ΔNp63 是一种启动因子,它可以结合不可及的染色质,并引发染色质重塑。

ΔNp63 is a pioneer factor that binds inaccessible chromatin and elicits chromatin remodeling.

机构信息

Department of Biochemistry, State University of New York at Buffalo, Buffalo, NY, 14203, USA.

Zhuhai Interventional Medical Center, Zhuhai Precision Medical Center, Zhuhai People's Hospital, Zhuhai Hospital Affiliated with Jinan University, Zhuhai, Guangdong, China.

出版信息

Epigenetics Chromatin. 2021 Apr 17;14(1):20. doi: 10.1186/s13072-021-00394-8.

Abstract

BACKGROUND

ΔNp63 is a master transcriptional regulator playing critical roles in epidermal development and other cellular processes. Recent studies suggest that ΔNp63 functions as a pioneer factor that can target its binding sites within inaccessible chromatin and induce chromatin remodeling.

METHODS

In order to examine if ΔNp63 can bind to inaccessible chromatin and to determine if specific histone modifications are required for binding, we induced ΔNp63 expression in two p63-naïve cell lines. ΔNp63 binding was then examined by ChIP-seq and the chromatin at ΔNp63 targets sites was examined before and after binding. Further analysis with competitive nucleosome binding assays was used to determine how ΔNp63 directly interacts with nucleosomes.

RESULTS

Our results show that before ΔNp63 binding, targeted sites lack histone modifications, indicating ΔNp63's capability to bind at unmodified chromatin. Moreover, the majority of the sites that are bound by ectopic ΔNp63 expression exist in an inaccessible state. Once bound, ΔNp63 induces acetylation of the histone and the repositioning of nucleosomes at its binding sites. Further analysis with competitive nucleosome binding assays reveal that ΔNp63 can bind directly to nucleosome edges with significant binding inhibition occurring within 50 bp of the nucleosome dyad.

CONCLUSION

Overall, our results demonstrate that ΔNp63 is a pioneer factor that binds nucleosome edges at inaccessible and unmodified chromatin sites and induces histone acetylation and nucleosome repositioning.

摘要

背景

ΔNp63 是一种主转录调控因子,在表皮发育和其他细胞过程中发挥着关键作用。最近的研究表明,ΔNp63 作为一种先驱因子发挥作用,可以靶向其在不可及染色质内的结合位点,并诱导染色质重塑。

方法

为了研究 ΔNp63 是否可以与不可及的染色质结合,并确定是否需要特定的组蛋白修饰来进行结合,我们在两个 p63 幼稚细胞系中诱导 ΔNp63 的表达。然后通过 ChIP-seq 检测 ΔNp63 的结合,并在结合前后检测 ΔNp63 靶位点的染色质。进一步采用竞争核小体结合测定法分析来确定 ΔNp63 如何直接与核小体相互作用。

结果

我们的结果表明,在 ΔNp63 结合之前,靶向位点缺乏组蛋白修饰,这表明 ΔNp63 能够结合未修饰的染色质。此外,大多数通过异位 ΔNp63 表达结合的位点处于不可及状态。一旦结合,ΔNp63 诱导组蛋白乙酰化和核小体在其结合位点的重新定位。进一步采用竞争核小体结合测定法分析表明,ΔNp63 可以直接结合核小体边缘,在核小体二联体 50bp 内发生明显的结合抑制。

结论

总体而言,我们的结果表明,ΔNp63 是一种先驱因子,它可以结合不可及和未修饰染色质位点的核小体边缘,并诱导组蛋白乙酰化和核小体重定位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ea2/8053304/2e3ac3dd638a/13072_2021_394_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索