RanBPM, a nuclear protein that interacts with and regulates transcriptional activity of androgen receptor and glucocorticoid receptor

被引:83
作者
Rao, MA
Cheng, H
Quayle, AN
Nishitani, H
Nelson, CC
Rennie, PS [1 ]
机构
[1] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC V6T 2B5, Canada
[2] Vancouver Gen Hosp, Prostate Ctr, Vancouver, BC V6H 3Z6, Canada
[3] Kyushu Univ, Grad Sch Med Sci, Dept Mol Biol, Higashi Ku, Fukuoka 8128582, Japan
关键词
D O I
10.1074/jbc.M209741200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The androgen receptor (AR) is a ligand-dependent transcription factor that has an essential role in the normal growth, development, and maintenance of the prostate gland. The AR is part of a large family of steroid receptors that also includes the glucocorticoid, progesterone, and mineralocorticoid receptors. Steroid receptor family members share significant homology at their DNA and ligand-binding domains. However, these receptors exhibit a high degree of sequence variability at their NH2-terminal domain, which suggests the possibility of receptor-specific interactions with co-regulator proteins. Transcriptional co-regulators that interact with the AR may have a role in defining AR activity and may be involved in directing AR-specific responses. Here we have identified Ran-binding protein in the microtubule-organizing center (RanBPM) to be a novel AR-interacting protein by yeast two-hybrid assay and have confirmed this interaction by glutathione S-transferase- and His-tagged pull-down assays. In addition, transient overexpression of RanBPM in prostate cancer cell lines resulted in enhanced AR activity in a ligand-dependent fashion. Glucocorticoid receptor activity was also enhanced when RanBPM was overexpressed, whereas estrogen receptor activity remained unchanged. These data demonstrate that RanBPM interacts with steroid receptors to selectively modify their activity.
引用
收藏
页码:48020 / 48027
页数:8
相关论文
共 40 条
[1]   Interaction of the putative androgen receptor-specific coactivator ARA70/ELE1α with multiple steroid receptors and identification of an internally deleted ELE1β isoform [J].
Alen, P ;
Claessens, F ;
Schoenmakers, E ;
Swinnen, JV ;
Verhoeven, G ;
Rombauts, W ;
Peeters, B .
MOLECULAR ENDOCRINOLOGY, 1999, 13 (01) :117-128
[2]   CATALYSIS OF GUANINE-NUCLEOTIDE EXCHANGE ON RAN BY THE MITOTIC REGULATOR RCC1 [J].
BISCHOFF, FR ;
PONSTINGL, H .
NATURE, 1991, 354 (6348) :80-82
[3]   MOLECULAR-CLONING OF HUMAN AND RAT COMPLEMENTARY-DNA ENCODING ANDROGEN RECEPTORS [J].
CHANG, CS ;
KOKONTIS, J ;
LIAO, SS .
SCIENCE, 1988, 240 (4850) :324-326
[4]   Analysis of estrogen response element binding by genetically selected steroid receptor DNA binding domain mutants exhibiting altered specificity and enhanced affinity [J].
Chusacultanachai, S ;
Glenn, KA ;
Rodriguez, AO ;
Read, EK ;
Gardner, JF ;
Katzenellenbogen, BS ;
Shapiro, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (33) :23591-23598
[5]   Running on ran: Nuclear transport and the mitotic spindle [J].
Dasso, M .
CELL, 2001, 104 (03) :321-324
[6]   Nuclear receptor-binding sites of coactivators glucocorticoid receptor interacting protein 1 (GRIP1) and steroid receptor coactivator 1 (SRC-1): Multiple motifs with different binding specificities [J].
Ding, XF ;
Anderson, CM ;
Ma, H ;
Hong, H ;
Uht, RM ;
Kushner, PJ ;
Stallcup, MR .
MOLECULAR ENDOCRINOLOGY, 1998, 12 (02) :302-313
[7]   THE N-TERMINAL DOMAIN OF THE HUMAN ANDROGEN RECEPTOR IS ENCODED BY ONE, LARGE EXON [J].
FABER, PW ;
KUIPER, GGJM ;
VANROOIJ, HCJ ;
VANDERKORPUT, JAGM ;
BRINKMANN, AO ;
TRAPMAN, J .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1989, 61 (02) :257-262
[8]   BAG-1L protein enhances androgen receptor function [J].
Froesch, BA ;
Takayama, S ;
Reed, JC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (19) :11660-11666
[9]   STRUCTURE AND DYNAMICS OF THE ESTROGEN-RECEPTOR [J].
GREENE, GL ;
PRESS, MF .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1986, 24 (01) :1-7
[10]  
Hayes SA, 2001, CANCER RES, V61, P2112