Ellis Timothy P, Helfenbein Kevin G, Tzagoloff Alexander, Dieckmann Carol L
Department of Biochemistry and Molecular Biophysics, University of Arizona, Tucson, Arizona 85721, USA.
J Biol Chem. 2004 Apr 16;279(16):15728-33. doi: 10.1074/jbc.M314162200. Epub 2004 Jan 23.
Subunits 6 and 8 of the mitochondrial ATPase in Saccharomyces cerevisiae are encoded by the mitochondrial genome and translated from bicistronic mRNAs containing both reading frames. The stability of the two major species of ATP8/6 mRNA, which differ in the length of the 5'-untranslated region, depends on the expression of several nuclear-encoded factors. In the present study, the product of the gene designated AEP3 (open reading frame YPL005W) is shown to be required for stabilization and/or processing of both ATP8/6 mRNA species. In an aep3-disruptant strain, the shorter ATP8/6 mRNA was undetectable, and the level of the longer mRNA was reduced to approximately 35% that of wild type. Localization of a hemagglutinin-tagged version of Aep3p showed that the protein is an extrinsic constituent of the mitochondrial inner membrane facing the matrix.
酿酒酵母线粒体ATP酶的亚基6和亚基8由线粒体基因组编码,并从包含两个阅读框的双顺反子mRNA翻译而来。两种主要的ATP8/6 mRNA,其5'-非翻译区长度不同,它们的稳定性取决于几种核编码因子的表达。在本研究中,名为AEP3(开放阅读框YPL005W)的基因产物被证明是稳定和/或加工这两种ATP8/6 mRNA所必需的。在aep3破坏菌株中,较短的ATP8/6 mRNA无法检测到,较长mRNA的水平降至野生型的约35%。带有血凝素标签的Aep3p的定位表明,该蛋白是线粒体内膜面向基质的外在成分。