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中链酰基辅酶A脱氢酶mRNA的核苷酸序列及其在酶缺陷型人体组织中的表达。

Nucleotide sequence of medium-chain acyl-CoA dehydrogenase mRNA and its expression in enzyme-deficient human tissue.

作者信息

Kelly D P, Kim J J, Billadello J J, Hainline B E, Chu T W, Strauss A W

出版信息

Proc Natl Acad Sci U S A. 1987 Jun;84(12):4068-72. doi: 10.1073/pnas.84.12.4068.

Abstract

Medium-chain acyl-CoA dehydrogenase (MCAD; acyl-CoA: (acceptor) 2,3-oxidoreductase, EC 1.3.99.3) is one of three similar enzymes that catalyze the initial step of fatty acid beta-oxidation. Definition of the primary structure of MCAD and the tissue distribution of its mRNA is of biochemical and clinical importance because of the recent recognition of inherited MCAD deficiency in humans. The MCAD mRNA nucleotide sequence was determined from two overlapping cDNA clones isolated from human liver and placental cDNA libraries, respectively. The MCAD mRNA includes a 1263-base-pair coding region and a 738-base-pair 3'-nontranslated region. A partial amino acid sequence (137 residues) determined on peptides derived from MCAD purified from porcine liver confirmed the identity of the cDNA clone. Comparison of the amino acid sequence predicted from the human MCAD cDNA with the partial protein sequence of the porcine MCAD revealed a high degree (88%) of interspecies sequence identity. RNA blot analysis shows that MCAD mRNA is expressed in a variety of rat (2.2 kilobases) and human (2.4 kilobases) tissues. Blot hybridization of RNA prepared from cultured skin fibroblasts from a patient with MCAD deficiency disclosed that mRNA was present and of similar size to MCAD mRNA derived from control fibroblasts. The isolation and characterization of MCAD cDNA is an important step in the definition of the defect underlying MCAD deficiency and in understanding its metabolic consequences.

摘要

中链酰基辅酶A脱氢酶(MCAD;酰基辅酶A:(受体)2,3-氧化还原酶,EC 1.3.99.3)是催化脂肪酸β-氧化第一步的三种相似酶之一。由于最近认识到人类中存在遗传性MCAD缺乏症,因此确定MCAD的一级结构及其mRNA的组织分布具有生化和临床重要性。MCAD mRNA核苷酸序列是分别从从人肝脏和胎盘cDNA文库中分离出的两个重叠cDNA克隆中确定的。MCAD mRNA包括一个1263个碱基对的编码区和一个738个碱基对的3'-非翻译区。从猪肝纯化的MCAD衍生的肽上确定的部分氨基酸序列(137个残基)证实了cDNA克隆的身份。将人MCAD cDNA预测的氨基酸序列与猪MCAD的部分蛋白质序列进行比较,发现种间序列同一性程度很高(88%)。RNA印迹分析表明,MCAD mRNA在多种大鼠(2.2千碱基)和人类(2.4千碱基)组织中表达。对一名MCAD缺乏症患者培养的皮肤成纤维细胞制备的RNA进行印迹杂交,结果显示存在mRNA,其大小与对照成纤维细胞来源的MCAD mRNA相似。MCAD cDNA的分离和表征是确定MCAD缺乏症潜在缺陷以及理解其代谢后果的重要一步。

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