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长链非编码RNA SNHG1与剪接因子相互作用影响红细胞分化

沈欣妍 郭嘉 马艳妮 余佳 刘思琪

基础医学与临床2026,Vol.46Issue(5):651-657,7.
基础医学与临床2026,Vol.46Issue(5):651-657,7.DOI:10.16352/j.issn.1001-6325.2026.05.0651

长链非编码RNA SNHG1与剪接因子相互作用影响红细胞分化

Long non-coding RNA SNHG1 interacting with splicing factors influences erythroid differentiation

沈欣妍 1郭嘉 1马艳妮 1余佳 1刘思琪1

作者信息

  • 1. 中国医学科学院北京协和医学院 基础医学研究所 生物化学与分子生物学系重大疾病共性机制研究全国重点实验室,北京 100005
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摘要

Abstract

Objective To investigate the function and molecular mechanism of long non-coding RNA(lncRNA)small nucleolar RNA host gene 1(SNHG1)in erythroid differentiation.Methods During erythroid differentiation of CD34+hematopoietic stem/progenitor cells derived from human umbilical cord blood,expression of SNHG1 was suppressed.Erythroid differentiation was assessed by flow cytometry with surface markers CD71 and CD235a,while the mRNA expression of globin genes was measured by reverse transcription quantitative PCR(RT-qPCR).Nucle-ar-cytoplasm fractionation and RNA fluorescence in situ hybridization(RNA-FISH)were applied to determine the sub-cellular localization of SNHG1.RNA pull-down and RNA immunoprecipitation(RIP)assays were applied to identify SNHG1-interacting proteins.Results Suppression of SNHG1 significantly decreased the proportion of CD71+/CD235a+erythroid progenitor cells(P<0.001)and reduced the expression of globingene(P<0.01).SNHG1 was found to be predominantly localized in the nucleus and interacted with multiple splicing regulators,including SFPQ and NONO.Conclusions SNHG1 may affect erythroid differentiation by recruiting splicing-related proteins such as SFPQ and NONO and thereby regulating RNA splicing and processing.

关键词

长链非编码 RNA(lncRNA)/红系分化/RNA 剪接

Key words

long non-coding RNA(lncRNA)/erythroid differentiation/RNA splicing

分类

医药卫生

引用本文复制引用

沈欣妍,郭嘉,马艳妮,余佳,刘思琪..长链非编码RNA SNHG1与剪接因子相互作用影响红细胞分化[J].基础医学与临床,2026,46(5):651-657,7.

基金项目

国家自然科学基金(32470847) (32470847)

基础医学与临床

1001-6325

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