Literature DB >> 15081407

Genomic organization, expression, and subcellular localization of mouse mitochondrial seryl-tRNA synthetase.

William J Gibbons1, Qingfeng Yan, Ronghua Li, Xiaoming Li, Min-Xin Guan.   

Abstract

We report here the identification and characterization of the mouse mitochondrial seryl-tRNA synthetase (mtSerRS). The genomic organization of mouse mtSerRS has been elucidated. The mouse mtSerRS gene containing 16 exons encodes a 519 residue protein with a strong homology to the mitochondria-like seryl-tRNA synthetase of bacteria, yeast, and other homologs. The mouse mtSerRS is ubiquitously expressed in various tissues, but more abundantly in tissues with high metabolic rates including heart and liver. Surprisingly, this gene, unlike other nuclear genes encoding mitochondrial proteins, exhibited a low expression in skeletal muscle and brain. Furthermore, immunofluorescence analysis of NIH3T3 cells expressing the mtSerRS-GFP fusion protein demonstrated that the mouse mtSerRS localizes in mitochondrion. These observations suggest that the mouse mtSerRS is an evolutionarily conserved protein involved in aminoacylation. Thus, it may play a role in the fidelity in mitochondrial translation and pathogenesis of deafness-associated mutations in the mitochondrial tRNA(Ser(UCN)).

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Year:  2004        PMID: 15081407     DOI: 10.1016/j.bbrc.2004.03.113

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  3 in total

1.  Genome-wide search of the genes tagged with the consensus of 33.6 repeat loci in buffalo Bubalus bubalis employing minisatellite-associated sequence amplification.

Authors:  Deepali Pathak; Jyoti Srivastava; Rana Samad; Iqbal Parwez; Sudhir Kumar; Sher Ali
Journal:  Chromosome Res       Date:  2010-05-18       Impact factor: 5.239

2.  Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndrome.

Authors:  Ruth Belostotsky; Efrat Ben-Shalom; Choni Rinat; Rachel Becker-Cohen; Sofia Feinstein; Sharon Zeligson; Reeval Segel; Orly Elpeleg; Suheir Nassar; Yaacov Frishberg
Journal:  Am J Hum Genet       Date:  2011-01-20       Impact factor: 11.025

3.  The bidirectional promoter of two genes for the mitochondrial translational apparatus in mouse is regulated by an array of CCAAT boxes interacting with the transcription factor NF-Y.

Authors:  Ernesto Zanotto; Zahid H Shah; Howard T Jacobs
Journal:  Nucleic Acids Res       Date:  2006-12-19       Impact factor: 16.971

  3 in total

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