Distinctive gene profiles occur at key points during natural metamorphosis in the Xenopus laevis tadpole tail

被引:41
作者
Veldhoen, N [1 ]
Crump, D [1 ]
Werry, K [1 ]
Helbing, CC [1 ]
机构
[1] Univ Victoria, Dept Biochem & Microbiol, Victoria, BC V8W 3P6, Canada
关键词
metamorphosis; Xenopus laevis; tadpole; thyroid hormone; cDNA array; gene expression;
D O I
10.1002/dvdy.10175
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Thyroid hormones (THs) are essential for tadpole metamorphosis into a juvenile frog; however, a complex interplay between additional hormones and signaling events also contributes to this dramatic developmental phase. A major mechanism of TH action is the nuclear receptor-mediated regulation of gene transcription of responsive genes. By using the precocious metamorphic model, several genes have been identified as TH responsive in the regressing tail. Many of these genes also exhibit altered expression during natural metamorphosis. Although identification of these genes provides insight into the mechanism whereby TH acts, complex interplay between TH and other hormones and the developmental stage-dependency of tissue responses contribute to the timing and coordination of metamorphic events. We investigated the temporal gene expression profile in Xenopus laevis tadpole tails from premetamorphosis through metamorphic climax by using a combination of a novel frog cDNA array containing 420 genes and quantitative real-time PCR. Seventy-nine genes were identified whose steady-state mRNA expression levels were altered in the tadpole tail during natural metamorphosis, of which 34 have previously been identified to be TH responsive in frogs or mammals. Of these genes, 75 clustered into 13 groups that displayed distinct developmental expression profiles. The levels of 28 transcripts were altered during premetamorphosis, 31 during prometamorphosis, and 43 with the onset of tail regression. This work establishes an important baseline for determining the mechanisms whereby tissues undergo differing metamorphic fates. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:457 / 468
页数:12
相关论文
共 64 条
[61]   Early gene expression changes preceding thyroid hormone-induced involution of a thyrotrope tumor [J].
Wood, WM ;
Sarapura, VD ;
Dowding, JM ;
Woodmansee, WW ;
Haakinson, DJ ;
Gordon, DF ;
Ridgway, EC .
ENDOCRINOLOGY, 2002, 143 (02) :347-359
[62]   ANTERIOR-PITUITARY AND ADRENAL-CORTICAL HORMONES ACCELERATE OR INHIBIT TADPOLE HINDLIMB GROWTH AND DEVELOPMENT DEPENDING ON STAGE OF SPONTANEOUS DEVELOPMENT OR THYROXINE CONCENTRATION IN INDUCED METAMORPHOSIS [J].
WRIGHT, ML ;
CYKOWSKI, LJ ;
LUNDRIGAN, L ;
HEMOND, KL ;
KOCHAN, DM ;
FASZEWSKI, EE ;
ANUSZEWSKI, CM .
JOURNAL OF EXPERIMENTAL ZOOLOGY, 1994, 270 (02) :175-188
[63]   XENOPUS-LAEVIS ALPHA-THYROID AND BETA-THYROID HORMONE RECEPTORS [J].
YAOITA, Y ;
SHI, YB ;
BROWN, DD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (18) :7090-7094
[64]   NOVEL PATHWAY FOR THYROID-HORMONE RECEPTOR ACTION THROUGH INTERACTION WITH JUN AND FOS ONCOGENE ACTIVITIES [J].
ZHANG, XK ;
WILLS, KN ;
HUSMANN, M ;
HERMANN, T ;
PFAHL, M .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (12) :6016-6025