Yoshihara T, Takaiwa F
Department of Cell Biology, National Institute of Agrobiological Resources, Tsukuba, Japan.
Plant Cell Physiol. 1996 Jan;37(1):107-11. doi: 10.1093/oxfordjournals.pcp.a028907.
The 897 bp 5' flanking region of the rice storage protein glutelin gene (GluA-3) was analyzed to define cis-regulatory elements responsible for the seed specific expression by progressive 5' deletions and gain-of-function experiments using a truncated CaMV 35S promoter (-90/+9). These constructs were transcriptionally fused either to the firefly luciferase (LUX) or beta-glucuronidase (GUS) reporter gene and introduced into tobacco. It was shown that a 121 bp sequence between -437 and -317 from the transcriptional start site is important for the quantitative regulation of the GluA-3 gene expression. This region contained at least two functionally different cis-regulatory elements. One acts as a general positive element and the other is involved in a specific negative regulation in non-seed tissues.
对水稻贮藏蛋白谷蛋白基因(GluA-3)的897 bp 5'侧翼区域进行了分析,通过使用截短的CaMV 35S启动子(-90/+9)进行逐步5'缺失和功能获得实验,以确定负责种子特异性表达的顺式调控元件。这些构建体与萤火虫荧光素酶(LUX)或β-葡萄糖醛酸酶(GUS)报告基因进行转录融合,并导入烟草中。结果表明,转录起始位点上游-437至-317之间的121 bp序列对GluA-3基因表达的定量调控很重要。该区域至少包含两个功能不同的顺式调控元件。一个作为一般的正调控元件,另一个参与非种子组织中的特异性负调控。