Haouas H, Morello D, Lavenu A, Billard M, Jasmin C, Boucheix C
INSERM U268, Hôpital Paul Brousse, Villejuif, Paris, France.
Biochem Biophys Res Commun. 1995 Feb 27;207(3):933-42. doi: 10.1006/bbrc.1995.1275.
We have characterized the 5' region of the CALLA/CD10 gene which has been shown to be identical to the membrane-associated enzyme neutral endopeptidase 24.11 (NEP). There is no CAAT or TATA box in the 5' flanking region, upstream of exon 1, but a GC rich region with several Sp1 binding sites. We have detected several putative initiation transcription sites by primer extension and by nuclease S1 analysis. Moreover by reverse transcriptase-polymerase chain reaction, we demonstrated the existence of a new exon: exon 1bis. This exon can be alternatively spliced as has already been described for exon 1 and exon 2.
我们已对CALLA/CD10基因的5'区域进行了特征分析,该区域已被证明与膜相关酶中性内肽酶24.11(NEP)相同。在第1外显子上游的5'侧翼区域中没有CAAT或TATA框,但有一个富含GC的区域,带有几个Sp1结合位点。我们通过引物延伸和核酸酶S1分析检测到了几个假定的起始转录位点。此外,通过逆转录聚合酶链反应,我们证实了一个新外显子的存在:第1双外显子。该外显子可以像已描述的第1外显子和第2外显子那样进行可变剪接。