| 摘要: |
| 为研究核基质结合区结合蛋白的功能及调控机制,PCR扩增杜氏盐藻MBP的cDNA全长序列及N端和C端序列,与绿色荧光蛋白基因融合构建真核表达载体,脂质体转染CHO细胞,Western blotting和荧光显微镜检测基因表达情况和细胞定位。结果显示:MBP及N端和C端融合蛋白成功在CHO细胞表达,MBP和C端部分定位于细胞核且聚集于核仁,N端部分分布整个细胞,说明MBP定位于细胞核且细胞定位信号位于C端,MBP可能与rRNA前体结合发挥作用。 |
| 关键词: 杜氏盐藻 核基质附着区 核基质结合区结合蛋白 真核表达载体 细胞定位 |
| DOI： |
| 分类号:Q781 |
| Fund project: |
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| Cellular localization of MAR binding protein of Dunaliella salina |
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WANG Peng-Ju1, WANG Tian-Yun2, FENG Ying-Cai1,
LIU Hong-Tao1, XUE Le-Xun1*
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1.Laboratory of Cell Biology, Zhengzhou University, Zhengzhou 450052, China;2.Department of Biochemistry and
Molecular Biology, Xinxiang Medical College, Xinxiang 453003, China
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| Abstract: |
| To study the function of Matrix attachment region(MAR)binding protein(MBP),full length,N-terminal and C-terminal of MBP gene from Dunaliella salina were amplified by RT-PCR,and fused to the green fluorescence protein gene to construct the eukaryotic vector. Then,the recombinant vectors were transfected into Chinese hamster ovary(CHO)cells by Lipofectamine 2000. Fluorescence microscope and western blotting were performed to determine the expression of the fusion proteins and cellular localization. The results showed that the fusion proteins were expressed in CHO cells,the proteins of MBP and C-terminal part were localized in the nucleus and clearly detected in nucleoli,however, the N-terminal part was distributed into all cells. |
| Key words: Dunaliella salina matrix attachment region MAR binding protein eukaryotic expression cellular localization |
