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Derepression by depolymerization; structural insights into the regulation of Yan by Mae.
- Source :
-
Cell [Cell] 2004 Jul 23; Vol. 118 (2), pp. 163-73. - Publication Year :
- 2004
-
Abstract
- Yan, an ETS family transcriptional repressor, is regulated by receptor tyrosine kinase signaling via the Ras/MAPK pathway. Phosphorylation and downregulation of Yan is facilitated by a protein called Mae. Yan and Mae interact through their SAM domains. We find that repression by Yan requires the formation of a higher order structure mediated by Yan-SAM polymerization. Moreover, a crystal structure of the Yan-SAM/Mae-SAM complex shows that Mae-SAM specifically recognizes a surface on Yan-SAM that is also required for Yan-SAM polymerization. Mae-SAM binds to Yan-SAM with approximately 1000-fold higher affinity than Yan-SAM binds to itself and can effectively depolymerize Yan-SAM. Mutations on Mae that specifically disrupt its SAM domain-dependent interactions with Yan disable the derepression function of Mae in vivo. Depolymerization of Yan by Mae represents a novel mechanism of transcriptional control that sensitizes Yan for regulation by receptor tyrosine kinases.
- Subjects :
- Amino Acid Sequence physiology
Animals
Binding Sites genetics
Carrier Proteins genetics
Carrier Proteins metabolism
Cell Line
Drosophila
Drosophila Proteins genetics
Drosophila Proteins metabolism
Eye Proteins genetics
Eye Proteins metabolism
Humans
Models, Molecular
Molecular Structure
Mutation genetics
Polymers chemistry
Polymers metabolism
Protein Binding genetics
Protein Structure, Tertiary genetics
Receptor Protein-Tyrosine Kinases genetics
Receptor Protein-Tyrosine Kinases metabolism
Repressor Proteins genetics
Repressor Proteins metabolism
Surface Plasmon Resonance
Carrier Proteins chemistry
Drosophila Proteins chemistry
Eye Proteins chemistry
Genes, Regulator physiology
Intracellular Signaling Peptides and Proteins
Repressor Proteins chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 0092-8674
- Volume :
- 118
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Cell
- Publication Type :
- Academic Journal
- Accession number :
- 15260987
- Full Text :
- https://doi.org/10.1016/j.cell.2004.07.010