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Serum Starvation Induces DRAM Expression in Liver Cancer Cells via Histone Modifications within Its Promoter Locus

机译:血清饥饿通过其启动子位点内的组蛋白修饰诱导肝癌细胞中的DRAM表达

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摘要

DRAM is a lysosomal membrane protein and is critical for p53-mediated autophagy and apoptosis. DRAM has a potential tumor-suppressive function and is downregulated in many human cancers. However, the regulation of DRAM expression is poorly described so far. Here, we demonstrated that serum deprivation strongly induces DRAM expression in liver cancer cells and a core DNA sequence in the DRAM promoter is essential for its responsiveness to serum deprivation. We further observed that euchromatin markers for active transcriptions represented by diacetyl-H3, tetra-acetyl-H4 and the trimethyl-H3K4 at the core promoter region of DRAM gene are apparently increased in a time-dependent manner upon serum deprivation, and concomitantly the dimethyl-H3K9, a herterochromatin marker associated with silenced genes, was time-dependently decreased. Moreover, the chromatin remodeling factor Brg-1 is enriched at the core promoter region of the DRAM gene and is required for serum deprivation induced DRAM expression. These observations lay the ground for further investigation of the DRAM gene expression.
机译:DRAM是一种溶酶体膜蛋白,对于p53介导的自噬和细胞凋亡至关重要。 DRAM具有潜在的肿瘤抑制功能,在许多人类癌症中均被下调。但是,到目前为止,对DRAM表达的调节描述得很差。在这里,我们证明血清剥夺强烈诱导肝癌细胞中的DRAM表达,而DRAM启动子中的核心DNA序列对于其对血清剥夺的反应性至关重要。我们进一步观察到,在血清基因剥夺后,DRAM基因核心启动子区域的以二乙酰基-H3,四乙酰基-H4和三甲基-H3K4表示的活性转录的常染色质标记明显以时间依赖性方式增加,并且随之而来的是二甲基-H3K9,一种与沉默基因相关的杂染色质标记,随时间而减少。此外,染色质重塑因子Brg-1在DRAM基因的核心启动子区域富集,并且是血清剥夺诱导的DRAM表达所必需的。这些观察为进一步研究DRAM基因表达奠定了基础。

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