首页|大豆油酸脱氢酶基因启动子的克隆及其表达活性分析

大豆油酸脱氢酶基因启动子的克隆及其表达活性分析

扫码查看
大豆油酸脱氢酶(FAD2-1B)基因是种子特异表达基因,利用PCR方法从大豆基因组DNA中分离FAD2-1B基因的启动子片段,命名为FP.PLACE在线启动子预测工具分析表明:序列中含有多种典型的种子特异性表达元件,如Skn-1 motif、AACACA、SEF4 motif、E-box、ACGT等.将克隆得到的FP片段替换pCAMBIA1301中的CaMV35S启动子,构建表达载体pCAM-FP.通过农杆菌介导法在大豆各组织中进行瞬时表达,GUS组织化学染色显示FP驱动GUS基因在大豆根、茎、叶中基本不表达,在种子中有较高的表达活性,推测FP启动子具有种子特异表达活性.
Cloning and Activity Analysis of Soybean FAD2-1B Promoter
The soybean oleate desaturase gene(FAD2-1B) has previously been shown to be expressed specifically in soybean seeds. The 5'-flanking upstream sequence of FAD2-1B gene, named FP, was isolated from the genomic DNA of soybean by PCR method. Sequence analysis by PLACE revealed that this fragment contains a series of motifs related to seed-specific promoters, such as Skn-1 motif,AACACA,SEF4 motif,E-box, ACGT. Replacing CaMV35S promoter of pCAMBIA1301 with FP fragment, the binary expression vector pCAM-FP was constructed. Transient expression in soybean tissues by Agrobacterium tumefaciens mediated method, the results of histochemical GUS analysis showed that there were little or not GUS activities in roots, stems and leaves, but there was higher activity in soybean seeds. It is inferred that FP promoter possess the function driven downstream gene expression exclusively in soybean seeds.

SoybeanFAD2-1BPromoterTransient expression

赵艳、沙伟、张梅娟、杨晓杰、范震宇、王艳梅

展开 >

齐齐哈尔大学生命科学与农林学院 齐齐哈尔161000

齐齐哈尔市龙沙公园 齐齐哈尔161006

大豆 油酸脱氢酶基因 启动子 瞬时表达

黑龙江省教育厅科学技术研究项目

12521611

2013

中国生物工程杂志
中国科学院文献情报中心 中国生物技术发展中心 中国生物工程学会

中国生物工程杂志

CSTPCDCSCD北大核心
影响因子:0.589
ISSN:1671-8135
年,卷(期):2013.33(4)
  • 1
  • 3