Takahashi T, Naito S, Komeda Y
Molecular Genetics Research Laboratory, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113, Japan.
Plant Physiol. 1992 Jun;99(2):383-90. doi: 10.1104/pp.99.2.383.
We have cloned and characterized two members of the family of genes for the 81-kilodalton heat-shock proteins from Arabidopsis thaliana, HSP81-1 and HSP81-2. Comparison of the entire genomic sequence of the HSP81-1 gene with the corresponding full-length cDNA previously reported as AtHS83 (TW Conner, PR LaFayette, RT Nagao, JL Key [1990] Plant Physiol 94: 1689-1695) reveals the presence of three introns of 315, 83, and 88 base pairs. By contrast, analysis of the HSP81-2 genomic and partial cDNA sequences suggests that the HSP81-2 gene is interrupted by only two introns of 304 and 106 base pairs. The 5'-initiation sites of the two corresponding mRNAs were mapped from results of experiments with S1 nuclease. The deduced amino acid sequences of the proteins encoded by these two genes show 88% identity, and they also show striking similarities to the hsp90 family of proteins in yeast and animal cells. From the results of northern blot analysis of transcripts, it appears that the expression of the HSP81-1 gene occurs at only very low levels in the absence of heat shock and is strongly induced by heat (35 degrees C). The HSP81-2 gene is constitutively expressed at much higher levels, and its expression is moderately enhanced by elevated temperatures. Severe heat shock appears to block the splicing of the pre-mRNA transcribed from HSP81-1. We also examined the effects of arsenite and cadmium on the expression of the HSP81 genes, as well as on other groups of hsp genes in Arabidopsis. Treatment with cadmium was marginally effective in inducing hsp genes, whereas arsenite stress strongly stimulated the accumulation of each mRNA in a coordinated fashion.
我们已经克隆并鉴定了拟南芥81千道尔顿热休克蛋白基因家族的两个成员,即HSP81-1和HSP81-2。将HSP81-1基因的完整基因组序列与先前报道为AtHS83(TW Conner、PR LaFayette、RT Nagao、JL Key [1990] Plant Physiol 94: 1689 - 1695)的相应全长cDNA进行比较,发现存在三个分别为315、83和88个碱基对的内含子。相比之下,对HSP81-2基因组和部分cDNA序列的分析表明,HSP81-2基因仅被两个分别为304和106个碱基对的内含子中断。通过S1核酸酶实验结果确定了两个相应mRNA的5'-起始位点。这两个基因编码的蛋白质的推导氨基酸序列显示出88%的同一性,并且它们与酵母和动物细胞中的hsp90蛋白家族也有显著的相似性。从转录本的Northern印迹分析结果来看,HSP81-1基因在无热激时仅以非常低的水平表达,而受热(35摄氏度)强烈诱导。HSP81-2基因以高得多的水平组成型表达,其表达在温度升高时适度增强。严重热激似乎会阻断从HSP81-1转录的前体mRNA的剪接。我们还研究了亚砷酸盐和镉对HSP81基因以及拟南芥中其他hsp基因表达的影响。镉处理在诱导hsp基因方面效果甚微,而亚砷酸盐胁迫以协同方式强烈刺激每种mRNA的积累。