Blanchard R K, Cousins R J
Food Science and Human Nutrition Department, Center for Nutritional Sciences, University of Florida, Gainesville, FL 32611, USA.
Proc Natl Acad Sci U S A. 1996 Jul 9;93(14):6863-8. doi: 10.1073/pnas.93.14.6863.
Regulation of gene expression by zinc is well established, especially through the metal response elements of the metallothionein genes; however, most other aspects of the functions of zinc in gene expression remain unknown. We have looked for intestinal mRNAs that are regulated by dietary zinc status. Using the reverse transcriptase-PCR method of mRNA differential display, we compared intestinal mRNA from rats that were maintained for 18 days in one of three dietary groups: zinc-deficient, zinc-adequate, and pair-fed zinc-adequate. At the end of this period, total RNA was prepared from the intestine and analyzed by mRNA differential display. Under these conditions, only differentially displayed cDNA bands that varied in the zinc-deficient group, relative to the zinc-adequate groups, were selected. Utilizing two anchored oligo-dT3' PCR primers and a total of 27 arbitrary decamers as 5' PCR primers, our results yielded 47 differentially displayed cDNA bands from intestinal RNA. Thirty were increased in zinc deficiency, and 17 were decreased. Nineteen bands were subcloned and sequenced. Eleven of these were detectable on Northern blots, of which four were confirmed as regulated. Three of these have homology to known genes: cholecystokinin, uroguanylin, and ubiquinone oxidoreductase. The fourth is a novel sequence as it has no significant homology in GenBank. The remainder of those cloned included novel sequences, as well as matches to reported expressed sequence tags, and functionally identified genes. Further characterization of the regulated sequences identified here will show whether they are primary or secondary effects of zinc deficiency.
锌对基因表达的调控作用已得到充分证实,特别是通过金属硫蛋白基因的金属反应元件;然而,锌在基因表达中功能的大多数其他方面仍不清楚。我们寻找了受膳食锌状态调控的肠道mRNA。使用mRNA差异显示的逆转录酶 - PCR方法,我们比较了在三种饮食组之一中维持18天的大鼠的肠道mRNA:缺锌组、锌充足组和配对喂养的锌充足组。在此期间结束时,从肠道制备总RNA并通过mRNA差异显示进行分析。在这些条件下,仅选择相对于锌充足组在缺锌组中变化的差异显示cDNA条带。利用两种锚定的oligo - dT3' PCR引物和总共27种任意的十聚体作为5' PCR引物,我们的结果从肠道RNA中产生了47条差异显示的cDNA条带。其中30条在缺锌时增加,17条减少。19条带被亚克隆并测序。其中11条在Northern印迹上可检测到,其中4条被确认为受调控。其中3条与已知基因有同源性:胆囊收缩素、尿鸟苷素和泛醌氧化还原酶。第四条是新序列,因为它在GenBank中没有明显的同源性。其余克隆的序列包括新序列,以及与报道的表达序列标签和功能鉴定基因的匹配。这里鉴定的受调控序列的进一步表征将表明它们是锌缺乏的主要还是次要影响。