4.1 Review

Mutations in cardiovascular connexin genes

Journal

BIOLOGY OF THE CELL
Volume 106, Issue 9, Pages 269-293

Publisher

WILEY
DOI: 10.1111/boc.201400038

Keywords

Connexins; Gap junctions; Gene mutations; Genetic diseases

Categories

Funding

  1. Swiss National Science Foundation [310030_143343, CRSII3_136207]
  2. Swiss Heart Foundation
  3. Fondation Leenaards
  4. Swiss National Science Foundation (SNF) [310030_143343] Funding Source: Swiss National Science Foundation (SNF)

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Connexins (Cxs) form a family of transmembrane proteins comprising 21 members in humans. Cxs differ in their expression patterns, biophysical properties and ability to combine into homomeric or heteromeric gap junction channels between neighbouring cells. The permeation of ions and small metabolites through gap junction channels or hemichannels confers a crucial role to these proteins in intercellular communication and in maintaining tissue homeostasis. Among others, Cx37, Cx40, Cx43, Cx45 and Cx47 are found in heart, blood and lymphatic vessels. Mutations or polymorphisms in the genes coding for these Cxs have not only been implicated in cardiovascular pathologies but also in a variety of other disorders. While mutations in Cx43 are mostly linked to oculodentodigital dysplasia, Cx47 mutations are associated with Pelizaeus-Merzbacher-like disease and lymphoedema. Cx40 mutations are principally linked to atrial fibrillation. Mutations in Cx37 have not yet been described, but polymorphisms in the Cx37 gene have been implicated in the development of arterial disease. This review addresses current knowledge on gene mutations in cardiovascular Cxs systematically and links them to alterations in channel properties and disease.

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