Schlesser A, Ulaszewski S, Ghislain M, Goffeau A
Unité de Biochimie Physiologique, Université de Louvain, Louvain-la-Neuve, Belgium.
J Biol Chem. 1988 Dec 25;263(36):19480-7.
A second transport ATPase gene from Saccharomyces cerevisiae has been identified by hybridization to a PMA1 probe and sequenced. The gene called PMA2 encodes a polypeptide of Mr = 102,157, which, with the exception of the 144 amino-terminal residues, is highly homologous to the structural gene PMA1 for the H+-ATPase. It is localized on the chromosome XVI at 16.7 centimorgan from gal4 and is not essential for haploid growth. Comparison between the upstream, noncoding DNA regions of PMA1 and PMA2 indicates that the two genes are controlled differently. The extensive amino acid sequence homology with the fungal H+-ATPases described so far indicates that the PMA2-encoded protein is also able to function as a H+ pump. This is supported by the observation that in pma1 mutants with reduced plasma membrane ATPase activity, disruption of the PMA2 gene confers the ability to grow under alkaline pH conditions. Slower development of diploids is also observed on normal minimal medium after bilateral disruption of PMA2 in the two parents.
通过与PMA1探针杂交,已经鉴定并测序了酿酒酵母的第二个转运ATP酶基因。这个名为PMA2的基因编码一种分子量为102,157的多肽,除了144个氨基末端残基外,它与H⁺-ATP酶的结构基因PMA1高度同源。它位于第XVI号染色体上,距离gal4基因16.7厘摩,对单倍体生长不是必需的。PMA1和PMA2上游非编码DNA区域的比较表明,这两个基因的调控方式不同。与迄今描述的真菌H⁺-ATP酶广泛的氨基酸序列同源性表明,PMA2编码的蛋白质也能够作为H⁺泵发挥作用。这一观点得到以下观察结果的支持:在质膜ATP酶活性降低的pma1突变体中,PMA2基因的破坏赋予了在碱性pH条件下生长的能力。在两个亲本中双侧破坏PMA2后,在正常基本培养基上也观察到二倍体的发育较慢。