NUCLEAR REMODELING IN RESPONSE TO STEROID-HORMONE ACTION

被引:5
作者
BRASCH, K
OCHS, RL
机构
[1] SCRIPPS RES INST, WM KECK AUTOIMMUNE DIS CTR, LA JOLLA, CA 92093 USA
[2] SCRIPPS RES INST, DEPT MOLEC & EXPTL MED, LA JOLLA, CA 92093 USA
来源
INTERNATIONAL REVIEW OF CYTOLOGY - A SURVEY OF CELL BIOLOGY, VOL 159 | 1995年 / 159卷
关键词
STEROID HORMONES; RECEPTORS; NUCLEUS; COILED BODIES; CANCER;
D O I
10.1016/S0074-7696(08)62107-5
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
Steroid and similar hormones comprise the broadest class of gene regulatory agents known, spanning vertebrates through the lower animals, and even fungi. Not unexpectedly, therefore, steroid receptors belong to an evolutionary highly conserved family of proteins. After complexing with their cognate ligands, receptors interact with hormone response elements on target genes and modulate transcription. These actions are multifaceted and only partly understood, and include large-scale changes in the structure and molecular composition of the affected cell nuclei. This chapter examines steroid hormone action and the resultant nuclear remodeling from the following perspectives: (1) Where are the receptors located? (2) Which nuclear domains are most affected? (3) Are there extended or permanent nuclear changes? (4) What is the role of coiled bodies and similar structures in this regard? To address these and related questions, information is drawn from several sources, including vertebrates, insects, and malignant tissues. Entirely new data are presented as well as a review of the literature. © 1995, Elsevier Inc. All rights reserved.
引用
收藏
页码:161 / 194
页数:34
相关论文
共 195 条
[51]   REVERSIBLE DISASSEMBLY OF TRANSCRIPTION DOMAINS IN LYMPHOCYTE NUCLEI DURING INHIBITION OF RNA-SYNTHESIS BY DRB [J].
DAVIS, L ;
CADRIN, M ;
BROWN, DL ;
CHALY, N .
BIOLOGY OF THE CELL, 1993, 78 (03) :163-180
[52]  
de la Espina S M, 1982, Cell Biol Int Rep, V6, P601, DOI 10.1016/0309-1651(82)90184-9
[53]  
DELAESPINA SMD, 1982, BIOL CELL, V44, P229
[54]   RELATIONSHIP BETWEEN ULTRASTRUCTURE AND FUNCTION OF HEPATOCYTE CHROMATIN - STUDY WITH ADRENALECTOMIZED RATS AFTER CORTISOL ADMINISTRATION [J].
DERENZINI, M ;
PESSIONBRIZZI, A ;
BONETTI, E ;
NOVELLO, F .
JOURNAL OF ULTRASTRUCTURE RESEARCH, 1979, 67 (02) :161-179
[55]   THE PML-RAR-ALPHA FUSION MESSENGER-RNA GENERATED BY THE T(15-17) TRANSLOCATION IN ACUTE PROMYELOCYTIC LEUKEMIA ENCODES A FUNCTIONALLY ALTERED RAR [J].
DETHE, H ;
LAVAU, C ;
MARCHIO, A ;
CHOMIENNE, C ;
DEGOS, L ;
DEJEAN, A .
CELL, 1991, 66 (04) :675-684
[56]   THE T(15-17) TRANSLOCATION OF ACUTE PROMYELOCYTIC LEUKEMIA FUSES THE RETINOIC ACID RECEPTOR-ALPHA GENE TO A NOVEL TRANSCRIBED LOCUS [J].
DETHE, H ;
CHOMIENNE, C ;
LANOTTE, M ;
DEGOS, L ;
DEJEAN, A .
NATURE, 1990, 347 (6293) :558-561
[57]   GENETIC STABILITY AND MODULATION OF METAZOAN NUCLEI TRANSPLANTED INTO EGGS AND OOCYTES [J].
DIBERARDINO, MA .
DIFFERENTIATION, 1980, 17 (01) :17-30
[58]   DEVELOPMENTAL PATHWAY OF GRANULAR AND BEADED NUCLEAR BODIES FROM NUCLEOLI [J].
DUPUYCOIN, AM ;
BOUTEILLE, M .
JOURNAL OF ULTRASTRUCTURE RESEARCH, 1972, 40 (1-2) :55-+
[59]   A NOVEL MACROMOLECULAR STRUCTURE IS A TARGET OF THE PROMYELOCYTE-RETINOIC ACID RECEPTOR ONCOPROTEIN [J].
DYCK, JA ;
MAUL, GG ;
MILLER, WH ;
CHEN, JD ;
KAKIZUKA, A ;
EVANS, RM .
CELL, 1994, 76 (02) :333-343
[60]  
ELICEIRI GL, 1994, J CELL PHYSL, V121, P449