The incorporation loci of H3.3K36M determine its preferential prevalence in chondroblastomas
Abstract The histone H3.3K36M mutation, identified in over 90% of chondroblastoma cases, reprograms the H3K36 methylation landscape and gene expression to promote tumorigenesis. However, it’s still unclear how the H3K36M mutation preferentially occurs in the histone H3 variant H3.3 in chondroblastom...
Main Authors: | Yanjun Zhang, Dong Fang |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Publishing Group
2021-03-01
|
Series: | Cell Death and Disease |
Online Access: | https://doi.org/10.1038/s41419-021-03597-9 |
Similar Items
-
H3.3 K36M Mutation as a Clinical Diagnosis Method of Suspected Chondroblastoma Cases
by: Haoran Mu, et al.
Published: (2021-04-01) -
Characterization of H3.3K36M as a tool to study H3K36 methylation in cancer cells
by: Saumya M. Sankaran, et al.
Published: (2017-11-01) -
Inhibition of a K9/K36 demethylase by an H3.3 point mutation found in paediatric glioblastoma
by: Hsiao P. J. Voon, et al.
Published: (2018-08-01) -
A histone H3.3K36M mutation in mice causes an imbalance of histone modifications and defects in chondrocyte differentiation
by: Shusaku Abe, et al.
Published: (2021-10-01) -
Chondroblastoma
by: IE Garin, et al.
Published: (2008-04-01)