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The polyQ expansion modulates the configuration and phosphorylation of huntingtin

Jung, T.-Y.; Shin, B.; Tamo, G.; Kim, H.; Vijayvargia, R.; Leitner, A.; Marcaida, M. J.; Astorga-Wells, J.; Jung, R.; Aebersold, R.; Dal Peraro, M.; Hebert, H.; Seong, I. S.; Song, J.-J.

2019-07-31 neuroscience
10.1101/721191 bioRxiv
Show abstract

The polyQ-expansion at the N-terminus of huntingtin (HTT) is the prime cause of Huntingtons disease. The recent cryo-EM structure of HTT with HAP40 provides information on the proteins prominent HEAT-repeats. Here, we present analyses of the impact of polyQ-length on the conformation of HTT by cryo-EM, the domain-interactions by cross-linking mass spectrometry and the phosphorylation of HTT. The cryo-EM analysis of normal (Q23-) and disease (Q78-) type HTTs in their apo forms shows that the structures of apo HTTs significantly differ from the structure of HTT-HAP40, and that the polyQ expansion induces global structural changes consisting of significant domain movements of the C-HEAT domain relative to the N-HEAT domain. In addition, we show that the polyQ-expansion alters the phosphorylation pattern across the full-length HTT and that the specific phosphorylation (Ser2116p) in turn affects the global structure of HTT, which influences the activity of polyQ-expanded HTT. These results provide a molecular basis for the effect of the N-terminal polyQ segment on HTT structure and activity, that may be important for the cell-selective toxicity of mutant HTT.

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