Department of Molecular Biology and Plant Physiology, University of Aarhus, C.F.Møllers Allé 130, 8000 Aarhus C, Denmark.
EMBO J. 1988 May;7(5):1265-71. doi: 10.1002/j.1460-2075.1988.tb02940.x.
Nuclear extracts from soybean nodules, leaves and roots were used to investigate protein-DNA interactions in the 5' upstream (promoter) region of the soybean leghaemoglobin lbc(3) gene. Two distinct regions were identified which strongly bind a nodule specific factor. A Bal31 deletion analysis delimited the DNA elements responsible for the binding of this factor, which map at nucleotides -223 to -246 (element 1) and -161 to -176 (element 2), relative to the start point of transcription. Competition experiments strongly suggest that both elements bind to the same nodule specific factor, but with different affinities. Elements 1 and 2 share a common motif, although their AT-rich DNA sequences differ. Element 2 is highly conserved at an analogous position in other soybean lb gene 5' upstream regions.
利用大豆根瘤、叶片和根的核提取物研究了大豆豆血红蛋白 lbc(3)基因的 5'上游(启动子)区域的蛋白-DNA 相互作用。鉴定出两个强烈结合豆科植物特异性因子的不同区域。Bal31 缺失分析限定了负责结合该因子的 DNA 元件,这些元件相对于转录起始点位于核苷酸 -223 至 -246(元件 1)和 -161 至 -176(元件 2)。竞争实验强烈表明,这两个元件都与相同的豆科植物特异性因子结合,但亲和力不同。虽然元件 1 和 2 的富含 AT 的 DNA 序列不同,但它们共享一个共同的基序。在其他大豆 lb 基因 5'上游区域的类似位置,元件 2 高度保守。