Bussereau F, Dupont C H, Boy-Marcotte E, Mallet L, Jacquet M
Université Paris-Sud, Institut de Génétique et de Microbiologie, Orsay, France.
Curr Genet. 1992 Apr;21(4-5):325-9. doi: 10.1007/BF00351690.
The ccs1-1 mutation of Saccharomyces cerevisiae, which has been previously described, is associated with an increase in cytochrome content, in respiration, and in ATP synthesis. In addition, this mutation leads to the same phenotype as cells de-regulated in the cAMP pathway. From a yeast genomic library, we have isolated a DNA fragment in a recombinant plasmid pCD1 which complements the ccs1-1 mutation. Homologous integration of this DNA in the genome occurs at the CCS1 locus. An 11 kb of the DNA insert is necessary for complementation. Sequencing part of the fragment identifies CCS1 as the IRA2 gene. The IRA2 gene is known to encode an attenuator of RAS gene product activity which stimulates the GTPase activity of the RAS proteins. This result underlines the involvement of cAMP-dependent phosphorylation in mitochondrial function. We present the sequence of 1 kb DNA upstream of the putative ATG of the IRA2/CCS1 gene product which is devoid of an ORF and could contain several regulatory sites.
先前已描述过的酿酒酵母ccs1-1突变,与细胞色素含量、呼吸作用及ATP合成的增加有关。此外,该突变导致的表型与cAMP途径失调的细胞相同。我们从酵母基因组文库中,在重组质粒pCD1中分离出一个能互补ccs1-1突变的DNA片段。该DNA在基因组中的同源整合发生在CCS1位点。11 kb的DNA插入片段是互补所必需的。对该片段部分测序确定CCS1为IRA2基因。已知IRA2基因编码一种RAS基因产物活性的衰减子,它能刺激RAS蛋白的GTP酶活性。这一结果强调了cAMP依赖性磷酸化在线粒体功能中的作用。我们给出了IRA2/CCS1基因产物推定的ATG上游1 kb DNA的序列,该序列没有开放阅读框,可能包含几个调控位点。