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一个2.2千碱基的重复DNA片段与弗氏链霉菌中的DNA扩增相关。

A 2.2-kilobase repeated DNA segment is associated with DNA amplification in Streptomyces fradiae.

作者信息

Fishman S E, Rosteck P R, Hershberger C L

出版信息

J Bacteriol. 1985 Jan;161(1):199-206. doi: 10.1128/jb.161.1.199-206.1985.

Abstract

We have previously identified a 10.5-kilobase DNA sequence which is highly amplified and tandemly repeated in the mutant Streptomyces fradiae JS85. A library of DNA was prepared from S. fradiae T776, which does not contain amplified DNA. The library was screened by plaque hybridization to identify phage clones containing the unamplified 10.5-kilobase DNA sequence. Four phage isolates were identified which contained DNA homology to the amplified DNA sequence. This sequence was designated the amplifiable unit of DNA. None of the clones carried an entire amplifiable unit of DNA, and so overlapping regions were aligned to create a map of the entire region. Detailed restriction mapping identified a 2.2-kilobase direct repeat at the ends of the amplifiable unit of DNA. Analysis by Southern hybridization confirmed that the direct repeats were homologous to each other. The DNA of S. fradiae contained at least two additional copies of DNA that was homologous to the repeat sequence.

摘要

我们之前鉴定出一个10.5千碱基的DNA序列,它在突变型弗氏链霉菌JS85中高度扩增且串联重复。从不含扩增DNA的弗氏链霉菌T776制备了一个DNA文库。通过噬菌斑杂交对该文库进行筛选,以鉴定含有未扩增的10.5千碱基DNA序列的噬菌体克隆。鉴定出四个噬菌体分离株,它们的DNA与扩增的DNA序列具有同源性。该序列被指定为DNA的可扩增单元。没有一个克隆携带完整的DNA可扩增单元,因此将重叠区域进行比对以创建整个区域的图谱。详细的限制性图谱分析在DNA可扩增单元的末端鉴定出一个2.2千碱基的正向重复序列。Southern杂交分析证实这些正向重复序列彼此同源。弗氏链霉菌的DNA含有至少另外两个与重复序列同源的DNA拷贝。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62d7/214856/0dc63b1c6ce4/jbacter00224-0219-a.jpg

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