Developmental expression of Commd1 in the liver of the Jackson toxic milk mouse

Biochemical and Biophysical Research Communications

Volumn 363, Issue 4, 2007, Pages 921-925

  Roberts, Eve A ^a,b,c   Lau, Calvin H F ^a   Silveira, Themis Reverbel da ^d   Yang, Suyun ^a  

^a HOSPITAL FOR SICK CHILDREN RESEARCH INSTITUTE   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c UNIVERSITY OF TORONTO   (Canada)

^d FEDERAL UNIVERSITY OF RIO GRANDE DO SUL   (Brazil)

Author keywords

ATP7B; COMMD1; Copper; Liver; Toxic milk mouse; XIAP

Indexed keywords

BINDING PROTEIN; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; PROTEIN COMMD1; UNCLASSIFIED DRUG; X LINKED INHIBITOR OF APOPTOSIS;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CELL STRAIN 3T3; CONTROLLED STUDY; IMMUNOBLOTTING; MISSENSE MUTATION; MOUSE; MOUSE STRAIN; NONHUMAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN EXPRESSION; REAL TIME POLYMERASE CHAIN REACTION;

ANIMALS; CYTOSOL; FEMALE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; LIVER; MALE; MICE; NF-KAPPA B; PROTEINS; RNA, MESSENGER; X-LINKED INHIBITOR OF APOPTOSIS PROTEIN;

MUS;

EID: 35048864294     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2007.09.059     Document Type: Article

References (33)

