| First Author | Haghighi K | Year | 1997 |
| Journal | Gene | Volume | 203 |
| Issue | 2 | Pages | 199-207 |
| PubMed ID | 9426251 | Mgi Jnum | J:44701 |
| Mgi Id | MGI:1101215 | Doi | 10.1016/s0378-1119(97)00514-3 |
| Citation | Haghighi K, et al. (1997) In vitro and in vivo promoter analyses of the mouse phospholamban gene. Gene 203(2):199-207 |
| abstractText | To determine the mechanisms responsible for regulation of the phospholamban (PLB) gene expression, a critical regulatory phosphoprotein in cardiac muscle, the mouse PLB gene was isolated and promoter analysis was performed in vitro and in vivo. The PLB gene consists of two exons separated by a single large intron. Deletion analysis revealed that a 7-kb 5' flanking fragment (including exon 1, the entire intron and part of exon 2) was necessary for maximal transcriptional activity in H9c2 and L6 cell lines. Interestingly, deletion of a 2.4-kb intronic region, which contained repetitive elements, caused a dramatic increase in CAT activity in both these cell lines. In vivo analysis indicated that the PLB fusion gene containing 7 kb of the 5'-flanking region was capable of cardiac specific gene expression in transgenic mice. Furthermore, these mice exhibited 3-fold higher levels of CAT activity in the ventricles compared with the atria, mimicking endogenous PLB mRNA expression. Our findings suggest that: (a) PLB gene expression may be regulated by the interplay of cis-acting regulatory elements located within the 5' flanking and intronic regions; and (b) the 7-kb upstream region is capable of directing cardiac-specific and compartment-specific expression in vivo. |
