Buzby J S, Yamada T, Tobin E M
Department of Biology, University of California, Los Angeles 90024-1606.
Plant Cell. 1990 Aug;2(8):805-14. doi: 10.1105/tpc.2.8.805.
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.
我们已鉴定出一种DNA结合活性,命名为光调节核因子(LRF-1),它与位于光敏色素调节的浮萍rbcS基因(SSU5B)转录起始位点上游150个核苷酸处的特定序列相互作用。从光照生长的植物细胞核中回收的LRF-1活性水平高于黑暗处理的植物。在经过1天黑暗处理的光照生长植物中,白光或单次2分钟的红光照射都会使该活性迅速增加两倍至三倍,这表明光敏色素系统可能参与了其调节。核提取物中还含有一种能与豌豆rbcS基因的Box II序列特异性结合的活性[格林,P.J.,勇,M.H.,科佐,M.,卡诺-村上,Y.,西尔弗斯坦,P.,和蔡,N.-H.(1988年)。《欧洲分子生物学组织杂志》7,4035 - 4044],但与黑暗处理的植物相比,这种活性在光照生长的植物中并不更高。将SSU5B转录起始位点上游约700个碱基对与另外两个浮萍rbcS基因的上游序列进行比较,发现了几个保守区域。其中一个区域存在于其他物种的rbcS基因上游,并且包含在已证明与LRF-1相互作用的序列中。