A splice variant of the human phosphohistidine phosphatase 1 (PHPT1) is degraded by the proteasome
2014 (English)In: International Journal of Biochemistry and Cell Biology, ISSN 1357-2725, E-ISSN 1878-5875, Vol. 57, 69-75 p.Article in journal (Refereed) Published
Regulation of protein activity by phosphorylation is central in many cellular processes. Phosphorylation of serine, threonine and tyrosine residues is well documented and studied. In addition, other amino acids, like histidine can be phosphorylated, but neither the mechanism nor the function of this modification is well understood. Nevertheless, there is a 14 kDa enzyme with phosphohistidine phosphatase activity, named PHPT1, found in most animals, but not in bacteria, plant or fungi. There are a few splice variant transcripts formed from the human PHPT1 locus and some of them are predicted to form variant proteins, but studies of these proteins are lacking. In order to get insight into the possible function of the variant transcripts encoded at the PHPT1 locus, ectopic expression of PHPT1 transcript variant 6, predicted to be degraded by the non-sense mediated mRNA decay pathway, in HeLa cells was undertaken. In HeLa cells the splice variant protein was degraded by the proteasome, unlike the wild type protein. Using an in silico modeling approach the variant C-terminal end of the proteins were predicted to form different secondary structures that might explain the different properties of the two proteins. The specific degradation of the PHPT1 splice variant indicates that at least for the PHPT1 protein, the quality control and the self-guarding of the cellular system works at two levels, first at the RNA level, aberrant transcripts are degraded by the non-sense mediated mRNA decay pathway, and the small amount of proteins that are formed will be degraded by the proteasome.
Place, publisher, year, edition, pages
Elsevier, 2014. Vol. 57, 69-75 p.
Phosphohistidine phosphatase, PHPT1, Proteasome, Splice variant, Nonsense-mediated decay
Research subject Biology with specialization in Molecular Cell Biology
IdentifiersURN: urn:nbn:se:uu:diva-235728DOI: 10.1016/j.biocel.2014.10.009ISI: 000347662300009PubMedID: 25450458OAI: oai:DiVA.org:uu-235728DiVA: diva2:761749
FunderSwedish Research Council, 6212011-4688Swedish Research Council, K2012-99X-21959-01-3Swedish Cancer Society, 13 0410