Dual functions of thyroid hormone receptors during Xenopus development

被引:106
作者
Sachs, LM
Damjanovski, S
Jones, PL
Li, Q
Amano, T
Ueda, S
Shi, YB [1 ]
Ishizuya-Oka, A
机构
[1] NICHHD, Mol Embryol Lab, NIH, Bethesda, MD 20892 USA
[2] Dokkyo Univ, Sch Med, Dept Histol & Neurobiol, Mibu, Tochigi 32102, Japan
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY | 2000年 / 126卷 / 02期
关键词
apoptosis; cell death; cell proliferation; metamorphosis; transcriptional regulation; Xenopus laevis; amphibian; thyroid hormone receptor;
D O I
10.1016/S0305-0491(00)00198-X
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
Thyroid hormone (TH) plays a causative role in anuran metamorphosis. This effect is presumed to be manifested through the regulation of gene expression by TH receptors (TRs). TRs can act as both activators and repressors of a TH-inducible gene depending upon the presence and absence of TH, respectively We have been investigating the roles of TRs during Xenopus laevis development, including premetamorphic and metamorphosing stages. In this review, we summarize some of the studies on the TRs by others and us. These studies reveal that TRs have dual functions in frog development as reflected in the following two aspects. First, TRs function initially as repressors of TH-inducible genes in premetamorphic tadpoles to prevent precocious metamorphosis, thus ensuring a proper period of tadpole growth, and later as activators of these genes to activate the metamorphic process. Second, TRs can promote both cell proliferation and apoptosis during metamorphosis, depending upon the cell type in which they are expressed. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:199 / 211
页数:13
相关论文
共 81 条
[21]  
GUERNSEY DL, 1983, MOL BASIS THYROID HO, P293
[22]  
HATZEL BS, 1989, STORY IODINE DEFICIE
[23]   A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression [J].
Heinzel, T ;
Lavinsky, RM ;
Mullen, TM ;
Soderstrom, M ;
Laherty, CD ;
Torchia, J ;
Yang, WM ;
Brard, G ;
Ngo, SD ;
Davie, JR ;
Seto, E ;
Eisenman, RN ;
Rose, DW ;
Glass, CK ;
Rosenfeld, MG .
NATURE, 1997, 387 (6628) :43-48
[24]   SEQUENTIAL UP-REGULATION OF THYROID-HORMONE BETA-RECEPTOR, ORNITHINE TRANSCARBAMYLASE, AND CARBAMYL-PHOSPHATE SYNTHETASE MESSENGER-RNAS IN THE LIVER OF RANA-CATESBEIANA TADPOLES DURING SPONTANEOUS AND THYROID HORMONE-INDUCED METAMORPHOSIS [J].
HELBING, C ;
GERGELY, G ;
ATKINSON, BG .
DEVELOPMENTAL GENETICS, 1992, 13 (04) :289-301
[25]   LIGAND-INDEPENDENT REPRESSION BY THE THYROID-HORMONE RECEPTOR-MEDIATED BY A NUCLEAR RECEPTOR CO-REPRESSOR [J].
HORLEIN, AJ ;
NAAR, AM ;
HEINZEL, T ;
TORCHIA, J ;
GLOSS, B ;
KUROKAWA, R ;
RYAN, A ;
KAMEL, Y ;
SODERSTROM, M ;
GLASS, CK ;
ROSENFELD, MG .
NATURE, 1995, 377 (6548) :397-404
[26]   Metamorphosis is inhibited in transgenic Xenopus laevis tadpoles that overexpress type III deiodinase [J].
Huang, HC ;
Marsh-Armstrong, N ;
Brown, DD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (03) :962-967
[27]  
IshizuyaOka A, 1997, DEV GENET, V20, P53, DOI 10.1002/(SICI)1520-6408(1997)20:1<53::AID-DVG7>3.0.CO
[28]  
2-8
[29]  
IshizuyaOka A, 1997, DEV GENET, V20, P329, DOI 10.1002/(SICI)1520-6408(1997)20:4<329::AID-DVG4>3.0.CO
[30]  
2-9