Skip navigation
Please use this identifier to cite or link to this item: http://arks.princeton.edu/ark:/88435/dsp016d56zz92g
Title: RNase L localization studies in human cells and potential applications of RNase L modulation in cancer immunotherapy
Authors: Chu, Jacqueline
Advisors: Korennykh, Alexei
Department: Molecular Biology
Class Year: 2015
Abstract: Ribonuclease L is an important effector of the type I IFN pathway in response to viral RNAs. In response to activation by 2-5As, RNase L cleaves both viral and cellular mRNAs. However, there is increasing interest in the roles of RNase L under homeostatic conditions. RNase L has been shown to cleave specific cellular mRNAs that have functions in proliferation and differentiation, but it is still unclear as to how RNase L is able to specifically target these RNAs. In order to elucidate the mechanism of RNase L substrate targeting, this study focused on determining the mechanism through which RNase L is localized. Deep sequencing, immunoblots, and a new localization assay developed for this study, all reveal a nuclear/cytoskeletal enrichment of both RNase L mRNA and protein. In addition, deep sequencing revealed an association of RNase L with RNAs of membrane-bound proteins. Based on this data, it is evident that studying the mechanism of RNase L mRNA localization can reveal how RNase L protein is localized, which has implications for how RNase L targets is substrates. In order to further study the connection between RNase L mRNA and localization of RNase L protein, two RNase L mutants were designed that study different possible mechanisms of RNase L mRNA spatial control of translation.
Extent: 79 pages
URI: http://arks.princeton.edu/ark:/88435/dsp016d56zz92g
Type of Material: Princeton University Senior Theses
Language: en_US
Appears in Collections:Molecular Biology, 1954-2016

Files in This Item:
File SizeFormat 
PUTheses2015-Chu_Jacqueline.pdf1.54 MBAdobe PDF    Request a copy


Items in Dataspace are protected by copyright, with all rights reserved, unless otherwise indicated.