Anthony Chan, a geneticist at Emory
University in Atlanta, GA, spent two years creating the first monkeys to be
genetically engineered with human mutations.
The primates were given the mutations for Huntington's disease. Three of the five monkeys developed severe
symptoms of the disease more quickly than anticipated and were put down within
a month of birth. The method in which
viruses were used to introduce the gene posed an issue; where the virus
inserted extra copies of the relevant gene randomly. Which caused the severe development of the
disease. This issue thus presented its
limitations when creating new animal disease models.
The use of transgenic monkeys as animal
disease models will more accurately mimic the disease symptoms and reaction to
treatments that is present in humans compared to mice models. Neuroscientists have waited for the ability to
use transgenic monkeys in research for disorders such as autism, schizophrenia,
and Alzheimer’s disease. Disorders such
as these cannot be replicated accurately in mice because they lack complex cognitive
and social abilities. Many neuro drugs
that have shown positive results actually ended up failing when tested on
humans.
Precision genome-editing techniques that may solve the problems presented by the viral technique are now being worked on. These techniques will work by using enzymes and RNA instead of viruses. A disadvantage with the use of monkeys instead of mice as a model is the lengthy time it takes for maturity. “Custom” monkeys have become a possibility due to efficient gene-editing techniques that support a method in which embryos are manipulated one at a time however. One method used is called CRISPR. A customizable RNA fragment is used to guide a DNA-cutting enzyme to the right spot. Feng Zhang, a synthetic biologist at the Massachusetts Institute of Technology (MIT) in Cambridge, showed that CRISPR could be used to make precise mutations in multiple genes in mouse embryos. This method could make it possible to use monkeys as models of human brain disorders that involve more than one gene. CRISPR is now being tested on fertilized monkey eggs.
Precision genome-editing techniques that may solve the problems presented by the viral technique are now being worked on. These techniques will work by using enzymes and RNA instead of viruses. A disadvantage with the use of monkeys instead of mice as a model is the lengthy time it takes for maturity. “Custom” monkeys have become a possibility due to efficient gene-editing techniques that support a method in which embryos are manipulated one at a time however. One method used is called CRISPR. A customizable RNA fragment is used to guide a DNA-cutting enzyme to the right spot. Feng Zhang, a synthetic biologist at the Massachusetts Institute of Technology (MIT) in Cambridge, showed that CRISPR could be used to make precise mutations in multiple genes in mouse embryos. This method could make it possible to use monkeys as models of human brain disorders that involve more than one gene. CRISPR is now being tested on fertilized monkey eggs.
I never thought they would start studying human diseases on monkeys. I mean I suppose if these transgenic monkeys can help humans find more efficient results as opposed to mice it would be good but I personally don't like the idea of creating transgenic monkeys and fertilized monkey eggs. Overall if its beneficial for disease study then I guess that is good, but studying on the monkeys and mice doesn't seem very humane.
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