In humans, ~60,000 initiation events occur each S phase, and ultimately trigger ~60,000 termination events. Proper execution of these events is necessary, as failure to replicate even a ~10 base pair stretch of DNA during termination would lead to catastrophic chromosome mis-segregation during the subsequent mitosis, or activate error-prone DNA repair pathways that would elevate the mutation rate. However, until recently the basic events of termination were unknown, and no termination-specific proteins were identified (Dewar and Walter, 2017, Nat Rev Mol Cell Biol). My lab studies replication termination, employing a variety of biochemical approaches and exploiting the power of frog egg extracts, which are a rich source of proteins involved in DNA replication. We are currently focused on the following areas:


1. The general mechanism of replication termination

Most termination events occur when pairs of replication forks converge upon the same stretch of DNA. Despite the high frequency of these termination events (~60,000 per cell cycle), they are difficult to monitor, as they occur asynchronously and are sequence non-specific. The difficulty of monitoring replication termination has hampered efforts to interrogate this fundamental process. To overcome this limitation, I developed a biochemical system to study termination, which was used to elucidate the basic mechanism of termination and identify novel regulators of this process (Dewar et al, 2015, Nature; Dewar et al, 2017, Genes Dev). In my lab, we are using this approach to probe the mechanism of replication termination. In particular, we are interested in how topoisomerases prevent the build-up of toxic amounts of topological stress, which would otherwise cause termination to stall. We have also performed mass spectrometry analyses and identified novel termination proteins, whose roles we are currently investigating.


2. Replication and termination at telomeres

In humans, ~100 termination events occur at telomeres each cell cycle, when individual replication forks travel unidirectionally towards chromosome ends. Telomeres are nucleoprotein  complexes that distinguish chromosome ends from DNA double strand breaks. This crucial role is fulfilled by the ‘Shelterin’ complex, which binds to telomeric repeat sequences and ensures that telomeres do not trigger checkpoint activation or undergo the processing associated with DSB repair. Although several Shelterin components and other telomere-interacting factors have been identified, multiple aspects of telomere replication, including the mechanisms of termination, are unclear. It is important to understand how telomeres are replicated, as defects in this process underlie both cellular aging and oncogenesis. We are currently developing in vitro systems to study telomere replication by adapting strategies that I previously developed to study DNA repair (Duxin et al, 2014, Cell; Zang et al, 2015, Nat Struct Mol Biol). Our goal is to study how telomeres are replicated and maintained, and ultimately use mass spectrometry to identify novel factors involved in these processes.