The GRHL3-regulated long non-coding RNA lnc-DC modulates keratinocytes differentiation by interacting with IGF2BP2 and up-regulating ZNF750

IF 4.6
Xue-ting Hu , Xiao-feng Wu , Lu-min Sui , Luo-quan Ao , Cheng-xiu Pu , Mu Yuan , Wei Xing , Xiang Xu
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引用次数: 0

Abstract

Background

Aberrant keratinocytes differentiation has been demonstrated to be associated with a number of skin diseases. The roles of lncRNAs in keratinocytes differentiation remain to be largely unknown.

Objective

Here we aim to investigate the role of lnc-DC in regulating epidermal keratinocytes differentiation.

Methods

Expression of lnc-DC in the skin was queried in AnnoLnc and verified by FISH. The lncRNA expression profiles during keratinocytes differentiation were reanalyzed and verified by qPCR and FISH. Gene knock-down and over-expression were used to explore the role of lnc-DC in keratinocytes differentiation. The downstream target of lnc-DC was screened by whole transcriptome sequencing. CUT&RUN assay and siRNAs transfection was used to reveal the regulatory effect of GRHL3 on lnc-DC. The mechanism of lnc-DC regulating ZNF750 was revealed by RIP assay and RNA stability assay.

Results

Lnc-DC was biasedly expressed in skin and up-regulated during epidermal keratinocytes differentiation. Knockdown lnc-DC repressed epidermal keratinocytes differentiation while over-express lnc-DC showed the opposite effect. GRHL3, a well-known transcription factor regulating keratinocytes differentiation, could bind to the promoter of lnc-DC and regulate its expression. By whole transcriptome sequencing, we identified that ZNF750 was a downstream target of lnc-DC during keratinocytes differentiation. Mechanistically, lnc-DC interacted with RNA binding protein IGF2BP2 to stabilize ZNF750 mRNA and up- regulated its downstream targets TINCR and KLF4.

Conclusion

Our study revealed the novel role of GRHL3/lnc-DC/ZNF750 axis in regulating epidermal keratinocytes differentiation, which may provide new therapeutic targets of aberrant keratinocytes differentiation related skin diseases.

GRHL3调控的长非编码RNA lnc-DC通过与IGF2BP2相互作用并上调ZNF750调节角朊细胞分化
背景已证实角质形成细胞分化异常与多种皮肤病有关。方法在AnnoLnc中查询lnc-DC在皮肤中的表达,并通过FISH进行验证。通过 qPCR 和 FISH 重新分析和验证了角朊细胞分化过程中 lncRNA 的表达谱。基因敲除和过表达被用来探索 lnc-DC 在角质形成细胞分化中的作用。通过全转录组测序筛选了lnc-DC的下游靶标。通过CUT&RUN检测和siRNAs转染揭示了GRHL3对lnc-DC的调控作用。结果lnc-DC在皮肤中偏向表达,并在表皮角朊细胞分化过程中上调。敲除lnc-DC会抑制表皮角质形成细胞的分化,而过表达lnc-DC则会产生相反的效果。GRHL3是一种著名的调控角质形成细胞分化的转录因子,它能与lnc-DC的启动子结合并调控其表达。通过全转录组测序,我们发现ZNF750是lnc-DC在角朊细胞分化过程中的下游靶标。结论:我们的研究揭示了GRHL3/lnc-DC/ZNF750轴在调控表皮角质形成细胞分化中的新作用,这可能为与角质形成细胞分化异常相关的皮肤病提供新的治疗靶点。
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
7.60
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