Chobert M N, Lahuna O, Lebargy F, Kurauchi O, Darbouy M, Bernaudin J F, Guellaen G, Barouki R, Laperche Y
Institut Unité National de la Santé et de la Recherche Médicale 99, Hôpital Henri Mondor, Créteil, France.
J Biol Chem. 1990 Feb 5;265(4):2352-7.
Two different cDNAs have been isolated and characterized from a rat kidney cDNA library. The two cDNA sequences are identical in the coding region and in the 144 bases upstream from the initiation codon but have alternate sequences (154 and 138 bases) at their 5' ends. Primer extension analysis on kidney mRNA reveals that both cDNAs are full-length and correspond to two mRNAs of nearly the same size (2142 and 2127 bases). Synthesis of two mRNAs with alternative 5' ends can be explained only by initiation at two separate promoters on the single rat gamma-glutamyl transpeptidase (GGT) gene. The alternate 5' end nucleotide sequences were used as probes to detect the corresponding mRNAs in several rat tissues. In the kidney, the expression of both RNAs was detected by in situ hybridization in the distal part of the proximal convolutions of the renal tubule. Northern blot analysis of kidney mRNAs reveals that the expression of both mRNAs increases from birth to the adult stage. Neither of these two transcripts is expressed in the liver or in seminal vesicles in which a larger mRNA (2.4 kilobase pairs) is transcribed from the same gene. Thus, two GGT mRNAs, initiated on two separate promoters on the single GGT gene, are expressed in the rat in a tissue-specific manner and coordinately regulated.
从大鼠肾脏cDNA文库中分离并鉴定了两种不同的cDNA。这两种cDNA序列在编码区以及起始密码子上游144个碱基处是相同的,但在其5'端具有交替序列(154和138个碱基)。对肾脏mRNA进行引物延伸分析表明,这两种cDNA都是全长的,并且对应于两种大小几乎相同的mRNA(2142和2127个碱基)。具有交替5'端的两种mRNA的合成只能通过在单个大鼠γ-谷氨酰转肽酶(GGT)基因上的两个单独启动子处起始来解释。交替的5'端核苷酸序列被用作探针来检测几种大鼠组织中的相应mRNA。在肾脏中,通过原位杂交在肾小管近端曲部的远端检测到了两种RNA的表达。对肾脏mRNA的Northern印迹分析表明,两种mRNA的表达从出生到成年阶段都增加。这两种转录本在肝脏或精囊中均未表达,在肝脏和精囊中,同一基因转录出一种更大的mRNA(2.4千碱基对)。因此,在单个GGT基因上的两个单独启动子处起始的两种GGT mRNA在大鼠中以组织特异性方式表达并受到协调调节。