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  <title><![CDATA[PhD Defense by Ruiqiao Yang]]></title>
  <body><![CDATA[<p>In partial fulfillment of the requirements for the degree of</p><p>&nbsp;</p><p>Doctor of Philosophy in Biology</p><p>In the</p><p>School of Biological Sciences</p><p>&nbsp;</p><p><strong>Ruiqiao Yang</strong></p><p>&nbsp;</p><p>Will defend her dissertation</p><p>&nbsp;</p><p><strong>ROLE OF H1 LINKER HISTONES IN GASTRULOID DEVELOPMENT</strong></p><p>&nbsp;</p><p>Time and Date: 1:00PM (Eastern Time), July 9th, 2026</p><p>Location: IBB 2316</p><p>&nbsp;</p><p>&nbsp;<strong>Thesis Advisor:</strong></p><p>Yuhong Fan, Ph.D.</p><p>School of Biological Sciences</p><p>Georgia Institute of Technology</p><p>&nbsp;</p><p><strong>Committee Members:</strong></p><p>Mirjana M. Brockett, Ph.D.</p><p>School of Biological Sciences</p><p>Georgia Institute of Technology</p><p>&nbsp;</p><p>Francesca Storici, Ph.D.</p><p>School of Biological Sciences</p><p>Georgia Institute of Technology</p><p>&nbsp;</p><p>Rabindranath De La Fuente, Ph.D.</p><p>&nbsp;&nbsp;&nbsp; Department of Physiology and Pharmacology</p><p>University of Georgia</p><p>&nbsp;</p><p>Jiyue Zhu, Ph.D.</p><p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; School of Pharmacy and Pharmaceutical Sciences</p><p>&nbsp;&nbsp;&nbsp; Washington State University</p><p>&nbsp;</p><p>ABSTRACT: H1 Linker histones are key chromatin proteins that bind to nucleosomes and linker DNA, facilitating the folding of higher-order chromatin structures. Linker histone H1 is essential for mammalian embryogenesis, and its depletion has been shown to impair embryonic stem cell differentiation. To dissect the role of H1 histones in coordinating developmental programs during embryogenesis, we first optimized a protocol for generating gastruloids, an in vitro 3D organoid model of gastrulation, from mouse embryonic stem cells (ESCs). By modeling gastruloid development and leveraging H1c/H1d/H1e triple-knockout (H1 TKO) ESCs, we investigated how H1 regulates developmental patterning and programming. Compared with wild-type gastruloids, H1 TKO gastruloids exhibited markedly impaired growth and temporal patterning and lacked clear axial organization and beating cardiomyocytes. Transcriptomic analysis of gastruloids by RNA sequencing revealed extensive changes in gene expression, with enrichment in multiple developmental programs and signaling processes, including myogenesis, epithelial–mesenchymal transition, hypoxia, glycolysis, and other signaling pathways. H1 depletion resulted in the dysregulation of genes associated with diverse developmental processes, including morphogenesis, muscle and heart development, nervous system development, and chromosome organization. These results demonstrate that H1 is required for the proper activation of multiple developmental programs during gastruloid formation and underscore the essential role of H1 in coordinating cell differentiation, migration, and morphogenesis during embryogenesis.</p><p>&nbsp;</p>]]></body>
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