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PMID: 15502158 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

von Hippel-Lindau partner Jade-1 is a transcriptional co-activator associated with histone acetyltransferase activity.

The Journal of biological chemistry ·Vol. 279 ·No. 53 ·2004-12-31 ·Pages 56032-41

Panchenko MV, Zhou MI, Cohen HT

Abstract

Jade-1 was identified as a protein partner of the von Hippel-Lindau tumor suppressor pVHL. The interaction of Jade-1 and pVHL correlates with renal cancer risk. We have investigated the molecular function of Jade-1. Jade-1 has two zinc finger motifs called plant homeodomains (PHD). A line of evidence suggests that the PHD finger functions in chromatin remodeling and protein-protein interactions. We determined the cellular localization of Jade-1 and examined whether Jade-1 might have transcriptional and histone acetyltransferase (HAT) functions. Biochemical cell fractionation studies as well as confocal images of cells immunostained with a specific Jade-1 antibody revealed that endogenous Jade-1 is localized predominantly in the cell nucleus. Tethering of Gal4-Jade-1 fusion protein to Gal4-responsive promoters in co-transfection experiments activated transcription 5-6-fold, indicating that Jade-1 is a possible transcriptional activator. It was remarkable that overexpression of Jade-1 in cultured cells specifically increased levels of endogenous acetylated histone H4, but not histone H3, strongly suggesting that Jade-1 associates with HAT activity specific for histone H4. Deletion of the two PHD fingers completely abolished Jade-1 transcriptional and HAT activities, indicating that these domains are indispensable for Jade-1 nuclear functions. In addition, we demonstrated that TIP60, a known HAT with histone H4/H2A specificity, physically associates with Jade-1 and is able to augment Jade-1 HAT function in live cells, strongly suggesting that TIP60 might mediate Jade-1 HAT activity. Thus, Jade-1 is a novel candidate transcriptional co-activator associated with HAT activity and may play a key role in the pathogenesis of renal cancer and von Hippel-Lindau disease.

MeSH Terms
Acetyltransferases/metabolism Cell Line Cell Nucleus/metabolism Chloramphenicol O-Acetyltransferase/metabolism Dose-Response Relationship, Drug Electrophoresis, Polyacrylamide Gel Genes, Reporter Genetic Vectors HeLa Cells Histone Acetyltransferases Histones/chemistry,metabolism Homeodomain Proteins/metabolism Humans Immunoprecipitation Lysine Acetyltransferase 5 Microscopy, Confocal Models, Biological Models, Genetic Promoter Regions, Genetic Protein Binding Protein Structure, Tertiary Sodium Chloride/pharmacology Subcellular Fractions Transcription, Genetic Transcriptional Activation Transfection Tumor Suppressor Proteins/metabolism Ubiquitin-Protein Ligases/metabolism Von Hippel-Lindau Tumor Suppressor Protein Zinc Fingers
Chemicals
Histones Homeodomain Proteins JADE1 protein, human Tumor Suppressor Proteins Sodium Chloride Acetyltransferases Chloramphenicol O-Acetyltransferase Histone Acetyltransferases KAT5 protein, human Lysine Acetyltransferase 5 Ubiquitin-Protein Ligases Von Hippel-Lindau Tumor Suppressor Protein VHL protein, human
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Panchenko Maria V
Department of Medicine, Sections of Nephrology and Hematology/Oncology, Boston University School of Medicine and Boston Medical Center, Boston, MA 02118, USA.
Zhou Mina I
Cohen Herbert T
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2004-12-31
Epub
2004-00-22
Pages
56032-41
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIDDK NIH HHS · T32 DK 07053-30 · United States
NCI NIH HHS · R01 CA079830 · United States
NIDDK NIH HHS · R01 DK 67569 · United States
NCI NIH HHS · R012 CA 79830 · United States
NIDDK NIH HHS · R01 DK067569 · United States
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