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苜蓿根中的一种新型锌指蛋白Alfin1,它能与盐诱导型MsPRP2基因的启动子元件结合。

Alfin1, a novel zinc-finger protein in alfalfa roots that binds to promoter elements in the salt-inducible MsPRP2 gene.

作者信息

Bastola D R, Pethe V V, Winicov I

机构信息

Department of Microbiology, School of Medicine, University of Nevada Reno, 89557, USA.

出版信息

Plant Mol Biol. 1998 Dec;38(6):1123-35. doi: 10.1023/a:1006081926699.

Abstract

Alfin1 cDNA, obtained by differential screening of a poly(A)+ library from salt-tolerant alfalfa cells, encodes a novel protein with a Cys4 and His/Cys3 putative zinc-binding domain that suggests a possible role for this protein in transcriptional regulation. We have expressed the cDNA in Escherichia coli and show that the recombinant Alfin1 protein binds DNA in a sequence-specific manner. The DNA recognition sequence was determined from individual clones isolated after four rounds of random oligonucleotide selection in gel retardation assays, coupled with PCR amplification of the selected sequences. The consensus binding site for Alfin1 is shown to contain two to five G-rich triplets with the conserved core of GNGGTG or GTGGNG in clones showing high-efficiency binding. DNA binding of the recombinant Alfin1 was inhibited by EDTA. Alfin1 mRNA was found predominantly in alfalfa roots. Growth of salt-sensitive Medicago sativa L on 171 mM NaCl led to a slight decrease in Alfin1 mRNA, while the salt-tolerant plants showed no decrease in Alfin1 mRNA levels. Interestingly, recombinant Alfin1 binds efficiently to three fragments of the MsPRP2 promoter, each containing consensus sequences identified by the random oligonucleotide selection. Since MsPRP2 transcripts were shown to be root-specific and accumulated in alfalfa roots in a salt-inducible manner, Alfin1 may play a role in the regulated expression of MsPRP2 in alfalfa roots and contribute to salt tolerance in these plants.

摘要

通过对耐盐苜蓿细胞的聚腺苷酸加尾文库进行差异筛选获得的Alfin1 cDNA,编码一种具有Cys4和His/Cys3推定锌结合结构域的新型蛋白质,这表明该蛋白质可能在转录调控中发挥作用。我们已在大肠杆菌中表达了该cDNA,并表明重组Alfin1蛋白以序列特异性方式结合DNA。DNA识别序列是通过凝胶阻滞试验中四轮随机寡核苷酸选择后分离的单个克隆确定的,同时对所选序列进行PCR扩增。结果显示,在高效结合的克隆中,Alfin1的共有结合位点包含两到五个富含G的三联体,其保守核心为GNGGTG或GTGGNG。重组Alfin1的DNA结合受到EDTA的抑制。Alfin1 mRNA主要在苜蓿根中发现。盐敏感型紫花苜蓿在171 mM NaCl上生长导致Alfin1 mRNA略有下降,而耐盐植物的Alfin1 mRNA水平没有下降。有趣的是,重组Alfin1能有效结合MsPRP2启动子的三个片段,每个片段都包含通过随机寡核苷酸选择鉴定的共有序列。由于MsPRP2转录本显示为根特异性,并以盐诱导的方式在苜蓿根中积累,Alfin1可能在苜蓿根中MsPRP2的调控表达中发挥作用,并有助于这些植物的耐盐性。

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