COMMD1
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هذا القسم فارغ أو غير مكتمل، ساهم بتحريره.
هذا القسم فارغ أو غير مكتمل، ساهم بتحريره.
COMMD1 (Copper metabolism domain containing 1) هوَ بروتين يُشَفر بواسطة جين COMMD1 في الإنسان.[1][2][3]
الوظيفة[عدل]

الأهمية السريرية[عدل]

المراجع[عدل]
- ^ "Entrez Gene: COMMD1 copper metabolism (Murr1) domain containing 1".
- ^ van De Sluis B، Rothuizen J، Pearson PL، van Oost BA، Wijmenga C (Jan 2002). "Identification of a new copper metabolism gene by positional cloning in a purebred dog population". Hum Mol Genet. 11 (2): 165–73. PMID 11809725. doi:10.1093/hmg/11.2.165.
- ^ Nabetani A، Hatada I، Morisaki H، Oshimura M، Mukai T (Feb 1997). "Mouse U2af1-rs1 is a neomorphic imprinted gene". Mol Cell Biol. 17 (2): 789–98. PMC 231805
. PMID 9001233.
قراءة متعمقة[عدل]
- Maruyama K، Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides.". Gene. 138 (1–2): 171–4. PMID 8125298. doi:10.1016/0378-1119(94)90802-8.
- Suzuki Y، Yoshitomo-Nakagawa K، Maruyama K، وآخرون. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library.". Gene. 200 (1–2): 149–56. PMID 9373149. doi:10.1016/S0378-1119(97)00411-3.
- Harrington JJ، Sherf B، Rundlett S، وآخرون. (2001). "Creation of genome-wide protein expression libraries using random activation of gene expression.". Nat. Biotechnol. 19 (5): 440–5. PMID 11329013. doi:10.1038/88107.
- Strausberg RL، Feingold EA، Grouse LH، وآخرون. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. PMC 139241
. PMID 12477932. doi:10.1073/pnas.242603899.
- Müller T، van de Sluis B، Zhernakova A، وآخرون. (2003). "The canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosis.". J. Hepatol. 38 (2): 164–8. PMID 12547404. doi:10.1016/S0168-8278(02)00356-2.
- Tao TY، Liu F، Klomp L، وآخرون. (2004). "The copper toxicosis gene product Murr1 directly interacts with the Wilson disease protein.". J. Biol. Chem. 278 (43): 41593–6. PMID 12968035. doi:10.1074/jbc.C300391200.
- Klomp AE، van de Sluis B، Klomp LW، Wijmenga C (2004). "The ubiquitously expressed MURR1 protein is absent in canine copper toxicosis.". J. Hepatol. 39 (5): 703–9. PMID 14568250. doi:10.1016/S0168-8278(03)00380-5.
- Biasio W، Chang T، McIntosh CJ، McDonald FJ (2004). "Identification of Murr1 as a regulator of the human delta epithelial sodium channel.". J. Biol. Chem. 279 (7): 5429–34. PMID 14645214. doi:10.1074/jbc.M311155200.
- Ganesh L، Burstein E، Guha-Niyogi A، وآخرون. (2004). "The gene product Murr1 restricts HIV-1 replication in resting CD4+ lymphocytes.". Nature. 426 (6968): 853–7. PMID 14685242. doi:10.1038/nature02171.
- Burstein E، Ganesh L، Dick RD، وآخرون. (2004). "A novel role for XIAP in copper homeostasis through regulation of MURR1.". EMBO J. 23 (1): 244–54. PMC 1271669
. PMID 14685266. doi:10.1038/sj.emboj.7600031.
- Stuehler B، Reichert J، Stremmel W، Schaefer M (2005). "Analysis of the human homologue of the canine copper toxicosis gene MURR1 in Wilson disease patients.". J. Mol. Med. 82 (9): 629–34. PMID 15205742. doi:10.1007/s00109-004-0557-9.
- Gerhard DS، Wagner L، Feingold EA، وآخرون. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121–7. PMC 528928
. PMID 15489334. doi:10.1101/gr.2596504.
- Burstein E، Hoberg JE، Wilkinson AS، وآخرون. (2005). "COMMD proteins, a novel family of structural and functional homologs of MURR1.". J. Biol. Chem. 280 (23): 22222–32. PMID 15799966. doi:10.1074/jbc.M501928200.
- Coronado VA، Bonneville JA، Nazer H، وآخرون. (2006). "COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiology.". Clin. Genet. 68 (6): 548–51. PMID 16283886. doi:10.1111/j.1399-0004.2005.00524.x.
- Zhang Z، Joh K، Yatsuki H، وآخرون. (2006). "Comparative analyses of genomic imprinting and CpG island-methylation in mouse Murr1 and human MURR1 loci revealed a putative imprinting control region in mice.". Gene. 366 (1): 77–86. PMID 16305817. doi:10.1016/j.gene.2005.08.020.
- de Bie P، van de Sluis B، Burstein E، وآخرون. (2006). "Characterization of COMMD protein-protein interactions in NF-kappaB signalling.". Biochem. J. 398 (1): 63–71. PMC 1525016
. PMID 16573520. doi:10.1042/BJ20051664.
- Sommerhalter M، Zhang Y، Rosenzweig AC (2007). "Solution structure of the COMMD1 N-terminal domain.". J. Mol. Biol. 365 (3): 715–21. PMC 2706016
. PMID 17097678. doi:10.1016/j.jmb.2006.10.030.
- Maine GN، Mao X، Komarck CM، Burstein E (2007). "COMMD1 promotes the ubiquitination of NF-kappaB subunits through a cullin-containing ubiquitin ligase.". EMBO J. 26 (2): 436–47. PMC 1783443
. PMID 17183367. doi:10.1038/sj.emboj.7601489.
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