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Mutator转座元件MuA2的克隆,MuA2是玉米a1-Mum2等位基因体细胞突变的一个假定调控因子。

Cloning of the Mutator transposable element MuA2, a putative regulator of somatic mutability of the a1-Mum2 allele in maize.

作者信息

Qin M M, Robertson D S, Ellingboe A H

机构信息

Department of Genetics, University of Wisconsin, Madison 53706.

出版信息

Genetics. 1991 Nov;129(3):845-54. doi: 10.1093/genetics/129.3.845.

DOI:10.1093/genetics/129.3.845
PMID:1661256
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1204751/
Abstract

The identification of the autonomous or transposase-encoding element of the Mutator (Mu) transposable element system of maize is necessary to the characterization of the system. We reported previously that a transcript homologous to the internal region of the MuA element is associated with activity of the Mutator system. We describe here the cloning of another Mu element, designated MuA2, that cosegregates with Mutator activity as assayed by somatic instability of the a1-Mum2 allele. The MuA2 element has features typical of the transposable elements of the Mutator family, including the 210-bp terminal inverted repeats. Several lines of evidence suggest that MuA2 is an autonomous or transposase-encoding element of the Mu family: (1) MuA2 cosegregates with a genetically defined element that regulates somatic mutability of the a1-Mum2 allele; (2) MuA2 is hypomethylated while most other MuA2-hybridizing sequences in the genome are extensively methylated; (3) the increase of the copy number of MuA2 is concomitant with the increase of regulator elements; (4) MuA2-like elements are found in Mutator lines but not in non-Mutator inbreds. We propose that autonomous or transposase-encoding elements of the Mu family may be structurally conserved and MuA2-like.

摘要

鉴定玉米Mutator(Mu)转座子系统的自主元件或转座酶编码元件对于该系统的特性描述至关重要。我们之前报道过,一种与MuA元件内部区域同源的转录本与Mutator系统的活性相关。我们在此描述另一种Mu元件MuA2的克隆,该元件与通过a1 - Mum2等位基因的体细胞不稳定性检测的Mutator活性共分离。MuA2元件具有Mutator家族转座子的典型特征,包括210bp的末端反向重复序列。几条证据表明MuA2是Mu家族的自主元件或转座酶编码元件:(1)MuA2与一个遗传定义的调节a1 - Mum2等位基因体细胞突变性的元件共分离;(2)MuA2发生低甲基化,而基因组中大多数其他与MuA2杂交的序列则被广泛甲基化;(3)MuA2拷贝数的增加与调节元件的增加同时发生;(4)在Mutator系中发现了MuA2样元件,但在非Mutator自交系中未发现。我们提出,Mu家族的自主元件或转座酶编码元件在结构上可能是保守的且类似MuA2。

相似文献

1
Cloning of the Mutator transposable element MuA2, a putative regulator of somatic mutability of the a1-Mum2 allele in maize.Mutator转座元件MuA2的克隆,MuA2是玉米a1-Mum2等位基因体细胞突变的一个假定调控因子。
Genetics. 1991 Nov;129(3):845-54. doi: 10.1093/genetics/129.3.845.
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本文引用的文献

1
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。
Genetics. 1986 Jul;113(3):765-73. doi: 10.1093/genetics/113.3.765.
2
Molecular cloning of the a1 locus of Zea mays using the transposable elements En and Mu1.利用转座元件En和Mu1对玉米a1基因座进行分子克隆。
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DNA insertion in the first intron of maize Adh1 affects message levels: cloning of progenitor and mutant Adh1 alleles.玉米醇脱氢酶1基因(Adh1)第一内含子中的DNA插入影响其信使核糖核酸水平:始祖和突变型Adh1等位基因的克隆
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4
Transposable element Mu1 is found in multiple copies only in Robertson's Mutator maize lines.转座因子Mu1仅在罗伯逊变异型玉米品系中以多个拷贝的形式存在。
J Mol Appl Genet. 1984;2(6):519-24.
5
Nucleotide sequence of the maize transposable element Mul.玉米转座因子Mul的核苷酸序列。
Nucleic Acids Res. 1984 Aug 10;12(15):5955-67. doi: 10.1093/nar/12.15.5955.
6
Inactivation of the maize transposable element Activator (Ac) is associated with its DNA modification.玉米转座因子激活子(Ac)的失活与其DNA修饰有关。
EMBO J. 1987 Feb;6(2):295-302. doi: 10.1002/j.1460-2075.1987.tb04753.x.
7
Molecular analysis of the maize anthocyanin regulatory locus C1.玉米花青素调控位点C1的分子分析
Proc Natl Acad Sci U S A. 1986 Dec;83(24):9631-5. doi: 10.1073/pnas.83.24.9631.
8
DNA modification of a maize transposable element correlates with loss of activity.玉米转座元件的DNA修饰与活性丧失相关。
Proc Natl Acad Sci U S A. 1986 Mar;83(6):1767-71. doi: 10.1073/pnas.83.6.1767.
9
The Mu transposable elements of maize: evidence for transposition and copy number regulation during development.玉米的Mu转座元件:发育过程中转座及拷贝数调控的证据
Genetics. 1986 Jan;112(1):107-19. doi: 10.1093/genetics/112.1.107.
10
Molecular characterization of suppressor-mutator (Spm)-induced mutations at the bronze-1 locus in maize: the bz-m13 alleles.玉米青铜-1位点上抑制突变体(Spm)诱导突变的分子特征:bz-m13等位基因
Basic Life Sci. 1988;47:261-78. doi: 10.1007/978-1-4684-5550-2_19.