Epigenomic interrogation of development and regeneration

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Abstract/Contents

Abstract
Mammalian development comprises the highly coordinated and robust processes of cellular proliferation, specification, and functionalization to form the diverse tissues of the adult body. A single cell, containing DNA from the mother and the father, divides and gives rise to increasingly specified stem and progenitor cells at controlled times during development. This process is driven by changes not to the DNA sequence itself, but to the activity of the DNA within each cell, and the genes that are turned on and off, through modifications to the epigenome. During adult regeneration these processes can be reversed and repeated to re-build tissue that has been lost due to aging or injury. Our understanding of these processes has accelerated over the last decade, as next-generation sequencing technologies have made it possible to measure the state of the epigenome and gene expression in diverse cell types and organisms. Despite the progress that has been made, there are still challenges to understanding the dynamics of the epigenome in developmental processes. These include both experimental challenges of making measurements in small numbers of homogeneous primary cells, and computational challenges including mapping the maternal and paternal genomes separately and mapping repetitive sequences in the genome. In this dissertation, we employ a technique for mapping regions of accessible DNA in the genome, the Assay for Transposase-Accessible Chromatin with sequencing (ATAC-seq), to discover novel mechanisms of developmental allelic gene regulation, gene regulation in regeneration, and evolution of gene regulatory programs.

Description

Type of resource text
Form electronic resource; remote; computer; online resource
Extent 1 online resource.
Place California
Place [Stanford, California]
Publisher [Stanford University]
Copyright date 2019; ©2019
Publication date 2019; 2019
Issuance monographic
Language English

Creators/Contributors

Author Carter, Ava Clayton
Degree supervisor Chang, Howard Y. (Howard Yuan-Hao), 1972-
Thesis advisor Chang, Howard Y. (Howard Yuan-Hao), 1972-
Thesis advisor Greenleaf, William James
Thesis advisor Oro, Anthony, 1958-
Degree committee member Greenleaf, William James
Degree committee member Oro, Anthony, 1958-
Associated with Stanford University, Department of Stem Cell Biology and Regenerative Medicine.

Subjects

Genre Theses
Genre Text

Bibliographic information

Statement of responsibility Ava Clayton Carter.
Note Submitted to the Department of Stem Cell Biology and Regenerative Medicine.
Thesis Thesis Ph.D. Stanford University 2019.
Location electronic resource

Access conditions

Copyright
© 2019 by Ava Clayton Carter
License
This work is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported license (CC BY-NC).

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