Marathe S V, McEwen J E
GRECC (Geriatrics Research and Education Clinical Center), John L. McClellan Memorial VA Hospital, Little Rock, AR 72205, USA.
Biochem Mol Biol Int. 1999 Jun;47(6):971-7. doi: 10.1080/15216549900202093.
The nuclear PET122 gene of S. cerevisiae encodes a mitochondrial-localized protein that activates initiation of translation of the mitochondrial mRNA from the COX3 gene, which encodes subunit III of cytochrome c oxidase. The PET122 locus contains two divergent transcription units: one is involved in expression of PET122 mRNA and the mRNA for an adjacent gene OXA1, which is also required for cytochrome c oxidase biogenesis, and the other is involved in expression of an antisense RNA that is complementary to about two thirds of the PET122 mRNA and an adjacent gene YER152C of unknown function. Steady state levels of OXA1, PET122 sense and PET122 antisense RNAs were measured after growth of yeast cells under catabolite repressing or derepressing conditions, or after deletion of portions of the 5' flanking DNA of the genes. The results reported here indicate that the PET122 and OXA1 genes are unconventional in terms of the control of their transcription. Neither possesses a canonical TATA element and they exhibit no apparent need for native upstream DNA. These results raise the interesting possibility that PET122 and OXA1 transcription is controlled by downstream DNA, perhaps located within the coding regions of the respective genes.
酿酒酵母的核PET122基因编码一种定位于线粒体的蛋白质,该蛋白质可激活细胞色素c氧化酶亚基III的编码基因COX3的线粒体mRNA的翻译起始。PET122基因座包含两个不同的转录单元:一个参与PET122 mRNA和相邻基因OXA1的mRNA的表达,细胞色素c氧化酶生物合成也需要OXA1;另一个参与与PET122 mRNA约三分之二互补的反义RNA和功能未知的相邻基因YER152C的表达。在酵母细胞于分解代谢物阻遏或去阻遏条件下生长后,或在缺失基因5'侧翼DNA的部分序列后,测定了OXA1、PET122正义和PET122反义RNA的稳态水平。此处报道的结果表明,PET122和OXA1基因在转录控制方面是非传统的。它们都不具有典型的TATA元件,并且对天然上游DNA没有明显需求。这些结果提出了一种有趣的可能性,即PET122和OXA1的转录受下游DNA控制,下游DNA可能位于各自基因的编码区内。