Characterization of Hepatoma-Derived Growth Factor-Related Protein 2 Interactions with Heterochromatin

被引:0
|
作者
Wistner, Sarah C. C. [1 ]
MacDonald, Ian A. A. [1 ]
Stanley, Karly A. A. [1 ]
Hathaway, Nathaniel A. A. [1 ,2 ]
机构
[1] Univ North Carolina Chapel Hill, Ctr Integrat Chem Biol & Drug Discovery, UNC Eshelman Sch Pharm, Div Chem Biol & Med Chem, Chapel Hill, NC 27599 USA
[2] Univ North Carolina Chapel Hill, UNC Lineberger Comprehens Canc Ctr, Sch Med, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
heterochromatin; HRP2; MPP8; HP1; gene regulation; chemical biology; H3; LYSINE-9; METHYLATION; HISTONE H3; DOMAIN; SPECIFICITY; ELONGATION; COMPLEX; SPT6; MPP8;
D O I
10.3390/cells12020325
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The expression of genetic information is tightly controlled by chromatin regulatory proteins, including those in the heterochromatin gene repression family. Many of these regulatory proteins work together on the chromatin substrate to precisely regulate gene expression during mammalian development, giving rise to many different tissues in higher organisms from a fixed genomic template. Here we identify and characterize the interactions of two related heterochromatin regulatory proteins, heterochromatin protein 1 alpha (HP1 alpha) and M-phase phosphoprotein 8 (MPP8), with hepatoma-derived growth factor-related protein 2 (HRP2). We find in biochemical experiments that HRP2 copurifies and co-sediments with heterochromatin-associated proteins, including HP1 alpha and MPP8. Using the Chromatin in vivo Assay in multiple cell types, we demonstrate that HP1 alpha-mediated gene repression dynamics are altered by the presence of HRP2. Furthermore, the knockout of HRP2 in MDA-MB-231 cells results in significant changes to chromatin structure and stability, which alter gene expression patterns. Here, we detail a mechanism by which HRP2 contributes to epigenetic transcriptional regulation through engagement with heterochromatin-associated proteins to stabilize the chromatin landscape and influence gene expression.
引用
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页数:18
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