A comparative investigation on efficiency of bacteriophage lambda and M13 based vectors for delivering and expression of transgene in eukaryote cells
محل انتشار: مجله سلول و تحقیقات مولکولی، دوره: 6، شماره: 2
سال انتشار: 1393
نوع سند: مقاله ژورنالی
زبان: فارسی
مشاهده: 593
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شناسه ملی سند علمی:
JR_JCMR-6-2_008
تاریخ نمایه سازی: 7 بهمن 1395
چکیده مقاله:
Gene delivery might be affected by several tribulations based on carrier/vector applied. Bacteriophages lambda and M13 have different genome conformations; linear double-stranded and circular single-stranded respectively.Therefore, it might be expected that these two common classes of gene delivery vehicles will have differentcapacity for gene delivery and expression in eukaryote cells. To address the possible effects of linear doublestrandedand circular single-stranded genome conformations of bacteriophages lambda and M13 on the transgene expression, the transfection efficacy of two vectors based on lambda and M13 were compared in AGS cell line. The GFP encoding sequence was inserted into the Lambda ZAP-CMV XR vector which resulted in λ-ZAP-CMV-GFPconstruct. The construct was then in vitro packaged using Gigapack® III Gold packaging extract and λ-GFP phage particles were obtained. The λ-GFP phage particles were then used for in vivo excisioning which resulted in M13- CMV-Script-GFP construct. 1011 copy of λ-ZAP-CMV-GFP or M13-CMV-Script-GFP constructs were transfected into AGS cells using lipofectamine 2000. Transfection efficiencies were analyzed by FACS. Results showed that linear double-stranded λ-ZAP-CMV-GFP was efficient than single-stranded form of M13-CMV-Script-GFP whileits double-stranded form was efficient than the linear double-stranded λ-ZAP-CMV-GFP construct for transgenedelivery and expression. Moreover the GFP signals resulted from transfections by single-stranded form of M13- CMV-Script-GFP construct faded more quickly in comparison to others. These findings highlight that genome conformation of gene carriers might be an important factor when seeking for an appropriate gene carrier/vehicle.
کلیدواژه ها:
نویسندگان
elham abedheydari
Department of Animal Biology, Faculty of Natural Science, University of Tabriz, Tabriz, Iran
mohammad khalaj kondori
Department of Animal Biology, Faculty of Natural Science, University of Tabriz, Tabriz, Iran
mohammad ali hosseinpour faizi
Department of Animal Biology, Faculty of Natural Science, University of Tabriz, Tabriz, Iran
morteza kosari nasab
Drug Applied Research Center, Tabriz University of Medical Sciences, PO Box 51656-65811, Tabriz, Iran