کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
9127340 | 1569976 | 2005 | 9 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Drag&Drop cloning in yeast
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
کلمات کلیدی
Recombinational cloningG418ORFMPRsGFPkDaGSTkiloDalton(s) - kiloDalton (s)amino acid(s) - آمینو اسیدهاTAGs - برچسب هاHeterologous gene expression - بیان ژن heterologousBase pair(s) - جفت پایه (ها)Myristoylation - خندیدنopen reading frame - قاب خواندن بازKanamycin resistance - مقاومت کانامایسینMyr - میرterminator of transcription - پایان نامه رونویسیgreen fluorescent protein - پروتئین فلورسنت سبزPromoter - پروموترPlasmid - پلاسمیدPoly (ethylene glycol) - پلی اتیلن گلیکول)PEG - پلیاتیلن گلیکول optical density - چگالی نوریGeneticin - ژنتیکKANR - کانرkilobase(s) - کیلو بایت (ها)glutathione-S-transferase - گلوتاتیون S-ترانسفراز
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
ژنتیک
پیش نمایش صفحه اول مقاله

چکیده انگلیسی
We have developed a set of vectors that have enhanced capabilities for efficiently constructing and expressing differentially tagged fusion proteins using Drag&Drop cloning in the yeast Saccharomyces cerevisiae. The pGREG vectors are based on the pRS series with an additional general kanR selection marker. In vivo homologous recombination is used to introduce genes of interest into galactose-inducible expression vectors (pGREGs), permitting the formation of amino-terminal fusions. The vectors all contain common regions for recombination that flank the stuffer fragment. Introduction of common recombination sequences at the end of PCR fragments will permit the cloning of genes without the need for specific restriction sites. In this process, the selectable stuffer HIS3 gene is replaced by successful gene integration, and a screen for loss of the selection marker identifies potential recombinants. Due to the modular structure of the vectors, genes introduced into one vector can be readily transferred by in vivo recombination to all other members of the vector system, thus permitting rapid and easy Drag&Drop construction of a series of tagged proteins. The pGREG series combines features for expression, tagging, integration, localization and library construction with the advantage of obtaining immediate results from sub-sequent experiments. This Drag&Drop system also allows efficient cloning and expression of heterologous genes in large-scale experiments.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Gene - Volume 344, 3 January 2005, Pages 43-51
Journal: Gene - Volume 344, 3 January 2005, Pages 43-51
نویسندگان
Gregor Jansen, Cunle Wu, Babette Schade, David Y. Thomas, Malcolm Whiteway,