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Monitoring transfected cells without selection agents by using the dual-cassette expression EGFP vectors

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TLDR
This vector has been modified to the dual-cassette expression vectors named pEGFP-Ks by the relocation of its EGFP expression cassette to determine transfection-induced cell toxicity and is a useful method to screen genes encoding potential toxic or useful proteins without performing undesirable selection agent.
Abstract
Conventional methods of selecting gene transfected cells by toxic agents may yield ambiguous results. It is difficult to determine whether cell death is due to selection agents or gene transfection, owing to the substantial overlap of the time-courses for both effects. Therefore, to determine transfection-induced cell toxicity, the mammalian expression vector pEGFP-N1 (CLONTECH Lab., Palo Alto, CA, USA) has been modified to the dual-cassette expression vectors named pEGFP-Ks by the relocation of its EGFP expression cassette. We have precisely monitored the cells transfected with this vector on our custom culture dishes, thereby bypassing the need for selection agent or fluorescent cell sorting. This is a useful method to screen genes encoding potential toxic or useful proteins without performing undesirable selection agent and also can be used to monitor the transfected cells for various purposes, either the inhibition or proliferation of mammalian cells for applications in biotechnology.

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TL;DR: In this paper, the authors used adenoviral overexpression of N -methylpurine DNA glycosylase (MPG or ANPG/AAG) in breast cancer cells to study its ability to imbalance base excision repair (BER) and sensitize cancer cells with alkylating agents.
References
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Journal ArticleDOI

Green fluorescent protein as a marker for gene expression

TL;DR: A complementary DNA for the Aequorea victoria green fluorescent protein produces a fluorescent product when expressed in prokaryotic or eukaryotic cells, which can be used to monitor gene expression and protein localization in living organisms.
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Primary structure of the Aequorea victoria green-fluorescent protein.

TL;DR: The cloning and sequencing of both cDNA and genomic clones of GFP from the cnidarian, Aequorea victoria, show three different restriction enzyme patterns which suggests that at least three different genes are present in the A. victoria population.
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The RNA component of human telomerase

TL;DR: Human cell lines that expressed hTR mutated in the template region generated the predicted mutant telomerase activity, and cells transfected with an antisense hTR lost telomeric DNA and began to die after 23 to 26 doublings.
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Generation of destabilized green fluorescent protein as a transcription reporter

TL;DR: A destabilized GFP is created by fusing amino acids 422–461 of the degradation domain of mouse ornithine decarboxylase to the C-terminal end of an enhanced variant of GFP (EGFP) to directly correlate gene induction with biochemical change, such as NFκB translocation to the nucleus.
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Implications for bcd mRNA localization from spatial distribution of exu protein in Drosophila oogenesis

TL;DR: In this article, a chimaeric gene encoding a fusion between the Acquorea victoria green fluorescent protein (GFP) and the exu protein (Exu) was expressed and localized in a temporal and spatial pattern similar to native Exu.
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