Heparanase Modulates Chromatin Accessibility

被引:0
作者
Li, Honglian [1 ]
Zhang, Hua [2 ]
Wenz, Amelie [2 ]
Kang, Ziqi [2 ]
Wang, Helen [1 ]
Vlodavsky, Israel [3 ]
Chen, Xingqi [2 ]
Li, Jinping [1 ]
机构
[1] Uppsala Univ, Biomed Ctr, Dept Med Biochem & Microbiol, SciLifeLab Uppsala, S-75237 Uppsala, Sweden
[2] Uppsala Univ, Dept Immunol Genet & Pathol, S-75237 Uppsala, Sweden
[3] Technion, Technion Integrated Canc Ctr TICC, Rappaport Fac Med, IL-31096 Haifa, Israel
基金
瑞典研究理事会;
关键词
heparanase; ATAC-seq; epigenetics; histone; TUMOR-GROWTH; ACTIVATION; SULFATE; EXPRESSION; NUCLEUS; TRANSCRIPTION; REVEALS; GENES; DRIVE; ACID;
D O I
10.3390/cells12060891
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Heparanase is the sole endoglucuronidase that degrades heparan sulfate in the cell surface and extracellular matrix (ECM). Several studies have reported the localization of heparanase in the cell nucleus, but the functional role of the nuclear enzyme is still obscure. Subjecting mouse embryonic fibroblasts (MEFs) derived from heparanase knockout (Hpse-KO) mice and applying transposase-accessible chromatin with sequencing (ATAC-seq), we revealed that heparanase is involved in the regulation of chromatin accessibility. Integrating with genome-wide analysis of chromatin states revealed an overall low activity in the enhancer and promoter regions of Hpse-KO MEFs compared with wild-type (WT) MEFs. Western blot analysis of MEFs and tissues derived from Hpse-KO vs. WT mice confirmed reduced expression of H3K27ac (acetylated lysine at N-terminal position 27 of the histone H3 protein). Our results offer a mechanistic explanation for the well-documented attenuation of inflammatory responses and tumor growth in Hpse-KO mice.
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页数:12
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