giw1p 将成熟的 Argonaute-siRNA 复合物导向细胞核。
Cell. 2010 Mar 5;140(5):692-703. doi: 10.1016/j.cell.2010.02.010.
7
2'-O-methylation stabilizes Piwi-associated small RNAs and ensures DNA elimination in Tetrahymena.2'-O-甲基化可稳定与Piwi相关的小RNA,并确保四膜虫中的DNA消除。
RNA. 2009 Apr;15(4):675-85. doi: 10.1261/rna.1455509. Epub 2009 Feb 24.
8
Microarray analyses of gene expression during the Tetrahymena thermophila life cycle.嗜热四膜虫生命周期中基因表达的微阵列分析。
PLoS One. 2009;4(2):e4429. doi: 10.1371/journal.pone.0004429. Epub 2009 Feb 10.
9
Nascent RNA sequencing reveals widespread pausing and divergent initiation at human promoters.新生RNA测序揭示了人类启动子处广泛的暂停和分歧起始。
Science. 2008 Dec 19;322(5909):1845-8. doi: 10.1126/science.1162228. Epub 2008 Dec 4.
10
An epigenetic role for maternally inherited piRNAs in transposon silencing.母系遗传的piRNA在转座子沉默中的表观遗传作用。
Science. 2008 Nov 28;322(5906):1387-92. doi: 10.1126/science.1165171.

偏转录和小 RNA 的选择性降解塑造了四膜虫 DNA 消除的模式。

Biased transcription and selective degradation of small RNAs shape the pattern of DNA elimination in Tetrahymena.

机构信息

Institute of Molecular Biotechnology of the Austrian Academy of Sciences, Vienna, Austria.

出版信息

Genes Dev. 2012 Aug 1;26(15):1729-42. doi: 10.1101/gad.196493.112.

DOI:10.1101/gad.196493.112
PMID:22855833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3418590/
Abstract

The ciliated protozoan Tetrahymena undergoes extensive programmed DNA elimination when the germline micronucleus produces the new macronucleus during sexual reproduction. DNA elimination is epigenetically controlled by DNA sequences of the parental macronuclear genome, and this epigenetic regulation is mediated by small RNAs (scan RNAs [scnRNAs]) of ∼28-30 nucleotides that are produced and function by an RNAi-related mechanism. Here, we examine scnRNA production and turnover by deep sequencing. scnRNAs are produced exclusively from the micronucleus and nonhomogeneously from a variety of chromosomal locations. scnRNAs are preferentially derived from the eliminated sequences, and this preference is mainly determined at the level of transcription. Despite this bias, a significant fraction of scnRNAs is also derived from the macronuclear-destined sequences, and these scnRNAs are degraded during the course of sexual reproduction. These results indicate that the pattern of DNA elimination in the new macronucleus is shaped by the biased transcription in the micronucleus and the selective degradation of scnRNAs in the parental macronucleus.

摘要

纤毛虫四膜虫在有性生殖过程中,当生殖系小核产生新的大核时,会经历广泛的程序性 DNA 消除。DNA 消除受亲代大核基因组 DNA 序列的表观遗传控制,这种表观遗传调控是由约 28-30 个核苷酸的小 RNA(扫描 RNA [scnRNA])介导的,这些小 RNA 通过 RNAi 相关机制产生并发挥作用。在这里,我们通过深度测序检查 scnRNA 的产生和周转。scnRNA 仅从小核产生,并且从各种染色体位置不均匀产生。scnRNA 优先从已消除的序列中衍生,这种偏好主要在转录水平上决定。尽管存在这种偏差,但相当一部分 scnRNA 也来自大核定向序列,并且这些 scnRNA 在有性生殖过程中被降解。这些结果表明,新大核中的 DNA 消除模式是由小核中的偏转录和亲代大核中 scnRNA 的选择性降解共同决定的。