Type of Document	Dissertation
Author	Lu, Junjie
Author's Email Address	jl06u@fsu.edu
URN	etd-03092010-095313
Title	Mechanism Of Replication Timing Program In Mammalian Systems
Degree	Doctor of Philosophy
Department	Biological Science, Department of
Advisory Committee	Advisor Name Title David M. Gilbert Committee Chair Hank W. Bass Committee Member Lloyd M. Epstein Committee Member Michael W. Davidson Committee Member Akash Gunjan University Representative
Keywords	DNA Replication Epigenetics Cell Cycle Chromatin Histone Modifications Transcription Heterochromatin Embryonic Stem Cell Chromatin Domain
Date of Defense	2010-03-02
Availability	unrestricted
Abstract DNA replication, the duplication of genetic and epigenetic information, is the basis of biological inheritance. In all eukaryotes, DNA replication follows a tightly regulated replication-timing program, which dynamically changes during development and has a lot of conserved characteristics across multiple species. However the molecular mechanism of replication timing program remains elusive. Using a Xenopus egg extract in vitro replication system, it was found that the replication timing program is established at a time point during early G1-phase of the cell cycle, termed the Timing Decision Point (TDP). The TDP is coincident with the re-positioning and anchorage of chromosome segments in the newly formed nucleus. Previous studies have found that many chromatin related factors were not able to determine replication timing. Here, I studied the roles of non-coding RNAs from mouse pericentric heterochromatin and histone methylatransferase G9a in replication timing determination and found that they were also not the main determinants. I further examined the replication timing property of chromatin in G2-phase and quiescent (G0) cells and demonstrated that G2-phase chromatin lacks determinants of replication timing but maintains the overall spatial organization of chromatin domains, using both in vitro system and in vivo cell culture. In contrast, chromatin from quiescent cells (G0) retains replication timing but exhibits disrupted spatial organization. These data support a model in which events at the TDP establish chromatin marks as replication timing determinants, potentially facilitated by spatial organization, which persist independent of such organization until the process of chromatin replication dilutes or disrupts those determinants. These results demonstrate that establishment and maintenance of replication timing program are mediated by different mechanisms, both of which potentially involve chromatin spatial organization. This work represents a major advance in our quest for the replication timing determinants and understanding of the mechanism of replication timing program.
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