Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.769950
Title: Reconstitution of eukaryotic DNA replication and replication-coupled chromatin assembly in vitro
Author: Hill, Jacob Hopkins
ISNI:       0000 0004 7660 242X
Awarding Body: King's College London
Current Institution: King's College London (University of London)
Date of Award: 2019
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Abstract:
Eukaryotic DNA replication machinery disrupts the structure of chromatin as the replication fork progresses through DNA. Importantly, the histone content must be duplicated every cell cycle in addition to the DNA. Whilst a number of insights into the initiation and elongation phases of replication on chromatin have been revealed from decades of work in vivo and in vitro, many mechanistic details of the later stages of replication remain poorly understood. In this study, I used an in vitro biochemical approach to build upon the work described by Yeeles et al. (2017) and Kurat et al. (2017). I reconstituted Okazaki fragment maturation and identified the minimal set of proteins involved in this process on both naked and chromatinised DNA: Fen1, DNA ligase I, PCNA, and DNA polymerase d. I then showed that these proteins - in addition to those required for replication initiation - are sufficient to generate relaxed, covalently closed daughter DNA. The process of termination is slow and inefficient relative to the rest of replication, however, and leads to the accumulation of late replication intermediates. I showed that Pif1 is able to enhance termination by (1) decreasing the amount of time it takes to occur and (2) resolving the late replication intermediates generated in the absence of Pif1. Furthermore, I found that excess Mcm2-7 are inhibitory to replication on chromatin and must be removed from the DNA. I then identified a novel pathway for Mcm2-7 removal during replication involving Pif1. It has been known for many years that cells licence more origins of replication than are used in each cell cycle. In fact, many species (including humans) have been shown to load many more Mcm2-7 than there are origins on DNA. This is the first indication that they need to be removed during replication, and the data presented in this thesis provides a mechanism for how they are removed from the DNA.
Supervisor: Thomas, Nicholas Shaun Bevan Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.769950  DOI: Not available
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