Koduri R, Ray D S
Mol Biochem Parasitol. 1984 Feb;10(2):151-60. doi: 10.1016/0166-6851(84)90003-3.
High frequency transformation of Saccharomyces cerevisiae was used as a functional assay to isolate autonomous replication sequences (ars) from the genomic and kinetoplast DNA of the insect trypanosomatid Crithidia fasciculata. Three independent cloned genomic sequences and one kinetoplast DNA sequence promoted high frequency transformation and extrachromosomal maintenance of the YIp5 plasmid DNA in yeast. The kinetoplast DNA clone was sub-cloned to further localize the DNA sequence essential for ars activity. This element was shown to be contained in a 2 kb HindIII-EcoRI fragment derived from a 8 kb HindIII fragment of the maxicircle component of the kinetoplast DNA. This 2 kb fragment is within a DNA sequence that has been shown to strongly hybridize to Trypanosoma brucei maxicircle DNA.
酿酒酵母的高频转化被用作一种功能分析方法,以从昆虫锥虫克氏锥虫的基因组和动质体DNA中分离自主复制序列(ars)。三个独立克隆的基因组序列和一个动质体DNA序列促进了酵母中YIp5质粒DNA的高频转化和染色体外维持。对动质体DNA克隆进行亚克隆,以进一步定位对ars活性至关重要的DNA序列。该元件被证明包含在一个2 kb的HindIII - EcoRI片段中,该片段源自动质体DNA大环成分的一个8 kb HindIII片段。这个2 kb的片段位于一个已被证明与布氏锥虫大环DNA强烈杂交的DNA序列内。