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Overlapping RdDM and non-RdDM mechanisms work together to maintain somatic repression of a paramutagenic epiallele of maize pericarp color1.重叠的RNA指导的DNA甲基化(RdDM)和非RdDM机制共同作用,以维持玉米果皮颜色1的一个副突变表等位基因的体细胞抑制。
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本文引用的文献

1
A paramutation phenomenon is involved in the genetics of maize low phytic acid1-241 (lpa1-241) trait.一种副突变现象与玉米低植酸1-241(lpa1-241)性状的遗传学有关。
Heredity (Edinb). 2009 Mar;102(3):236-45. doi: 10.1038/hdy.2008.96. Epub 2008 Sep 10.
2
Targets of RNA-directed DNA methylation.RNA定向DNA甲基化的靶点。
Curr Opin Plant Biol. 2007 Oct;10(5):512-9. doi: 10.1016/j.pbi.2007.06.007. Epub 2007 Aug 16.
3
Noncoding RNAs and gene silencing.非编码RNA与基因沉默
Cell. 2007 Feb 23;128(4):763-76. doi: 10.1016/j.cell.2007.02.016.
4
Paramutation: from maize to mice.副突变:从玉米到小鼠
Cell. 2007 Feb 23;128(4):641-5. doi: 10.1016/j.cell.2007.02.007.
5
A Genetic Change Associated with the R Locus in Maize Which Is Directed and Potentially Reversible.与玉米R基因座相关的一种定向且可能可逆的基因变化。
Genetics. 1956 Nov;41(6):872-89. doi: 10.1093/genetics/41.6.872.
6
An RNA-dependent RNA polymerase is required for paramutation in maize.玉米的副突变需要一种依赖RNA的RNA聚合酶。
Nature. 2006 Jul 20;442(7100):295-8. doi: 10.1038/nature04884.
7
RNA-mediated non-mendelian inheritance of an epigenetic change in the mouse.RNA介导的小鼠表观遗传变化的非孟德尔遗传
Nature. 2006 May 25;441(7092):469-74. doi: 10.1038/nature04674.
8
Transcriptionally silenced transgenes in maize are activated by three mutations defective in paramutation.玉米中转录沉默的转基因被三个副突变缺陷型突变激活。
Genetics. 2006 Jul;173(3):1637-47. doi: 10.1534/genetics.106.058669. Epub 2006 May 15.
9
A REGULAR AND CONTINUING CONVERSION-TYPE PHENOMENON AT THE B LOCUS IN MAIZE.玉米B位点上一种规律且持续的转换型现象。
Proc Natl Acad Sci U S A. 1959 Jun;45(6):828-32. doi: 10.1073/pnas.45.6.828.
10
The mop1 (mediator of paramutation1) mutant progressively reactivates one of the two genes encoded by the MuDR transposon in maize.mop1(副突变介导因子1)突变体逐渐重新激活玉米中由MuDR转座子编码的两个基因之一。
Genetics. 2006 Jan;172(1):579-92. doi: 10.1534/genetics.105.051383. Epub 2005 Oct 11.

RNA依赖的RNA聚合酶是与玉米p1基因副突变相关的增强子介导的转录沉默所必需的。

RNA-dependent RNA polymerase is required for enhancer-mediated transcriptional silencing associated with paramutation at the maize p1 gene.

作者信息

Sidorenko Lyudmila, Chandler Vicki

机构信息

The BIO5 Institute and Department of Plant Sciences, University of Arizona, Tucson, Arizona 85721, USA.

出版信息

Genetics. 2008 Dec;180(4):1983-93. doi: 10.1534/genetics.108.095281. Epub 2008 Oct 9.

DOI:10.1534/genetics.108.095281
PMID:18845841
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2600936/
Abstract

Paramutation is the ability of an endogenous gene or a transgene to heritably silence another closely related allele or gene. At the maize p1 (pericarp color1) gene, paramutation is associated with decreases in transcript levels and reduced pigmentation of the endogenous allele that normally specifies red seed coat (pericarp) and cob pigmentation. Herein we demonstrate that this silencing occurs at the transcriptional level and that a specific enhancer fragment from p1 is sufficient to induce all aspects of paramutation. Further, we demonstrate that a mutation in the mop1 gene (mediator of paramutation1), which encodes a RNA-dependent RNA polymerase, is absolutely required for establishing the silencing associated with p1 paramutation. In contrast to its effects on other paramutation loci, the mop1 mutation does not immediately reactivate a previously silenced allele; several generations in the presence of the mop1 mutation are required. In addition, the mop1 mutation was also able to release tissue-specific silencing of another p1 allele that does not participate in paramutation, but does contain a tandem repeated structure and is likely regulated through epigenetic mechanisms. These results demonstrate that RNA-mediated gene-silencing mechanisms play key roles in p1 paramutation and the spectrum of roles for MOP1 is broadened to include tissue-specific expression patterns.

摘要

副突变是指一个内源基因或转基因能够遗传地沉默另一个密切相关的等位基因或基因的能力。在玉米的p1(果皮颜色1)基因中,副突变与转录水平的降低以及内源等位基因色素沉着的减少有关,该内源等位基因通常决定红色种皮(果皮)和穗轴色素沉着。在此我们证明这种沉默发生在转录水平,并且来自p1的一个特定增强子片段足以诱导副突变的所有方面。此外,我们证明编码RNA依赖性RNA聚合酶的mop1基因(副突变介导因子1)中的一个突变对于建立与p1副突变相关的沉默是绝对必需的。与其对其他副突变位点的影响相反,mop1突变不会立即重新激活一个先前沉默的等位基因;在存在mop1突变的情况下需要几代时间。此外,mop1突变还能够解除另一个不参与副突变但确实含有串联重复结构且可能通过表观遗传机制调控的p1等位基因的组织特异性沉默。这些结果表明RNA介导的基因沉默机制在p1副突变中起关键作用,并且MOP1的作用范围扩大到包括组织特异性表达模式。