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case1274900106.pdf (3.54 MB)
ETD Abstract Container
Abstract Header
The Interplay of Eukaryotic mRNA Translation and Degradation
Author Info
Hu, Wenqian
Permalink:
http://rave.ohiolink.edu/etdc/view?acc_num=case1274900106
Abstract Details
Year and Degree
2010, Doctor of Philosophy, Case Western Reserve University, Biochemistry.
Abstract
The regulation of mRNA translation and degradation is essential for proper gene expression. In eukaryotes, a major mRNA degradation pathway is initiated by deadenylation, followed by decapping, and ultimately 5’-3’ exonucleolytic digestion. Removal of the mRNA 5’ cap is an irreversible step in mRNA degradation, and is postulated to require dissociation of the mRNA from the ribosomes and packaging into sub-cellular, ribosome-free granules termed P-bodies. Based on this and other observations, a “two-step” model of eukaryotic mRNA degradation had been proposed that mRNA translation and degradation occur in different compartments within the cell. Recent findings suggest, however, that mRNA degradation may occur independent of P-bodies. Consequently, an important but unresolved issue in the field is to determine the context in which mRNA is degraded. In my study, I have demonstrated that the three steps of mRNA decay, deadenylation, decapping, and 5’-3’ exonucleolytic digestion, occur co-translationally. Specifically, mRNA deadenylation does not lead to ribosome dissociation. Second, I found that decapped mRNA mainly bound to polyribosomes, suggesting that decapping occurs during translation. In addition, using kinetic analysis, I demonstrated that mRNA decapping is initiated while the mRNA is on polyribosomes. Third, I observed that in wild-type cells, exonucleolytic decay fragments are polyribosome associated when ribosome transit is slowed in cis. Lastly, using an innovative assay I designed, I detected decapping products from endogenous mRNAs mainly on polyribosomes in wild type cells. These results clearly demonstrate that under normal physiological conditions, mRNA degradation occurs while the mRNA is still associated with ribosomes. In addition to the normal mRNA turnover pathway, I observed that mRNA decapping triggered by nonsense-mediated mRNA decay, an important mRNA quality control mechanism, also occurs on polyribosomes. Collectively, these results indicate that polyribosomes are the major sites for destroying both normal and aberrant mRNAs within eukaryotic cells
Committee
Jeff Coller (Advisor)
Eckhard Jankowsky (Committee Chair)
Timothy Nilsen (Committee Member)
Alan Tartakoff (Committee Member)
Maria Hatzoglou (Committee Member)
Pages
121 p.
Subject Headings
Biochemistry
;
Cellular Biology
;
Genetics
;
Molecular Biology
Keywords
mRNA turnover
;
mRNA decapping
;
mRNA translation
;
polyribosomes
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Citations
Hu, W. (2010).
The Interplay of Eukaryotic mRNA Translation and Degradation
[Doctoral dissertation, Case Western Reserve University]. OhioLINK Electronic Theses and Dissertations Center. http://rave.ohiolink.edu/etdc/view?acc_num=case1274900106
APA Style (7th edition)
Hu, Wenqian.
The Interplay of Eukaryotic mRNA Translation and Degradation.
2010. Case Western Reserve University, Doctoral dissertation.
OhioLINK Electronic Theses and Dissertations Center
, http://rave.ohiolink.edu/etdc/view?acc_num=case1274900106.
MLA Style (8th edition)
Hu, Wenqian. "The Interplay of Eukaryotic mRNA Translation and Degradation." Doctoral dissertation, Case Western Reserve University, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=case1274900106
Chicago Manual of Style (17th edition)
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Document number:
case1274900106
Download Count:
804
Copyright Info
© 2010, all rights reserved.
This open access ETD is published by Case Western Reserve University School of Graduate Studies and OhioLINK.