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本文引用的文献

1
Molecular analysis of ds controlling element mutations at the adh1 locus of maize.玉米 adh1 基因座 ds 控制元件突变的分子分析。
Science. 1984 Mar 23;223(4642):1265-8. doi: 10.1126/science.223.4642.1265.
2
Twin Mutations in Medium Variegated Pericarp Maize.中花斑纹果皮玉米中的双突变
Genetics. 1962 Apr;47(4):489-501. doi: 10.1093/genetics/47.4.489.
3
A chromosome replication pattern deduced from pericarp phenotypes resulting from movements of the transposable element, modulator, in maize.从可移动转座因子 modulator 引起的果皮表型变化推断出的染色体复制模式,在玉米中。
Genetics. 1984 Oct;108(2):471-85. doi: 10.1093/genetics/108.2.471.
4
Molecular analysis of paramutant plants of Antirrhinum majus and the involvement of transposable elements.金鱼草副突变体植株的分子分析及转座元件的作用
Mol Gen Genet. 1987 Oct;209(3):499-507. doi: 10.1007/BF00331156.
5
Plant transposable elements generate the DNA sequence diversity needed in evolution.植物转座元件产生进化所需的DNA序列多样性。
EMBO J. 1985 Mar;4(3):591-7. doi: 10.1002/j.1460-2075.1985.tb03671.x.
6
Transposition in plants: a molecular model.植物中的转座:一个分子模型。
EMBO J. 1985 Mar;4(3):585-90. doi: 10.1002/j.1460-2075.1985.tb03670.x.
7
Variable Patterns of Transposition of the Maize Element Activator in Tobacco.玉米激活因子元件在烟草中的可变转座模式
Plant Cell. 1991 May;3(5):473-482. doi: 10.1105/tpc.3.5.473.
8
Factors affecting the excision frequency of the maize transposable element Ds in Arabidopsis thaliana.影响玉米转座因子Ds在拟南芥中切除频率的因素。
Mol Gen Genet. 1993 Jul;240(1):65-72. doi: 10.1007/BF00276885.
9
The calf 5'- to 3'-exonuclease is also an endonuclease with both activities dependent on primers annealed upstream of the point of cleavage.小牛5'-至3'-外切核酸酶也是一种核酸内切酶,两种活性均依赖于在切割点上游退火的引物。
J Biol Chem. 1994 Jan 14;269(2):1191-6.
10
Analysis of the frequency of inheritance of transposed Ds elements in Arabidopsis after activation by a CaMV 35S promoter fusion to the Ac transposase gene.分析CaMV 35S启动子与Ac转座酶基因融合激活后拟南芥中转座Ds元件的遗传频率。
Mol Gen Genet. 1993 Dec;241(5-6):627-36. doi: 10.1007/BF00279905.

相邻序列影响玉米转座子切除过程中的DNA修复。

Adjacent sequences influence DNA repair accompanying transposon excision in maize.

作者信息

Scott L, LaFoe D, Weil C F

机构信息

Department of Biological Sciences, University of Idaho, Moscow 83844, USA.

出版信息

Genetics. 1996 Jan;142(1):237-46. doi: 10.1093/genetics/142.1.237.

DOI:10.1093/genetics/142.1.237
PMID:8770601
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1206952/
Abstract

Mobile elements transposing via DNA intermediates often leave small rearrangements, or "transposon footprints," at sites where they excise. Each excision event leaves its own footprint and, at any given site, these vary in size and sequence. Footprint formation involves DNA repair of sequences flanking the element. We have analyzed the footprints formed by a 2-kb Ds element excising from six different sites in exons of the maize waxy (Wx) gene. We find that groups of footprints left at individual sites are surprisingly nonrandom; different excision products predominate consistently at each site. Less frequent footprints left by each insertion appear related to the predominant type. The data suggest that flanking sequences affect the DNA repair processes associated with element excision. Two models have been proposed to explain footprint formation, one featuring a 5' exonuclease and the other featuring hairpin loop formation and an endonuclease. Our data have interesting implications for both these models. Evidence is also presented to support the presence of a separate excision mechanism that can remove Ac/Ds elements without leaving any footprint and that operates in parallel with the footprint-forming mechanism.

摘要

通过DNA中间体进行转座的移动元件通常会在其切除的位点留下小的重排,即“转座子足迹”。每次切除事件都会留下其自身的足迹,并且在任何给定位点,这些足迹的大小和序列各不相同。足迹形成涉及元件侧翼序列的DNA修复。我们分析了从玉米蜡质(Wx)基因外显子的六个不同位点切除的一个2kb Ds元件形成的足迹。我们发现,在各个位点留下的足迹组出人意料地并非随机;在每个位点,不同的切除产物始终占主导。每次插入留下的较少见的足迹似乎与主要类型相关。数据表明,侧翼序列会影响与元件切除相关的DNA修复过程。已经提出了两种模型来解释足迹形成,一种以5'核酸外切酶为特征,另一种以发夹环形成和内切酶为特征。我们的数据对这两种模型都有有趣的启示。还提供了证据来支持存在一种单独的切除机制,该机制可以去除Ac/Ds元件而不留下任何足迹,并且与形成足迹的机制并行运作。