posted on 2022-01-18, 21:08authored byXin Li, Sha Liu, Xiang Li, Xiang David Li
Interpretation of the histone posttranslational
modifications (PTMs)
by effector proteins, or readers, is an important epigenetic mechanism
to regulate gene function. YEATS domains have been recently identified
as novel readers of histone lysine acetylation and a variety of nonacetyl
acylation marks. Accumulating evidence has revealed the association
of dysregulated interactions between YEATS domains and histone PTMs
with human diseases, suggesting the therapeutic potential of YEATS
domain inhibition. Here, we discuss the molecular mechanisms adopted
by YEATS domains in recognizing their preferred histone marks and
the biological significance of such recognitions in normal cell physiology
and pathogenesis of human diseases. Recent progress in the development
of YEATS domain inhibitors is also discussed.