Cyclic-AMP-responsive transcriptional activation of CREB-327 involves interdependent phosphorylated subdomains
- PMID: 2176153
- PMCID: PMC552238
- DOI: 10.1002/j.1460-2075.1990.tb07896.x
Cyclic-AMP-responsive transcriptional activation of CREB-327 involves interdependent phosphorylated subdomains
Retraction in
-
Cyclic AMP-responsive transcriptional activation domain of CREB-327 involves interdependent phosphorylated subdomains.EMBO J. 1994 Jun 1;13(11):2736. doi: 10.1002/j.1460-2075.1994.tb06564.x. EMBO J. 1994. PMID: 8013471 Free PMC article. No abstract available.
Abstract
Cyclic AMP-regulated gene expression is mediated by specific phosphoproteins (CREBs) which bind to cAMP-responsive elements of gene promoters. By analyzing the transactivation activities and phosphorylations in vivo of deletion and point mutated chimeric fusion proteins of the placental CREB-327, in which the DNA-binding domain is replaced by the heterologous binding-domain of the yeast transcription factor GAL4, we localized the cAMP-responsive and phosphorylated domain to a minimal-essential sequence module of 46 amino acids (residues 92-137). This serine-rich, multiply-phosphorylated sequence consists of at least three interdependent subdomains required for transcriptional activation. Although phosphorylation of serine-119 by cyclic AMP-dependent protein kinase A is necessary for transcriptional activation, such activation requires both a phosphorylated heptadecapeptide domain located ten residues amino terminal to the serine-119 and an eleven-residue domain carboxyl terminal to the serine-119. Deletion of these two domains does not impair phosphorylation of serine-119. Further, deletion of the carboxyl-terminal domain does not alter phosphorylation of the heptadecapeptide domain. We propose that akin to the phosphorylation-dependent activation of enzymes, the transcriptional transactivation functions of CREB-327 involve a phosphorylation-dependent allosteric conformational mechanism.
Comment in
-
Findings of scientific misconduct.NIH Guide Grants Contracts (Bethesda). 1996 Mar 29;25(10):2-3. NIH Guide Grants Contracts (Bethesda). 1996. PMID: 8615993 Free PMC article. No abstract available.
Similar articles
-
Genetic characterization of transactivation of the human T-cell leukemia virus type 1 promoter: Binding of Tax to Tax-responsive element 1 is mediated by the cyclic AMP-responsive members of the CREB/ATF family of transcription factors.Mol Cell Biol. 1996 May;16(5):2174-82. doi: 10.1128/MCB.16.5.2174. Mol Cell Biol. 1996. PMID: 8628284 Free PMC article.
-
Transcriptional regulation of the transforming growth factor-beta2 promoter by cAMP-responsive element-binding protein (CREB) and activating transcription factor-1 (ATF-1) is modulated by protein kinases and the coactivators p300 and CREB-binding protein.J Biol Chem. 1999 Nov 26;274(48):34020-8. doi: 10.1074/jbc.274.48.34020. J Biol Chem. 1999. PMID: 10567368
-
A secondary phosphorylation of CREB341 at Ser129 is required for the cAMP-mediated control of gene expression. A role for glycogen synthase kinase-3 in the control of gene expression.J Biol Chem. 1994 Dec 23;269(51):32187-93. J Biol Chem. 1994. PMID: 7798217
-
Transcriptional regulation by cyclic AMP-responsive factors.Prog Nucleic Acid Res Mol Biol. 2000;64:343-69. doi: 10.1016/s0079-6603(00)64009-6. Prog Nucleic Acid Res Mol Biol. 2000. PMID: 10697414 Review.
-
What turns CREB on?Cell Signal. 2004 Nov;16(11):1211-27. doi: 10.1016/j.cellsig.2004.05.001. Cell Signal. 2004. PMID: 15337521 Review.
Cited by
-
Lipopolysaccharide stimulation of trophoblasts induces corticotropin-releasing hormone expression through MyD88.Am J Obstet Gynecol. 2008 Sep;199(3):317.e1-6. doi: 10.1016/j.ajog.2008.06.091. Am J Obstet Gynecol. 2008. PMID: 18771998 Free PMC article.
-
Sexual dimorphism of stress response and immune/ inflammatory reaction: the corticotropin releasing hormone perspective.Mediators Inflamm. 1995;4(3):163-74. doi: 10.1155/S0962935195000275. Mediators Inflamm. 1995. PMID: 18475634 Free PMC article.
-
The cAMP response element binding protein, CREB, is a potent inhibitor of diverse transcriptional activators.Nucleic Acids Res. 1993 Jun 25;21(12):2907-11. doi: 10.1093/nar/21.12.2907. Nucleic Acids Res. 1993. PMID: 8332500 Free PMC article.
-
Expression of a peptide inhibitor of protein phosphatase 1 increases phosphorylation and activity of CREB in NIH 3T3 fibroblasts.Mol Cell Biol. 1994 Jul;14(7):4398-407. doi: 10.1128/mcb.14.7.4398-4407.1994. Mol Cell Biol. 1994. PMID: 7516466 Free PMC article.
-
Phosphorylation of CREB affects its binding to high and low affinity sites: implications for cAMP induced gene transcription.EMBO J. 1992 Sep;11(9):3337-46. doi: 10.1002/j.1460-2075.1992.tb05412.x. EMBO J. 1992. PMID: 1354612 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases