Pericentromeric repetitive ncRNA regulates chromatin interaction and inflammatory gene expression.

Kenichi Miyata, Akiko Takahashi
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Abstract

Cellular senescence provokes a dramatic alteration of chromatin organization and gene expression profile of proinflammatory factors, thereby contributing to various age-related pathologies via the senescence-associated secretory phenotype (SASP). Chromatin organization and global gene expression are maintained through the CCCTC-binding factor (CTCF). However, the molecular mechanism underlying CTCF regulation and its association with SASP gene expression remains to be fully elucidated. A recent study by our team showed that noncoding RNA (ncRNA) derived from normally silenced pericentromeric repetitive sequences directly impair the DNA binding of CTCF. This CTCF disturbance increases the accessibility of chromatin at the loci of SASP genes and caused the transcription of inflammatory factors. This mechanism may promote malignant transformation.

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中心粒周围重复ncRNA调节染色质相互作用和炎症基因表达。
细胞衰老引起染色质组织和促炎因子基因表达谱的显著改变,从而通过衰老相关分泌表型(SASP)促进各种与年龄相关的病理。染色质组织和整体基因表达是通过ccctc结合因子(CTCF)维持的。然而,CTCF调控的分子机制及其与SASP基因表达的关系仍未完全阐明。我们团队最近的一项研究表明,非编码RNA (ncRNA)来源于正常沉默的周中心粒重复序列,直接损害CTCF的DNA结合。这种CTCF干扰增加了SASP基因位点染色质的可及性,并引起炎症因子的转录。这一机制可能促进恶性转化。
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