Unconventional tonicity-regulated nuclear trafficking of NFAT5 mediated by KPNB1, XPOT and RUVBL2

J Cell Sci. 2022 Jul 1;135(13):jcs259280. doi: 10.1242/jcs.259280. Epub 2022 Jul 12.

Abstract

NFAT5 is the only known mammalian tonicity-responsive transcription factor with an essential role in cellular adaptation to hypertonic stress. It is also implicated in diverse physiological and pathological processes. NFAT5 activity is tightly regulated by extracellular tonicity, but the underlying mechanisms remain elusive. Here, we demonstrate that NFAT5 enters the nucleus via the nuclear pore complex. We found that NFAT5 utilizes a unique nuclear localization signal (NFAT5-NLS) for nuclear import. siRNA screening revealed that only karyopherin β1 (KPNB1), but not karyopherin α, is responsible for the nuclear import of NFAT5 via direct interaction with the NFAT5-NLS. Proteomics analysis and siRNA screening further revealed that nuclear export of NFAT5 under hypotonicity is driven by exportin-T (XPOT), where the process requires RuvB-like AAA-type ATPase 2 (RUVBL2) as an indispensable chaperone. Our findings have identified an unconventional tonicity-dependent nucleocytoplasmic trafficking pathway for NFAT5 that represents a critical step in orchestrating rapid cellular adaptation to change in extracellular tonicity. These findings offer an opportunity for the development of novel NFAT5 targeting strategies that are potentially useful for the treatment of diseases associated with NFAT5 dysregulation.

Keywords: Exportin-T; Importin; NFAT5; Nucleocytoplasmic trafficking; RUVBL2.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • ATPases Associated with Diverse Cellular Activities / genetics
  • ATPases Associated with Diverse Cellular Activities / metabolism
  • Active Transport, Cell Nucleus
  • Animals
  • Carrier Proteins / metabolism
  • Cell Nucleus* / metabolism
  • DNA Helicases
  • Humans
  • Karyopherins* / metabolism
  • Mammals / metabolism
  • Nuclear Localization Signals / metabolism
  • Nucleocytoplasmic Transport Proteins
  • RNA, Small Interfering / metabolism
  • Transcription Factors / metabolism
  • beta Karyopherins / genetics
  • beta Karyopherins / metabolism

Substances

  • Carrier Proteins
  • KPNB1 protein, human
  • Karyopherins
  • NFAT5 protein, human
  • Nuclear Localization Signals
  • Nucleocytoplasmic Transport Proteins
  • RNA, Small Interfering
  • Transcription Factors
  • XPOT protein, human
  • beta Karyopherins
  • ATPases Associated with Diverse Cellular Activities
  • DNA Helicases
  • RUVBL2 protein, human