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小鼠线粒体3,2-反式烯酰辅酶A异构酶的分子克隆与基因结构

Molecular cloning and gene organization of the mouse mitochondrial 3,2-trans-enoyl-CoA isomerase.

作者信息

Stoffel W, Düker M, Hofmann K

机构信息

Institut für Biochemie, Medizinische Fakultät, Universität zu Köln, Germany.

出版信息

FEBS Lett. 1993 Oct 25;333(1-2):119-22. doi: 10.1016/0014-5793(93)80387-a.

Abstract

3,2-trans-enoyl-CoA isomerase (mECI, E.C. 5.3.3.8) is the key enzyme of mitochondrial beta-oxidation of unsaturated fatty acids. A mouse cDNA clone spanning the entire coding region of mECI was isolated and sequenced. Subsequently, two overlapping genomic clones containing the complete mECI gene were isolated and characterized. The mouse mECI cDNA comprises an open reading frame of 867 bp, encoding a protein of 32 kDa. The mECI gene, spanning about 15 kb, consists of seven exons. Multiple transcription starts were determined by primer extension experiments. Knowledge of the gene organization and availability of genomic clones for mouse mECI will facilitate the study of unsaturated fatty acid metabolism in normal and pathological states.

摘要

3,2-反式烯酰辅酶A异构酶(mECI,E.C. 5.3.3.8)是不饱和脂肪酸线粒体β氧化的关键酶。分离并测序了跨越mECI整个编码区的小鼠cDNA克隆。随后,分离并鉴定了两个包含完整mECI基因的重叠基因组克隆。小鼠mECI cDNA包含一个867 bp的开放阅读框,编码一个32 kDa的蛋白质。mECI基因跨度约15 kb,由七个外显子组成。通过引物延伸实验确定了多个转录起始位点。小鼠mECI基因组织的知识和基因组克隆的可用性将有助于研究正常和病理状态下的不饱和脂肪酸代谢。

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