Mutations in the basic domain and the loop-helix II junction of TWIST abolish DNA binding in Saethre-Chotzen syndrome.

Abstract

Saethre-Chotzen syndrome is an autosomal dominant skull disorder resulting from premature fusion of coronal sutures (craniosynostosis). It is caused by mutations in the TWIST gene encoding a basic Helix-Loop-Helix transcription factor. Here we report on the identification of a novel mutation affecting a highly conserved residue of the basic domain. Unlike nonsense and missense mutations lying within helices, this mutation does not affect protein stability or heterodimerisation of TWIST with its partner E12. However, it does abolish TWIST binding capacity to a target E-box as efficiently as two missense mutations in the loop-helix II junction. By contrast, elongation of the loop through a 7 amino acid insertion appears not to hamper binding to the DNA target. We conclude that loss of TWIST protein function in Saethre-Chotzen patients can occur at three different levels, namely protein stability, dimerisation, and DNA binding and that the loop-helix II junction is essential for effective protein-DNA interaction.

• Authors: V El Ghouzzi, L Legeai-Mallet, C Benoist-Lasselin, E Lajeunie, D Renier, A Munnich, J Bonaventure
• Journal: FEBS letters (FEBS Lett) Vol. 492 Issue 1-2 Pg. 112-8 (Mar 09 2001) ISSN: 0014-5793 [Print] England
• PMID: 11248247 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• DNA-Binding Proteins
• Nuclear Proteins
• TCF Transcription Factors
• TCF7L1 protein, human
• TWIST1 protein, human
• Transcription Factor 7-Like 1 Protein
• Transcription Factors
• Twist-Related Protein 1
• DNA

Topics

• Acrocephalosyndactylia (genetics)
• Amino Acid Substitution
• Animals
• Binding Sites
• COS Cells
• DNA (metabolism)
• DNA-Binding Proteins (chemistry, genetics, metabolism)
• Dimerization
• Humans
• Models, Molecular
• Mutation
• Nuclear Proteins
• Protein Conformation
• TCF Transcription Factors
• Transcription Factor 7-Like 1 Protein
• Transcription Factors (chemistry, genetics, metabolism)
• Twist-Related Protein 1