TY - JOUR
T1 - Entrapment of a Histone Tail by a DNA Lesion in a Nucleosome Suggests the Lesion Impacts Epigenetic Marking
T2 - A Molecular Dynamics Study
AU - Fu, Iwen
AU - Cai, Yuqin
AU - Zhang, Yingkai
AU - Geacintov, Nicholas E.
AU - Broyde, Suse
N1 - Publisher Copyright:
© 2015 American Chemical Society.
PY - 2016/1/19
Y1 - 2016/1/19
N2 - Errors in epigenetic markings are associated with human diseases, including cancer. We have used molecular dynamics simulations of a nucleosome containing the 10S (+)-trans-anti-B[a]P-N2-dG lesion, derived from the environmental pro-carcinogen benzo[a]pyrene, to elucidate the impact of the lesion on the structure and dynamics of a nearby histone N-terminal tail. Our results show that a lysine-containing part of this H2B tail that is subject to post-translational modification is engulfed by the enlarged DNA minor groove imposed by the lesion. The tail entrapment suggests that epigenetic markings could be hampered by this lesion, thereby impacting critical cellular functions, including transcription and repair.
AB - Errors in epigenetic markings are associated with human diseases, including cancer. We have used molecular dynamics simulations of a nucleosome containing the 10S (+)-trans-anti-B[a]P-N2-dG lesion, derived from the environmental pro-carcinogen benzo[a]pyrene, to elucidate the impact of the lesion on the structure and dynamics of a nearby histone N-terminal tail. Our results show that a lysine-containing part of this H2B tail that is subject to post-translational modification is engulfed by the enlarged DNA minor groove imposed by the lesion. The tail entrapment suggests that epigenetic markings could be hampered by this lesion, thereby impacting critical cellular functions, including transcription and repair.
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U2 - 10.1021/acs.biochem.5b01166
DO - 10.1021/acs.biochem.5b01166
M3 - Article
C2 - 26709619
AN - SCOPUS:84955245051
SN - 0006-2960
VL - 55
SP - 239
EP - 242
JO - Biochemistry
JF - Biochemistry
IS - 2
ER -