Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Dates: Last 2 Years

You searched for +publisher:"Rutgers University" +contributor:("Woychik, Nancy"). One record found.

Search Limiters

Last 2 Years | English Only

No search limiters apply to these results.

▼ Search Limiters


Rutgers University

1. Cristovao Barth Junior, Valdir. Functional dissection of tRNA-cleaving toxins in mycobacteria.

Degree: PhD, tRNA, 2020, Rutgers University

Tuberculosis (TB) is the leading cause of infectious disease-related deaths world-wide. The most common infectious agent of TB, Mycobacterium tuberculosis, is a highly resistant bacterium that evades the human immune response, presumably allowing it to persist in a dormant state in the lungs for decades. The factors that lead to its high persistence are not completely understood, but bacterial toxin-antitoxin (TA) systems have been implicated. Most TA systems do not have their mode of action elucidated, limiting our understanding of how they participate in bacterial persistence and latent TB. Therefore, the aim of this work was to identify the specific targets of VapC and MazF toxins and their physiological effects in M. tuberculosis and in the fast-growing model organism, Mycobacterium smegmatis. To do so, we applied 5’ RNA-seq to accurately detect toxin-cleaved RNAs differentiating them from other cellular RNAs by their distinct 5’ end left by the toxin. Knowing that VapCs and MazFs leave 5’ monophosphate and 5’ hydroxyl (OH) ends upon cleavage, respectively, our method analyzes enrichment of those cleavage markers in mycobacterial cells expressing these TA toxins. We first found by 5’ OH RNA-seq that MazF-mt9 is an isoacceptor-specific tRNAse which targets tRNALys-UUU in M. tuberculosis. 5’ OH RNA-seq also suggested that ribosomes were selectively stalling at lysine AAA codons due to the low levels of tRNALys-UUU , which we confirmed using Ribo-seq. Expressing MazF-mt9 in the model organism M. smegmatis generates a shift in translational output favoring protein synthesis from transcripts with low levels of AAA codons and lowering the levels of AAA-rich proteins. Therefore, we documented a possible new mechanism of post-transcriptional regulation by tRNAs that dictates gene expression by codon usage. We predict this resulting cellular AAA-depleted proteome may induce persistence against antibiotics and protection against the host’s immune system. In the second Chapter, we show that the only MazF toxin described in M. smegmatis genome (here named MazF-ms) is also a tRNALys-specific tRNA-cleaving toxin. Expression of MazF-ms in M. smegmatis generates similar effects as observed for MazF-mt9 in M. tuberculosis. Newly synthesized protein production is heavily dictated by the transcript’s Lys AAA codon content. The change in proteome favors genes involved in stress response and reduces expression of genes involved in cell division and DNA replication. In the third Chapter, we show that in vitro studies may be misleading. As we report for VapC-mt11, the toxin is highly specific when studied in vivo in its original host (M. tuberculosis) and loses specificity in in vitro assays. We propose the actual targets of VapC-mt11 are tRNAGln and tRNALeu, even though additional targets can be observed in vitro or when expressing in M. smegmatis. In the fourth and last Chapter, we show that VapC-mt4 is another tRNA-cleaving toxin that behaves promiscuously in in vitro assays. We report that VapC-mt4 targets the only tRNACys in vivo… Advisors/Committee Members: Copeland, Paul (chair), Woychik, Nancy A (internal member), Brewer, Gary (internal member), Husson, Robert (outside member), School of Graduate Studies.

Subjects/Keywords: Microbiology and Molecular Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Cristovao Barth Junior, V. (2020). Functional dissection of tRNA-cleaving toxins in mycobacteria. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/65068/

Chicago Manual of Style (16th Edition):

Cristovao Barth Junior, Valdir. “Functional dissection of tRNA-cleaving toxins in mycobacteria.” 2020. Doctoral Dissertation, Rutgers University. Accessed May 09, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/65068/.

MLA Handbook (7th Edition):

Cristovao Barth Junior, Valdir. “Functional dissection of tRNA-cleaving toxins in mycobacteria.” 2020. Web. 09 May 2021.

Vancouver:

Cristovao Barth Junior V. Functional dissection of tRNA-cleaving toxins in mycobacteria. [Internet] [Doctoral dissertation]. Rutgers University; 2020. [cited 2021 May 09]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/65068/.

Council of Science Editors:

Cristovao Barth Junior V. Functional dissection of tRNA-cleaving toxins in mycobacteria. [Doctoral Dissertation]. Rutgers University; 2020. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/65068/

.