Smart E J, Selman B R
Department of Cell Biology, Texas Southwestern Medical Center, Dallas 75235-9053.
J Bioenerg Biomembr. 1993 Jun;25(3):275-84. doi: 10.1007/BF00762588.
Chlamydomonas reinhardtii strain atpC1 is a mutant defective in the nuclear gene that encodes the CF1 ATP synthase gamma-subunit polypeptide. Photoautotrophic growth was restored to atpC1 after it was transformed with wild-type DNA. Transformed strains were acetate-independent and arsenate-sensitive, similar in phenotype to the progenitor wild-type strain from which atpC1 was generated. Three transformed strains were examined in detail. Southern blot analyses demonstrated that the transformants were complements and not revertants. The transforming DNA integrated into the nuclear genome in a nonhomologous manner and at a low copy number. Northern blot analyses showed that the gamma-subunit mRNA in the complemented strains was expressed at the same relative level as that of wild-type. Western blots of total protein showed that whereas atpC1 was unable to synthesize any CF1 gamma-subunit, all three complemented strains could. Furthermore, the Western blot analyses demonstrated that the mutation in atpC1 had a pleiotropic effect on the accumulation of the CF1 beta-subunit which was relieved upon complementation. Cell extracts from atpC1 did not have any CF1-dependent catalytic activity, whereas extracts from all of the complemented strains and the wild-type strain had identical activities.
莱茵衣藻菌株atpC1是一种核基因缺陷型突变体,该核基因编码CF1 ATP合酶γ亚基多肽。用野生型DNA转化atpC1后,其光自养生长得以恢复。转化后的菌株不依赖乙酸盐且对砷酸盐敏感,其表型与产生atpC1的原始野生型菌株相似。对三个转化菌株进行了详细研究。Southern印迹分析表明,转化体是互补体而非回复体。转化DNA以非同源方式且低拷贝数整合到核基因组中。Northern印迹分析表明,互补菌株中的γ亚基mRNA表达水平与野生型相同。总蛋白的Western印迹显示,atpC1无法合成任何CF1γ亚基,而所有三个互补菌株都可以。此外,Western印迹分析表明,atpC1中的突变对CF1β亚基的积累具有多效性作用,互补后这种作用得以缓解。atpC1的细胞提取物没有任何CF1依赖性催化活性,而所有互补菌株和野生型菌株的提取物具有相同的活性。