Morioka H, Magnuson M A, Mitsuhashi T, Song M K, Rall J E, Nikodem V M
Clinical Endocrinology Branch, National Institute of Diabetes, Digestive, and Kidney Diseases, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1989 Jul;86(13):4912-6. doi: 10.1073/pnas.86.13.4912.
We have identified and characterized lambda bacteriophage clones containing genomic DNA encoding rat malic enzyme [(S)-malate:NADP+ oxidoreductase (oxaloacetate-decarboxylating); EC 1.1.1.40]. The malic enzyme gene is unexpectedly large, spanning at least 95 kilobases. It is divided into 14 exons that range in size from 76 to 1513 base pairs. The sizes and boundaries of the exons were determined by Southern blotting and DNA sequencing. The sequences at the 5' and 3' ends of each intron conformed to the consensus sequence for mammalian introns. S1 nuclease and primer-extension assays showed that transcription of the malic enzyme gene initiates at multiple sites, the strongest one at position -31 relative to the ATG. "TATA and CCAAT box" homologies are not present in the proximal promoter region. Analysis of the 3' end of the gene showed that the utilization of alternate polyadenylylation signals in exon 14 results in two mRNAs with 3' untranslated regions of 345 and 1345 nucleotides, respectively.
我们已经鉴定并表征了含有编码大鼠苹果酸酶[(S)-苹果酸:NADP +氧化还原酶(草酰乙酸脱羧);EC 1.1.1.40]基因组DNA的λ噬菌体克隆。苹果酸酶基因出乎意料地大,跨度至少为95千碱基。它被分为14个外显子,大小从76到1513个碱基对不等。外显子的大小和边界通过Southern印迹和DNA测序确定。每个内含子5'和3'末端的序列符合哺乳动物内含子的共有序列。S1核酸酶和引物延伸分析表明,苹果酸酶基因的转录起始于多个位点,最强的一个位于相对于ATG的-31位。近端启动子区域不存在“TATA和CCAAT框”同源性。对该基因3'末端的分析表明,外显子14中交替多聚腺苷酸化信号的利用导致两种mRNA,其3'非翻译区分别为345和1345个核苷酸。