Zelikson R, Luzzati M
Mol Cell Biol. 1982 Apr;2(4):457-66. doi: 10.1128/mcb.2.4.457-466.1982.
The Saccharomyces cerevisiae tmp3 mutant is deficient in the mitochondrial enzyme complex that participates in the formation of one-carbon-group-tetrahydrofolate coenzymes, serine transhydroxymethylase, dihydrofolate reductase, and thymidylate synthetase, thus leading to multiple nutritional requirements of dTMP, adenine, histidine, and methionine. The tmp3 mutant quickly loses its mitochondrial genome even when grown on fully supplemented medium or on a high concentration of 5-formyl tetrahydrofolate, which replaces all the four requirements. A study of the loss of the mitochondrial genome by following several mitochondrial genetic markers showed that there was a preferential specific loss of a large region of the mitochondrial genome, covering mit ts983, Er, Cr, and mit ts982 up to OrI, and retention of the region of Pr and mit tscs1297. A kinetic study showed that there was a preferentially rapid loss of the region covering the mit+ alleles ts983 to tscs902 at the rate of 10% per generation.
酿酒酵母tmp3突变体在参与一碳基团四氢叶酸辅酶形成的线粒体酶复合物、丝氨酸转羟甲基酶、二氢叶酸还原酶和胸苷酸合成酶方面存在缺陷,从而导致对dTMP、腺嘌呤、组氨酸和蛋氨酸的多种营养需求。即使在完全补充培养基上或在高浓度的5-甲酰四氢叶酸上生长,tmp3突变体也会迅速丢失其线粒体基因组,5-甲酰四氢叶酸可替代所有这四种需求。通过追踪几个线粒体遗传标记对线粒体基因组丢失的研究表明,线粒体基因组的一个大区域存在优先特异性丢失,该区域覆盖mit ts983、Er、Cr以及直至OrI的mit ts982,而Pr和mit tscs1297区域得以保留。动力学研究表明,覆盖mit+等位基因ts983至tscs902的区域以每代10%的速率优先快速丢失。