1. Gitlin J.D. Wilson disease. Gastroenterology 125 (2003) 1868-1877
2. Bull P.C., Thomas G.R., Rommens J.M., Forbes J.R., and Cox D.W. The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene. Nat. Genet. 5 (1993) 327-337
3. Petrukhin K., Fischer S.G., Pirastu M., Tanzi R.E., Chernov I., Devoto M., Brzustowicz L.M., Cayanis E., Vitale E., Russo J.J., et al. Mapping, cloning and genetic characterization of the region containing the Wilson disease gene. Nat. Genet. 5 (1993) 338-343
4. Cater M.A., La Fontaine S., Shield K., Deal Y., and Mercer J.F. ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion. Gastroenterology 130 (2006) 493-506
5. Huster D., Hoppert M., Lutsenko S., Zinke J., Lehmann C., Mossner J., Berr F., and Caca K. Defective cellular localization of mutant ATP7B in Wilson's disease patients and hepatoma cell lines. Gastroenterology 124 (2003) 335-345
6. Thomas G.R., Forbes J.R., Roberts E.A., Walshe J.M., and Cox D.W. The Wilson disease gene: spectrum of mutations and their consequences. Nat. Genet. 9 (1995) 210-217
7. Muller T., Feichtinger H., H B., and Muller W. Endemic Tyrolean infantile cirrhosis: an ecogenetic disorder. Lancet 347 (1996) 877-880
8. Pankit A.N., and Bhave S.A. Copper metabolic defects and liver disease: environmental aspects. J. Gastroenterol. Hepatol. 17 Suppl. 3 (2002) S403-S407
9. Nanji M.S., and Cox D.W. The copper chaperone atox1 in canine copper toxicosis in bedlington terriers. Genomics 62 (1999) 108-112
10. Klomp A.E., van de Sluis B., Klomp L.W., and Wijmenga C. The ubiquitously expressed MURR1 protein is absent in canine copper toxicosis. J. Hepatol. 39 (2003) 703-709
11. Burstein E., Hoberg J.E., Wilkinson A.S., Rumble J.M., Csomos R.A., Komarck C.M., Maine G.N., Wilkinson J.C., Mayo M.W., and Duckett C.S. COMMD proteins: A novel family of structural and functional homologs of MURR1. J. Biol. Chem. 280 (2005) 22222-22232
12. Muller T., van de Sluis B., Zhernakova A., van Binsbergen E., Janecke A.R., Bavdekar A., Pandit A., Weirich-Schwaiger H., Witt H., Ellemunter H., Deutsch J., Denk H., Muller W., Sternlieb I., Tanner M.S., and Wijmenga C. The canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosis. J. Hepatol. 38 (2003) 164-168
13. Coronado V.A., Bonneville J.A., Nazer H., Roberts E.A., and Cox D.W. COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiology. Clin Genet 68 (2005) 548-551
14. Weiss K.H., Merle U., Schaefer M., Ferenci P., Fullekrug J., and Stremmel W. Copper toxicosis gene MURR1 is not changed in Wilson disease patients with normal blood ceruloplasmin levels. World J. Gastroenterol. 12 (2006) 2239-2242
15. Huffman D.L., and O'Halloran T.V. Function, structure, and mechanism of intracellular copper trafficking proteins. Annu. Rev. Biochem. 70 (2001) 677-701
16. Smith S.D., She Y.M., Roberts E.A., and Sarkar B. Using immobilized metal affinity chromatography, two-dimensional electrophoresis and mass spectrometry to identify hepatocellular proteins with copper-binding ability. J. Proteome Res. 3 (2004) 834-840
17. Lim C.M., Cater M.A., Mercer J.F., and La Fontaine S. Copper-dependent interaction of dynactin subunit p62 with the N terminus of ATP7B but not ATP7A. J. Biol. Chem. 281 (2006) 14006-14014
18. Coronado V., Nanji M., and Cox D.W. The Jackson toxic milk mouse as a model for copper loading. Mamm. Genome 12 (2001) 793-795
19. Livak K.J., and Schmittgen T.D. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 25 (2001) 402-408
20. Mufti A.R., Burstein E., Csomos R.A., Graf P.C., Wilkinson J.C., Dick R.D., Challa M., Son J.K., Bratton S.B., Su G.L., Brewer G.J., Jakob U., and Duckett C.S. XIAP Is a copper binding protein deregulated in Wilson's disease and other copper toxicosis disorders. Mol. Cell 21 (2006) 775-785
21. Ganesh L., Burstein E., Guha-Niyogi A., Louder M.K., Mascola J.R., Klomp L.W., Wijmenga C., Duckett C.S., and Nabel G.J. The gene product Murr1 restricts HIV-1 replication in resting CD4+ lymphocytes. Nature 426 (2003) 853-857
22. Greene W.C. How resting T cells deMURR HIV infection. Nat. Immunol. 5 (2004) 18-19
23. Biasio W., Chang T., McIntosh C.J., and McDonald F.J. Identification of Murr1 as a regulator of the human delta epithelial sodium channel. J. Biol. Chem. 279 (2004) 5429-5434
24. de Bie P., van de Sluis B., Burstein E., Duran K.J., Berger R., Duckett C.S., Wijmenga C., and Klomp L.W. Characterization of COMMD protein-protein interactions in NF-kappaB signalling. Biochem. J. 398 (2006) 63-71
25. Maine G.N., and Burstein E. COMMD proteins and the control of the NF kappa B pathway. Cell Cycle 6 (2007) 672-676
26. Burstein E., Ganesh L., Dick R.D., van De Sluis B., Wilkinson J.C., Klomp L.W., Wijmenga C., Brewer G.J., Nabel G.J., and Duckett C.S. A novel role for XIAP in copper homeostasis through regulation of MURR1. EMBO J. 23 (2004) 244-254
27. Tao T.Y., Liu F., Klomp L., Wijmenga C., and Gitlin J.D. The copper toxicosis gene product Murr1 directly interacts with the Wilson disease protein. J. Biol. Chem. 278 (2003) 41593-41596
28. Narindrasorasak S., Kulkarni P., Deschamps P., She Y.M., and Sarkar B. Characterization and copper binding properties of human COMMD1 (MURR1). Biochemistry 46 (2007) 3116-3128
29. Roberts E.A., Yang S., and Wanless I.R. Wilsonian liver disease in the Jackson Laboratory toxic milk (tx-j) mouse (abstr.). Clin. Biochem. 36 (2004) 1140
30. Biempica L., Rauch H., Quintana N., and Sternlieb I. Morphologic and chemical studies on a murine mutation (toxic milk mice) resulting in hepatic copper toxicosis. Lab Invest. 59 (1988) 500-508
31. Allen K.J., Buck N.E., Cheah D.M., Gazeas S., Bhathal P., and Mercer J.F. Chronological changes in tissue copper, zinc and iron in the toxic milk mouse and effects of copper loading. Biometals 19 (2006) 555-564
32. Huster D., Finegold M.J., Morgan C.T., Burkhead J.L., Nixon R., Vanderwerf S.M., Gilliam C.T., and Lutsenko S. Consequences of copper accumulation in the livers of the Atp7b-/- (Wilson disease gene) knockout mice. Am. J. Pathol. 168 (2006) 423-434
33. Spee B., Mandigers P.J., Arends B., Bode P., van den Ingh T.S., Hoffmann G., Rothuizen J., and Penning L.C. Differential expression of copper-associated and oxidative stress related proteins in a new variant of copper toxicosis in Doberman pinschers. Comp. Hepatol. 4 (2005) 3