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大型人工染色体的扩增

Amplification of large artificial chromosomes.

作者信息

Smith D R, Smyth A P, Moir D T

机构信息

Department of Human Genetics, Collaborative Research, Inc., Bedford, MA 01730.

出版信息

Proc Natl Acad Sci U S A. 1990 Nov;87(21):8242-6. doi: 10.1073/pnas.87.21.8242.

Abstract

Yeast artificial chromosome cloning is an attractive technology for genomic mapping studies because very large DNA segments can be readily propagated. However, detailed analyses often require the extensive application of blotting-hybridization techniques because artificial chromosomes are normally present at only one copy per haploid genome. We have developed a cloning vector and host strain that alleviate this problem by permitting copy number amplification of artificial chromosomes. The vector includes a conditional centromere that can be turned on or off by changing the carbon source. Strong selective pressure for extra copies of the artificial chromosome can be applied by selecting for the expression of a heterologous thymidine kinase gene. When this system was used, artificial chromosomes ranging from about 100 to 600 kilobases in size were readily amplified 10- to 20-fold. The selective conditions did not induce obvious rearrangements in any of the clones tested. Reactivation of the centromere in amplified artificial chromosome clones resulted in stable maintenance of an elevated copy number for 20 generations. Applications of copy number control to various aspects of artificial chromosome analysis are addressed.

摘要

酵母人工染色体克隆对于基因组图谱研究而言是一项颇具吸引力的技术,因为非常大的DNA片段能够轻易地进行增殖。然而,详细分析往往需要广泛应用印迹杂交技术,这是由于人工染色体通常在每个单倍体基因组中仅以一个拷贝存在。我们已经开发出一种克隆载体和宿主菌株,通过允许人工染色体的拷贝数扩增来缓解这一问题。该载体包含一个可通过改变碳源来开启或关闭的条件性着丝粒。通过选择异源胸苷激酶基因的表达,可以对人工染色体的额外拷贝施加强大的选择压力。当使用这个系统时,大小约为100至600千碱基的人工染色体能够轻易地扩增10至20倍。在任何测试的克隆中,选择条件都未诱导明显的重排。在扩增的人工染色体克隆中着丝粒的重新激活导致高拷贝数稳定维持20代。文中还讨论了拷贝数控制在人工染色体分析各个方面的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1779/54931/dc6ce844c1e6/pnas01046-0067-a.jpg

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