Cloning and expression of full-length cDNA encoding human vitamin D receptor.

Andrew R. Baker(Planet Biotechnology (United States)), Donald P. McDonnell(Planet Biotechnology (United States)), Mark Hughes(Planet Biotechnology (United States)), Thomas M. Crisp(Planet Biotechnology (United States)), David J. Mangelsdorf(Planet Biotechnology (United States)), Mark R. Haussler(Planet Biotechnology (United States)), J. Wesley Pike(Planet Biotechnology (United States)), John Shine(Planet Biotechnology (United States)), B W O'Malley(Planet Biotechnology (United States))
Proceedings of the National Academy of Sciences
May 1, 1988
Cited by 961Open Access
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Abstract

Complementary DNA clones encoding the human vitamin D receptor have been isolated from human intestine and T47D cell cDNA libraries. The nucleotide sequence of the 4605-base pair (bp) cDNA includes a noncoding leader sequence of 115 bp, a 1281-bp open reading frame, and 3209 bp of 3' noncoding sequence. Two polyadenylylation signals, AATAAA, are present 25 and 70 bp upstream of the poly(A) tail, respectively. RNA blot hybridization indicates a single mRNA species of approximately equal to 4600 bp. Transfection of the cloned sequences into COS-1 cells results in the production of a single receptor species indistinguishable from the native receptor. Sequence comparisons demonstrate that the vitamin D receptor belongs to the steroid-receptor gene family and is closest in size and sequence to another member of this family, the thyroid hormone receptor.


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