Journal
JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 287, Issue 7, Pages 5122-5132Publisher
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M111.297192
Keywords
-
Categories
Funding
- National Institutes of Health from NIDCR [Z1A-DE000735]
- Machiah Foundation [2008-0702]
- foundation of the Jewish Community Federation of San Francisco
- Peninsula, Marin, and Sonoma Counties
Ask authors/readers for more resources
Slc26a2 is a ubiquitously expressed SO42- transporter with high expression levels in cartilage and several epithelia. Mutations in SLC26A2 are associated with diastrophic dysplasia. The mechanism by which Slc26a2 transports SO42- and the ion gradients that mediate SO42- uptake are poorly understood. We report here that Slc26a2 functions as an SO42-/2OH(-), SO42-/2Cl(-), andSO(4)(2-)/OH-/Cl- exchanger, depending on the Cl- and OH- gradients. At inward Cl- and outward pH gradients (high Cl-o(-) and low pH(o)) Slc26a2 functions primarily as an SO4o2-/2OH(i)(-) exchanger. At low Cl-o(-) and high pH(o) Slc26a2 functions increasingly as an SO4o2-/2Cl(i)(-) exchanger. The reverse is observed for SO4i2-/2OH(o)(-) and SO4i2-/2Cl(o)(-) exchange. Slc26a2 also exchanges Cl- for I-, Br-, and NO3- and Cl-o(-) competes with SO42- on the transport site. Interestingly, Slc26a2 is regulated by an extracellular anion site, required to activate SO4i2-/2OH(o)(-) exchange. Slc26a2 can transport oxalate in exchange for OH- and/or Cl- with properties similar to SO42- transport. Modeling of the Slc26a2 transmembrane domain (TMD) structure identified a conserved extracellular sequence (367)GFXXP(371) between TMD7 and TMD8 close to the conserved Glu(417) in the permeation pathway. Mutation of Glu(417) eliminated transport by Slc26a2, whereas mutation of Phe(368) increased the affinity for SO4o2- 8-fold while reducing the affinity for Cl-o(-) 2 fold, but without affecting regulation by Cl-o(-). These findings clarify the mechanism of net SO42- transport and describe a novel regulation of Slc26a2 by an extracellular anion binding site and should help in further understanding aberrant SLC26A2 function in diastrophic dysplasia.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available