Brennan L E, Nakagawa J, Egger D, Bienz K, Moroni C
Institute for Medical Microbiology, University of Basel, Petersplatz 10, CH-4003, Basel, Switzerland.
Gene. 1999 Mar 4;228(1-2):85-91. doi: 10.1016/s0378-1119(99)00003-7.
AU-rich elements function as instability elements which direct rapid mRNA degradation. AUH protein exhibits an AU-specific RNA-binding property and an intrinsic enoyl-CoA hydratase activity and may therefore function to link mRNA decay to metabolic processes (. Proc. Natl. Acad. Sci. USA 92, 2051-2055). The sequence encoding the murine protein, muAUH, was established by cloning, and the corresponding polypeptide predicted to have a molecular mass of 37kDa. As shown for the human protein, muAUH is expressed in a 32kDa form and there is 94% homology between the two species. Recombinant muAUH was shown to be an RNA-binding enoyl-CoA hydratase. All murine cells studied contained a single AUH transcript of approx. 1.7kb and an investigation of tissue-specific expression revealed highest levels in kidney, skeletal muscle, heart, liver and spleen. It was further determined, using immunoelectron microscopy, that AUH is located in the mitochondria of mouse cells.
富含AU元件作为不稳定元件,可直接导致mRNA快速降解。AUH蛋白具有AU特异性RNA结合特性和内在的烯酰辅酶A水合酶活性,因此可能起到将mRNA衰变与代谢过程联系起来的作用(《美国国家科学院院刊》92, 2051 - 2055)。通过克隆确定了编码小鼠蛋白muAUH的序列,预测相应的多肽分子量为37kDa。如人类蛋白所示,muAUH以32kDa的形式表达,两种物种之间的同源性为94%。重组muAUH被证明是一种RNA结合烯酰辅酶A水合酶。所研究的所有小鼠细胞都含有一个约1.7kb的单一AUH转录本,对组织特异性表达的研究表明,在肾脏、骨骼肌、心脏、肝脏和脾脏中的水平最高。使用免疫电子显微镜进一步确定,AUH位于小鼠细胞的线粒体中。