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dc.contributor.advisorOliver J. Rando
dc.contributor.authorChan, Io Long
dc.date2022-08-11T08:08:38.000
dc.date.accessioned2022-08-23T16:02:10Z
dc.date.available2022-08-23T16:02:10Z
dc.date.issued2019-09-23
dc.date.submitted2019-11-11
dc.identifier.doi10.13028/ksrn-nb69
dc.identifier.urihttp://hdl.handle.net/20.500.14038/31273
dc.description.abstractOrganisms modulate their response to changing environmental conditions through changes in gene expression, and extensive variations in gene expression are prevalent among individuals even within a population. This widespread plasticity and variability of gene expression is thought to play roles in adaptation and drive novel phenotypes in species. Understanding the mechanisms that contribute to such variations requires the analysis of interactions between the genome and its environment and sequence variations within the genome. This work consists of two projects investigating the plasticity and variation of gene expression during post-embryonic development in the nematode C. elegans. In the first study, I examined the response to changes in population density in developmentally arrested L1 larvae. I systematically characterized arrested L1 larvae from low to high densities using single-worm RNA-seq and uncovered that the density of resuspended L1 larvae regulates the expression of hundreds of mRNAs. Further analysis revealed that the physiological response to changes in density is rapid and signaled by a non-canonical daf-22 ascaroside independent pathway. In the second study, I investigated the evolution of gene expression within species using two genetically divergent C. elegans strains (N2 and CB4856). I carried out RNA-seq and allele-specific analysis across six different conditions and four developmental stages, and we examined gene expression divergence using the homozygous parent and F1 hybrid system. This work provides a new experimental model for studying the evolution of gene expression and a comprehensive view of gene expression variation during development in C. elegans.
dc.language.isoen_US
dc.publisherUniversity of Massachusetts Medical Schoolen_US
dc.rightsCopyright is held by the author, with all rights reserved.
dc.subjectc elegans
dc.subjectgene regulation
dc.subjectdevelopment
dc.subjectRNA-seq
dc.subjectevolution
dc.subjectmetabolism
dc.subjectepigenetics
dc.subjectbleaching
dc.subjectsynchronization
dc.subjectgene expression
dc.subjectBiology
dc.subjectDevelopmental Biology
dc.subjectGenetics and Genomics
dc.subjectGenomics
dc.subjectMolecular Genetics
dc.titleThe Plasticity and Variation in Gene Expression during Development in C. elegans
dc.typeDoctoral Dissertation
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2060&context=gsbs_diss&unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_diss/1051
dc.legacy.embargo2020-11-11T00:00:00-08:00
dc.identifier.contextkey15752106
dc.file.descriptionFile 2.1 Summary of sequencing from single L1 RNA-seq samples. Mapping statistics for all individual worm RNA-Seq datasets in this study. (.xlsx)
dc.file.descriptionFile 2.2 fog-2 dataset. Single-animal RNA-Seq data for fog-2 animals arrested at 1, 5, 20, or 100 eggs/mL, as indicated. (.xlsx)
dc.file.descriptionFile 2.3 N2 dataset. Single-animal RNA-Seq data for N2 animals arrested at 1, 5, 20, or 100 eggs/mL, as indicated. (.xlsx)
refterms.dateFOA2022-08-28T04:15:22Z
html.description.abstract<p>Organisms modulate their response to changing environmental conditions through changes in gene expression, and extensive variations in gene expression are prevalent among individuals even within a population. This widespread plasticity and variability of gene expression is thought to play roles in adaptation and drive novel phenotypes in species. Understanding the mechanisms that contribute to such variations requires the analysis of interactions between the genome and its environment and sequence variations within the genome. This work consists of two projects investigating the plasticity and variation of gene expression during post-embryonic development in the nematode <em>C. elegans</em>.</p> <p>In the first study, I examined the response to changes in population density in developmentally arrested L1 larvae. I systematically characterized arrested L1 larvae from low to high densities using single-worm RNA-seq and uncovered that the density of resuspended L1 larvae regulates the expression of hundreds of mRNAs. Further analysis revealed that the physiological response to changes in density is rapid and signaled by a non-canonical <em>daf-22 </em>ascaroside independent pathway. In the second study, I investigated the evolution of gene expression within species using two genetically divergent <em>C. elegans</em> strains (N2 and CB4856). I carried out RNA-seq and allele-specific analysis across six different conditions and four developmental stages, and we examined gene expression divergence using the homozygous parent and F1 hybrid system. This work provides a new experimental model for studying the evolution of gene expression and a comprehensive view of gene expression variation during development in <em>C. elegans</em>.</p>
dc.identifier.submissionpathgsbs_diss/1051
dc.contributor.departmentBiochemistry and Molecular Pharmacology
dc.description.thesisprogramInterdisciplinary Graduate Program
dc.identifier.orcid0000-0002-0790-3793


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