Gain-of-function mutations in STIM1 and ORAI1 causing tubular aggregate myopathy and Stormorken syndrome.

Abstract

Calcium (Ca2+) is a key regulator for a large number of cellular functions in all kinds of cells, and small disturbances of Ca2+ homeostasis can severely compromise normal physiology in various tissues and organs. A major mechanism controlling Ca2+ homeostasis is store-operated Ca2+ entry (SOCE), which relies on the concerted action of the reticular Ca2+ sensor STIM1 and the plasma membrane Ca2+ channel ORAI1. Gain-of-function mutations in the respective genes induce excessive Ca2+ entry, and cause tubular aggregate myopathy (TAM) and Stormorken syndrome. Both disorders are part of a clinical continuum and involve muscle weakness and additional variably pronounced features including miosis, thrombocytopenia, hyposplenism, ichthyosis, dyslexia, and short stature. Mutations in the reticular Ca2+ buffer calsequestrin (CASQ1) have moreover been associated with the mild end of the TAM/Stormorken syndrome spectrum. Here we review the clinical and histological characteristics of both disorders, provide an overview on the genetic causes, and thereby focus on the pathomechanisms leading to muscle dysfunction and the multi-systemic phenotype of tubular aggregate myopathy and Stormorken syndrome.

• Authors: Johann Böhm, Jocelyn Laporte
• Journal: Cell calcium (Cell Calcium) Vol. 76 Pg. 1-9 (12 2018) ISSN: 1532-1991 [Electronic] Netherlands
• PMID: 30243034 (Publication Type: Journal Article, Review)
• Copyright: Copyright © 2018 Elsevier Ltd. All rights reserved.

Chemical References

• ORAI1 Protein
• Stromal Interaction Molecule 1
• Calcium

Topics

• Blood Platelet Disorders (genetics, metabolism)
• Calcium (metabolism)
• Dyslexia (genetics, metabolism)
• Erythrocytes, Abnormal (metabolism)
• Gain of Function Mutation
• Humans
• Ichthyosis (genetics, metabolism)
• Migraine Disorders (genetics, metabolism)
• Miosis (genetics, metabolism)
• Muscle Fatigue (genetics)
• Myopathies, Structural, Congenital (genetics, metabolism)
• ORAI1 Protein (genetics, metabolism)
• Spleen (abnormalities, metabolism)
• Stromal Interaction Molecule 1 (genetics, metabolism)