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iASPP preferentially binds p53 proline-rich region and modulates apoptotic function of codon 72-polymorphic p53.
- Source :
-
Nature genetics [Nat Genet] 2006 Oct; Vol. 38 (10), pp. 1133-41. Date of Electronic Publication: 2006 Sep 10. - Publication Year :
- 2006
-
Abstract
- iASPP is one of the most evolutionarily conserved inhibitors of p53, whereas ASPP1 and ASPP2 are activators of p53. We show here that, in addition to the DNA-binding domain, the ASPP family members also bind to the proline-rich region of p53, which contains the most common p53 polymorphism at codon 72. Furthermore, the ASPP family members, particularly iASPP, bind to and regulate the activity of p53Pro72 more efficiently than that of p53Arg72. Hence, escape from negative regulation by iASPP is a newly identified mechanism by which p53Arg72 activates apoptosis more efficiently than p53Pro72.
- Subjects :
- Amino Acid Sequence
Arginine
Binding Sites
Breast Neoplasms genetics
Carcinoma genetics
Cells, Cultured
Codon
Conserved Sequence
Female
Gene Expression Regulation
Homozygote
Humans
Intracellular Signaling Peptides and Proteins genetics
Molecular Sequence Data
Repressor Proteins
Tumor Suppressor Protein p53 metabolism
Tyrosine metabolism
Apoptosis physiology
Intracellular Signaling Peptides and Proteins metabolism
Polymorphism, Genetic
Proline metabolism
Tumor Suppressor Protein p53 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1061-4036
- Volume :
- 38
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Nature genetics
- Publication Type :
- Academic Journal
- Accession number :
- 16964264
- Full Text :
- https://doi.org/10.1038/ng1879