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丁酸钠可增强重组质粒在哺乳动物细胞中的表达。

Expression of recombinant plasmids in mammalian cells is enhanced by sodium butyrate.

作者信息

Gorman C M, Howard B H, Reeves R

出版信息

Nucleic Acids Res. 1983 Nov 11;11(21):7631-48. doi: 10.1093/nar/11.21.7631.

DOI:10.1093/nar/11.21.7631
PMID:6316266
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC326508/
Abstract

We have studied the effects of sodium butyrate on DNA-mediated gene transfer in an effort to investigate interrelationships between chromatin structure and expression of recombinant plasmids. Our results demonstrate that butyrate affects the early stages of gene activity following DNA uptake at least two levels. First, the number of cells able to express foreign DNA increases from 10% to up to 40%. Second, there is an increase in enhancer-dependent transcription, approximately 30 fold in HeLa cells, involving the SV40 early promoter. Stable transformation efficiencies increase to 4% and 10% in HeLa S3 and monkey kidney CV-1 cells, respectively. Finally, expression of integrated recombinant plasmid genes is reinducible by a second treatment five weeks after initial exposure to this agent.

摘要

我们研究了丁酸钠对DNA介导的基因转移的影响,旨在探究染色质结构与重组质粒表达之间的相互关系。我们的结果表明,丁酸钠至少在两个水平上影响DNA摄取后基因活性的早期阶段。首先,能够表达外源DNA的细胞数量从10%增加到高达40%。其次,增强子依赖性转录增加,在HeLa细胞中约为30倍,涉及SV40早期启动子。在HeLa S3细胞和猴肾CV-1细胞中,稳定转化效率分别提高到4%和10%。最后,在初次接触该试剂五周后,通过第二次处理可再次诱导整合的重组质粒基因的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf94/326508/276920b6d121/nar00366-0378-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf94/326508/276920b6d121/nar00366-0378-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf94/326508/276920b6d121/nar00366-0378-a.jpg

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Expression of recombinant plasmids in mammalian cells is enhanced by sodium butyrate.丁酸钠可增强重组质粒在哺乳动物细胞中的表达。
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本文引用的文献

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Mol Cell Biol. 1982 Dec;2(12):1608-18. doi: 10.1128/mcb.2.12.1608-1618.1982.
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Template structural requirements for transcription in vivo by RNA polymerase II.RNA聚合酶II在体内进行转录的模板结构要求。
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A study of the dopamine transporter using the TRACT assay, a novel in vitro tool for solute carrier drug discovery.使用新型体外溶质载体药物发现工具——TRACTS 测定法研究多巴胺转运体。
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Investigating Phosphorylation Patterns of the Ion Channel TRPM7 Using Multiple Extraction and Enrichment Techniques Reveals New Phosphosites.采用多种提取和富集技术研究离子通道 TRPM7 的磷酸化模式揭示新的磷酸化位点。
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