Abstract
Spatial and temporal regulation of developmental gene transcription often involves regulatory sequences found in noncoding DNA separate from the gene’s promoter. Conservation of a noncoding region (CNR) across divergent species may indicate a regulatory region critical to basic morphogenesis. CNR-green fluorescent protein (GFP) constructs can demonstrate spatial and temporal CNR activity by microscopy visualization. However, characterization of regulatory modules within a CNR requires quantitative, in addition to qualitative, analysis. The study presented here describes the development and implementation of a novel application of flow cytometry in the quantitative characterization of CNRs. The technique couples fluorescent microscopy localization with flow cytometry distribution and expression level analysis, creating a technique more powerful than either on its own. To optimize the flow cytometric analysis technique, we examined the limb-specific Shh regulatory region, LSSRR. LSSRR is a CNR that tightly regulates the specific spatiotemporal expression of Shh, a crucial morphogen for limb patterning. Our data demonstrate that flow cytometric analysis can identify and quantify changes in the distribution and intensity of CNR activity. Thus, this technique can be used to characterize conserved regulatory modules necessary for limb morphogenesis. However, it is likely that other organs and tissues utilize specific CNRs. The technique developed here is widely applicable outside of limb development. This enhances our ability to characterize CNR-related regulatory modules in general, and the technique can be used to advance knowledge of organ patterning during development.
LLU Discipline
Biochemistry
Department
Basic Sciences
School
School of Medicine
First Advisor
Oberg, Kerby C.
Second Advisor
Langridge, William
Third Advisor
Payne, Kimberly J.
Degree Name
Master of Science (MS)
Degree Level
M.S.
Year Degree Awarded
2014
Date (Title Page)
6-2014
Language
English
Library of Congress/MESH Subject Headings
Flow Cytometry; Gene Expression Profiling; Reverse Transcriptase Polymerase Chain Reaction; Fibroblast Growth Factors; Receptor Protein-Tyrosine Kinases; Receptors - Retinoic Acid; Mesoderm; Electroporation; Limb buds; Models - Biological
Subject - Local
Development Gene Transcription; Noncoding DNA; Morphogenesis; CNR-Green flourescent protein; Fluorescent Microscopy Localization;
Type
Thesis
Page Count
115
Digital Format
Digital Publisher
Loma Linda University Libraries
Copyright
Author
Usage Rights
This title appears here courtesy of the author, who has granted Loma Linda University a limited, non-exclusive right to make this publication available to the public. The author retains all other copyrights.
Recommended Citation
Brown, Amber, "Quantitative Characterization of Conserved Noncoding Regions by Flow Cytometry" (2014). Loma Linda University Electronic Theses, Dissertations & Projects. 200.
https://scholarsrepository.llu.edu/etd/200
Collection
Loma Linda University Electronic Theses and Dissertations
Collection Website
http://scholarsrepository.llu.edu/etd/
Repository
Loma Linda University. Del E. Webb Memorial Library. University Archives