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摘要:
The P19CL6 mouse embryonic carcinoma cells efficiently differentiate into cardiac muscle cells in the presence of DMSO. A reporter plasmid for cardiac muscle differentiation was constructed by connecting the CMV enhancer and a 250 bp MLC-2v promoter in front of the GFP gene to further evaluate the role of the CMV enhancer. This plasmid (pCBVenh/MLC-2vpro/EGFP) was stably introduced into P19CL6 cells, and the transfectant differentiated into cardiomyocytes with DMSO. Upon DMSO addition, GFP was immediately transcribed (within 2 days) and the amount of the transcript increased with cultivation. Concomitantly, GFP fluorescence was detected in the cells under a microscope. However, native MLC-2v was transcribed later on day 4. This expression time course is different from that of GFP. Clearly the CMV enhancer responded immediately to DMSO. Since GATA DNA-binding proteins play crucial roles in the initiation of cardiomyocyte differentiation, such a response could be ascribed to the presence of multiple GATA motifs in the enhancer sequence but not in the native MLC-2v promoter. Thus the CMV enhancer may be not only useful for gene therapy and monitoring cell differentiation but also the study of the role of GATA transcription factors expressed in P19CL6 cells.
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篇名 The Cytomegalovirus Enhancer Induces an Immediate Response to the Myosin Light Chain 2v Promoter during P19CL6 Cell Differentiation
来源期刊 美国分子生物学期刊(英文) 学科 医学
关键词 CYTOMEGALOVIRUS ENHANCER Differentiation GATA TRANSCRIPTION Factor Gene Expression Heart MUSCLE MLC-2v P19CL6 Cells PROMOTER
年,卷(期) 2017,(4) 所属期刊栏目
研究方向 页码范围 190-203
页数 14页 分类号 R73
字数 语种
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CYTOMEGALOVIRUS
ENHANCER
Differentiation
GATA
TRANSCRIPTION
Factor
Gene
Expression
Heart
MUSCLE
MLC-2v
P19CL6
Cells
PROMOTER
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研究来源
研究分支
研究去脉
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期刊影响力
美国分子生物学期刊(英文)
季刊
2161-6620
武汉市江夏区汤逊湖北路38号光谷总部空间
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191
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0
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