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编码心脏6-磷酸果糖-2-激酶/果糖-2,6-二磷酸酶的大鼠基因:异常启动子区域的特征及四种mRNA的鉴定

Rat gene coding for heart 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase: characterization of an unusual promoter region and identification of four mRNAs.

作者信息

Chikri M, Rousseau G G

机构信息

Hormone and Metabolic Research Unit, University of Louvain Medical School, Brussels, Belgium.

出版信息

Biochemistry. 1995 Jul 11;34(27):8876-84. doi: 10.1021/bi00027a040.

DOI:10.1021/bi00027a040
PMID:7612629
Abstract

We have cloned previously a 22-kb rat gene which codes for heart 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase from an ATG located in exon 2. To characterize the promoter of the gene, we have now cloned and sequenced 1.9 kb of its 5' region and show here that it has an unusual structural and functional organization. By S1 nuclease mapping and primer extension we found that this region contains the first, noncoding, exon of a mRNA that we call R3. The sequence upstream from this exon behaved as a promoter in transient transfection assays. These assays also suggested that the gene possesses more than one promoter. Indeed, by reverse transcription-polymerase chain reaction techniques we identified three additional mRNAs that differ by their 5' noncoding exons upstream from the common, coding, exon 2. mRNA R1 contains two 5' noncoding exons located upstream from the first exon of mRNA R3. mRNA R2 contains one 5' noncoding exon located upstream from, and partially overlapping with, the first exon of mRNA R3. mRNA R4 contains one 5' noncoding exon located downstream from the first exon of mRNA R3 but overlapping partially with it. The distribution of these mRNAs in rat tissues was evaluated by reverse transcription--polymerase chain reaction. We conclude that the gene contains four more exons than the 16 previously described and at least three promoters, two of which correspond to exonic sequences. The gene gives rise to at least four mRNAs which are expressed not only in heart but also in most tissues.

摘要

我们先前已从位于外显子2中的一个ATG开始克隆了一个22 kb的大鼠基因,该基因编码心脏6-磷酸果糖-2-激酶/果糖-2,6-二磷酸酶。为了表征该基因的启动子,我们现在克隆并测序了其5'区域的1.9 kb,并在此表明它具有不同寻常的结构和功能组织。通过S1核酸酶图谱分析和引物延伸,我们发现该区域包含一种我们称为R3的mRNA的第一个非编码外显子。该外显子上游的序列在瞬时转染实验中表现为启动子。这些实验还表明该基因拥有不止一个启动子。实际上,通过逆转录-聚合酶链反应技术,我们鉴定出另外三种mRNA,它们在共同的编码外显子2上游的5'非编码外显子不同。mRNA R1包含位于mRNA R3第一个外显子上游的两个5'非编码外显子。mRNA R2包含一个位于mRNA R3第一个外显子上游并与之部分重叠的5'非编码外显子。mRNA R4包含一个位于mRNA R3第一个外显子下游但与之部分重叠的5'非编码外显子。通过逆转录-聚合酶链反应评估了这些mRNA在大鼠组织中的分布。我们得出结论,该基因比先前描述的16个外显子多四个外显子,并且至少有三个启动子,其中两个对应于外显子序列。该基因产生至少四种mRNA,它们不仅在心脏中表达,而且在大多数组织中也表达。

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