THE CYCLOPHILIN COMPONENT OF THE UNACTIVATED ESTROGEN-RECEPTOR CONTAINS A TETRATRICOPEPTIDE REPEAT DOMAIN AND SHARES IDENTITY WITH P59 (FKBP59)
Details
Publication Year 1993-06-25,Volume 268,Issue #18,Page 13187-13192
Journal Title
JOURNAL OF BIOLOGICAL CHEMISTRY
Publication Type
Journal Article
Abstract
Using a rapid single-step affinity chromatography procedure we have isolated the unactivated estrogen receptor from bovine uterus. Results of sodium dodecyl sulfate-polyacrylamide gel electrophoresis and Western analyses for protein extracts recovered from affinity chromatography of receptor cytosols, either preincubated or untreated with estradiol, suggest a component structure for the intact oligomeric receptor which includes hsp90, hsp70, p59, a 40-kDa cyclophilin-related protein, and an uncharacterized 22-kDa protein species. We have chemically determined the amino acid sequences of eight peptides derived from the 40-kDa component and now report the cloning and primary sequence of a cDNA encoding this protein, which is designated estrogen receptor-binding cyclophilin (ERBC). Homology analyses confirm that ERBC is a new member of the cyclophilin family and contains a C-terminal domain with significant sequence homology to an internal region of p59, a binding protein for the immunosuppressant FK506 (FKBP59). This conserved region includes a 3-unit tetratricopeptide repeat domain bounded at the C terminus by a putative calmodulin binding site. We propose that the tetratricopeptide repeat domain mediates the protein interaction properties of ERBC and p59. Both immunophilins may have important roles in receptor assembly and may represent a new category of ligand- and calcium-dependent modulators of protein function.
Publisher
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
Keywords
HEAT-SHOCK PROTEIN; CELL GLUCOCORTICOID RECEPTOR; AMINO-ACID SEQUENCE; NON-DNA-BINDING; SACCHAROMYCES-CEREVISIAE; PROGESTERONE-RECEPTOR; 59-KILODALTON PROTEIN; STEROID-RECEPTORS; GENE; COMPLEXES
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Creation Date: 1993-06-25 12:00:00
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