Literature DB >> 1711358

A comparison of phenotype and copper distribution in blotchy and brindled mutant mice and in nutritionally copper deficient controls.

M Phillips1, J Camakaris, D M Danks.   

Abstract

The murine mottled mutants brindled, Mo br, and blotchy, Mo blo, are valuable animal models for the study of mammalian copper metabolism. In this paper, we present data showing that a nutritionally copper deficient suckling mouse, Cu-, with strong phenotypic similarities to the brindled mutant can be produced by feeding genetically normal dams a copper deficient diet (0.1-0.4 ppm Cu2+) from the day of mating. Comparisons of copper distribution between the Cu- mice and brindled mutants indicate that when a small dose of copper (0.5-0.9 micrograms Cu2+) was administered by intracardiac injection, the copper was abnormally distributed, and that the pattern of tissue distribution was very similar in Cu- mice and brindled mutants 24 h after injection. When, however, a treatment dose (50 micrograms Cu2+) was injected subcutaneously, and tissues assayed 3 d after injection, copper distribution in Cu- mice and brindled mutants was clearly different. Copper deficiency in Cu- suckling mice is entirely derived from maternal effects. Evidence that maternal effects may also influence the survival and phenotype of the brindled and blotchy mutants was obtained by comparing the viability of mutants born to dams carrying mottled mutations on one or both X chromosomes.

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Year:  1991        PMID: 1711358     DOI: 10.1007/bf03032670

Source DB:  PubMed          Journal:  Biol Trace Elem Res        ISSN: 0163-4984            Impact factor:   3.738


  17 in total

1.  A study of copper treatment and tissue copper levels in the murine congenital copper deficiency, mottled.

Authors:  D M Hunt
Journal:  Life Sci       Date:  1976-12-15       Impact factor: 5.037

2.  Type IX Ehlers-Danlos syndrome and Menkes syndrome: the decrease in lysyl oxidase activity is associated with a corresponding deficiency in the enzyme protein.

Authors:  H Kuivaniemi; L Peltonen; K I Kivirikko
Journal:  Am J Hum Genet       Date:  1985-07       Impact factor: 11.025

3.  Report of the American Institute of Nurtition ad hoc Committee on Standards for Nutritional Studies.

Authors: 
Journal:  J Nutr       Date:  1977-07       Impact factor: 4.798

4.  Alterations in copper and collagen metabolism in the Menkes syndrome and a new subtype of the Ehlers-Danlos syndrome.

Authors:  L Peltonen; H Kuivaniemi; A Palotie; N Horn; I Kaitila; K I Kivirikko
Journal:  Biochemistry       Date:  1983-12-20       Impact factor: 3.162

5.  Abnormal copper metabolism and deficient lysyl oxidase activity in a heritable connective tissue disorder.

Authors:  H Kuivaniemi; L Peltonen; A Palotie; I Kaitila; K I Kivirikko
Journal:  J Clin Invest       Date:  1982-03       Impact factor: 14.808

6.  Copper metabolism in mottled mouse mutants: copper concentrations in tissues during development.

Authors:  J Camakaris; J R Mann; D M Danks
Journal:  Biochem J       Date:  1979-06-15       Impact factor: 3.857

7.  Copper metabolism in mottled mouse mutants: distribution of 64Cu in brindled (Mobr) mice.

Authors:  J R Mann; J Camakaris; D M Danks
Journal:  Biochem J       Date:  1979-06-15       Impact factor: 3.857

8.  Copper metabolism in mottled mouse mutants: copper therapy of brindled (Mobr) mice.

Authors:  J R Mann; J Camakaris; D M Danks; E G Walliczek
Journal:  Biochem J       Date:  1979-06-15       Impact factor: 3.857

Review 9.  Mutations in humans and animals which affect copper metabolism.

Authors:  J Camakaris; M Phillips; D M Danks; R Brown; T Stevenson
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

10.  Altered copper metabolism in cultured cells from human Menkes' syndrome and mottled mouse mutants.

Authors:  J Camakaris; D M Danks; L Ackland; E Cartwright; P Borger; R G Cotton
Journal:  Biochem Genet       Date:  1980-02       Impact factor: 1.890

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  5 in total

1.  Pathological structure of the kidney from adult mice with mosaic mutation.

Authors:  M Lenartowicz; M Kowal; D Buda-Lewandowska; J Styrna
Journal:  J Inherit Metab Dis       Date:  2002-12       Impact factor: 4.982

2.  Counteract of bone marrow of blotchy mice against the increases of plasma copper levels induced by high-fat diets in LDLR-/- mice.

Authors:  Jessica Yao; Zhenyu Qin
Journal:  J Trace Elem Med Biol       Date:  2015-02-21       Impact factor: 3.849

3.  Bone marrow from blotchy mice is dispensable to regulate blood copper and aortic pathologies but required for inflammatory mediator production in LDLR-deficient mice during chronic angiotensin II infusion.

Authors:  Devon Harris; Yuanyuan Liang; Cang Chen; Senlin Li; Om Patel; Zhenyu Qin
Journal:  Ann Vasc Surg       Date:  2014-10-29       Impact factor: 1.466

4.  Prenatal treatment of mosaic mice (Atp7a mo-ms) mouse model for Menkes disease, with copper combined by dimethyldithiocarbamate (DMDTC).

Authors:  Małgorzata Lenartowicz; Wojciech Krzeptowski; Paweł Koteja; Katarzyna Chrząścik; Lisbeth Birk Møller
Journal:  PLoS One       Date:  2012-07-18       Impact factor: 3.240

Review 5.  Mottled Mice and Non-Mammalian Models of Menkes Disease.

Authors:  Małgorzata Lenartowicz; Wojciech Krzeptowski; Paweł Lipiński; Paweł Grzmil; Rafał Starzyński; Olga Pierzchała; Lisbeth Birk Møller
Journal:  Front Mol Neurosci       Date:  2015-12-18       Impact factor: 5.639

  5 in total

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