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A light-regulated DNA-binding activity interacts with a conserved region of a Lemna gibba rbcS promoter.

机译:光调节的DNA结合活性与Lemna gibba rbcS启动子的保守区域相互作用。

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摘要

We have characterized a DNA-binding activity, designated light-regulated nuclear factor (LRF-1), which interacted with a specific sequence located 150 nucleotides upstream from the transcription start site of a phytochrome-regulated Lemna gibba rbcS gene (SSU5B). There was a higher level of LRF-1 activity recovered from nuclei of light-grown plants than from dark-treated plants. In light-grown plants given a 1-day dark treatment, either white light or a single 2-min red illumination caused a rapid twofold to threefold increase in this activity, suggesting that the phytochrome system is probably involved in its regulation. The nuclear extracts also contained an activity that bound specifically to Box II sequences from a pea rbcS gene [Green, P.J., Yong, M.H., Cuozzo, M., Kano-Murakami, Y., Silverstein, P., and Chua, N.-H. (1988). EMBO J. 7, 4035-4044], but this activity was not higher in the light-grown compared with the dark-treated plants. Comparison of about 700 base pairs upstream from the SSU5B transcription start site with the upstream sequences of two other Lemna rbcS genes revealed several conserved regions. One of these regions is found upstream of rbcS genes in other species and is contained in the sequence which was shown to interact with LRF-1.
机译:我们已经表征了一种DNA结合活性,称为光调节核因子(LRF-1),它与位于植物色素调节的Lemna gibba rbcS基因(SSU5B)转录起始位点上游150个核苷酸的特定序列相互作用。从光生植物的核中回收的LRF-1活性水平高于从黑暗处理的植物中回收的LRF-1活性水平。在经过1天黑暗处理的光生植物中,白光或2分钟红色单次照射都会使这种活性迅速增加两倍至三倍,这表明植物色素系统可能参与了其调节。核提取物还含有与豌豆rbcS基因的Box II序列特异性结合的活性[Green,PJ,Yong,MH,Cuozzo,M.,Kano-Murakami,Y.,Silverstein,P.和Chua,N. -H。 (1988)。 EMBO J. 7,4035-4044],但是与深色处理的植物相比,浅色种植的这种活性并不高。 SSU5B转录起始位点上游约700个碱基对与另外两个Lemna rbcS基因的上游序列的比较显示了几个保守区。在其他物种的rbcS基因上游发现了这些区域之一,该区域包含在已显示与LRF-1相互作用的序列中。

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