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Mu 杀手介导的和自发的玉米突变子家族转座元件沉默定义了不同的表观遗传失活途径。

Mu killer-Mediated and Spontaneous Silencing of Zea mays Mutator Family Transposable Elements Define Distinctive Paths of Epigenetic Inactivation.

机构信息

Department of Biology, Stanford University Stanford, CA, USA.

出版信息

Front Plant Sci. 2012 Sep 13;3:212. doi: 10.3389/fpls.2012.00212. eCollection 2012.

DOI:10.3389/fpls.2012.00212
PMID:22993515
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3440606/
Abstract

Mu killer contains a partial inverted duplication of the mudrA transposase gene and two copies of the terminal inverted repeat A (TIRA) region of the master MuDR element of maize. Mu killer can effectively silence single copy MuDR/Mu lines, and it is proposed that a ∼4 kb hairpin RNA is generated by read through transcription from a flanking gene and that this transcript serves as a substrate for siRNA production. Mu killer was sequenced, except for a recalcitrant portion in the center of the locus, and shown to be co-linear with mudrA as originally proposed. The ability of the dominant Mu killer locus to silence a standard high copy number MuDR/Mu transposon line was evaluated. After two generations of exposure, about three quarters of individuals were silenced indicating reasonable effectiveness as measured by the absence of mudrA transposase transcripts. Mu killer individuals that effectively silenced MuDR expressed two short antisense transcripts. In contrast, Mu killer individuals that failed to silence MuDR expressed multiple sense transcripts, derived from read through transcription initiating in a flanking gene, but no antisense transcripts were detected.

摘要

Mu 杀手含有玉米 MuDR 主元件末端反向重复 A(TIRA)区域的两个拷贝和 mudrA 转座酶基因的部分反向重复。Mu 杀手可以有效地沉默单拷贝 MuDR/Mu 系,据推测,一个约 4kb 的发夹 RNA 是由侧翼基因的通读转录产生的,该转录物作为 siRNA 产生的底物。Mu 杀手进行了测序,除了位于基因座中心的一个顽固部分外,与最初提出的 mudrA 共线性。显性 Mu 杀手基因座沉默标准高拷贝数 MuDR/Mu 转座子系的能力进行了评估。经过两代暴露,大约四分之三的个体被沉默,表明沉默效果合理,因为没有检测到 mudrA 转座酶转录本。有效沉默 MuDR 的 Mu 杀手个体表达了两个短的反义转录本。相比之下,未能沉默 MuDR 的 Mu 杀手个体表达了多个正义转录本,这些转录本来源于侧翼基因起始的通读转录,但未检测到反义转录本。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/0f9125e624ec/fpls-03-00212-a001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/97755ea30e99/fpls-03-00212-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/77afdd40a29f/fpls-03-00212-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/633bd0be5d5e/fpls-03-00212-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/86f760028bbc/fpls-03-00212-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/2ac72046be81/fpls-03-00212-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/6e90c28fbe6f/fpls-03-00212-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/fa77eda9f155/fpls-03-00212-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/3799d46d5f7b/fpls-03-00212-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/489d9e141209/fpls-03-00212-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/0f9125e624ec/fpls-03-00212-a001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/97755ea30e99/fpls-03-00212-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/77afdd40a29f/fpls-03-00212-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/633bd0be5d5e/fpls-03-00212-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/86f760028bbc/fpls-03-00212-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/2ac72046be81/fpls-03-00212-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/6e90c28fbe6f/fpls-03-00212-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/fa77eda9f155/fpls-03-00212-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/3799d46d5f7b/fpls-03-00212-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/489d9e141209/fpls-03-00212-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/966a/3440606/0f9125e624ec/fpls-03-00212-a001.jpg

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本文引用的文献

1
Extraction of DNA from milligram amounts of fresh, herbarium and mummified plant tissues.从新鲜植物组织、标本植物组织和木乃伊植物组织中提取毫克级 DNA。
Plant Mol Biol. 1985 Mar;5(2):69-76. doi: 10.1007/BF00020088.
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Mutator transposon activity reprograms the transcriptomes and proteomes of developing maize anthers.诱变转座子活性对发育中的玉米花药的转录组和蛋白质组进行重编程。
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Epigenetic silencing and unstable inheritance of MuDR activity monitored at four bz2-mu alleles in maize (Zea mays L.).
在玉米(Zea mays L.)的四个bz2-mu等位基因处监测到的MuDR活性的表观遗传沉默和不稳定遗传。
Genes Genet Syst. 2007 Oct;82(5):387-401. doi: 10.1266/ggs.82.387.
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Genetic studies on the loss of mu mutator activity in maize.玉米中 mu 突变子失活的遗传研究。
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Initiation, establishment, and maintenance of heritable MuDR transposon silencing in maize are mediated by distinct factors.玉米中可遗传的MuDR转座子沉默的起始、建立和维持由不同因素介导。
PLoS Biol. 2006 Oct;4(10):e339. doi: 10.1371/journal.pbio.0040339.
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Heritable transposon silencing initiated by a naturally occurring transposon inverted duplication.由自然发生的转座子反向重复引发的可遗传转座子沉默。
Nat Genet. 2005 Jun;37(6):641-4. doi: 10.1038/ng1576. Epub 2005 May 22.
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Mu killer causes the heritable inactivation of the Mutator family of transposable elements in Zea mays.Mu杀手导致玉米中转座因子Mutator家族的遗传性失活。
Genetics. 2003 Oct;165(2):781-97. doi: 10.1093/genetics/165.2.781.
9
Deletion derivatives of the MuDR regulatory transposon of maize encode antisense transcripts but are not dominant-negative regulators of mutator activities.玉米MuDR调控转座子的缺失衍生物编码反义转录本,但不是突变体活性的显性负调控因子。
Plant Cell. 2003 Oct;15(10):2430-47. doi: 10.1105/tpc.014605. Epub 2003 Sep 24.
10
Initiation of silencing of maize MuDR/Mu transposable elements.玉米MuDR/Mu转座元件沉默的起始
Plant J. 2003 Mar;33(6):1013-25. doi: 10.1046/j.1365-313x.2003.01683.x.