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关于基因重组的机制:重组中间体的电子显微镜观察

On the mechanism of genetic recombination: electron microscopic observation of recombination intermediates.

作者信息

Potter H, Dressler D

出版信息

Proc Natl Acad Sci U S A. 1976 Sep;73(9):3000-4. doi: 10.1073/pnas.73.9.3000.

DOI:10.1073/pnas.73.9.3000
PMID:787981
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC430907/
Abstract

This paper deals with the nature of recombination intermediates. Using the electron microscope to study the DNA of the plasmid colicin E1, we have observed more than 800 molecules that appear to represent intermediates in the process of recombination. Specifically, after isolating colicin DNA and linearizing it with the restriction enzyme EcoRI, we find crossed molecules with twice the normal colicin DNA content. These forms consist of two genome-length elements held together at a region of DNA homology. The molecules can be recovered from wild type and Rec B-C host cells but are not present among the colicin DNA forms isolated from recombination-deficient Rec A cells. We have termed the experimentally observed molecules "chi forms" and believe that they represent the recombination intermediate of the Holliday model.

摘要

本文探讨了重组中间体的性质。利用电子显微镜研究质粒大肠杆菌素E1的DNA,我们观察到800多个分子,它们似乎代表了重组过程中的中间体。具体而言,在分离大肠杆菌素DNA并用限制性内切酶EcoRI将其线性化后,我们发现了DNA含量为正常大肠杆菌素DNA两倍的交叉分子。这些形式由两个基因组长度的元件在DNA同源区域结合在一起组成。这些分子可以从野生型和Rec B-C宿主细胞中回收,但在从重组缺陷型Rec A细胞中分离的大肠杆菌素DNA形式中不存在。我们将实验观察到的分子称为“χ形式”,并认为它们代表了霍利迪模型的重组中间体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ac/430907/f06a3e524677/pnas00039-0064-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ac/430907/ddcde5ae4280/pnas00039-0062-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ac/430907/5b8445f1fb89/pnas00039-0063-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ac/430907/48a3b39b58be/pnas00039-0063-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ac/430907/f06a3e524677/pnas00039-0064-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ac/430907/ddcde5ae4280/pnas00039-0062-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ac/430907/5b8445f1fb89/pnas00039-0063-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ac/430907/48a3b39b58be/pnas00039-0063-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ac/430907/f06a3e524677/pnas00039-0064-a.jpg

相似文献

1
On the mechanism of genetic recombination: electron microscopic observation of recombination intermediates.关于基因重组的机制:重组中间体的电子显微镜观察
Proc Natl Acad Sci U S A. 1976 Sep;73(9):3000-4. doi: 10.1073/pnas.73.9.3000.
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Excision of a DNA sequence determining kanamycin resistance from a ColE1-Km recombinant plasmid.从ColE1-Km重组质粒中切除决定卡那霉素抗性的DNA序列。
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Replication of colicin E1 plasmid DNA in minicells from a unique replication initiation site.大肠杆菌素E1质粒DNA在来自独特复制起始位点的微小细胞中的复制。
Proc Natl Acad Sci U S A. 1974 Jun;71(6):2256-9. doi: 10.1073/pnas.71.6.2256.
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Replicative intermediates of colicin E1 plasmid DNA in minicells.微小细胞中大肠杆菌素E1质粒DNA的复制中间体
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Replication of colicin E1 plasmid DNA in cell extracts. Origin and direction of replication.大肠杆菌素E1质粒DNA在细胞提取物中的复制。复制起点及方向
Proc Natl Acad Sci U S A. 1974 Jun;71(6):2260-4. doi: 10.1073/pnas.71.6.2260.
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Discontinuous replication of colicin E1 plasmid deoxyribonucleic acid.大肠杆菌素E1质粒脱氧核糖核酸的不连续复制
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A DNA segment within the colicin E1 structural gene on ColE1 affecting immunity to colicin.大肠杆菌素E1上大肠杆菌素E1结构基因内的一段DNA,影响对大肠杆菌素的免疫性。
Mol Gen Genet. 1978 Sep 8;164(3):259-64. doi: 10.1007/BF00333155.
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Specialized transduction of colicin E1 DNA in Escherichia coli K-12.大肠杆菌K-12中大肠杆菌素E1 DNA的特异性转导
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Cleavage map of colicin E1 plasmid.大肠杆菌素E1质粒的切割图谱。
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引用本文的文献

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Search and processing of Holliday junctions within long DNA by junction-resolving enzymes.连接点解析酶对长 DNA 内 Holliday 连接点的搜索和处理。
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2
Changes in the architecture and abundance of replication intermediates delineate the chronology of DNA damage tolerance pathways at UV-stalled replication forks in human cells.在人类细胞中,复制叉因紫外线受阻时,复制中间体结构和丰度的变化可描绘出 DNA 损伤容忍途径的时间顺序。
Nucleic Acids Res. 2022 Sep 23;50(17):9909-9929. doi: 10.1093/nar/gkac746.
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The structural ensemble of a Holliday junction determined by X-ray scattering interference.

本文引用的文献

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