| First Author | Anderson KP | Year | 1995 |
| Journal | Mol Cell Biol | Volume | 15 |
| Issue | 11 | Pages | 5957-65 |
| PubMed ID | 7565748 | Mgi Jnum | J:29401 |
| Mgi Id | MGI:76925 | Doi | 10.1128/mcb.15.11.5957 |
| Citation | Anderson KP, et al. (1995) Isolation of a gene encoding a functional zinc finger protein homologous to erythroid Kruppel-like factor: identification of a new multigene family. Mol Cell Biol 15(11):5957-65 |
| abstractText | We have identified and characterized the gene for a novel zinc finger transcription factor which we have termed lung Kruppel-like factor (LKLF). LKLF was isolated through the use of the zinc finger domain of erythroid Kruppel-like factor (ELKF) as a hybridization probe and is closely related to this erythroid cell-specific gene. LKLF is expressed in a limited number of tissues, with the predominant expression seen in the lungs and spleen. The gene is developmentally controlled, with expression noted in the 7-day embryo followed by a down-regulation at 11 days and subsequent reactivation. A high degree of similarity is noted in the zinc finger regions of LKLF and EKLF. Beyond this domain, the sequences diverge significantly, although the putative transactivation domains for both LKLF and EKLF are proline-rich regions. In the DNA-binding domain, the three zinc finger motifs are so closely conserved that the predicted DNA contact sites are identical, suggesting that both proteins may bind to the same core sequence. This was further suggested by transactivation assays in which mouse fibroblasts were transiently transfected with a human beta-globin reporter gene in the absence and presence of an LKLF cDNA construct. Expression of the LKLF gene activates this human beta-globin promoter containing the CACCC sequence previously shown to be a binding site for EKLF. Mutation of this potential binding site results in a significant reduction in the reporter gene expression. LKLF and EKLF can thus be grouped as members of a unique family of transcription factors which have discrete patterns of expression in different tissues and which appear to recognize the same DNA-binding site. |
