TY - JOUR
T1 - Histone isoforms and the oncohistone code
AU - Flaus, Andrew
AU - Downs, Jessica A.
AU - Owen-Hughes, Tom
N1 - Publisher Copyright:
© 2020 Elsevier Ltd
PY - 2021/4
Y1 - 2021/4
N2 - Recent studies have highlighted the potential for missense mutations in histones to act as oncogenic drivers, leading to the term ‘oncohistones’. While histone proteins are highly conserved, they are encoded by multigene families. There is heterogeneity among these genes at the level of the underlying sequence, the amino acid composition of the encoded histone isoform, and the expression levels. One question that arises, therefore, is whether all histone-encoding genes function equally as oncohistones. In this review, we consider this question and explore what this means in terms of the mechanisms by which oncohistones can exert their effects in chromatin.
AB - Recent studies have highlighted the potential for missense mutations in histones to act as oncogenic drivers, leading to the term ‘oncohistones’. While histone proteins are highly conserved, they are encoded by multigene families. There is heterogeneity among these genes at the level of the underlying sequence, the amino acid composition of the encoded histone isoform, and the expression levels. One question that arises, therefore, is whether all histone-encoding genes function equally as oncohistones. In this review, we consider this question and explore what this means in terms of the mechanisms by which oncohistones can exert their effects in chromatin.
UR - http://www.scopus.com/inward/record.url?scp=85097423335&partnerID=8YFLogxK
U2 - 10.1016/j.gde.2020.11.003
DO - 10.1016/j.gde.2020.11.003
M3 - Review article
C2 - 33285512
AN - SCOPUS:85097423335
SN - 0959-437X
VL - 67
SP - 61
EP - 66
JO - Current Opinion in Genetics and Development
JF - Current Opinion in Genetics and Development
ER -