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Production of transgenic goats expressing human coagulation factor IX in the mammary glands after nuclear transfer using transfected fetal fibroblast cells
Authors:Amir Amiri Yekta  Azam Dalman  Poopak Eftekhari-Yazdi  Mohammad Hossein Sanati  Abdol Hossein Shahverdi  Rahman Fakheri  Hamed Vazirinasab  Mohammad Taghi Daneshzadeh  Mahdi Vojgani  Alireza Zomorodipour  Nayeralsadat Fatemi  Zeinab Vahabi  Shahab Mirshahvaladi  Fariba Ataei  Elmira Bahraminejad  Najmehsadat Masoudi  Mojtaba Rezazadeh Valojerdi  Hamid Gourabi
Institution:1. Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, 12 Hafez St, Banihashem St, Resalat St, PO Box 19395?C4644, Tehran, Iran
2. Department of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, 12 Hafez St, Banihashem St, Resalat St, PO Box 19395?C4644, Tehran, Iran
3. Department of Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran
5. Animal Core Facility, Reproductive Biomedicine Research Center, Royan Institute for Animal Biotechnology, ACECR, Tehran, Iran
6. Department of Clinical Science, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran
4. Department of Molecular Genetics, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran
7. Department of Molecular Systems Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran
Abstract:There are growing numbers of recombinant proteins that have been expressed in milk. Thus one can consider the placement of any gene of interest under the control of the regulatory elements of a milk protein gene in a dairy farm animal. Among the transgene introducing techniques, only nuclear transfer (NT) allows 100?% efficiency and bypasses the mosaicism associated with counterpart techniques. In this study, in an attempt to produce a transgenic goat carrying the human coagulation factor IX (hFIX) transgene, goat fetal fibroblasts were electroporated with a linearized marker-free construct in which the transgene was juxtaposed to ??-casein promoter designed to secret the recombinant protein in goat milk. Two different lines of transfected cells were used as donors for NT to enucleated oocytes. Two transgenic goats were liveborn. DNA sequencing of the corresponding transgene locus confirmed authenticity of the cloning procedure and the complementary experiments on the whey demonstrated expression of human factor IX in the milk of transgenic goats. In conclusion, our study has provided the groundwork for a prosperous and promising approach for large-scale production and therapeutic application of hFIX expressed in transgenic goats.
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