Leucine-rich pentatricopeptide repeat-containing protein (LRPPRC)-stabilized lncRNA small nucleolar RNA host gene 15 (Snhg15) modulates hematopoietic injury induced by γ-ray irradiation via m6A modification.

IF 6.3 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shuqin Zhang, Yajia Cheng, Yujia Gao, Feifei Xu, Yuna Wang, Junling Zhang, Yue Shang, Deguan Li, Saijun Fan
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引用次数: 0

Abstract

With advancements in radiotherapy technologies, the detrimental effects of ionizing radiation on biological systems, particularly the hematopoietic system, have caused significant concern. N6-methyladenosine (m6A), the most pervasive representative of post-transcriptional modifications, plays critical roles in diverse biological events. Non-coding RNA comprises the vast majority of the human genome. This study aimed to explore the role of long non-coding RNA (lncRNA) m6A modification in γ-ray irradiation-induced hematopoietic injury. By using mouse models, it was found that γ-radiation rapidly damaged hematopoietic bone marrow cells (BMCs), triggering apoptosis, oxidative stress and DNA damage, along with up-regulation of m6A Reader proteins. We revealed the time-conditioned landscape of lncRNA m6A methylome of BMCs in the short term after radiation and found that a dynamic "change-then-recover" trend involved. LncRNA Snhg15 was identified as a key regulator through integration analysis of the methylome and transcriptome data. Its m6A modification was closely related to progression of radiation injury in BMCs. Further research demonstrated that the novel m6A Reader LRPPRC could interact with the modification site of Snhg15, stabilize Snhg15 and promote its expression, thereby exacerbating radiation-induced injury to BMCs both in vitro and in vivo. Knockdown of Lrpprc or Snhg15 could alleviate the radiation injury to the hematopoietic system. Additionally, the LRPPRC-Snhg15 axis was involved in the radio-protective efficacy of gut microbiota-derived valeric acid. These findings uncover a novel mechanism by which m6A-modified lncRNA Snhg15 is stabilized by LRPPRC modulates γ-irradiation-induced hematopoietic injury, providing potential therapeutic targets for the prevention and treatment of radiation injuries.

富含亮氨酸的五肽重复序列蛋白(LRPPRC)稳定lncRNA小核仁RNA宿主基因15 (Snhg15)通过m6A修饰调节γ射线照射诱导的造血损伤。
随着放射治疗技术的进步,电离辐射对生物系统,特别是造血系统的有害影响引起了人们的极大关注。n6 -甲基腺苷(n6 - methylladenosine, m6A)是转录后修饰最普遍的代表,在多种生物事件中发挥着重要作用。非编码RNA构成了人类基因组的绝大部分。本研究旨在探讨长链非编码RNA (lncRNA) m6A修饰在γ射线照射诱导的造血损伤中的作用。通过小鼠模型研究发现,γ辐射可快速损伤造血骨髓细胞(BMCs),引发细胞凋亡、氧化应激和DNA损伤,m6A Reader蛋白上调。我们揭示了放射后短时间内bmmc的lncRNA m6A甲基化组的时间条件景观,并发现了一个动态的“变化-恢复”趋势。通过对甲基组和转录组数据的整合分析,LncRNA Snhg15被确定为一个关键的调节因子。其m6A修饰与bmmc放射损伤的进展密切相关。进一步研究表明,新型m6A Reader LRPPRC可与Snhg15的修饰位点相互作用,稳定Snhg15并促进其表达,从而在体外和体内均加剧辐射对BMCs的损伤。低表达Lrpprc或Snhg15可减轻辐射对造血系统的损伤。此外,LRPPRC-Snhg15轴参与了肠道微生物源戊酸的辐射保护作用。这些发现揭示了m6a修饰的lncRNA Snhg15被LRPPRC稳定调控γ辐射诱导的造血损伤的新机制,为预防和治疗辐射损伤提供了潜在的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.30
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