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Histone isoforms and the oncohistone code
被引:14
|作者:
Flaus, Andrew
[1
]
Downs, Jessica A.
[2
]
Owen-Hughes, Tom
[3
]
机构:
[1] Natl Univ Ireland, Ctr Chromosome Biol, Sch Nat Sci, Biochem, Galway, Ireland
[2] Inst Canc Res, Epigenet & Genome Stabil Team, 237 Fulham Rd, London SW3 6JB, England
[3] Univ Dundee, Ctr Gene Regulat & Express, Sch Life Sci, Dundee DD1 5EH, Scotland
基金:
英国医学研究理事会;
关键词:
VARIANTS TH2A;
MUTATIONS;
STABILITY;
GAIN;
H2AX;
D O I:
10.1016/j.gde.2020.11.003
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
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.
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页码:61 / 66
页数:6
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