Literature DB >> 11127411

Individual variability in the zinc inducibility of metallothionein-IIA mRNA in human lymphocytes.

M T Wu1, B Demple, R A Bennett, D C Christiani, R Fan, H Hu.   

Abstract

The metallothionein-III gene (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-IIA polymorphisms 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-IIA mRNA in human lymphocytes treated with zinc (Zn), the major known inducer of MT-IIA in vitro. Fresh lymphocytes obtained from 16 healthy volunteers, aged 23-38 yr, were genotyped for the MT-IIA gene and tested for expression. A 43.5-bp HindIII-Taql fragment of the MT-IIA promoter was used to probe for the two known polymorphisms (a 7.8-kb vs. a 5.3-kb fragmnent, 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-II mRNA levels were induced over a wide range of Zn concentrations during 2-h exposures; specifcally, levels increased by 9- to 115-fold with exposure to 100 microM ZnCl, and by 16- to 311-fold with exposure to 200 microM ZnCl2. However, no significant differences in MT-IIA inducibility 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-IIA is strongly inducible by Zn in human lymphocytes, but individual variations exceed those that can be attributed to the known promoter-region polymorphisms.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11127411     DOI: 10.1080/00984100050194081

Source DB:  PubMed          Journal:  J Toxicol Environ Health A        ISSN: 0098-4108


  7 in total

1.  Increased copper bioremediation ability of new transgenic and adapted Saccharomyces cerevisiae strains.

Authors:  Polina Geva; Rotem Kahta; Faina Nakonechny; Stella Aronov; Marina Nisnevitch
Journal:  Environ Sci Pollut Res Int       Date:  2016-07-08       Impact factor: 4.223

2.  Early life inorganic lead exposure induces testicular teratoma and renal and urinary bladder preneoplasia in adult metallothionein-knockout mice but not in wild type mice.

Authors:  Erik J Tokar; Bhalchandra A Diwan; Michael P Waalkes
Journal:  Toxicology       Date:  2010-06-23       Impact factor: 4.221

3.  The metallothionein-null phenotype is associated with heightened sensitivity to lead toxicity and an inability to form inclusion bodies.

Authors:  Wei Qu; Bhalchandra A Diwan; Jie Liu; Robert A Goyer; Tammy Dawson; John L Horton; M George Cherian; Michael P Waalkes
Journal:  Am J Pathol       Date:  2002-03       Impact factor: 4.307

Review 4.  Metallothionein protection of cadmium toxicity.

Authors:  Curtis D Klaassen; Jie Liu; Bhalchandra A Diwan
Journal:  Toxicol Appl Pharmacol       Date:  2009-04-09       Impact factor: 4.219

5.  Recombinational micro-evolution of functionally different metallothionein promoter alleles from Orchesella cincta.

Authors:  Thierry K S Janssens; Janine Mariën; Peter Cenijn; J Legler; Nico M van Straalen; Dick Roelofs
Journal:  BMC Evol Biol       Date:  2007-06-11       Impact factor: 3.260

6.  Blood metallothionein transcript as a biomarker for metal sensitivity: low blood metallothionein transcripts in arsenicosis patients from Guizhou, China.

Authors:  Jie Liu; Min-Liang Cheng; Qin Yang; Ke-Ren Shan; Jun Shen; Yushu Zhou; Xinjiang Zhang; Anna L Dill; Michael P Waalkes
Journal:  Environ Health Perspect       Date:  2007-07       Impact factor: 9.031

Review 7.  Mammalian Metallothionein-2A and Oxidative Stress.

Authors:  Xue-Bin Ling; Hong-Wei Wei; Jun Wang; Yue-Qiong Kong; Yu-You Wu; Jun-Li Guo; Tian-Fa Li; Ji-Ke Li
Journal:  Int J Mol Sci       Date:  2016-09-06       Impact factor: 5.923

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.