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Characterization of a novel human putative mitochondrial transporter homologous to the yeast mitochondrial RNA splicing proteins 3 and 4.
Li, F Y; Nikali, K; Gregan, J; Leibiger, I; Leibiger, B; Schweyen, R; Larsson, C; Suomalainen, A.
Afiliação
  • Li FY; Department of Molecular Medicine, CMM, Karolinska Hospital, Stockholm, Sweden. fangyuan.li@cmm.ki.se
FEBS Lett ; 494(1-2): 79-84, 2001 Apr 06.
Article em En | MEDLINE | ID: mdl-11297739
ABSTRACT
We report here a novel human gene, hMRS3/4, encoding a putative mitochondrial transporter structurally and functionally homologous to the yeast mitochondrial RNA splicing proteins 3 and 4. These proteins belong to the family of mitochondrial carrier proteins (MCF) and are likely to function as solute carriers. hMRS3/4 spans approximately 10 kb of genomic DNA on chromosome 10q24 and consists of four exons that encode a 364-aa protein with six transmembrane domains. A putative splice variant, encoding a 177-aa protein with three transmembrane domains, was also identified. hMRS3/4 has a well-conserved signature sequence of MCF and is targeted into the mitochondria. When expressed in yeast, hMRS3/4 efficiently restores the mitochondrial functions in mrs3(o)mrs4(o) knock-out mutants. Ubiquitous expression in human tissues and a well-conserved structure and function suggest an important role for hMRS3/4 in human cells.
Assuntos
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Base de dados: MEDLINE Assunto principal: Proteínas de Membrana Transportadoras / Proteínas Repressoras / Cromossomos Humanos Par 10 / Proteínas de Transporte / Processamento Alternativo / Proteínas de Transporte de Cátions / Proteínas de Saccharomyces cerevisiae / Mitocôndrias Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2001 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Proteínas de Membrana Transportadoras / Proteínas Repressoras / Cromossomos Humanos Par 10 / Proteínas de Transporte / Processamento Alternativo / Proteínas de Transporte de Cátions / Proteínas de Saccharomyces cerevisiae / Mitocôndrias Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2001 Tipo de documento: Article