Saijoh K, Katsuyama H, Sumino K
Department of Public Health, Kobe University School of Medicine, Japan.
Biol Signals. 1994 May-Jun;3(3):150-6. doi: 10.1159/000109538.
Metallothionein (MT) gene expression in the brain has been most thoroughly studied using rodents. Although MT is considered to be a 'housekeeping' protein even in the brain, the basal MT mRNA expression level is not always high. Differences in the responses of rats and mice have made it difficult to interpret the data. Moreover, the response to inducers is not always apparent, probably because the brain is protected by the blood-brain barrier and initial responses to inducers in peripheral tissues modulate their accumulation in the brain. A relatively high content of MT protein in the brain might be sufficient to elicit minute alterations in the level of inducers. Nonetheless, regulation of MT gene expression in the brain seems to be important in e.g. maintaining the levels of trace elements and controlling redox potentials. The localization and utilization of trans elements such as MTF-I and MEP-I in the brain will provide new aspects for study. The high homology among MT isoforms with respect to nucleotide as well as amino acid sequences has made it difficult to obtain cDNA probes or antibodies capable of distinguishing MT isoforms. Thus, their cross-reactivity might make changes in MT mRNAs appear minimal when MT isoforms are differently regulated. The rapid developments in methodology permitting sensitive, rapid, high-resolution analysis could clarify the background of tissue- and cell-specific gene regulation as well as differential induction.
利用啮齿动物对大脑中金属硫蛋白(MT)基因表达进行了最为深入的研究。尽管MT即使在大脑中也被视为一种“管家”蛋白,但其基础MT mRNA表达水平并不总是很高。大鼠和小鼠反应的差异使得对数据的解读变得困难。此外,对诱导剂的反应并不总是明显的,这可能是因为大脑受到血脑屏障的保护,并且外周组织对诱导剂的初始反应会调节其在大脑中的积累。大脑中相对较高的MT蛋白含量可能足以引发诱导剂水平的微小变化。尽管如此,大脑中MT基因表达的调节在例如维持微量元素水平和控制氧化还原电位方面似乎很重要。大脑中MTF-I和MEP-I等反式作用元件的定位和利用将为研究提供新的方向。MT同工型在核苷酸和氨基酸序列方面的高度同源性使得难以获得能够区分MT同工型的cDNA探针或抗体。因此,当MT同工型受到不同调节时,它们的交叉反应性可能会使MT mRNA的变化显得很小。允许进行灵敏、快速、高分辨率分析的方法学的迅速发展可能会阐明组织和细胞特异性基因调节以及差异诱导的背景。