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Epigenetically modified N6-methyladenine inhibits DNA replication by human DNA polymerase iota.
- Source :
-
Biochimie . Jan2020, Vol. 168, p134-143. 10p. - Publication Year :
- 2020
-
Abstract
- Among human four Y-family DNA polymerases, hPol ι is exceptionally error-prone in DNA synthesis. 6 mA plays significant roles in epigenetic regulation of numerous biological processes. Nonetheless, its effects on DNA replication by hPol ι is still unclear. In this work, we found that 6 mA and Hyp, the intermediate of 6 mA, inhibited the replication of DNA by hPol ι. 6 mA lost priority in extension beyond 6 mA:T pair, partially reducing dTTP incorporation efficiency and inhibiting next-base extension. Hyp was prone to dCTP incorporation and extension beyond Hyp:C instead of Hyp:T pair. Statistically, 6 mA primarily reduced the burst incorporation rate (k pol) and slightly increased the dissociation constant (K d,dTTP). However, Hyp mainly increased the K d,dCTP yet did not affect the k pol , both reducing the burst incorporation efficiency (k pol / K d,dCTP). 6 mA together with Hyp weakened the binding affinity of hPol ι to DNA in binary or ternary complex. The misincorporation opposite 6 mA or Hyp further weakened this binding affinity. The methyl group in 6 mA doesn't almost affect the H-bond formation with dTTP, therefore mildly inhibiting dTTP incorporation. As an analogue of G, Hyp can form only two H-bonds with dCTP, thus reducing dCTP incorporation. This work provides a new insight in how the epigenetically modified 6 mA and its intermediate Hyp affect replication of DNA by human DNA polymerase ι. Image 1 • 6 mA and its intermediate Hyp inhibited DNA replication by hPol ι. • 6 mA reduced dTTP incorporation efficiency and lost extension priority. • Hyp was prone to dCTP incorporation and extension beyond Hyp:C pair. • 6 mA and Hyp weakened the binding affinity of hPol ι to DNA. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 03009084
- Volume :
- 168
- Database :
- Academic Search Index
- Journal :
- Biochimie
- Publication Type :
- Academic Journal
- Accession number :
- 140423766
- Full Text :
- https://doi.org/10.1016/j.biochi.2019.10.018