Ben-Aroya Shay, Pan Xuewen, Boeke Jef D, Hieter Philip
Michael Smith Laboratories, Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
Methods Enzymol. 2010;470:181-204. doi: 10.1016/S0076-6879(10)70008-2. Epub 2010 Mar 1.
The study of temperature-sensitive (Ts) mutant phenotypes is fundamental to gene identification and for dissecting essential gene function. In this chapter, we describe two "shuffling" methods for producing Ts mutants using a combination of PCR, in vivo recombination, and transformation of diploid strains heterozygous for a knockout of the desired mutation. The main difference between the two methods is the type of strain produced. In the "plasmid" version, the product is a knockout mutant carrying a centromeric plasmid carrying the Ts mutant. In the "chromosomal" version, The Ts alleles are integrated directly into the endogenous locus, albeit not in an entirely native configuration. Both variations have their strengths and weaknesses, which are discussed here.
对温度敏感(Ts)突变体表型的研究是基因鉴定和剖析必需基因功能的基础。在本章中,我们描述了两种“洗牌”方法,用于通过结合PCR、体内重组以及对所需突变敲除杂合的二倍体菌株进行转化来产生Ts突变体。这两种方法的主要区别在于产生的菌株类型。在“质粒”版本中,产物是一个敲除突变体,携带一个携带Ts突变体的着丝粒质粒。在“染色体”版本中,Ts等位基因直接整合到内源性位点,尽管并非完全处于天然构型。两种变体都有其优缺点,在此进行讨论。