Basic transcription element binding protein is a thyroid hormone‐regulated transcription factor expressed during metamorphosis in Xenopus laevis

Basic transcription element binding protein (BTEB) is a member of the Krüppel family of zinc finger transcription factors. It has been shown that BTEB plays a role in promoting neuronal process formation during postembryonic development. In the present study, the biochemical properties, transactivation function, and the developmental and hormone‐regulated expression of BTEB in Xenopus laevis (xBTEB) are described. xBTEB binds the GC‐rich basic transcription element (BTE) with high affinity and functions as a transcriptional activator on promoters containing multiple or single GC boxes. xBTEB mRNA levels increase in the tadpole brain, intestine and tail during metamorphosis, and are correlated with tissue‐specific morphological and biochemical transformations. xBTEB mRNA expression can be induced precociously in premetamorphic tadpole tissues by treatment with thyroid hormone. In situ hybridization histochemistry showed that thyroid hormone upregulates xBTEB mRNA throughout the brain of premetamorphic tadpoles, with the highest expression found in the subventricular zones of the telencephalon, diencephalon, optic tectum, cerebellum and spinal cord. xBTEB protein parallels changes in its mRNA, and it was found that xBTEB is not expressed in mitotic cells in the developing brain, but is expressed just distal to the proliferative zone, supporting the hypothesis that this protein plays a role in neural cell differentiation.

[1]  J. Puymirat,et al.  Suppression of the basic transcription element-binding protein in brain neuronal cultures inhibits thyroid hormone-induced neurite branching. , 2002, Endocrinology.

[2]  D. Dang,et al.  The biology of the mammalian Krüppel-like family of transcription factors. , 2000, The international journal of biochemistry & cell biology.

[3]  J. Metcalfe,et al.  Mouse BTEB3, a new member of the basic transcription element binding protein (BTEB) family, activates expression from GC-rich minimal promoter regions. , 2000, The Biochemical journal.

[4]  D. D. Brown,et al.  In vitro and in vivo analysis of the regulation of a transcription factor gene by thyroid hormone during Xenopus laevis metamorphosis. , 1999, Molecular endocrinology.

[5]  Yunbo Shi Amphibian Metamorphosis: From Morphology to Molecular Biology , 1999 .

[6]  R J Denver,et al.  Basic Transcription Element-binding Protein (BTEB) Is a Thyroid Hormone-regulated Gene in the Developing Central Nervous System , 1999, The Journal of Biological Chemistry.

[7]  D. D. Brown,et al.  The expression pattern of thyroid hormone response genes in remodeling tadpole tissues defines distinct growth and resorption gene expression programs. , 1998, Developmental biology.

[8]  R. Koenig,et al.  Protein-protein interaction domains and the heterodimerization of thyroid hormone receptor variant alpha2 with retinoid X receptors. , 1998, Molecular endocrinology.

[9]  J. Oppenheimer,et al.  Molecular basis of thyroid hormone-dependent brain development. , 1997, Endocrine reviews.

[10]  B. Demeneix,et al.  Adenovirus enhancement of polyethylenimine-mediated transfer of regulated genes in differentiated cells , 1997, Gene Therapy.

[11]  Oppenheimer Jh Citation for the 1997 Edwin B. Astwood Lecture Award of The Endocrine Society to John D. Baxter. , 1997 .

[12]  T. Takeda,et al.  Oct-1, silencer sequence, and GC box regulate thyroid hormone receptor β1 promoter , 1997, Molecular and Cellular Endocrinology.

[13]  Yunbo Shi,et al.  Thyroid Hormone-dependent Gene Expression Program for Xenopus Neural Development* , 1997, The Journal of Biological Chemistry.

[14]  Z. Wang,et al.  The thyroid hormone-induced tail resorption program during Xenopus laevis metamorphosis. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[15]  K. Hashizume,et al.  Importance of the most proximal GC box for activity of the promoter of human thyroid hormone receptor beta 1. , 1995, Molecular endocrinology.

[16]  J. Gurdon,et al.  Normal table of Xenopus laevis (Daudin) , 1995 .

[17]  A. Seasholtz,et al.  Molecular and biochemical characterization of the mouse brain corticotropin-releasing hormone-binding protein , 1995, Molecular and Cellular Endocrinology.

[18]  H. Akil,et al.  Mu, delta, and kappa opioid receptor mRNA expression in the rat CNS: An in situ hybridization study , 1994, The Journal of comparative neurology.

[19]  J. Wong,et al.  Transcriptional repression of Xenopus TR beta gene is mediated by a thyroid hormone response element located near the start site. , 1994, The Journal of biological chemistry.

