Marco, Antonio and Cuesta, Ana and Pedrola, Laia and Palau, Francesc and Marín, Ignacio (2004) 'Evolutionary and structural analyses of GDAP1, involved in Charcot-Marie-Tooth disease, characterize a novel class of glutathione transferase-related genes.' Mol Biol Evol, 21 (1). 176 - 187. ISSN 0737-4038

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Abstract

Mutations in the Ganglioside-induced differentiation-associated protein-1 (GDAP1) gene cause autosomal recessive Charcot-Marie-Tooth disease type 4A. The protein encoded by GDAP1 shows clear similarity to glutathione transferases (also known as glutathione S-transferases or GSTs). The human genome contains a paralog of GDAP1 called GDAP1L1. Using comparative genomics, we show that orthologs of GDAP1 and GDAP1L1 are found in mammals, birds, amphibians, and fishes. Likely orthologs of those genes in invertebrates and a low but consistent similarity with some plant and eubacterial genes have also been found. We demonstrate that GDAP1 and GDAP1L1 do not belong to any of the known classes of GST genes. In addition to having distinctive sequences, GDAP1 and its relatives are also characterized by an extended region in GST domain II, absent in most other GSTs, and by a C-terminal end predicted to contain transmembrane domains. Mutations affecting any of those characteristic domains are known to cause Charcot-Marie-Tooth disease. These features define the GDAP1 class of GST-like proteins.

Item Type:	Article
Uncontrolled Keywords:	Amino Acid Sequence, Charcot-Marie-Tooth Disease, Cluster Analysis, Databases, Genetic, Evolution, Molecular, Glutathione Transferase, Humans, Molecular Sequence Data, Multigene Family, Nerve Tissue Proteins, Phylogeny, Protein Conformation, Sequence Alignment
Subjects:	Q Science > Q Science (General)
Divisions:	Faculty of Science and Health > Life Sciences, School of
Depositing User:	Antonio Marco
Date Deposited:	23 Mar 2015 19:39
Last Modified:	19 Aug 2019 23:15
URI:	http://repository.essex.ac.uk/id/eprint/8505

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