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H3K36 methylation is a reprogramming barrier
被引:1
|作者:
Cohen, Lea Rachel Zehava
[1
,2
]
Meshorer, Eran
[1
,2
]
机构:
[1] Hebrew Univ Jerusalem, Edmond & Lily Safra Ctr Brain Sci, Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Alexander Silberman Inst Life Sci, Dept Genet, Jerusalem, Israel
关键词:
PLASTICITY;
D O I:
10.1038/s41556-023-01147-3
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Reprogramming of somatic cells is an inherently inefficient process. A new study has now identified histone H3K36 methylation as a crucial reprogramming barrier that operates downstream of TGF beta signalling. Global inhibition of H3K36 methylation induced PRC2-dependent silencing of mesenchymal genes and dramatically increased reprogramming efficiency.
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页码:1077 / 1078
页数:2
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