The long term goal of this project is to fully define the function and role of PRKX protein kmase in normal renal development and in PKD mutants. Using a degenerate PCR cloning strategy and library screening techniques, I identified the full length PRKX gene from a human fetal kidney library. Since its distribution patterns are developmentally regulated and differ in ADPKD and ARPKD versus normal kidneys, this has led us to the hypothesis that PRKX kinase is important for the regulation and signal transduction of the PKDl-encoded protein, polycystin-1. Our preliminary studies also suggest that PRKX is bona fide cAMP-responsive kinase that signal to the nucleus via CREB proteins to stimulate gene transcription via CRE elements. In vitro phosphorylation study showed that PRKX fusion protein can phosphorylate PKD 1 C terminal domain. Our hypothesis, therefore is that PRKX protein kinase -is responsible for serine phosphorylation of polycystin-1 protein and that this has important consequences for the regulation of appropriate signal transduction and gene transcription.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32DK010130-02
Application #
6523944
Study Section
General Medicine B Study Section (GMB)
Program Officer
Rankin, Tracy L
Project Start
2002-08-15
Project End
Budget Start
2002-08-15
Budget End
2003-08-14
Support Year
2
Fiscal Year
2002
Total Cost
$54,352
Indirect Cost
Name
Mount Sinai School of Medicine
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
114400633
City
New York
State
NY
Country
United States
Zip Code
10029
Li, Xiaohong; Burrow, Christopher R; Polgar, Katalin et al. (2008) Protein kinase X (PRKX) can rescue the effects of polycystic kidney disease-1 gene (PKD1) deficiency. Biochim Biophys Acta 1782:1-9
Polgar, Katalin; Burrow, Christopher R; Hyink, Deborah P et al. (2005) Disruption of polycystin-1 function interferes with branching morphogenesis of the ureteric bud in developing mouse kidneys. Dev Biol 286:16-30
Li, Xiaohong; Hyink, Deborah P; Polgar, Katalin et al. (2005) Protein kinase X activates ureteric bud branching morphogenesis in developing mouse metanephric kidney. J Am Soc Nephrol 16:3543-52
Li, Xiaohong; Li, Hsi-Ping; Amsler, Kurt et al. (2002) PRKX, a phylogenetically and functionally distinct cAMP-dependent protein kinase, activates renal epithelial cell migration and morphogenesis. Proc Natl Acad Sci U S A 99:9260-5