期刊
CURRENT OPINION IN GENETICS & DEVELOPMENT
卷 67, 期 -, 页码 61-66出版社
CURRENT BIOLOGY LTD
DOI: 10.1016/j.gde.2020.11.003
关键词
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资金
- Cancer Research UK [C7905/A25715]
- Medical Research Council, UK [MR/SO21647/1]
Recent studies have revealed the potential for missense mutations in histones to act as oncogenic drivers, leading to the term 'oncohistones'. Despite the highly conserved nature of histone proteins, there is heterogeneity among the genes encoding them, raising the question of whether all histone-encoding genes function equally as oncohistones. This review explores the implications of this question and delves into the mechanisms by which oncohistones can exert their effects in chromatin.
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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