Steroid hormones regulate gene expression posttranscriptionally by altering the stabilities of messenger RNAs

被引:138
作者
Ing, NH [1 ]
机构
[1] Texas A&M Univ, Dept Anim Sci, College Stn, TX 77843 USA
关键词
gene regulation; mechanisms of hormone action; steroid hormones; steroid hormone receptors;
D O I
10.1095/biolreprod.105.040014
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hormones exert powerful effects on reproductive physiology by regulating gene expression. Recent discoveries in hormone action emphasize that regulation of gene expression is not restricted to their alterations of the rate of gene transcription. On the contrary, hormonal effects on the stability of it specific mRNA can profoundly alter its steady-state concentration. The mRNAs encoding hormone receptors are commonly regulated by their own hormones to create autoregulatory feedback loops. Negative and positive autoregulatory feedback loops serve to limit or augment hormonal responses, respectively. After introducing the topics of mRNA degradation and regulated stability, this review focuses on steroid hormone effects on mRNA stabilities. Autoregulation of the mRNAs encoding estrogen, progesterone, androgen, and glucocorticoid receptors by the steroid hormones in reproductive tissues is discussed. In addition, steroid hormone effects on the stabilities of many other mRNAs that are important to reproductive biology are reviewed. These include mRNAs that encode gonadotropin hormones, integrins, growth factors, and inflammatory response proteins. Through these posttranscriptional effects, steroid hormones impact the expression of a large population of genes. Studies of the molecular mechanisms of hormonally regulated mRNA stabilities continue to identify critical mRNA sequence elements and their interactions with proteins. Increased understanding of how hormones affect mRNA stability may yield novel approaches to the therapeutic control of hormone effects, including those essential to reproductive physiology in animals.
引用
收藏
页码:1290 / 1296
页数:7
相关论文
共 81 条
[31]   Estradiol-regulated expression of the immunophilins cyclophilin 40 and FKBP52 in MCF-7 breast cancer cells [J].
Kumar, P ;
Mark, PJ ;
Ward, BK ;
Minchin, RF ;
Ratajczak, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 284 (01) :219-225
[32]  
Kuwahara S, 2003, J NEUROSCI, V23, P10231
[33]   Progesterone mediates decreases in uterine smooth muscle cell interleukin-1α by a mechanism involving decreased stability of IL-1α mRNA. [J].
Lan, L ;
Vinci, JM ;
Melendez, JA ;
Jeffrey, JJ ;
Wilcox, BD .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1999, 155 (1-2) :123-133
[34]   Dexamethasone causes sustained expression of mitogen-activated protein kinase (MAPK) phosphatase 1 and phosphatase-mediated inhibition of MAPK p38 [J].
Lasa, M ;
Abraham, SM ;
Boucheron, C ;
Saklatvala, J ;
Clark, AR .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (22) :7802-7811
[35]   ESTROGEN ENHANCES ALPHA(V)BETA(3) INTEGRIN EXPRESSION BY AVIAN OSTEOCLAST PRECURSORS VIA STABILIZATION OF BETA(3) INTEGRIN MESSENGER-RNA [J].
LI, CF ;
ROSS, FP ;
CAO, X ;
TEITELBAUM, SL .
MOLECULAR ENDOCRINOLOGY, 1995, 9 (07) :805-813
[36]   RNase-L-dependent destabilization of interferon-induced mRNAs - A role for the 2-5A system in attenuation of the interferon response [J].
Li, XL ;
Blackford, JA ;
Judge, CS ;
Liu, MJ ;
Xiao, WH ;
Kalvakolanu, DV ;
Hassel, BA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (12) :8880-8888
[37]   Tissue distribution of AU-rich mRNA-binding proteins involved in regulation of mRNA decay [J].
Lu, JY ;
Schneider, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (13) :12974-12979
[38]  
Mahonen A, 1998, J CELL BIOCHEM, V68, P151, DOI 10.1002/(SICI)1097-4644(19980201)68:2<151::AID-JCB2>3.3.CO
[39]  
2-V
[40]   An extensive network of coupling among gene expression machines [J].
Maniatis, T ;
Reed, R .
NATURE, 2002, 416 (6880) :499-506