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A more recent version of this article appeared on September 14, 2001
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M101269200v1
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Papers In Press, published online ahead of print July 10, 2001
J. Biol. Chem, 10.1074/jbc.M101269200
Submitted on February 8, 2001
Revised on June 26, 2001
Accepted on July 10, 2001

Ldhc expression in non-germ cell nuclei is repressed by NF-I binding

Poonam Jethanandani and Erwin Goldberg

Biochem.MolBiol.&CellBiol., Northwestern University, Evanston, IL 60208-3500

Corresponding Author: erv{at}northwestern.edu

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 bp promoter sequence upstream of the transcription initiation site. This promoter fragment has a TATA box and an overlapping 31 bp 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 to 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.


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