Rhaissi H, Béchet D, Ferrara M
Unité Expression des Protéases Lysosomales, INRA Theix, Saint-Genès-Champanelle, France.
Biochimie. 1993;75(10):899-904. doi: 10.1016/0300-9084(93)90046-u.
We previously described the gene structure of murine cathepsin B. Our results suggested that the 5'-untranslated region (leader) is interrupted by a large intron. The second exon (exon-2) contains the translation initiation site. To characterize the leader region, a rapid amplification of cDNA ends (RACE) procedure was developed. The PCR products were directly cloned and sequenced. Nucleotide sequence analyses revealed three different 5'-cDNA ends, suggesting the existence of three different leader regions. In addition to the leader (LA) previously characterized, we now describe two other 5'-untranslated regions, LB and LC. Leader LB is located 2.3 kb upstream exon-2, and leader LC corresponds to the 3'-end of the first intron and is thus contiguous to exon-2. Our results suggest for murine cathepsin B gene the presence of multiple promoters, and possibly the expression of multiple mRNAs differing in their leader region.
我们之前描述了小鼠组织蛋白酶B的基因结构。我们的结果表明,5'-非翻译区(前导序列)被一个大的内含子打断。第二个外显子(外显子2)包含翻译起始位点。为了表征前导序列区域,我们开发了一种cDNA末端快速扩增(RACE)方法。PCR产物直接克隆并测序。核苷酸序列分析揭示了三个不同的5'-cDNA末端,表明存在三个不同的前导序列区域。除了之前表征的前导序列LA,我们现在描述另外两个5'-非翻译区,LB和LC。前导序列LB位于外显子2上游2.3 kb处,前导序列LC对应于第一个内含子的3'-末端,因此与外显子2相邻。我们的结果表明,小鼠组织蛋白酶B基因存在多个启动子,并且可能表达前导序列区域不同的多种mRNA。