Literature DB >> 8768438

Primary structure and phylogenetic relationships of glyceraldehyde-3-phosphate dehydrogenase genes of free-living and parasitic diplomonad flagellates.

C Rozario1, L Morin, A J Roger, M W Smith, M Müller.   

Abstract

Complete nucleotide sequences have been established for two genes (gap1 and gap2) coding for glyceraldehyde-3-phosphate dehydrogenase (GAPDH, EC 1.2.1.12) homologs in the diplomonad Giardia lamblia. In addition, almost complete sequences of the GAPDH open reading frames were obtained from PCR products for two free-living diplomonad species, Trepomonas agillis and Hexamita inflata, and a parasite of Atlantic salmon, an as yet unnamed species with morphological affinities to Spironucleus. Giardia lamblia gap1 and the genes from the three other diplomonad species show high similarity to each other and to other glycolytic GAPDH genes. All amino-acyl residues known to be highly conserved in this enzyme are also conserved in these sequences. Giardia lamblia gap2 gene is more divergent and its putative translation reveals the presence of a cysteine and serine-rich insertion resembling a metal binding finger. This motif has not yet been noted in other GAPDH molecules. All sequences contain an S-loop signature with characteristics close to those of eukaryotes. In phylogenetic reconstructions based on the derived amino acid sequences with neighbor-joining, parsimony and maximum-likelihood methods the four typical GAPDH sequences of diplomonads cluster into a single clade. Within this clade, G. lambia gap1 shares a common ancestor with the rest of the genes. The latter are more closely related to each other, indicating an early separation of the lineage leading to the genus Giardia from the lineage encompassing the morphologically less differentiated genera, Trepomonas, Hexamita and that of the unnamed species. This result is discordant with the orthogonal evolution of diplomonads suggested on the basis of comparative morphology. In neighbor-joining reconstructions G. lamblia gap2 occupies a variable position, due to its great divergence. In parsimony and maximum likelihood analysis however, it shares a most recent common ancestor with the typical G. lamblia gap1 gene, suggesting that it diverged after the separation of the Giardia lineage. The position of the diplomonad clade in broader phylogenetic reconstructions is firmly within the typical cytosolic glycolytic representatives of GAPDH of eukaryotes.

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Year:  1996        PMID: 8768438     DOI: 10.1111/j.1550-7408.1996.tb03997.x

Source DB:  PubMed          Journal:  J Eukaryot Microbiol        ISSN: 1066-5234            Impact factor:   3.346


  5 in total

Review 1.  Origin and evolution of the mitochondrial proteome.

Authors:  C G Kurland; S G Andersson
Journal:  Microbiol Mol Biol Rev       Date:  2000-12       Impact factor: 11.056

Review 2.  Biology of Giardia lamblia.

Authors:  R D Adam
Journal:  Clin Microbiol Rev       Date:  2001-07       Impact factor: 26.132

3.  A possible mitochondrial gene in the early-branching amitochondriate protist Trichomonas vaginalis.

Authors:  A J Roger; C G Clark; W F Doolittle
Journal:  Proc Natl Acad Sci U S A       Date:  1996-12-10       Impact factor: 11.205

4.  In vivo determination of the gap2 gene promoter activity in Giardia lamblia.

Authors:  Hye-Won Yang; Juri Kim; Tai-Soon Yong; Soon-Jung Park
Journal:  Korean J Parasitol       Date:  2006-03       Impact factor: 1.341

5.  A Detailed Gene Expression Map of Giardia Encystation.

Authors:  Laura Rojas-López; Sascha Krakovka; Elin Einarsson; Ulf Ribacke; Feifei Xu; Jon Jerlström-Hultqvist; Staffan G Svärd
Journal:  Genes (Basel)       Date:  2021-11-30       Impact factor: 4.096

  5 in total

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