Modulation of cl signaling and ion transport by recruitment of kinases and phosphatases mediated by the regulatory protein IRBIT

Laura Vachel, Nikolay Shcheynikov, Osamu Yamazaki, Moran Fremder, Ehud Ohana, Aran Son, Dong Min Shin, Ai Yamazaki-Nakazawa, Chin Rang Yang, Mark A. Knepper, Shmuel Muallem

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5 Citations (Scopus)

Abstract

IRBIT is a multifunctional protein that controls the activity of various epithelial ion transporters including NBCe1-B. Interaction with IRBIT increases NBCe1-B activity and exposes two cryptic Cl-sensing GXXXP sites that enable regulation of NBCe1-B by intracellular Cl (Cl in). Here, phosphoproteomic analysis revealed that IRBIT controlled five phosphorylation sites in NBCe1-B that determined both the active conformation of the transporter and its regulation by Cl in. Mutational analysis suggested that the phosphorylation status of Ser232, Ser233, and Ser235 was regulated by IRBIT and determined whether NBCe1 transporters are in active or inactive conformations. The absence of phosphorylation at Ser232, Ser233, or Ser235 produced NBCe1-B in the conformations pSer233/pSer235, pSer232/pSer235, or pSer232/pSer233, respectively. The activity of the pSer233/pSer235 form was similar to that of IRBIT-activated NBCe1-B, but it was insensitive to inhibition by Cl in. The properties of the pSer232/pSer235 form were similar to those of wild-type NBCe1-B, whereas the pSer232/pSer233 form was partially active, further activated by IRBIT, but retained inhibition by Cl in. Furthermore, IRBIT recruited the phosphatase PP1 and the kinase SPAK to control phosphorylation of Ser65, which affected Cl in sensing by the 32GXXXP36 motif. IRBIT also recruited the phosphatase calcineurin and the kinase CaMKII to control phosphorylation of Ser12, which affected Cl in sensing by the194GXXXP198 motif. Ser232, Ser233, and Ser235 are conserved in all NBCe1 variants and affect their activity. These findings reveal how multiple kinase and phosphatase pathways use phosphorylation sites to fine-tune a transporter, which have important implications for epithelial fluid and HCO3 secretion.

Original languageEnglish
Article numbereaat5018
JournalScience Signaling
Volume11
Issue number554
DOIs
Publication statusPublished - 2018 Oct 30

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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    Vachel, L., Shcheynikov, N., Yamazaki, O., Fremder, M., Ohana, E., Son, A., Shin, D. M., Yamazaki-Nakazawa, A., Yang, C. R., Knepper, M. A., & Muallem, S. (2018). Modulation of cl signaling and ion transport by recruitment of kinases and phosphatases mediated by the regulatory protein IRBIT. Science Signaling, 11(554), [eaat5018]. https://doi.org/10.1126/scisignal.aat5018