MEP50/PRMT5 Reduces Gene Expression by Histone Arginine Methylation and this Is Reversed by PKCδ/p38δ Signaling

被引:24
|
作者
Saha, Kamalika [1 ]
Adhikary, Gautam [1 ]
Eckert, Richard L. [1 ,2 ,3 ,4 ]
机构
[1] Univ Maryland, Sch Med, Dept Biochem & Mol Biol, 108 N Greene St, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Dept Dermatol, Baltimore, MD 21201 USA
[3] Univ Maryland, Sch Med, Dept Obstet & Gynecol, Baltimore, MD 21201 USA
[4] Univ Maryland, Sch Med, Marlene & Stewart Greenebaum Canc Ctr, Baltimore, MD 21201 USA
关键词
PROTEIN-KINASE-C; HUMAN INVOLUCRIN PROMOTER; REGULATED KERATINOCYTE DIFFERENTIATION; PKC-DELTA; EPIDERMAL DIFFERENTIATION; METHYLTRANSFERASE; P38-DELTA MAPK; CANCER CELLS; SKIN-CANCER; CROSS-TALK;
D O I
10.1038/JID.2015.400
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Protein kinase C delta (PKC delta) and p38 delta are key proteins in a cascade that stimulates keratinocyte differentiation. This cascade activates transcription of involucrin (hINV) and other genes associated with differentiation. Protein arginine methyltransferase 5 (PRMT5) is an arginine methyltransferase that symmetrically dimethylates arginine residues. This protein interacts with a cofactor, methylosome protein 50 (MEP50), and symmetrically dimethylates arginine eight of histone 3 (H3R8me2s) and arginine three of histone 4 (H4R3me2s) to silence gene expression. We use the hINV gene as a tool to understand the relationship between PKC delta/p38 delta and PRMT5/MEP50 signaling. MEP50 suppresses hINV mRNA level and promoter activity. This is associated with increased arginine dimethylation of hINV gene-associated H3/H4. We further show that the PKC delta/p38 delta keratinocyte differentiation cascade reduces PRMT5 and MEP50 expression, association with the hINV gene promoter, and H3R8me2s and H4R2me2s formation. We propose that PRMT5/MEP50-dependent methylation is an epigenetic mechanism that assists in silencing of hINV expression, and that PKC delta signaling activates gene expression by directly activating transcription and by suppressing PRMT5/MEP50-dependent arginine dimethylation of promoter-associated histones. This is an example of crosstalk between PKC delta/p38 delta signaling and PRMT5/MEP50 epigenetic silencing.
引用
收藏
页码:214 / 224
页数:11
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