染色质
核小体
组蛋白
先锋因素
生物
转录因子
细胞生物学
组蛋白修饰酶
遗传学
二价染色质
嘉雅宠物
染色质重塑
转录协同调节子
芯片排序
组蛋白密码
抄写(语言学)
支架/基质附着区域
异染色质
DNA
基因表达调控
计算生物学
组蛋白H1
作者
Andrew Katznelson,Jingchao Zhang,Greg Donahue,Kenneth S. Zaret
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-01-09
卷期号:12 (2): eadz7409-eadz7409
标识
DOI:10.1126/sciadv.adz7409
摘要
Pioneer transcription factors target transcriptionally silent chromatin, thereby enabling gene activation in development, regeneration, and cell reprogramming. However, silent chromatin is heterogeneous, varying in nucleosome stability, nucleosome compaction, and repressive histone modifications, and how pioneer factors may differentially overcome these different chromatin barriers is unknown. We systematically compared the chromatin targeting of 13 embryonic transcription factors and found that the DNA binding domain (DBD) type predicts whether a pioneer factor targets low-turnover nucleosomes in compact chromatin, dynamic nucleosomes in compact chromatin or functions as a nonpioneer factor targeting accessible chromatin. By contrast, non-DBD domains enable targeting of repressed chromatin marked by H3K9me3 or H3K27me3 . Fusions of different non-DBD segments of heterochromatin-targeting pioneer factors to the transcription factor SOX2 can expand binding of SOX2 target motifs within heterochromatin and improve cellular reprogramming. Our study unveils how different forms of silent chromatin are coordinately targeted by lineage-specifying factors.
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