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Originally published In Press as doi:10.1074/jbc.M910152199 on March 9, 2000

J. Biol. Chem., Vol. 275, Issue 21, 15685-15690, May 26, 2000
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A Broad Role for the Zinc Finger Protein ZNF202 in Human Lipid Metabolism*

Susanne WagnerDagger §, Mark A. HessDagger , Patricia Ormonde-HansonDagger , Jennifer MalandroDagger , Heping HuDagger , Mike ChenDagger , Robert KehrerDagger , Michael FrodshamDagger , Christoph Schumacher, Michael Beluch, Christian Honer, Mark SkolnickDagger , Dennis BallingerDagger , and Benjamin R. Bowen

From the Dagger  Myriad Genetics, Inc., Salt Lake City, Utah 84108 and  Novartis Institute for Biomedical Research, Summit, New Jersey 07901

The ZNF202 gene resides in a chromosomal region linked genetically to low high density lipoprotein cholesterol in Utah families. Here we show that the ZNF202 gene product is a transcriptional repressor that binds to elements found predominantly in genes that participate in lipid metabolism. Among its targets are structural components of lipoprotein particles (apolipoproteins AIV, CIII, and E), enzymes involved in lipid processing (lipoprotein lipase, lecithin cholesteryl ester transferase), and several genes involved in processes related to energy metabolism and vascular disease. Based on the linkage and apparent transcriptional function of ZNF202, we propose that ZNF202 is a candidate susceptibility gene for human dyslipidemia.


* The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

§ To whom correspondence should be addressed: Myriad Genetics, Inc., 320 Wakara Way, Salt Lake City, UT 84108. Tel.: 801-584-3724; Fax: 801-584-3650; E-mail: swagner@myriad.com.


Copyright © 2000 by The American Society for Biochemistry and Molecular Biology, Inc.
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