Zhao Y, Okita T W
Institute of Biological Chemistry, Washington State University, Pullman 99164, USA.
Plant Cell Physiol. 1995 Dec;36(8):1657-67.
Three DNA binding activities, BP-1, BP-2 and BP-3, which interact with the 5' flanking region of the rice glutelin Gt3 gene, were identified by gel retardation assays of rice seed nuclear extracts. The DNA binding activities were seed-specific as identical DNA-protein complexes were not observed when nuclear extracts from leaf tissue or suspension culture cells were analyzed, suggesting that these DNA binding activities are involved in seed-specific expression of the Gt3 gene. The DNA sequences recognized by these DNA binding activities were identified by DNaseI foot-printing and Bal 31 nuclease mapping analyses. BP-1 recognizes DNA sequences located at -272 bp to -259 bp relative to the transcriptional start site. This DNA segment contains a sequence motif that is conserved among several seed protein genes, implicating that the motif may be a common cis-regulatory element determining seed-specific expression of these genes. BP-2 interacts with sequences located between -861 bp to -838 bp while BP-3 interacts with sequences upstream of -788 bp. The temporal levels of BP-2 binding activity parallel the steady state levels of the Gt3 mRNAs during seed development. Overall, these results and those obtained from in vivo promoter analysis in transgenic plants [Zhao et al. (1994) Plant Mol. Biol. 25: 429] indicate that multiple regulatory elements located at two spatially separated regions of the Gt3 promoter are involved in endosperm-specific and temporal regulation.
通过对水稻种子核提取物进行凝胶阻滞分析,鉴定出三种与水稻谷蛋白Gt3基因5'侧翼区域相互作用的DNA结合活性,即BP-1、BP-2和BP-3。这些DNA结合活性具有种子特异性,因为当分析叶片组织或悬浮培养细胞的核提取物时,未观察到相同的DNA-蛋白质复合物,这表明这些DNA结合活性参与了Gt3基因的种子特异性表达。通过DNaseI足迹分析和Bal 31核酸酶图谱分析鉴定了这些DNA结合活性所识别的DNA序列。BP-1识别相对于转录起始位点位于-272 bp至-259 bp的DNA序列。该DNA片段包含一个在几个种子蛋白基因中保守的序列基序,这意味着该基序可能是决定这些基因种子特异性表达的常见顺式调控元件。BP-2与位于-861 bp至-838 bp之间的序列相互作用,而BP-3与-788 bp上游的序列相互作用。在种子发育过程中,BP-2结合活性的时间水平与Gt3 mRNA的稳态水平平行。总体而言,这些结果以及从转基因植物体内启动子分析中获得的结果[Zhao等人(1994年),植物分子生物学25:429]表明,位于Gt3启动子两个空间分离区域的多个调控元件参与胚乳特异性和时间调控。