Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/199058
Type: Artigo de periódico
Title: Transcriptional Activity Analysis Of Promoter Region Of Human Pax9 Gene Under Dexamethasone, Retinoic Acid, And Ergocalciferol Treatment In Mcf-7 And Mdpc23.
Author: Ramenzoni, Liza L
Saito, Cristiane P B
McCormick, J Justin
Line, Sérgio R P
Abstract: PAX9 gene is a member of the family homeobox of transcription factors and performs important function in development and organogenesis. Mutations in PAX9 coding sequences have been implicated in autosomal dominant oligodontia affecting predominantly permanent molars and second premolars. Previous studies have shown that PAX9 is required for secondary palate development and teratogens have been identified as inducers of a tooth and craniofacial malformations. This work focused on the analysis on the 5'-flanking region of the PAX9 gene studying the influence of retinoic acid, dexamethasone, and vitamin D on the expression of PAX9 by expression constructs that carry the reporter gene luciferase. As results, retinoic acid and dexamethasone showed progressive decrease of PAX9 expression. PAX9-pGL3B1 and PAX9-pGL3B2 promoter was inhibited under the treatment of dexamethasone and ergocalciferol. Retinoic acid and dexamethasone did not alter PAX9-pGL3B3 behavior indicating that sequences present between -1106 and +92 were important for the transcriptional activity of PAX9 promoter. In this study, we characterized the transcriptional activity of specific regions of the PAX9 promoter gene and we demonstrated that retinoic acid and ergocalciferol can modulate the transcriptional activity of PAX9 gene.
Subject: 5' Flanking Region
Amino Acid Sequence
Animals
Anti-inflammatory Agents
Cell Line
Dexamethasone
Ergocalciferols
Gene Expression Regulation
Genes, Reporter
Humans
Mice
Osmolar Concentration
Pax9 Transcription Factor
Promoter Regions, Genetic
Rna, Messenger
Reverse Transcriptase Polymerase Chain Reaction
Sequence Alignment
Sequence Homology, Amino Acid
Transcriptional Activation
Tretinoin
Rights: fechado
Identifier DOI: 10.1002/cbf.1688
Address: http://www.ncbi.nlm.nih.gov/pubmed/20941745
Date Issue: 2010
Appears in Collections:Unicamp - Artigos e Outros Documentos

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