The N-terminal region of DNMT3A engages the nucleosome surface to aid chromatin recruitment.

IF 6.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hannah Wapenaar, Gillian Clifford, Willow Rolls, Moira Pasquier, Hayden Burdett, Yujie Zhang, Gauri Deák, Juan Zou, Christos Spanos, Mark R D Taylor, Jacquie Mills, James A Watson, Dhananjay Kumar, Richard Clark, Alakta Das, Devisree Valsakumar, Janice Bramham, Philipp Voigt, Duncan Sproul, Marcus D Wilson
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引用次数: 0

Abstract

DNA methyltransferase 3A (DNMT3A) plays a critical role in establishing and maintaining DNA methylation patterns in vertebrates. Here we structurally and biochemically explore the interaction of DNMT3A1 with diverse modified nucleosomes indicative of different chromatin environments. A cryo-EM structure of the full-length DNMT3A1-DNMT3L complex with a H2AK119ub nucleosome reveals that the DNMT3A1 ubiquitin-dependent recruitment (UDR) motif interacts specifically with H2AK119ub and makes extensive contacts with the core nucleosome histone surface. This interaction facilitates robust DNMT3A1 binding to nucleosomes, and previously unexplained DNMT3A disease-associated mutations disrupt this interface. Furthermore, the UDR-nucleosome interaction synergises with other DNMT3A chromatin reading elements in the absence of histone ubiquitylation. H2AK119ub does not stimulate DNMT3A DNA methylation activity, as observed for the previously described H3K36me2 mark, which may explain low levels of DNA methylation on H2AK119ub marked facultative heterochromatin. This study highlights the importance of multivalent binding of DNMT3A to histone modifications and the nucleosome surface and increases our understanding of how DNMT3A1 chromatin recruitment occurs.

DNMT3A 的 N 端区域与核小体表面接触,帮助染色质招募。
DNA 甲基转移酶 3A (DNMT3A) 在建立和维持脊椎动物的 DNA 甲基化模式中发挥着关键作用。在这里,我们从结构和生物化学角度探讨了 DNMT3A1 与不同染色质环境中各种修饰核小体的相互作用。全长 DNMT3A1-DNMT3L 与 H2AK119ub 核小体复合物的低温电子显微镜结构显示,DNMT3A1 泛素依赖性招募(UDR)基序与 H2AK119ub 有特异性相互作用,并与核心核小体组蛋白表面有广泛接触。这种相互作用促进了 DNMT3A1 与核小体的牢固结合,而以前无法解释的 DNMT3A 疾病相关突变会破坏这一界面。此外,在没有组蛋白泛素化的情况下,UDR-核小体相互作用与其他 DNMT3A 染色质阅读元件协同作用。H2AK119ub 并不刺激 DNMT3A 的 DNA 甲基化活性,就像在之前描述的 H3K36me2 标记中观察到的那样,这可能是 H2AK119ub 标记的变异异染色质上 DNA 甲基化水平较低的原因。这项研究强调了 DNMT3A 与组蛋白修饰和核小体表面多价结合的重要性,并加深了我们对 DNMT3A1 染色质招募如何发生的理解。
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来源期刊
EMBO Reports
EMBO Reports 生物-生化与分子生物学
CiteScore
11.20
自引率
1.30%
发文量
267
审稿时长
1 months
期刊介绍: EMBO Reports is a scientific journal that specializes in publishing research articles in the fields of molecular biology, cell biology, and developmental biology. The journal is known for its commitment to publishing high-quality, impactful research that provides novel physiological and functional insights. These insights are expected to be supported by robust evidence, with independent lines of inquiry validating the findings. The journal's scope includes both long and short-format papers, catering to different types of research contributions. It values studies that: Communicate major findings: Articles that report significant discoveries or advancements in the understanding of biological processes at the molecular, cellular, and developmental levels. Confirm important findings: Research that validates or supports existing knowledge in the field, reinforcing the reliability of previous studies. Refute prominent claims: Studies that challenge or disprove widely accepted ideas or hypotheses in the biosciences, contributing to the correction and evolution of scientific understanding. Present null data: Papers that report negative results or findings that do not support a particular hypothesis, which are crucial for the scientific process as they help to refine or redirect research efforts. EMBO Reports is dedicated to maintaining high standards of scientific rigor and integrity, ensuring that the research it publishes contributes meaningfully to the advancement of knowledge in the life sciences. By covering a broad spectrum of topics and encouraging the publication of both positive and negative results, the journal plays a vital role in promoting a comprehensive and balanced view of scientific inquiry. 
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