• ثبت نام
    • ورود به سامانه
    مشاهده مورد 
    •   صفحهٔ اصلی
    • نشریات انگلیسی
    • Iranian Journal of Biotechnology
    • Volume 12, Issue 4
    • مشاهده مورد
    •   صفحهٔ اصلی
    • نشریات انگلیسی
    • Iranian Journal of Biotechnology
    • Volume 12, Issue 4
    • مشاهده مورد
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Identification of a Specific Pseudo attP Site for Phage PhiC31 Integrase in Bovine Genome

    (ندگان)پدیدآور
    Sekhavati, Mohammad HadiTahmoorespur, MojtabaJafarpour, FarnooshDormiani, KianoushKhazaie, YahyaGhaedi, KamranHosseini, Sayyed MortezaForouzanfar, MahboobehNasr Esfahani, Mohammad Hossein
    Thumbnail
    دریافت مدرک مشاهده
    FullText
    اندازه فایل: 
    786.0کیلوبایت
    نوع فايل (MIME): 
    PDF
    نوع مدرک
    Text
    Research Paper
    زبان مدرک
    English
    نمایش کامل رکورد
    چکیده
    Background: PhiC31 integrase system provides a new platform in various felid of research, mainly in gene therapy and creation of transgenic animals. This system enables integration of exogenous DNA into preferred locations in mammalian genomes, which results in robust, long-term expression of the integrated transgene. Objectives: Identification of a novel pseudo attP site. Materials and Methods: Genomic DNA was extracted from primary bovine fetal fibroblast cells, which were stably transfected with EGFP and phiC31 integrase cDNAs carrying vectors. An inverse PCR was carried out for production of mini-circle DNAs and followed by sequencing. Results: A new specific pseudo attP site termed BF5 was identified in bovine genome.  This site is located in an intergenic AT rich region on chromosome 5 with similar features of other mammalian attP pseudo sites.  Furthermore, direct sequencing of generated attL site confirmed that site-specific transgene recombination was occurred at this site. Conclusions: This finding confirmed that phiC31 integrase could be feasible for production of transgenic animals for biotechnological applications.
    کلید واژگان
    PhiC31 intagrase
    Pseudo attP site
    Protein expression
    Recombination

    شماره نشریه
    4
    تاریخ نشر
    2014-12-01
    1393-09-10
    ناشر
    National Institute of Genetic Engineering and Biotechnology
    سازمان پدید آورنده
    Department of Animal Science, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, Iran
    Department of Animal Science, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, I.R. IRAN
    Department of Reproduction and Development at Reproductive Biomedicine Center, Royan Institute for Biotechnology, ACECR, Isfahan, I.R. IRAN
    Department of Molecular Biotechnology at Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, I.R. IRAN
    Department of Molecular Biotechnology at Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, I.R. IRAN
    Department of Biology, School of Sciences, University of Isfahan & Department of Cellular Biotechnology at Cell Science Research Center, Royan Institute for Biotechnology
    Department of Reproduction and Development at Reproductive Biomedicine Center, Royan Institute for Biotechnology, ACECR, Isfahan, I.R. IRAN
    Department of Molecular Biotechnology at Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, I.R. IRAN
    Department of Molecular Biotechnology at Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, I.R. IRAN

    شاپا
    1728-3043
    2322-2921
    URI
    https://dx.doi.org/10.15171/ijb.1013
    http://www.ijbiotech.com/article_7571.html
    https://iranjournals.nlai.ir/handle/123456789/85762

    مرور

    همه جای سامانهپایگاه‌ها و مجموعه‌ها بر اساس تاریخ انتشارپدیدآورانعناوینموضوع‌‌هااین مجموعه بر اساس تاریخ انتشارپدیدآورانعناوینموضوع‌‌ها

    حساب من

    ورود به سامانهثبت نام

    آمار

    مشاهده آمار استفاده

    تازه ترین ها

    تازه ترین مدارک
    © کليه حقوق اين سامانه برای سازمان اسناد و کتابخانه ملی ایران محفوظ است
    تماس با ما | ارسال بازخورد
    قدرت یافته توسطسیناوب