Cellular DNA is continually altered by mutagenic agents from the environment (e.g. UV light, radiation etc.) and cellular metabolism (e.g. reactive oxygen). This DNA damage, and the resulting mutation, contributes to many interesting phenomena in biology– evolution, antibiotic resistance in bacteria, toxicity, initiation of cancerous cells in animals, treatments for cancer, to name a few. My lab is focused on the mechanisms that protect genes and genomes from excess DNA damage and mutation, using the plant Arabidopsis thaliana as a model system. Because the types of damage to DNA are so diverse, it is not surprising that the mechanisms and molecular pathways that monitor and repair DNA damage are very complex. What may be surprising, however, is that DNA maintenance and repair pathways are very well conserved, from single-celled microorganisms (such as yeasts), to plants, to humans. In other words, yeast and plant genomes encode the same general DNA repair pathways that are present in humans. Therefore, organisms such as yeasts and plants are useful “model systems” for the study of DNA repair and genome maintenance.
Two general mechanisms that we are actively pursuing in the lab are the regulation of DNA repair pathways, and how cells monitor and regulate cell-cycle progression in response to DNA damage. When a cell incurs DNA damage, the cell must first recognize the type of damage, and then mount an appropriate response. This response is not simply just a decision of the type of repair pathway to activate (Non-homologous end joining versus recombinational repair, for example), but also involves activating so-called cell-cycle “checkpoints” if DNA damage persists, and in the case of animals often involves a cellular life or death decision termed apoptosis. Consequently, we are interested in identifying novel genes and pathways involved in the initial response to DNA damage in Arabidopsis thaliana to gain insights into how plant cells protect themselves from genomic stress, potentially leading to insights into animal DNA repair and maintenance.
The protein kinases ATR and ATM are known master regulators of both the DNA repair and cell-cycle checkpoint responses to DNA damage in mammalian cells. These master regulators are key components of cellular decisions in how to respond appropriately to cellular DNA damage. Currently, my lab is interested in upstream activators of ATR and ATM. One example is activation of ATR pathways through Replication Protein A (RPA) by DNA damage. We have recently characterized a unique plant gene family of RPA, and are interested in how the various functions of RPA are integrated into the DNA damage response.
Overall, our goal is to better understand the highly complex pathways involved in DNA repair and genome maintenance in Arabidopsis, and apply this knowledge to better improve crop species, and potentially aid in the understanding of these pathways in humans as it relates to disease and cancer biology.
If you are currently an undergraduate (preferably majoring in biological sciences) in good academic standing, and would like to gain some research experience, please visit the COLSA Research Opportunities Webpage, to see what current opportunities are available in the lab.
Ph.D., Cell and Molecular Biology, Oregon State University
B.S., Molecular Biology, University of California - San Diego
BCHM 999: Doctoral Research
BMCB 795W: Invest in Molecular & Cell Bio
GEN 799H: Honors Senior Thesis
INCO 590: Rsrch Exp/MCBS
INCO 790: Adv Rsrch Exp/MCBS
MCBS 999: Doctoral Thesis
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