K.R. Blasier and M.K. Humsi contributed equally to this work.
Live cell imaging reveals differential modifications to cytoplasmic dynein properties by phospho- and dephosphomimic mutations of the intermediate chain 2C S84
Article first published online: 5 MAY 2014
© 2014 Wiley Periodicals, Inc.
Journal of Neuroscience Research
Volume 92, Issue 9, pages 1143–1154, September 2014
How to Cite
Blasier, K. R., Humsi, M. K., Ha, J., Ross, M. W., Smiley, W. R., Inamdar, N. A., Mitchell, D. J., Lo, K. W.-H. and Pfister, K. K. (2014), Live cell imaging reveals differential modifications to cytoplasmic dynein properties by phospho- and dephosphomimic mutations of the intermediate chain 2C S84. J. Neurosci. Res., 92: 1143–1154. doi: 10.1002/jnr.23388
- Issue published online: 12 JUL 2014
- Article first published online: 5 MAY 2014
- Manuscript Accepted: 26 FEB 2014
- Manuscript Revised: 25 FEB 2014
- Manuscript Received: 16 JAN 2014
- NIH Institute of General Medical Science. Grant Number: RO1 GM086472
- motor protein;
- axonal transport;
- cytoplasmic dynein
Cytoplasmic dynein is a multisubunit motor protein responsible for intracellular cargo transport toward microtubule minus ends. There are multiple isoforms of the dynein intermediate chain (DYNC1I, IC), which is encoded by two genes. One way to regulate cytoplasmic dynein is by IC phosphorylation. The IC-2C isoform is expressed in all cells, and the functional significance of phosphorylation on IC-2C serine 84 was investigated by using live cell imaging of fluorescent protein-tagged IC-2C wild type (WT) and phospho- and dephosphomimic mutant isoforms in axonal transport model systems. Both mutations modulated dynein functional properties. The dephosphomimic mutant IC-2C S84A had greater colocalization with mitochondria than the IC-2C WT or the phosphomimic mutant IC-2C S84D. The dephosphomimic mutant IC-2C S84A was also more likely to be motile than the phosphomimic mutant IC-2C S84D or the IC-2C WT. In contrast, the phosphomimic mutant IC-2C S84D mutant was more likely to move in the retrograde direction than was the IC-2C S84A mutant. The phosphomimic IC-2C S84D was also as likely as the IC-2C WT to colocalize with mitochondria. Both the S84D phospho- and the S84A dephosphomimic mutants were found to be capable of microtubule minus-end-directed (retrograde) movement in axons. They were also observed to be passively transported in the anterograde direction. These data suggest that the IC-2C S84 has a role in modulating dynein properties. © 2014 Wiley Periodicals, Inc.