Dominant functional role of the novel phosphorylation site S811 in the human renal NaCl cotransporter. Issue 8 (16th March 2018)
- Record Type:
- Journal Article
- Title:
- Dominant functional role of the novel phosphorylation site S811 in the human renal NaCl cotransporter. Issue 8 (16th March 2018)
- Main Title:
- Dominant functional role of the novel phosphorylation site S811 in the human renal NaCl cotransporter
- Authors:
- Tutakhel, Omar A. Z.
Bianchi, Frans
Smits, Daniel A.
Bindels, Rene J. M.
Hoenderop, Joost G. J.
van der Wijst, Jenny - Abstract:
- Abstract : The NaCl cotransporter (NCC) is essential for electrolyte homeostasis and control of blood pressure. The human SLC12A3 gene, which encodes NCC, gives rise to 3 isoforms, of which only the shortest isoform [NaCl cotransporter isoform 3 (NCC3 )] has been studied extensively. All NCC isoforms share key phosphorylation sites at T55 and T60 that are essential mediators of NCC function. Recently, a novel phosphorylation site at S811 was identified in isoforms 1 and 2 [NaCl cotransporter splice variant (NCCSV )], which are only present in humans and higher primates. The aim of the current study, therefore, is to investigate the role of S811 phosphorylation in the regulation of NCC by a combination of biochemical and fluorescent microscopy analyses. We demonstrate that hypotonic low‐chloride buffer increases S811 phosphorylation, whereas phosphorylation‐deficient S811A mutant hinders phosphorylation at T55 and T60 in NCCSV and NCC3 .NCCSV S811A impairs NCC3 activity in a dominantnegative fashion, although it does not affect plasma membrane abundance. This effect may be explained by the heterodimerization of NCCSV with NCC3 . Taken together, our study highlights the dominant‐negative effect of NCCSV on T55 and T60 phosphorylation and NCC activity. Here, we reveal a new function of NCCSV in humans that broadens the understanding on NCC regulation in blood pressure control.—Tutakhel, O. A. Z., Bianchi, F., Smits, D. A., Bindels, R. J. M., Hoenderop, J. G. J., van der Wijst,Abstract : The NaCl cotransporter (NCC) is essential for electrolyte homeostasis and control of blood pressure. The human SLC12A3 gene, which encodes NCC, gives rise to 3 isoforms, of which only the shortest isoform [NaCl cotransporter isoform 3 (NCC3 )] has been studied extensively. All NCC isoforms share key phosphorylation sites at T55 and T60 that are essential mediators of NCC function. Recently, a novel phosphorylation site at S811 was identified in isoforms 1 and 2 [NaCl cotransporter splice variant (NCCSV )], which are only present in humans and higher primates. The aim of the current study, therefore, is to investigate the role of S811 phosphorylation in the regulation of NCC by a combination of biochemical and fluorescent microscopy analyses. We demonstrate that hypotonic low‐chloride buffer increases S811 phosphorylation, whereas phosphorylation‐deficient S811A mutant hinders phosphorylation at T55 and T60 in NCCSV and NCC3 .NCCSV S811A impairs NCC3 activity in a dominantnegative fashion, although it does not affect plasma membrane abundance. This effect may be explained by the heterodimerization of NCCSV with NCC3 . Taken together, our study highlights the dominant‐negative effect of NCCSV on T55 and T60 phosphorylation and NCC activity. Here, we reveal a new function of NCCSV in humans that broadens the understanding on NCC regulation in blood pressure control.—Tutakhel, O. A. Z., Bianchi, F., Smits, D. A., Bindels, R. J. M., Hoenderop, J. G. J., van der Wijst, J. Dominant functional role of the novel phosphorylation site S811 in the human renal NaCl cotransporter. FASEB J . 32, 4482–4493 (2018). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 32:Issue 8(2018)
- Journal:
- FASEB journal
- Issue:
- Volume 32:Issue 8(2018)
- Issue Display:
- Volume 32, Issue 8 (2018)
- Year:
- 2018
- Volume:
- 32
- Issue:
- 8
- Issue Sort Value:
- 2018-0032-0008-0000
- Page Start:
- 4482
- Page End:
- 4493
- Publication Date:
- 2018-03-16
- Subjects:
- hypertension -- kidney -- NCC -- splice variant
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.201701047R ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13222.xml