Literature DB >> 1588441

Hepatic metallothionein gene expression in toxic milk mice.

J F Mercer1, A Grimes, H Rauch.   

Abstract

The toxic milk mutation (tx) in mice is an autosomal recessive condition that causes a marked hepatic accumulation of copper in adults and severe copper deficiency in the pups of tx/tx dams. We determined the concentration of metallothionein-I (MT-I) mRNA in mutant and normal animals at various stages of development and following administration of copper and zinc. In two tx/tx males the average MT-I mRNA was 329 molecules/pg RNA compared with 38 molecules/pg in normal animals. In fetal and neonatal animals the concentration of MT-I mRNA was generally the same in normal and mutant mice and was independent of copper status. Copper or zinc administration to 7-d-old pups caused a marked induction of MT-I mRNA. There was an increased response to copper administration in one mutant group, but no clear pattern of hyper-induction of the MT gene in tx/tx animals was demonstrated. The elevation of MT-I mRNA in adult toxic milk mice is likely to be a secondary consequence of copper accumulation and not a primary effect of the mutation, because high MT-I mRNA levels would have been observed in the mutant neonates and fetuses. However, the possibility that the tx mutation causes overexpression of MT in post-weaning animals cannot be excluded by these data. The results also show that copper deficiency has no effect on the fetal or neonatal expression of the MT genes.

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Year:  1992        PMID: 1588441     DOI: 10.1093/jn/122.6.1254

Source DB:  PubMed          Journal:  J Nutr        ISSN: 0022-3166            Impact factor:   4.798


  4 in total

1.  The toxic milk mouse does have elevated hepatic metallothionein mRNA.

Authors:  J F Mercer; J A Paynter; A Grimes
Journal:  Biochem J       Date:  1994-11-15       Impact factor: 3.857

2.  Decreased carbonic anhydrase III levels in the liver of the mouse mutant 'toxic milk' (tx) due to copper accumulation.

Authors:  A Grimes; J Paynter; I D Walker; M Bhave; J F Mercer
Journal:  Biochem J       Date:  1997-01-15       Impact factor: 3.857

3.  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 4.  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

  4 in total

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