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DNA复制的单分子分析

Single molecule analysis of DNA replication.

作者信息

Herrick J, Bensimon A

机构信息

Laboratoire de Biophysique de l'ADN, Département des Biotechnologies, Institut Pasteur, 25, rue du Dr.-Roux, 75724 Paris Cedex 15, France.

出版信息

Biochimie. 1999 Aug-Sep;81(8-9):859-71. doi: 10.1016/s0300-9084(99)00210-2.

Abstract

We describe here a novel approach for the study of DNA replication. The approach is based on a process called molecular combing and allows for the genome wide analysis of the spatial and temporal organization of replication units and replication origins in a sample of genomic DNA. Molecular combing is a process whereby molecules of DNA are stretched and aligned on a glass surface by the force exerted by a receding air/water interface. Since the stretching occurs in the immediate vicinity of the meniscus, all molecules are identically stretched in a size and sequence independent manner. The application of fluorescence hybridization to combed DNA results in a high resolution (1 to 4 kb) optical mapping that is simple, controlled and reproducible. The ability to comb up to several hundred haploid genomes on a single coverslip allows for a statistically significant number of measurements to be made. Direct labeling of replicating DNA sequences in turn enables origins of DNA replication to be visualized and mapped. These features therefore make molecular combing an attractive tool for genomic studies of DNA replication. In the following, we discuss the application of molecular combing to the study of DNA replication and genome stability.

摘要

我们在此描述一种研究DNA复制的新方法。该方法基于一种称为分子梳拉的过程,可对基因组DNA样本中复制单元和复制起点的空间和时间组织进行全基因组分析。分子梳拉是一个过程,通过后退的空气/水界面施加的力,使DNA分子在玻璃表面伸展并排列。由于伸展发生在弯月面的紧邻区域,所有分子都以大小和序列无关的方式被相同地拉伸。将荧光杂交应用于梳拉后的DNA可产生高分辨率(1至4 kb)的光学图谱,该图谱简单、可控且可重复。在单个盖玻片上梳拉多达数百个单倍体基因组的能力使得能够进行具有统计学意义的大量测量。对复制DNA序列的直接标记进而能够可视化并绘制DNA复制起点。因此,这些特性使分子梳拉成为DNA复制基因组研究的一个有吸引力的工具。在接下来的内容中,我们将讨论分子梳拉在DNA复制和基因组稳定性研究中的应用。

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