PLEASE HELP; 'Can genetic engineering determine a community's crime rate?'
Posted: Sun Mar 24, 2019 5:20 am
I've recently switched my project topic from neurology to genetics. I hope someone can tell me if my procedure makes sense since I didn't get a chance to read too intensively on genetic engineering.
Can genetically engineering the hereditary MAOA gene in a human embryo affect behaviour, and ultimately a community’s crime rate? This project is a simulation of such a situation, to show that genetic engineering can affect not just the single individual but the whole community. I will exhibit this claim by mutating another species’ gene, the Brewer’s yeast cells’ FLO1, to see if there’s an increase in the number of flocs overtime, and how that affects other factors, like their reproduction rate.
Prepare three normal Brewer’s yeast culture on petri dishes, observe behaviour
Perform bacterial knock-out on FLO1 gene of yeast cells on one dish
Prepare a plasmid with the sgRNA, a plasmid carrying Cas9 + lambda red genes, and the repair template, ssDNA oligo
Transform pCas9 on dish; wait to grow at 30०C on kanamycin plates
Make cells electrocompetent by introducing lambda red genes
Cotransform p-target carrying sgRNA as well as repair template by electroporation
Screen cells for FLO1 gene knockouts
Place edited cells in second petri dish so that the number of cells on both dishes are relatively similar
Report, daily, the number of flocs in each dish, as well as any growth.
Can genetically engineering the hereditary MAOA gene in a human embryo affect behaviour, and ultimately a community’s crime rate? This project is a simulation of such a situation, to show that genetic engineering can affect not just the single individual but the whole community. I will exhibit this claim by mutating another species’ gene, the Brewer’s yeast cells’ FLO1, to see if there’s an increase in the number of flocs overtime, and how that affects other factors, like their reproduction rate.
Prepare three normal Brewer’s yeast culture on petri dishes, observe behaviour
Perform bacterial knock-out on FLO1 gene of yeast cells on one dish
Prepare a plasmid with the sgRNA, a plasmid carrying Cas9 + lambda red genes, and the repair template, ssDNA oligo
Transform pCas9 on dish; wait to grow at 30०C on kanamycin plates
Make cells electrocompetent by introducing lambda red genes
Cotransform p-target carrying sgRNA as well as repair template by electroporation
Screen cells for FLO1 gene knockouts
Place edited cells in second petri dish so that the number of cells on both dishes are relatively similar
Report, daily, the number of flocs in each dish, as well as any growth.