WBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor network.
Détails
ID Serval
serval:BIB_B2DCC33D5ABF
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
WBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor network.
Périodique
Human Molecular Genetics
ISSN
0964-6906 (Print)
ISSN-L
0964-6906
Statut éditorial
Publié
Date de publication
2001
Volume
10
Numéro
6
Pages
617-627
Langue
anglais
Résumé
Williams-Beuren syndrome (WBS) is a developmental disorder associated with haploinsufficiency of multiple genes at 7q11.23. Here, we report the functional characterization of WBS critical region gene 14 (WBSCR14), a gene contained in the WBS commonly deleted region. It encodes a basic-helix--loop--helix leucine zipper (bHLHZip) transcription factor of the Myc/Max/Mad superfamily. WBSCR14 is expressed in multiple tissues, including regions of the brain and the intestinal tract. WBSCR14 forms heterodimers with the bHLHZip protein Mlx to bind the DNA sequence CACGTG. Like Max, Mlx has no intrinsic transcriptional activity, but its association with Mad1, Mad4, Mnt or WBSCR14 can repress E-box-dependent transcription. Preliminary results suggest a possible role of WBSCR14 in growth control. Our data support the view that the Max-like bHLHZip protein, Mlx, is a key element of a transcription factor network. We thus suggest that WBSCR14 may contribute to some aspects of the WBS pathology.
Mots-clé
Amino Acid Sequence, Animals, Basic Helix-Loop-Helix Leucine Zipper Transcription Factors, Cell Differentiation/genetics, Cell Division/genetics, Cells, Cultured, Chromosome Mapping, Chromosomes, Human, Pair 7, DNA/metabolism, DNA-Binding Proteins/metabolism, Dimerization, Gene Deletion, Gene Expression, Humans, Mice, Molecular Sequence Data, Sequence Homology, Amino Acid, Transcription Factors/genetics, Transcription Factors/metabolism, Transcription, Genetic/genetics, Transfection, Williams Syndrome/genetics, Williams Syndrome/metabolism
Pubmed
Web of science
Open Access
Oui
Création de la notice
24/01/2008 15:52
Dernière modification de la notice
20/08/2019 15:21