MS Defense by Kirti Karunakaran

Event Details
  • Date/Time:
    • Monday March 30, 2020
      10:00 am - 12:00 pm
  • Location: REMOTE
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  • URL: BlueJeans Link
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Summaries

Summary Sentence: Analysis of the Impact of a p53 Mutation in a Homogeneous Genetic Background

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In partial fulfillment of the requirements for the degree of

 

Master of Science in Biology

in the

School of Biological Sciences

 

Kirti Karunakaran

 

Will defend her thesis

 

“Analysis of the Impact of a p53 Mutation in a Homogeneous Genetic Background ”

 

Monday, March 30, 2020

10:00 AM

IBB 1128

 

Thesis Advisor:

Dr. John F. McDonald

School of Biological Sciences

Georgia Institute of Technology

 

Committee Members:

Dr. Matthew Torres

School of Biological Sciences

Georgia Institute of Technology

 

 J. Leonard Lichtenfeld, MD, MACP

Deputy Chief Medical Office

American Cancer Society

  

Abstract:

In more than 50% of cancers, p53, a tumor suppressor gene involved cell cycle arrest and apoptosis, has been seen to be heavily mutated making it an important gene to study. There are several studies on p53 and its role in cancer, but they ignore the impact of genetic background. Past studies have shown that genetic background can have a significant effect on the phenotypic consequences of cancer driver mutations, however, all these studies are carried out in a heterogenous environment. The goal of my study was to utilize the CRISPR Cas 9 system to create a loss of function mutation in the p53 gene in a well characterized human cell line (HEYA8F8) and to evaluate the impact of this mutation on cell growth and apoptotic function in identical genetic backgrounds. The resulting mutation was a deletion in codons 33-36 of exon 4 which decreased the length of the protein from 393 to 389 amino acids. Using the cell lines with the specified deletion, growth rates over 96 hours were compared, which resulted in higher cell counts for the mutant in comparison to the wildtype. Assay for drug sensitivity using cisplatin, the standard of care for many cancers, showed that mutant cell lines had higher cell viability in comparison to the wild type. The overall results demonstrated that mutations in p53 increase cell viability when treated with chemotherapy and an increase in cell proliferation. We believe that the cell lines with the loss of function mutations in p53 generated will provide an ideal experimental set up to study how the genetic background can evolve to enhance cancer in future studies. 

 

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ms defense
Status
  • Created By: Tatianna Richardson
  • Workflow Status: Published
  • Created On: Mar 12, 2020 - 12:28pm
  • Last Updated: Mar 26, 2020 - 2:47pm