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通过多线染色体DNA的显微切割和用非特异性引物进行聚合酶链式反应克隆果蝇基因组区域。

Cloning regions of the Drosophila genome by microdissection of polytene chromosome DNA and PCR with nonspecific primer.

作者信息

Wesley C S, Ben M, Kreitman M, Hagag N, Eanes W F

机构信息

Department of Ecology and Evolution, State University of New York, Stony Brook 11794.

出版信息

Nucleic Acids Res. 1990 Feb 11;18(3):599-603. doi: 10.1093/nar/18.3.599.

Abstract

A simple and rapid procedure to isolate clones carrying sequences from a specific region of the polytene chromosome of Drosophila is demonstrated. The procedure involves microdissection of the region of interest, amplification of the DNA by PCR using a primer designed to prime the synthesis nonspecifically, labeling of the amplified DNA using the random primer method, and screening of a standard library with the probe to identify and isolate clones carrying sequences homologous to the dissected region. This procedure has the potential to replace the difficult procedure of microcloning, as well as facilitate chromosome walking.

摘要

本文展示了一种简单快速的方法,用于从果蝇多线染色体的特定区域分离携带序列的克隆。该方法包括对感兴趣区域进行显微切割,使用设计用于非特异性引发合成的引物通过PCR扩增DNA,使用随机引物法标记扩增的DNA,以及用该探针筛选标准文库,以鉴定和分离携带与切割区域同源序列的克隆。该方法有可能取代困难的微克隆程序,并有助于染色体步移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c63/333467/afbe33300cc7/nar00187-0193-a.jpg

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