Translation-dependent mRNA localization in the Caenorhabditis elegans embryo
Date
2022
Authors
Winkenbach, Lindsay P., author
Osborne Nishimura, Erin, advisor
Wilusz, Carol, committee member
Stasevich, Tim, committee member
Di Pietro, Santiago, committee member
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Abstract
Though each animal cell contains the same genetic information, cell-specific gene expression is required for embryos to develop into mature organisms. Embryos rely on maternally inherited components during early development to guide cell fate specification. In animals, de novo transcription is paused after fertilization until zygotic genome activation. Consequently, early embryos rely on post-transcriptional regulation of maternal mRNA to spatially and temporally regulate protein production. Caenorhabditis elegans has emerged as a powerful developmental model for studying mRNA localization of maternally-inherited transcripts. We have identified subsets of maternal mRNAs with cell-specific and subcellular patterning in the early C. elegans embryo. Previous RNA localization studies in C. elegans focused on maternal transcripts that cluster in the posterior lineage and showed mRNA localization occurs in a translation-independent manner through localization sequence elements in the 3'UTR. However, little is known about the mechanisms directing RNA localization to other subcellular locales in early embryos. Therefore, we sought to understand the localization of maternal transcripts found enriched at the plasma membrane and nuclear periphery, erm-1 (Ezrin/Radixin/Moesin) and imb-2 (Importin Beta), respectively. In this thesis, I characterize two different translation-dependent pathways for mRNA localization of maternal transcripts at the plasma membrane and nuclear periphery. I identified the PIP2-membrane binding region of the ERM-1 proteins is necessary for erm-1 mRNA localization while identifying additional membrane localized maternal transcripts through the presence of encoded PIP2-membrane binding domains. Additionally, I observed that mRNA localization patterns can change over developmental time corresponding to changes in translation status. For imb-2 mRNA localization, I found localization to the nuclear periphery is also translation-dependent. Through recoding the imb-2 mRNA sequence while maintaining the translated peptide sequence using alternative codons, I found both localization and transcript stability additionally depends on mRNA sequence context. These findings represent the first report of a translation-dependent localization pathway for two maternally-inherited transcripts in C. elegans and demonstrate the utility of C. elegans as a model for studying translation-dependent mRNA localization during development.
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Subject
ERM-1
RNA localization
Caenorhabditis elegans
translation
IMB-2