Wenzlau J M, Perlman P S
Department of Molecular Genetics, Ohio State University, Columbus 43210.
Genetics. 1990 Sep;126(1):53-62. doi: 10.1093/genetics/126.1.53.
Yeast mtDNA contains two different kinds of mobile optional sequences, two group I introns and a short G + C-rich insertion to some var1 genes. Movement of each element in crosses has been called gene conversion though little is known about the mechanism of G + C cluster conversion. A new allele of the var1 gene found in mtDNA of Saccharomyces capensis is described that permitted a more detailed comparison between intron mobility and G + C cluster conversion. The S. capensis var1 gene lacks the cc+ element present in all S. cerevisiae var 1 genes and the previously described optional a+ element. In crosses with cc+ a- and cc+ a+ S. cerevisiae strains, both clusters were found to be mobile and, in the latter cross, appear to convert independently and only to homologous insertion sites. No evidence for flanking marker coconversion (a hallmark feature of intron conversion) was obtained despite the availability of nearby physical markers on both sides of cluster conversion sites. These data indicate that G + C cluster conversion has only a superficial resemblance to intron mobility; analogies to procaryotic transposition mechanisms are considered.
酵母线粒体DNA包含两种不同类型的可移动选择序列、两个I类内含子以及一些var1基因中的富含G + C的短插入序列。在杂交过程中,每个元件的移动都被称为基因转换,尽管对G + C簇转换的机制知之甚少。本文描述了在卡氏酵母线粒体DNA中发现的var1基因的一个新等位基因,它使得对内含子移动性和G + C簇转换进行更详细的比较成为可能。卡氏酵母var1基因缺乏所有酿酒酵母var1基因中存在的cc+元件以及先前描述的可选a+元件。在与cc+ a-和cc+ a+酿酒酵母菌株的杂交中,发现这两个簇都是可移动的,并且在后一种杂交中,它们似乎独立转换,并且仅转换到同源插入位点。尽管在簇转换位点两侧都有附近的物理标记,但未获得侧翼标记共转换的证据(内含子转换的一个标志性特征)。这些数据表明,G + C簇转换与内含子移动性仅表面相似;文中考虑了与原核转座机制的类比。