Two thyroid hormone-mediated gene expression patterns in vivo identified by cDNA expression arrays in rat

被引:90
作者
Weitzel, JM [1 ]
Radtke, C [1 ]
Seitz, HJ [1 ]
机构
[1] Univ Klinikum Hamburg Eppendorf, Inst Med Biochem & Mol Biol, D-20246 Hamburg, Germany
关键词
D O I
10.1093/nar/29.24.5148
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 (T3) is essential for normal development, differentiation and metabolic balance. Only a limited number of T3-target genes have been identified so far and their complex regulation pattern is poorly understood. We performed cDNA expression array hybridisation to identify T3-regulated genes and to investigate their expression pattern after various time points in vivo. Radioactively labelled cDNA was prepared from hepatic RNA of hypothyroid and hyperthyroid rats 6, 24 and 48 h after the administration of T3. Labelled cDNA probes were hybridised to rat Atlas Arrays. Twenty-three of 588 genes were shown to be differentially regulated, 18 of which were previously not known to be regulated by T3. The expression of 19 genes was verified by independent northern blot hybridisation. Two different expression time courses of T3 expression were observed. In a first expression profile ('early' expression) the transcription level of the target genes rises within 6 h, drops by 24 h and increases again within 48 h after the administration of T3. In a second expression profile ('late' expression) the mRNA level rose in the first 6 h and rose further by 48 h, indicating an additional regulation mechanism. Nuclear respiratory factor (NRF)-1 and peroxisome proliferator-activated receptor gamma coactivator 1 (PGC-1), but not NRF-2, were up-regulated within 6 h after T3 adminstration, suggesting NRF-1 and/or PGC-1 as key regulators for mediating the 'late' expression pattern.
引用
收藏
页码:5148 / 5155
页数:8
相关论文
共 47 条
[1]   The expression pattern of thyroid hormone response genes in the tadpole tail identifies multiple resorption programs [J].
Berry, DL ;
Schwartzman, RA ;
Brown, DD .
DEVELOPMENTAL BIOLOGY, 1998, 203 (01) :12-23
[2]  
CARTER WJ, 1975, J BIOL CHEM, V250, P3588
[3]   Making and reading microarrays [J].
Cheung, VG ;
Morley, M ;
Aguilar, F ;
Massimi, A ;
Kucherlapati, R ;
Childs, G .
NATURE GENETICS, 1999, 21 (Suppl 1) :15-19
[4]   Identification of redox-sensitive cysteines in GA binding protein-α that regulate DNA binding and heterodimerization [J].
Chinenov, Y ;
Schmidt, T ;
Yang, XY ;
Martin, ME .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (11) :6203-6209
[5]   Nuclear receptors: coactivators, corepressors and chromatin remodeling in the control of transcription [J].
Collingwood, TN ;
Urnov, FD ;
Wolffe, AP .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 1999, 23 (03) :255-275
[6]   Nongenomic actions of thyroid hormone [J].
Davis, PJ ;
Davis, FB .
THYROID, 1996, 6 (05) :497-504
[7]   Thyroid hormone-dependent gene expression program for Xenopus neural development [J].
Denver, RJ ;
Pavgi, S ;
Shi, YB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (13) :8179-8188
[8]   Expression profiling using cDNA microarrays [J].
Duggan, DJ ;
Bittner, M ;
Chen, YD ;
Meltzer, P ;
Trent, JM .
NATURE GENETICS, 1999, 21 (Suppl 1) :10-14
[9]  
Dummler K, 1996, BIOCHEM J, V317, P913
[10]   Thyroid hormone regulation of hepatic genes in vivo detected by complementary DNA microarray [J].
Feng, X ;
Jiang, Y ;
Meltzer, P ;
Yen, PM .
MOLECULAR ENDOCRINOLOGY, 2000, 14 (07) :947-955