[20]  Y. B. Shi,et al.  Cloning and characterization of the ribosomal protein L8 gene from Xenopus laevis. , 1994, Biochimica et biophysica acta.

[21]  Y. Fujii‐Kuriyama,et al.  Comparison of DNA-binding properties between BTEB and Sp1. , 1993, Journal of biochemistry.

[22]  D. D. Brown,et al.  The earliest changes in gene expression in tadpole intestine induced by thyroid hormone. , 1993, The Journal of biological chemistry.

[23]  Zhou Wang,et al.  Thyroid hormone-induced gene expression program for amphibian tail resorption. , 1993, The Journal of biological chemistry.

[24]  É. M. Rabelo,et al.  Autoinduction of nuclear receptor genes and its significance , 1993, The Journal of Steroid Biochemistry and Molecular Biology.

[25]  Y Fujii-Kuriyama,et al.  cDNA cloning and transcriptional properties of a novel GC box-binding protein, BTEB2. , 1993, Nucleic acids research.

[26]  S. P. Porterfield,et al.  The role of thyroid hormones in prenatal and neonatal neurological development--current perspectives. , 1993, Endocrine reviews.

[27]  L. Buckbinder,et al.  Thyroid hormone-induced gene expression changes in the developing frog limb. , 1992, The Journal of biological chemistry.

[28]  Y. Fujii‐Kuriyama,et al.  Two regulatory proteins that bind to the basic transcription element (BTE), a GC box sequence in the promoter region of the rat P‐4501A1 gene. , 1992, The EMBO journal.

[29]  J. Tata,et al.  Autoinduction of thyroid hormone receptor during metamorphosis is reproduced in Xenopus XTC-2 cells , 1992, Molecular and Cellular Endocrinology.

[30]  J. Dixon,et al.  Eukaryotic proteins expressed in Escherichia coli: an improved thrombin cleavage and purification procedure of fusion proteins with glutathione S-transferase. , 1991, Analytical biochemistry.

[31]  Y. Yaoita,et al.  A correlation of thyroid hormone receptor gene expression with amphibian metamorphosis. , 1990, Genes & development.

[32]  Y. Fujii‐Kuriyama,et al.  A novel cis-acting DNA element required for a high level of inducible expression of the rat P-450c gene , 1990, Molecular and cellular biology.

[33]  R. Tjian,et al.  Transcriptional regulation in mammalian cells by sequence-specific DNA binding proteins. , 1989, Science.

[34]  R. Tjian,et al.  Analysis of Sp1 in vivo reveals mutiple transcriptional domains, including a novel glutamine-rich activation motif , 1988, Cell.

[35]  P. Licht,et al.  Thyroid hormones act at the level of the pituitary to regulate thyrotropin and growth hormone secretion in hatchling slider turtles (Pseudemys scripta elegans) , 1988 .

[36]  H. Jäckle,et al.  A conserved family of nuclear proteins containing structural elements of the finger protein encoded by Krüppel, a Drosophila segmentation gene , 1986, Cell.

[37]  R. Tjian,et al.  Transcription factor Sp1 recognizes promoter sequences from the monkey genome that are simian virus 40 promoter. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[38]  P. Licht,et al.  Studies on the specificity of thyroid response to pituitary glycoprotein hormones. , 1984, General and comparative endocrinology.

[39]  B. Howard,et al.  Recombinant genomes which express chloramphenicol acetyltransferase in mammalian cells , 1982, Molecular and cellular biology.

[40]  C. Dournon,et al.  [Effects of thyroid hormone on cell proliferation in the amphibian larva (author's transl)]. , 1974, Annales d'endocrinologie.

[41]  P. Weiss,et al.  Growth Responses of Opposite Sign Among Different Neuron Types Exposed to Thyroid Hormone. , 1951, Proceedings of the National Academy of Sciences of the United States of America.

[42]  R. Denver 12 – Neuroendocrine Control of Amphibian Metamorphosis , 1996 .

[43]  J. Tata,et al.  Analysis of structure and expression of the Xenopus thyroid hormone receptor-beta gene to explain its autoinduction. , 1995, Molecular endocrinology.

[44]  Y. Fujii‐Kuriyama,et al.  Analysis of functional domains of a GC box-binding protein, BTEB. , 1995, Journal of biochemistry.

[45]  R. Tjian,et al.  Transcription factor Spl recognizes promoter sequences from the monkey genome that are similar to the simian virus 40 promoter , 2022 .