Title page for ETD etd-04082009-113609

Type of Document Master's Thesis
Author Wilson, Jessica A.
URN etd-04082009-113609
Title Determining Gene Copy Number in Transfected Caprine Fibroblast Cells
Degree Master of Science (M.S.)
Department Animal Science (Animal, Dairy, & Poultry Sciences)
Advisory Committee
Advisor Name Title
Dr. Kenneth Bondioli Committee Chair
Dr. Gary Hay Committee Member
Dr. Robert Godke Committee Member
  • Transgenic
  • Transgene copy number
  • Transfection
  • Quantitative PCR
  • Plasmid
  • Liposome mediated transfection
  • Electroporation
  • Caprine
Date of Defense 2009-04-01
Availability unrestricted
Transgene expression in stably transgenic organisms is affected by many factors, including the copy number of the transgene in the genome, and by interactions between the transgene and flanking DNA sequences. Transgene copy number has also been shown to effect genetic stability in transgenic plants. Two commonly used methods for transfecting cells are liposome mediated transfection and electroporation. Little is known about the mean transgene copy number or variability of the copy number with these techniques. Quantitative PCR (Q-PCR) has been shown to be an effective method for determining transgene copy number.

The objective of this study was to determine transgene copy number after liposome mediated transfection and electroporation. The mean transgene copy number and variability between individual integration events have been determined.

Q-PCR conditions were optimized for primer annealing temperature and concentration when amplifying a region of the plasmid hEFGFP used for transfection. The quantitative nature of the Q-PCR reaction was confirmed by amplifying 10-fold dilutions of the plasmid and plotting the threshold cycle (CT) value against the log of the plasmid concentration. A correlation coefficient of 1.00 and a calculated PCR efficiency of 93.3% were obtained from this analysis. Caprine fibroblasts were transfected by electroporation or FuGENEŽ HD reagent with either a circular or linearized hEFGFP plasmid and plated at low density in medium containing GeneticinŽ. After 10 days of culture, single cell colonies were isolated and expanded. When cultures reached 1-2 million cells, genomic DNA was isolated. Transgene copy number was determined by amplifying genomic DNA from individual clones representing 1x105 cells with Q-PCR. Transgene copy number was calculated by comparing CT values to a standard curve. The transgene copy number for electroporation circular was 2.7  0.75 (n=32) and 1.3  0.65 (n=19) when using a linear DNA construct. FuGENEŽ HD using a circular plasmid construct generated a gene copy number of 0.5  0.11 (n=14) and 0.64  0.13 (n=16) for the linear plasmid construct. There were significant differences when comparing electroporation circular to all other treatments, however, there were no differences when comparing electroporation linear, FuGENEŽ HD circular and FuGENEŽ HD linear to each other.

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