Supplementary Figures 1 - 5 from ASH1L Links Histone H3 Lysine 36 Dimethylation to MLL Leukemia

Li, Zhu; Li, Qin; Wong, Stephen H.K.; Huang, Min; Klein, Brianna J.; Ikenouye, Larissa; Onishi, Masayuki; Schneidawind, Dominik; Buechele, Corina; Hansen, Larry G.; Duque‐Afonso, Jesús; Zhu, Fuliang; Martín, Glòria Mas; Gozani, Or; Majeti, Ravindra; Kutateladze, Tatiana G.; Cleary, Michael L.

doi:10.1158/2159-8290.22531023.v1

Cited by 1 publication

(1 citation statement)

References 0 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…As an H3K36 methyltransferase, ASH1L remains relatively understudied. However, nonsense and missense variants have been linked with autism spectrum disorder and brain development, and its overexpression has been identified in both anaplastic thyroid cancer and acute leukemia (22,23,24).…”

Section: Introductionmentioning

confidence: 99%

Systematic perturbations of SETD2, NSD1, NSD2, NSD3 and ASH1L reveals their distinct contributions to H3K36 methylation

Shipman,

Padilla,

Horth

et al. 2023

Preprint

View full text Add to dashboard Cite

BackgroundMethylation of histone 3 lysine 36 (H3K36me) has emerged as an essential epigenetic component for the faithful regulation of gene expression. Despite its importance in development, disease, and cancer, how the molecular agents collectively shape the H3K36me landscape is unclear.ResultsWe use a mouse mesenchymal stem cell model to perturb the H3K36me deposition machinery and infer the activities of the five most prominent players: SETD2, NSD1, NSD2, NSD3, and ASH1L. We find that H3K36me2 is the most abundant of the three methylation states and is predominantly deposited at intergenic regions by NSD1, and partly by NSD2. In contrast, H3K36me1/3 are most abundant within exons and are positively correlated with gene expression. We demonstrate that while SETD2 deposits most H3K36me3, it also deposits H3K36me2 within transcribed genes. Additionally, loss of SETD2 results in an increase of exonic H3K36me1, suggesting other H3K36 methyltransferases (K36MTs) prime gene bodies with lower methylation states ahead of transcription. Through a reductive approach, we uncover the distribution patterns of NSD3- and ASH1L-catalyzed H3K36me2. While NSD1/2 establish broad intergenic H3K36me2 domains, NSD3 deposits H3K36me2 peaks on active promoters and enhancers. Meanwhile, the activity of ASH1L is restricted to the regulatory elements of developmentally relevant genes, and our analyses implicate PBX2 as a potential recruitment factor.ConclusionsWithin genes, SETD2 deposits both H3K36me2/3, while the other K36MTs are capable of depositing H3K36me1/2 independently of SETD2 activity. For the deposition of H3K36me1/2, we find a hierarchy of K36MT activities where NSD1>NSD2>NSD3>ASH1L. While NSD1 and NSD2 are responsible for most genome-wide propagation of H3K36me2, the activities of NSD3 and ASH1L are confined to active regulatory elements.

show abstract

Section: Introductionmentioning

confidence: 99%