Protein Kinase A Regulates Molecular Chaperone Transcription and Protein Aggregation
DSpace/Manakin Repository
Protein Kinase A Regulates Molecular Chaperone Transcription and Protein Aggregation
| Title: | Protein Kinase A Regulates Molecular Chaperone Transcription and Protein Aggregation |
| Author: |
Prince, Thomas; Zhang, Yue; Calderwood, Stuart K.; Murshid, Ayesha
Note: Order does not necessarily reflect citation order of authors. |
| Citation: | Zhang, Yue, Ayesha Murshid, Thomas Prince, and Stuart K. Calderwood. 2011. Protein kinase a regulates molecular chaperone transcription and protein aggregation. PLoS ONE 6(12): e29850. |
| Full Text & Related Files: |
3245242.pdf (1.840Mb; PDF) 
|
| Abstract: | Heat shock factor 1 (HSF1) regulates one of the major pathways of protein quality control and is essential for deterrence of protein-folding disorders, particularly in neuronal cells. However, HSF1 activity declines with age, a change that may open the door to progression of neurodegenerative disorders such as Huntington's disease. We have investigated mechanisms of HSF1 regulation that may become compromised with age. HSF1 binds stably to the catalytic domain of protein kinase A (PKAcα) and becomes phosphorylated on at least one regulatory serine residue (S320). We show here that PKA is essential for effective transcription of HSP genes by HSF1. PKA triggers a cascade involving HSF1 binding to the histone acetylase p300 and positive translation elongation factor 1 (p-TEFb) and phosphorylation of the c-terminal domain of RNA polymerase II, a key mechanism in the downstream steps of HSF1-mediated transcription. This cascade appears to play a key role in protein quality control in neuronal cells expressing aggregation-prone proteins with long poly-glutamine (poly-Q) tracts. Such proteins formed inclusion bodies that could be resolved by HSF1 activation during heat shock. Resolution of the inclusions was inhibited by knockdown of HSF1, PKAcα, or the pTEFb component CDK9, indicating a key role for the HSF1-PKA cascade in protein quality control. |
| Published Version: | doi:10.1371/journal.pone.0028950 |
| Other Sources: | http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245242/ |
| Terms of Use: | This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA |
| Citable link to this page: | http://nrs.harvard.edu/urn-3:HUL.InstRepos:8519284 |
| Downloads of this work: |
This item appears in the following Collection(s)
-
HMS Scholarly Articles [16253]
Contact administrator regarding this item (to report mistakes or request changes)
