Target intelligence / Profile preview

Coordinator of PRMT5 and differentiation stimulator (COPRS)

Target
COPRS
Molecular classification
Histone-binding protein, Chromatin remodeling factor, Adaptor protein, Other
01

Overview

COPRS (Coordinator of PRMT5 and differentiation stimulator) is a nuclear histone-binding adaptor protein essential for the recruitment and substrate specificity of PRMT5, a protein arginine methyltransferase. COPRS binds specifically to the N-terminus of histone H4, promoting PRMT5-mediated methylation of H4 arginine 3 (H4R3) and is implicated in the repression of cell cycle genes such as cyclin E1 (CCNE1). COPRS is expressed in most tissues, localizes to the nucleus, and functions in chromatin remodeling, cell differentiation (especially muscle cell differentiation), and cell cycle exit. It has been associated with chromosomal deletion syndromes and studied in cancer proliferation pathways, but is not currently a direct drug target. COPRS appears to function as a bridging adaptor, linking PRMT5 to chromatin at specific loci, thereby regulating gene expression and cellular differentiation[1][2][4][7].

Other names
COPR5C17orf79HSA272196TTP1cooperator of PRMT5Protein TTP1
02

Mechanism of action

Facilitation of PRMT5-dependent histone methylation (COPRS acts as an adaptor, recruiting PRMT5 to nucleosomes for specific methylation of histone H4 arginine 3[2])

03

Biological functions

Chromatin remodelingHistone H4 arginine methylationRegulation of cell cycle exitMuscle cell differentiationPromoter repression (e.g., CCNE1 promoter)
04

Disease associations

Cancer (implicated in cell proliferation and regulation of cyclin E1; also studied as a possible modifier in NF1 microdeletion syndrome and tumorigenesis[1][7])Other (chromatin deficiencies arising from chromosome 17q11.2 deletions[1])
05

Biomarkers

Histone H4R3 symmetrical dimethylation marks (a consequence of COPRS-PRMT5 complex activity, associated with repression at target gene loci like CCNE1[2])

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