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Complementation analyses suggest species-specific functions of the SNF5 homology domain.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2005 Oct 21; Vol. 336 (2), pp. 634-8. - Publication Year :
- 2005
-
Abstract
- Inactivation on both alleles of the hSNF5/INI1 tumor suppressor gene which encodes a subunit of the human SWI/SNF chromatin remodelling complex occurs in most malignant rhabdoid tumors. No paralog of hSNF5/INI1 is identified in the human genome. In contrast, it has two homologs in the yeast Saccharomyces cerevisiae, SNF5 and SFH1 which encode core components of the ySWI/SNF and RSC complexes, respectively. The homology mainly concerns an approximately 200 amino acid region termed the SNF5 homology domain. We have tested the ability of the hSNF5/INI1-wild type gene product and of chimerical constructs in which the yeast SNF5 domains were replaced by that of the human protein, to complement yeast snf5 and sfh1 phenotypes. Neither growth deficiencies on different carbon sources of snf5 yeasts nor the lethality of the sfh1 phenotype could be rescued. This strongly suggests that the SNF5 homology domain presents species-specific functions.
- Subjects :
- Amino Acid Sequence
Amino Acid Substitution
Binding Sites
Cell Proliferation
Cell Survival
Chromosomal Proteins, Non-Histone
DNA-Binding Proteins genetics
Humans
Molecular Sequence Data
Mutagenesis, Site-Directed
Protein Binding
Protein Structure, Tertiary
Recombinant Proteins chemistry
Recombinant Proteins metabolism
SMARCB1 Protein
Saccharomyces cerevisiae Proteins
Sequence Homology, Amino Acid
Species Specificity
Structure-Activity Relationship
Transcription Factors genetics
DNA-Binding Proteins chemistry
DNA-Binding Proteins metabolism
Saccharomyces cerevisiae physiology
Transcription Factors chemistry
Transcription Factors metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 336
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 16154112
- Full Text :
- https://doi.org/10.1016/j.bbrc.2005.08.133