TY - JOUR
T1 - Production of transgenic goats expressing human coagulation factor IX in the mammary glands after nuclear transfer using transfected fetal fibroblast cells
AU - Amiri Yekta, Amir
AU - Dalman, Azam
AU - Eftekhari-Yazdi, Poopak
AU - Sanati, Mohammad Hossein
AU - Shahverdi, Abdol Hossein
AU - Fakheri, Rahman
AU - Vazirinasab, Hamed
AU - Daneshzadeh, Mohammad Taghi
AU - Vojgani, Mahdi
AU - Zomorodipour, Alireza
AU - Fatemi, Nayeralsadat
AU - Vahabi, Zeinab
AU - Mirshahvaladi, Shahab
AU - Ataei, Fariba
AU - Bahraminejad, Elmira
AU - Masoudi, Najmehsadat
AU - Rezazadeh Valojerdi, Mojtaba
AU - Gourabi, Hamid
PY - 2013/2
Y1 - 2013/2
N2 - 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 β-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.
AB - 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 β-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.
KW - Fibroblast
KW - Goat
KW - Human Coagulation Factor IX
KW - Somatic cell nuclear transfer
KW - Transgenic
UR - http://www.scopus.com/inward/record.url?scp=84871361365&partnerID=8YFLogxK
U2 - 10.1007/s11248-012-9634-y
DO - 10.1007/s11248-012-9634-y
M3 - Article
C2 - 22869287
AN - SCOPUS:84871361365
SN - 0962-8819
VL - 22
SP - 131
EP - 142
JO - Transgenic Research
JF - Transgenic Research
IS - 1
ER -