| Literature DB >> 20054825 |
Mainul Hoque1, Michael B Mathews, Tsafi Pe'ery.
Abstract
Progranulin (also known as granulin/epithelin precursor, GEP) is composed of seven granulin/epithelin repeats (granulins) and functions both as a full-length protein and as individual granulins. It is a secretory protein but a substantial amount of GEP is found inside cells, some in complexes with positive transcription elongation factor b (P-TEFb). GEP and certain granulins interact with the cyclin T1 subunit of P-TEFb, and with its HIV-1 Tat co-factor, leading to repression of transcription from the HIV promoter. We show that GEP lacking the signal peptide (GEPspm) remains inside cells and, like wild-type GEP, interacts with cyclin T1 and Tat. GEPspm represses transcription from the HIV-1 promoter at the RNA level. Granulins that bind cyclin T1 are phosphorylated by P-TEFb in vivo and in vitro on serine residues. GEPspm and those granulins that interact with cyclin T1 also inhibit transcription from cellular cad and c-myc promoters, which are highly dependent on P-TEFb, but not from the PCNA promoter. In addition, GEPspm and granulins repress transcriptional activation by VP16 or c-Myc, proteins that bind and recruit P-TEFb to responsive promoters. These data suggest that intracellular GEP is a promoter-specific transcriptional repressor that modulates the function of cellular and viral transcription factors. J. Cell. Physiol. 223: 224-233, 2010. (c) 2010 Wiley-Liss, Inc.Entities:
Keywords: CDK9; GEP; HIV-1; P-TEFb; Progranulin; c-Myc; c-myc promoter; cad promoter; cyclin T1; transcription elongation
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Year: 2010 PMID: 20054825 PMCID: PMC2904068 DOI: 10.1002/jcp.22031
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384