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小鼠长链脂酰辅酶A脱氢酶基因的RNA表达及染色体定位

RNA expression and chromosomal location of the mouse long-chain acyl-CoA dehydrogenase gene.

作者信息

Hinsdale M E, Farmer S C, Johnson K R, Davisson M T, Hamm D A, Tolwani R J, Wood P A

机构信息

Department of Comparative Medicine, School of Medicine, University of Alabama at Birmingham 35294-0019, USA.

出版信息

Genomics. 1995 Jul 20;28(2):163-70. doi: 10.1006/geno.1995.1127.

Abstract

The cDNA for mouse long-chain acyl-CoA dehydrogenase (Acadl, gene symbol; LCAD, enzyme) was cloned and characterized. The cDNA was obtained by library screening and reverse transcription-polymerase chain reaction (RT-PCR). The deduced amino acid sequence showed a high degree of homology to both the rat and the human LCAD sequence. Northern analysis of multiple tissues using the mouse Acadl cDNA as a probe showed two bands in all tissues examined. We found a total of three distinct mRNAs for Acadl. These three mRNAs were encoded by a single gene that we mapped to mouse chromosome 1. The three transcripts differed in the 3' untranslated region due to use of alternative polyadenylation sites. Quantitative evaluation of a multitissue Northern blot showed a varied ratio of the larger transcript as compared with the smaller transcripts.

摘要

克隆并鉴定了小鼠长链酰基辅酶A脱氢酶(Acadl,基因符号;LCAD,酶)的cDNA。通过文库筛选和逆转录-聚合酶链反应(RT-PCR)获得了该cDNA。推导的氨基酸序列与大鼠和人LCAD序列均显示出高度同源性。使用小鼠Acadl cDNA作为探针,对多个组织进行Northern分析,结果显示在所有检测的组织中均有两条带。我们总共发现了三种不同的Acadl mRNA。这三种mRNA由一个单一基因编码,我们将该基因定位到小鼠1号染色体上。由于使用了不同的聚腺苷酸化位点,这三种转录本在3'非翻译区存在差异。对多组织Northern印迹的定量评估显示,与较小的转录本相比,较大转录本的比例各不相同。

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