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http://purl.uniprot.org/citations/16631601http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/16631601http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/16631601http://www.w3.org/2000/01/rdf-schema#comment"M-LP (Mpv17-like protein) is a protein that was initially identified in mouse tissues and shows high sequence homology with Mpv17 protein, a peroxisomal membrane protein involved in the development of early-onset glomerulosclerosis [R. Iida, T. Yasuda, E. Tsubota, H. Takatsuka, M. Masuyama, T. Matsuki, K. Kishi, M-LP, Mpv17-like protein, has a peroxisomal membrane targeting signal comprising a transmembrane domain and a positively charged loop and up-regulates expression of the manganese superoxide dismutase gene, J. Biol. Chem. 278 (2003) 6301-6306]. Here we report the identification and characterization of a human homolog of the M-LP (M-LPH) gene. The M-LPH gene is composed of four exons, extends over 14kb on chromosome 16p13.1, and is expressed as two alternatively spliced variants comprising four and three exons, respectively, which include open-reading frames encoding two distinct isoforms composed of 196 (M-LPH1) and 147 (M-LPH2) amino acids, respectively. These two variants were expressed ubiquitously in human tissues, however only M-LPH1 was detected at the protein level. Dual-color confocal analysis of COS-7 cells transfected with a green fluorescent protein-tagged M-LPH1 demonstrated that M-LPH1 is localized in peroxisomes. In order to elucidate the function of M-LPH1, we examined the mRNA levels of several enzymes involved in the metabolism of reactive oxygen species in COS-7 cells and found that transfection with M-LPH1 down-regulates expression of the plasma glutathione peroxidase and catalase genes. These results show the existence of the human homolog of M-LP and its participation in reactive oxygen species metabolism."xsd:string
http://purl.uniprot.org/citations/16631601http://purl.org/dc/terms/identifier"doi:10.1016/j.bbrc.2006.04.008"xsd:string
http://purl.uniprot.org/citations/16631601http://purl.org/dc/terms/identifier"doi:10.1016/j.bbrc.2006.04.008"xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/author"Yasuda T."xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/author"Yasuda T."xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/author"Matsuki T."xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/author"Matsuki T."xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/author"Kishi K."xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/author"Kishi K."xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/author"Takatsuka H."xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/author"Takatsuka H."xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/author"Iida R."xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/author"Iida R."xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/author"Tsubota E."xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/author"Tsubota E."xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/date"2006"xsd:gYear
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/date"2006"xsd:gYear
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/name"Biochem. Biophys. Res. Commun."xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/name"Biochem. Biophys. Res. Commun."xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/pages"948-954"xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/pages"948-954"xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/title"Human Mpv17-like protein is localized in peroxisomes and regulates expression of antioxidant enzymes."xsd:string
http://purl.uniprot.org/citations/16631601http://purl.uniprot.org/core/title"Human Mpv17-like protein is localized in peroxisomes and regulates expression of antioxidant enzymes."xsd:string