Abstract
The Brain Tumor (Brat) protein is recruited to the 3′ untranslated region (UTR) of hunchback mRNA to regulate its translation. Recruitment is mediated by interactions between the Pumilio RNA-binding Puf repeats and the NHL domain of Brat, a conserved structural motif present in a large family of growth regulators. In this report, we describe the crystal structure of the Brat NHL domain and present a model of the Pumilio-Brat complex derived from in silico docking experiments and supported by mutational analysis of the protein-protein interface. A key feature of the model is recognition of the outer, convex surface of the Pumilio Puf domain by the top, electropositive face of the six-bladed Brat β-propeller. In particular, an extended loop in Puf repeat 8 fits in the entrance to the central channel of the Brat β-propeller. Together, these interactions are likely to be prototypic of the recruitment strategies of other NHL-containing proteins in development.
| Original language | English |
|---|---|
| Pages (from-to) | 2508-2513 |
| Number of pages | 6 |
| Journal | Genes and Development |
| Volume | 17 |
| Issue number | 20 |
| DOIs | |
| State | Published - 15 Oct 2003 |
Keywords
- Brain Tumor
- Crystal structure
- MRNA translation
- NHL domain
- Pumilio
- β-propellor
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