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Originally published In Press as doi:10.1074/jbc.M101269200 on July 10, 2001

J. Biol. Chem., Vol. 276, Issue 38, 35414-35421, September 21, 2001
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ldhc Expression in Non-germ Cell Nuclei Is Repressed by NF-I Binding*

Poonam JethanandaniDagger and Erwin Goldberg§

From the Department of Biochemistry, Molecular Biology and Cell Biology, Northwestern University, Evanston, Illinois 60208-3500

Developmental and testis-specific expression of the mouse lactate dehydrogenase C (mldhc) gene requires mechanisms for activation in germ cells and repression in somatic cells. Promoter activity restricted to the testis has been demonstrated using in vitro transcription assays with a 60-base pair promoter sequence upstream of the transcription initiation site. This promoter fragment has a TATA box and an overlapping 31-base pair palindromic sequence. Here we have explored the role of the palindrome as a silencer of the ldhc gene in somatic tissues. A gel retardation assay detected two sites within the palindrome that were important for protein binding. A member of the NF-I/CTF family was identified as the protein binding to one of the sites. In transiently transfected mouse L cells, a promoter fragment in which the NF-I site was mutated showed a 4-fold greater activity as compared with the wild-type sequence. Overexpression of the four NF-I proteins, NF-IA, -B, -C, or -X, in mouse L cells transiently transfected with an ldhc promoter-reporter construct resulted in a 20-50% decrease in activity of the wild-type promoter but had no effect when the NF-I binding element in the palindrome was mutated. These results indicate a role for the NF-I proteins in regulation of the mldhc gene.


* This work was supported in part by National Institutes of Health Grants R01 HD05863 and U54HD29099.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.

Dagger Fogarty International Fellow. Present address: Dept. of Stomatology, University of California, San Francisco, CA 94143-0512.

§ To whom correspondence should be addressed: Dept. of Biochemistry, Molecular Biology and Cell Biology, Northwestern University, Evanston, IL 60208-3500. Tel.: 847-491-5416; Fax: 847-467-1380; E-mail: erv@northwestern.edu.


Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.


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