Esposito M S, Bruschi C V
Lawrence Berkeley Laboratory, University of California, Berkeley 94720.
Curr Genet. 1993 May-Jun;23(5-6):430-4. doi: 10.1007/BF00312630.
A leucine-requiring hybrid of Saccharomyces cerevisiae, homoallelic at the LEU1 locus (leu1-12/leu1-12) and heterozygous for three chromosome-VII genetic markers distal to the LEU1 locus, was employed to inquire: (1) whether spontaneous gene mutation and mitotic segregation of heterozygous markers occur in positive nonrandom association and (2) whether homozygous LEU1/LEU1 mutant diploids are generated. The results demonstrate that gene mutation of leu1-12 to LEU1 and mitotic segregation of heterozygous chromosome-VII markers occur in strong positive nonrandom association, suggesting that the stimulatory DNA lesion is both mutagenic and recombinogenic. In addition, genetic analysis of diploid Leu+ revertants revealed that approximately 3% of mutations of leu1-12 to LEU1 result in LEU1/LEU1 homozygotes. Red-white sectored Leu+ colonies exhibit genotypes that implicate post-replicational chromatid breakage and exchange near the site of leu1-12 reversion, chromosome loss, and subsequent restitution of diploidy, in the sequence of events leading to mutational homozygosis. By analogy, diploid cell populations can yield variants homozygous for novel recessive gene mutations at biologically significant rates. Mutational homozygosis may be relevant to both carcinogenesis and the evolution of asexual diploid organisms.
使用了一种酿酒酵母亮氨酸需求型杂种,其在LEU1位点为同型等位基因(leu1 - 12/leu1 - 12),并且在LEU1位点远端的三个VII号染色体遗传标记上为杂合子,以探究:(1)杂合标记的自发基因突变和有丝分裂分离是否以正向非随机关联发生,以及(2)是否产生纯合的LEU1/LEU1突变二倍体。结果表明,leu1 - 12突变为LEU1以及杂合的VII号染色体标记的有丝分裂分离以强正向非随机关联发生,这表明刺激性DNA损伤既是诱变的又是重组的。此外,对二倍体亮氨酸原养型回复体的遗传分析表明,leu1 - 12突变为LEU1的突变中约3%导致LEU1/LEU1纯合子。红白扇形的亮氨酸原养型菌落显示出的基因型暗示在leu1 - 12回复位点附近的复制后染色单体断裂和交换、染色体丢失以及随后的二倍体恢复,这是导致突变纯合化的事件顺序。以此类推,二倍体细胞群体可以以生物学上显著的速率产生新的隐性基因突变的纯合变体。突变纯合化可能与致癌作用和无性二倍体生物的进化都相关。