摘要
为了研究马铃薯StHb1蛋白的亚细胞定位情况,采用RT-PCR技术克隆到马铃薯StHb1基因cDNA序列,并成功构建了StHb1基因与绿色荧光蛋白基因的融合表达载体pBI121-StHb1-GFP.利用农杆菌介导法将重组载体转化洋葱内表皮细胞,通过荧光显微镜观察融合蛋白的瞬时表达以确定StHb1蛋白在细胞内的分布.结果表明StHb1蛋白主要分布于细胞核中.
To identify the subcellular location of StHb1 protein,a cDNA encoding nonsymbiotic hemoglobin(StHb1) was cloned from Solanum tuberosum by RT-PCR,and fused to the 5′ end of the green fluorescent protein gene to generate plant binary vector pBI121-StHb1-GFP.It was introduced into onion epidermal cells via Agrobacterium-mediated transformation.Subcellular localization of StHb1 protein was detected by fluorescent microscopy.The results showed that the StHb1-GFP fusion proteins were predominantly present in the nucleus.
出处
《河北大学学报(自然科学版)》
CAS
北大核心
2012年第5期523-527,共5页
Journal of Hebei University(Natural Science Edition)
基金
河北大学博士基金资助项目(2007-097)
河北省教育厅资助项目(2007412)
河北省科技支撑计划项目(11215529)
关键词
非共生血红蛋白
绿色荧光蛋白(GFP)
亚细胞定位
融合表达载体
农杆菌介导转化
non-symbiotic hemoglobin
green fluorescent protein(GFP)
subcellular localization
fusion expression vector
Agrobacterium-mediated transformation