由 CDKN1A 基因通过替代多基化生成的长非编码RNA 在DNA损伤反应过程中调节p21表达
Michael R Murphy1,2, Anthony Ramadei1,2, Ahmet Doymaz1
1Chemistry Department, Hunter College, The City University of New York, New York, NY 10021, USA.
Nucleic acids research
|October 23, 2023
概括
一个新的lncRNA,SPUD,是由DNA损伤诱导的,增加p21蛋白水平并促进细胞循环的进展. 这一发现揭示了DNA损伤反应中一种新的转录后调节机制.
科学领域:
- 分子生物学分子生物学
- 遗传学 遗传学是一种遗传学.
- 细胞生物学 细胞生物学
背景情况:
- 替代多氨基基化 (APA) 动态调节基因表达.
- 广泛的APA发生在DNA损伤反应 (DDR) 期间的内子中.
研究的目的:
- 调查DDR激活的APA事件及其功能后果.
- 识别和表征一种参与DDR的新型lncRNA.
主要方法:
- 在DDR期间对CDKN1A中APA事件的分析.
- 鉴定和表征的 lncRNA SPUD. 的识别和表征.
- 研究SPUD在p21调节和细胞循环控制中的作用.
主要成果:
- 在CDKN1A中的DDR激活的APA事件产生了lncRNASPUD.
- SPUD是由DNA损伤引起的,部分通过p53,并由HuR.稳定.
- 通过调节转化调节剂,SPUD可提高p21蛋白水平,影响细胞循环和生长.
结论:
- SPUD代表了一种新的lncRNA介导的转录后调节机制,用于DDR期间的p21表达.
- 这一发现突显了lncRNAs在DDR和细胞循环控制中的重要作用.
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