Preprint Review Version 1 Preserved in Portico This version is not peer-reviewed

The Phosphoinositide 5-Phosphatase inpp5k: From Gene Structure to in Vivo Functions

Version 1 : Received: 16 September 2020 / Approved: 17 September 2020 / Online: 17 September 2020 (11:19:10 CEST)

How to cite: Schurmans, S.; Vande Catsyne, C.; Desmet, C.; Möes, B. The Phosphoinositide 5-Phosphatase inpp5k: From Gene Structure to in Vivo Functions. Preprints 2020, 2020090399 (doi: 10.20944/preprints202009.0399.v1). Schurmans, S.; Vande Catsyne, C.; Desmet, C.; Möes, B. The Phosphoinositide 5-Phosphatase inpp5k: From Gene Structure to in Vivo Functions. Preprints 2020, 2020090399 (doi: 10.20944/preprints202009.0399.v1).

Abstract

INPP5K (Inositol Polyphosphate 5-Phosphatase K, or SKIP (for Skeletal muscle and Kidney enriched Inositol Phosphatase) is a member of the phosphoinositide 5-phosphatases family. Its protein structure is comprised of a N-terminal catalytic domain which hydrolyses both PtdIns(4,5)P2 and PtdIns(3,4,5)P3, followed by a SKICH domain at the C-terminus which is responsible for protein-protein interactions and subcellular localization of INPP5K. Strikingly, INPP5K is mostly concentrated in the endoplasmic reticulum, although it is also detected at the plasma membrane, in the cytosol and the nucleus. Recently, mutations in INPP5K have been detected in patients with a rare form of autosomal recessive congenital muscular dystrophy with cataract, short stature and intellectual disability. INPP5K functions extend from control of insulin signaling, endoplasmic reticulum stress response and structural integrity, myoblast differentiation, cytoskeleton organization, cell adhesion and migration, renal osmoregulation, to cancer. The goal of this review is thus to summarize and comment recent and less recent data in the literature on INPP5K, in particular on the structure, expression, intracellular localization, interactions and functions of this specific member of the 5-phosphatases family.

Subject Areas

inositide; phosphoinositide; 5-phosphatase; INPP5K; SKIP; phosphatidylinositol 3,4,5-trisphosphate; phosphatidylinositol 4,5-bisphosphate; congenital muscular dystrophy; cataract; intellectual disability; insulin signaling; insulin resistance; endoplasmic reticulum; endoplasmic reticulum stress; unfolded protein response

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