Histone H3.3 G34 Mutations Alter Histone H3K36 and H3K27 Methylation In Cis

被引:68
|
作者
Shi, Leilei [1 ]
Shi, Jiejun [2 ]
Shi, Xiaobing [1 ]
Li, Wei [2 ]
Wen, Hong [1 ,3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Epigenet & Mol Carcinogenesis, Houston, TX 77030 USA
[2] Baylor Coll Med, Dan L Duncan Canc Ctr, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[3] Van Andel Res Inst, 333 Bostwick Ave NE, Grand Rapids, MI 49503 USA
关键词
histone variant H3.3; G34; mutations; SETD2; giant cell tumor of the bone; PEDIATRIC GLIOBLASTOMA; DRIVER MUTATIONS; REPROGRAMS;
D O I
10.1016/j.jmb.2018.04.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Histone H3 encoding genes, particularly H3F3A and H3F3B, the genes encoding the variant histone H3.3, are mutated at high frequency in pediatric brain and bone malignancies. Compared to the extensive studies on K27M and K36M mutations, little is known about the mechanism of G34 mutations found in pediatric glioblastoma or giant cell tumors of the bone. Here we report that unlike the K27M or K36M that affect global histone methylation, the giant cell tumors of the bone G34 mutations (G34L/W) only affect histone H3K36 and H3K27 methylation on the same mutated histone tails (in cis), a mechanism distinct from known histone mutations. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1562 / 1565
页数:4
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