Please use this identifier to cite or link to this item: https://doi.org/10.1074/jbc.M110.132423
Title: Cooperativity between the phosphorylation of Thr95and Ser 77 of NHERF-1 in the hormonal regulation of renal phosphate transport
Authors: Weinman, E.J.
Steplock, D.
Zhang, Y.
Biswas, R.
Bloch, R.J.
Shenolikar, S. 
Issue Date: 13-Aug-2010
Citation: Weinman, E.J., Steplock, D., Zhang, Y., Biswas, R., Bloch, R.J., Shenolikar, S. (2010-08-13). Cooperativity between the phosphorylation of Thr95and Ser 77 of NHERF-1 in the hormonal regulation of renal phosphate transport. Journal of Biological Chemistry 285 (33) : 25134-25138. ScholarBank@NUS Repository. https://doi.org/10.1074/jbc.M110.132423
Abstract: The phosphorylation of the sodium-hydrogen exchanger regulatory factor-1 (NHERF-1) plays a key role in the regulation of renal phosphate transport by parathyroid hormone (PTH) and dopamine. Ser77 in the first PDZ domain of NHERF-1 is a downstream target of both hormones. The current experiments explore the role of Thr95, another phosphate acceptor site in the PDZ I domain, on hormone-mediated regulation of phosphate transport in the proximal tubule of the kidney. The substitution of alanine for threonine at position 95 (T95A) significantly decreased the rate and extent of in vitro phosphorylation of Ser77 by PKC. In NHERF-1-null proximal tubule cells, neither PTH nor dopamine inhibited sodium-dependent phosphate transport. Infection of the cells with adenovirus expressing full-length WT GFP-NHERF-1 increased basal phosphate transport and restored the inhibitory effect of both PTH and dopamine. Infection with full-length NHERF-1 containing a T95A mutation, however, increased basal phosphate transport but not the responsiveness to either hormone. As determined by surface plasmon resonance, the substitution of serine for aspartic acid (S77D) in the PDZ I domain decreased the binding affinity to the sodium-dependent phosphate transporter 2a (Npt2a) as compared with WTPDZ I, but a T95D mutation had no effect on binding. Finally, cellular studies indicated that both PTH and dopamine treatment increased the phosphorylation of Thr95. These studies indicate a remarkable cooperativity between the phosphorylation of Thr95 and Ser77 of NHERF-1 in the hormonal regulation of renal phosphate transport. The phosphorylation of Thr95 facilitates the phosphorylation of Ser77. This, in turn, results in the dissociation of NHERF-1 from Npt2a and a decrease in phosphate transport in renal proximal tubule cells.
Source Title: Journal of Biological Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/128606
ISSN: 00219258
DOI: 10.1074/jbc.M110.132423
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

SCOPUSTM   
Citations

39
checked on Dec 10, 2018

WEB OF SCIENCETM
Citations

34
checked on Dec 10, 2018

Page view(s)

6
checked on Mar 10, 2018

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.