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INDIVIDUAL VARIABILITY IN THE ZINC INDUCIBILITY OF METALLOTHIONEIN-IIAmRNA IN HUMAN LYMPHOCYTES

 

作者: Ming-Tsang Wu,   Bruce Demple,   Richard A. O. Bennett,   David C. Christiani,   Rong Fan,   Howard Hu,  

 

期刊: Journal of Toxicology and Environmental Health, Part A  (Taylor Available online 2000)
卷期: Volume 61, issue 7  

页码: 553-567

 

ISSN:1528-7394

 

年代: 2000

 

DOI:10.1080/00984100050194081

 

出版商: Informa UK Ltd

 

数据来源: Taylor

 

摘要:

The metallothionein-IIAgene (MT-IIA) is a major member of the human MT gene family. Metallothioneins (MTs) are low-molecular-weight, cysteine-rich proteins that bind and detoxify heavy metals. At least two different MT-IIApolymorphisms have been identified in humans, one or both of which may affect susceptibility to metal toxicity. The purpose of this study was to investigate whether these different genotypes affect the inducibility of MT-IIAmRNA in human lymphocytes treated with zinc (Zn), the major known inducer of MT-IIAin vitro. Fresh lymphocytes obtained from 16 healthy volunteers, aged 23-38 yr, were genotyped for the MT-IIAgene and tested for expression. A 435-bp Hin dIII- Taq I fragment of the MT-IIApromoter was used to probe for the two knownpolymorphisms (a 7.8-kb vs. a 5.3-kb fragment, and a 1.7-kb vs. a 1.6-kb fragment). The allele frequencies of the 16 subjects were 14% for 5.3-kb allele and 19% for 1.6-kb allele. In Northern blotting experiments, MT-IIAmRNA levels were induced over a wide range of Zn concentrations during 2-h exposures; specifically, levels increased by 9- to 115-fold with exposure to 100 µ M ZnCl2and by 16- to 311-fold with exposure to 200 µ M ZnCl2. However, no significant differences in MT-IIAinducibility were found between the 7.8/5.3 -kb allele pair (n = 4) and the 7.8/7.8 -kb allele pair (n = 12) or between the 1.7/1.6 -kb allele pair (n = 5) and the 1.7/1.7 -kb allele pair (n = 11). Thus, MT-IIAis strongly inducible by Zn in human lymphocytes, but individual variations exceed those that can be attributed to the known promoter-region polymorphisms.

 

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