Cloning and characterization of human and mouse mitochondrial elongation factor G, GFM and Gfm, and mapping of GFM to human chromosome 3q25.1-q26.2
- PMID: 11374907
- DOI: 10.1006/geno.2001.6536
Cloning and characterization of human and mouse mitochondrial elongation factor G, GFM and Gfm, and mapping of GFM to human chromosome 3q25.1-q26.2
Abstract
Similar to the translational system in the cell cytoplasm, the initiation, elongation, and termination of protein synthesis in the mitochondria of eukaryotes are catalyzed by several protein factors. These factors, from the viewpoint of evolution, are more closely related to the corresponding prokaryotic factors than to those in the eukaryotic cytoplasm. In this paper, we isolated two cDNAs coding for human and mouse mitochondrial elongation factor G (GFM and Gfm, respectively). The GFM cDNA, which is 3481 bp in length, predicts a protein of 751 amino acids sharing 84 and 42% identity and 88 and 62% similarity to rat EF-G(mt) and Escherichia coli EF-G, respectively, and 24% identity and 39% similarity to human EF-2, the equivalent of EF-G in the cytoplasm. The mouse Gfm cDNA is 2564 bp and contains an intact open reading frame that encodes 751 amino acids showing 89% sequence identity and 94% similarity to human GFM. Northern blot analysis of human GFM revealed three transcripts of 3.8, 3.4, and 2.9 kb. The first two were expressed at high levels in heart, skeletal muscle, and testis, at moderate levels in liver and kidney, and at low levels in other tissues including brain, placenta, and lung, while the last transcript was expressed only in testis. The relative abundance of GFM was consistent with the observations for human EF-Tu(mt) and EF-Ts(mt), the other two mitochondrial elongation factors, indicating that the three factors were expressed at corresponding levels. The expression pattern of mouse Gfm was also determined, which showed that Gfm was expressed as a 3.0-kb transcript, abundantly in heart, skeletal muscle, kidney, and testis. In addition, GFM was assigned to human chromosome 3q25.1-q26.2 by the radiation hybrid mapping method. The genomic organization of GFM was also analyzed by comparing this cDNA with a genomic DNA sequence (Accession No. AC010936), which showed that GFM contained 18 exons and spanned at least 40 kb.
Copyright 2001 Academic Press.
Similar articles
-
Identification and characterization of two novel human mitochondrial elongation factor genes, hEFG2 and hEFG1, phylogenetically conserved through evolution.Hum Genet. 2001 Nov;109(5):542-50. doi: 10.1007/s00439-001-0610-5. Epub 2001 Oct 13. Hum Genet. 2001. PMID: 11735030
-
Cloning, expression patterns, and chromosome localization of three human and two mouse homologues of GABA(A) receptor-associated protein.Genomics. 2001 Jun 15;74(3):408-13. doi: 10.1006/geno.2001.6555. Genomics. 2001. PMID: 11414770
-
Orthologues of the Caenorhabditis elegans longevity gene clk-1 in mouse and human.Genomics. 1999 Jun 15;58(3):293-301. doi: 10.1006/geno.1999.5838. Genomics. 1999. PMID: 10373327
-
Human dehydroepiandrosterone sulfotransferase: molecular cloning of cDNA and genomic DNA.Chem Biol Interact. 1994 Jun;92(1-3):145-59. doi: 10.1016/0009-2797(94)90060-4. Chem Biol Interact. 1994. PMID: 8033249 Review.
-
Genomics of the human carnitine acyltransferase genes.Mol Genet Metab. 2000 Sep-Oct;71(1-2):139-53. doi: 10.1006/mgme.2000.3055. Mol Genet Metab. 2000. PMID: 11001805 Review.
Cited by
-
A novel composition of two heterozygous GFM1 mutations in a Chinese child with epilepsy and mental retardation.Brain Behav. 2020 Oct;10(10):e01791. doi: 10.1002/brb3.1791. Epub 2020 Aug 9. Brain Behav. 2020. PMID: 32776492 Free PMC article.
-
Ribosome-Targeting Antibiotics Impair T Cell Effector Function and Ameliorate Autoimmunity by Blocking Mitochondrial Protein Synthesis.Immunity. 2021 Jan 12;54(1):68-83.e6. doi: 10.1016/j.immuni.2020.11.001. Epub 2020 Nov 24. Immunity. 2021. PMID: 33238133 Free PMC article.
-
Infantile Progressive Hepatoencephalomyopathy with Combined OXPHOS Deficiency due to Mutations in the Mitochondrial Translation Elongation Factor Gene GFM1.JIMD Rep. 2012;5:113-22. doi: 10.1007/8904_2011_107. Epub 2011 Dec 21. JIMD Rep. 2012. PMID: 23430926 Free PMC article.
-
[Analysis of GFM1 gene mutations in a family with combined oxidative phosphorylation deficiency 1].Zhejiang Da Xue Xue Bao Yi Xue Ban. 2020 Oct 25;49(5):574-580. doi: 10.3785/j.issn.1008-9292.2020.10.04. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2020. PMID: 33210482 Free PMC article. Chinese.
-
Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations.Front Genet. 2015 Mar 23;6:102. doi: 10.3389/fgene.2015.00102. eCollection 2015. Front Genet. 2015. PMID: 25852744 Free PMC article.
Publication types
MeSH terms
Substances
Associated data
- Actions
- Actions
LinkOut - more resources
Full Text Sources
Molecular Biology Databases