| First Author | Mericskay M | Year | 2000 |
| Journal | Dev Biol | Volume | 226 |
| Issue | 2 | Pages | 192-208 |
| PubMed ID | 11023680 | Mgi Jnum | J:65247 |
| Mgi Id | MGI:1913243 | Doi | 10.1006/dbio.2000.9865 |
| Citation | Mericskay M, et al. (2000) An overlapping CArG/Octamer element is required for regulation of desmin gene transcription in arterial smooth muscle cells. Dev Biol 226(2):192-208 |
| abstractText | The desmin gene encodes an intermediate filament protein that is present in skeletal, cardiac, and smooth muscle cells. This study shows that the 4-kb upstream region of the murine desmin promoter directs expression of a lacZ reporter gene throughout the heart from E7.5 and in skeletal muscle and vascular smooth muscle cells from E9. 5. The distal fragment (-4005/-2495) is active in arterial smooth muscle cells but not in venous smooth muscle cells or in the heart in vivo. It contains a CArG/octamer overlapping element (designated CArG4) that can bind the serum response factor (SRF) and an Oct-like factor. The desmin distal fragment can replace a SM22alpha regulatory region (-445/-126) that contains two CArG boxes, to cis-activate a minimal (-125/+65) SM22alpha promoter fragment in arterial smooth muscle cells of transgenic embryos. lacZ expression was abolished when mutations were introduced into the desmin CArG4 element that abolished the binding of SRF and/or Oct-like factor. These data suggest that a new type of combined CArG/octamer element plays a prominent role in the regulation of the desmin gene in arterial smooth muscle cells, and SRF and Oct-like factor could cooperate to drive specific expression in these cells. Copyright 2000 Academic Press. |
