Liao X, Butow R A
Department of Biochemistry, University of Texas, Southwestern Medical Center, Dallas 75235.
Cell. 1993 Jan 15;72(1):61-71. doi: 10.1016/0092-8674(93)90050-z.
The expression of some nuclear genes is sensitive to the functional state of mitochondria, a process we term retrograde regulation. Here we show that retrograde regulation of the yeast CIT2 gene encoding peroxisomal citrate synthase depends on a new class of upstream activation site element (UASr) and two previously unidentified genes, RTG1 and RTG2. RTG1 encodes a protein of 177 amino acids with similarity to basic helix-loop-helix transcription factors that likely functions at the CIT2 UASr. RTG2 encodes a protein of 394 amino acids of unknown function. Cells containing null alleles of RTG1 and RTG2 are viable and respiratory competent. However, they are auxotrophic for glutamic or aspartic acid and cannot use acetate as a sole carbon source, suggesting that both the tricarboxylic acid and glyoxylate cycles are compromised. Thus, RTG1 and RTG2 are pivotal genes in controlling interorganelle communication between mitochondria, peroxisomes, and the nucleus.
一些核基因的表达对线粒体的功能状态敏感,我们将这一过程称为逆向调控。在此我们表明,酵母中编码过氧化物酶体柠檬酸合酶的CIT2基因的逆向调控依赖于一类新的上游激活位点元件(UASr)以及两个先前未鉴定的基因RTG1和RTG2。RTG1编码一个由177个氨基酸组成的蛋白质,与碱性螺旋-环-螺旋转录因子相似,可能在CIT2 UASr处发挥作用。RTG2编码一个由394个氨基酸组成的功能未知的蛋白质。含有RTG1和RTG2无效等位基因的细胞是有活力的且具有呼吸能力。然而,它们对谷氨酸或天冬氨酸营养缺陷,并且不能将乙酸盐作为唯一碳源利用,这表明三羧酸循环和乙醛酸循环均受到损害。因此,RTG1和RTG2是控制线粒体、过氧化物酶体和细胞核之间细胞器间通讯的关键基因。