| Literature DB >> 10050886 |
H Yamamoto1, F Kihara-Negishi, T Yamada, Y Hashimoto, T Oikawa.
Abstract
Yeast two-hybrid system was employed to isolate novel proteins that physically interact with PU.1, a member of Ets family transcription factors. Sequence analyses of several isolated clones positive for beta-galactosidase activity revealed that one of these clones was confirmed to encode a transcriptional coactivator, CREB binding protein (CBP). GST binding assay showed that the interacting sites were located at the transcriptional activation domain of PU.1 through 74-122 and the region spanning residues 1283-1915 of CBP. CBP potentiated PU.1-mediated transcription of the reporter gene driven by the multimerized PU.1-binding sites, suggesting that CBP functions as a coactivator for PU.1. Considering that CBP is a limited cellular component to function as a coactivator for several transcription factors, CBP may mediate synergistic and antagonistic interactions between PU.1 and other transcription factors during the process of hematopoietic cell differentiation.Entities:
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Year: 1999 PMID: 10050886 DOI: 10.1038/sj.onc.1202427
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867