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Analysis of GapJunction AssemblyUsing MutatedConnexins Detected inCharcot—Marie—ToothX‐Linked Disease Patricia E. MartinElvira T. MambetisaevaDeborah A. Archer2000 год

Analysis of Gap Junction Assembly Using Mutated Connexins Detected in Charcot—Marie—Tooth X‐Linked Disease
статья из журнала

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Аннотация: The assembly of gap junction intercellular communication channels was studied by analysis of the molecular basis of the dysfunction of connexin 32 mutations associated with the X-linked form of Charcot-Marie-Tooth disease in which peripheral nervous transmission is impaired. A cell-free translation system showed that six recombinant connexin 32 mutated proteins-four point mutations at the cytoplasmic amino terminus, one at the membrane aspect of the cytoplasmic carboxyl terminus, and a deletion in the intracellular loop-were inserted into microsomal membranes and oligomerised into connexon hemichannels with varying efficiencies. The functionality of the connexons was determined by the ability of HeLa cells expressing the respective connexin cDNAs to transfer Lucifer yellow. The intracellular trafficking properties of the mutated connexins were determined by immunocytochemistry. The results show a relationship between intracellular interruption of connexin trafficking, the efficiency of intercellular communication, and the severity of the disease phenotype. Intracellular retention was explained either by deficiencies in the ability of connexins to oligomerise or by mutational changes at two targeting motifs. The results point to dominance of two specific targeting motifs: one at the amino terminus and one at the membrane aspect of the cytoplasmically located carboxyl tail. An intracellular loop deletion of six amino acids, associated with a mild phenotype, showed partial oligomerisation and low intercellular dye transfer compared with wild-type connexin 32. The results show that modifications in trafficking and assembly of gap junction channels emerge as a major feature of Charcot-Marie-Tooth X-linked disease.
Год издания: 2000
Авторы: Patricia E. Martin, Elvira T. Mambetisaeva, Deborah A. Archer, Christopher H. George, W. Howard Evans
Издательство: Wiley
Источник: Journal of Neurochemistry
Ключевые слова: Connexins and lens biology, Hereditary Neurological Disorders, Heat shock proteins research
Другие ссылки: Journal of Neurochemistry (HTML)
PubMed (HTML)