Georgakopoulos T, Koutroubas G, Vakonakis I, Tzermia M, Prokova V, Voutsina A, Alexandraki D
Foundation for Research and Technology-HELLAS, Institute of Molecular Biology and Biotechnology, PO Box 1527, Heraklion 711 10, Crete, Greece.
Yeast. 2001 Sep 15;18(12):1155-71. doi: 10.1002/yea.764.
Saccharomyces cerevisiae YFR021w, YGR223c and YPL100w are paralogous ORFs of unknown function. Phenotypic analysis of overexpression, single-, double- and triple-ORF deletion strains under various growth conditions indicated mitochondria-related functions for all three ORFs. Two-hybrid screens of a yeast genomic library identified potentially interacting proteins for the three ORFs. Among these, the transcriptional activator Rtg3p interacted with both Yfr021wp and Ypl100wp and both ORF single deletions reduced the constitutive expression of the RTG-regulated CIT2 and DLD3 genes and caused typical retrograde response of CIT2 and DLD3 under growth conditions requiring functional mitochondria, indicating that YFR021w and YPL100w are also involved in unidentified mitochondrial functions. Ptr3p, a component of the amino acid sensor Ssy1p/Ptr3p, was also found as a two-hybrid interactant of Yfr021wp. Of the three single-ORF deletions, ypl100w Delta exhibited ptr3 Delta-similar phenotypes. These findings, combined with the fact that RTG-dependent expression is modulated by specific amino acids, suggested possible relations of Yfr021wp and Ypl100wp to amino acid signalling pathways. Under most conditions examined, the effects of the single- and double-ORF deletions indicated that YFR021w, YPL100w and YGR223c are not parts of the same pathway. We found no unique phenotype attributed to the deletion of YGR223c. However, its function interferes with the function of the other two ORFs, as revealed by the effects of double- and triple-ORF deletions.
酿酒酵母YFR021w、YGR223c和YPL100w是功能未知的旁系同源开放阅读框。在各种生长条件下对过表达菌株、单开放阅读框缺失菌株、双开放阅读框缺失菌株和三开放阅读框缺失菌株进行的表型分析表明,这三个开放阅读框均具有与线粒体相关的功能。对酵母基因组文库进行的双杂交筛选确定了这三个开放阅读框可能相互作用的蛋白质。其中,转录激活因子Rtg3p与Yfr021wp和Ypl100wp都相互作用,并且两个开放阅读框的单缺失都降低了RTG调控的CIT2和DLD3基因的组成型表达,并在需要功能性线粒体的生长条件下导致CIT2和DLD3出现典型的逆行反应,这表明YFR021w和YPL100w也参与了未知的线粒体功能。氨基酸传感器Ssy1p/Ptr3p的组成部分Ptr3p也被发现是Yfr021wp的双杂交相互作用蛋白。在三个单开放阅读框缺失中,ypl100wΔ表现出与ptr3Δ相似的表型。这些发现,再加上RTG依赖性表达受特定氨基酸调节这一事实,表明Yfr021wp和Ypl100wp可能与氨基酸信号通路有关。在大多数检测条件下,单开放阅读框和双开放阅读框缺失的影响表明YFR021w、YPL100w和YGR223c不属于同一途径。我们没有发现YGR223c缺失所特有的表型。然而,如双开放阅读框和三开放阅读框缺失的影响所示,它的功能会干扰其他两个开放阅读框的功能。