Suppr超能文献

[MEIS1和miR-425对慢性髓性白血病细胞增殖的调控作用]

[Function of MEIS1 and miR-425 to the Regulating of Chronic Myeloid Leukemia Cell Proliferation].

作者信息

Zhao Xu-Hong, Yang Gui-Hua, Li Dan-Dan

机构信息

Department of Clinical Laboratorial Examination, Beijing Geneplus, Beijing 102206, China.

Department of Clinical Laboratorial Examination, Beijing Giantmed Medical Dignostics Lab, Beijing 101300, China.

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020 Jun;28(3):802-807. doi: 10.19746/j.cnki.issn.1009-2137.2020.03.014.

Abstract

OBJECTIVE

To investigate the function and mechanism of transcription factor of MEIS1 and miR-425 to the proliferation of chronic myeloid leukemia cell K562.

METHODS

Bioinformatic prediction was used to analyze the binding of MEIS1 in miR-425 promoter region. ChIP-qPCR coupled with dual luciferase assay was used to detect the combination of MEIS1 and the transcription activity of miR-425, and its regulative role in the transcription activity miR-425. CCK-8 was used to detect the effect of MEIS1 and miR-425 on cell proliferation. Flow cytometry with PI staining was used to detected the effect of MEIS1 and miR-425 on K562 cell cycle progression. Western blot was used to examine the effect of miR-452 on the expression level of MEIS1.

RESULTS

MEIS1 could bind the promoter of miR-425 and repressed its transcription. After K562 was transfected by shRNA, the K562 cell proliferation and cell cycle progression was significantly inhibitied. Moreover, after K562 cells were transfected by miR-425 mimic, cell proliferation and cell cycle was inhibited. The expression level of MEIS1 could be inhibited by the combination of miR-425 and MEIS1 3'UTR.

CONCLUSION

MEIS1 can inhibit the activity of miR-425 in transcriptional level, while the miR-425 can suppress the expression of MEIS1 protein in post-transnational level. Therefore, a regulatory circuit comprising from MEIS1 and miR-425 regulates K562 cell proliferation.

摘要

目的

探讨转录因子MEIS1和miR - 425对慢性髓性白血病细胞K562增殖的作用及机制。

方法

采用生物信息学预测分析MEIS1在miR - 425启动子区域的结合情况。运用染色质免疫沉淀-定量聚合酶链反应(ChIP-qPCR)结合双荧光素酶报告基因检测法检测MEIS1与miR - 425的结合情况及其对miR - 425转录活性的调控作用。采用细胞计数试剂盒-8(CCK-8)检测MEIS1和miR - 425对细胞增殖的影响。用碘化丙啶(PI)染色的流式细胞术检测MEIS1和miR - 425对K562细胞周期进程的影响。采用蛋白质免疫印迹法检测miR - 425对MEIS1表达水平的影响。

结果

MEIS1可结合miR - 425的启动子并抑制其转录。K562细胞经短发夹RNA(shRNA)转染后,K562细胞增殖和细胞周期进程受到显著抑制。此外,K562细胞经miR - 425模拟物转染后,细胞增殖和细胞周期也受到抑制。miR - 425与MEIS1的3'非翻译区(3'UTR)结合可抑制MEIS1的表达水平。

结论

MEIS1可在转录水平抑制miR - 425的活性,而miR - 425可在翻译后水平抑制MEIS1蛋白的表达。因此,由MEIS1和miR - 425组成的调控环路调节K562细胞的增殖。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验