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Sufu的突变位点对Sonic Hedgehog信号通路调控机制的研究

王美 程雁

南京医科大学学报(自然科学版)2018,Vol.38Issue(4):429-434,6.
南京医科大学学报(自然科学版)2018,Vol.38Issue(4):429-434,6.DOI:10.7655/NYDXBNS20180402

Sufu的突变位点对Sonic Hedgehog信号通路调控机制的研究

Effect of Sufu mutations on regulation of Sonic Hedgehog signaling pathway

王美 1程雁1

作者信息

  • 1. 南京医科大学病理学与病理生理学系,江苏 南京 211166
  • 折叠

摘要

Abstract

Objective:To investigate the mechanism of aberrant Sonic Hedgehog(Shh)signaling which found in medulloblastom patients' Suppressor of Fused(Sufu)mutations, and to reveal the relationship between Shh pathway and tumor growth or development. Methods:To create Sufu variants expression plasmids, the influence of Sufu mutants on the expression level of Sufu-/-cell endogenous Gli1 were detected by quantitative real-time PCR and Western blot. The combination of Sufu mutants and Gli were detected by CO-IP assay. MTT assay were used to evaluate the effects of Sufu variants on growth and proliferation of human medulloblastoma cells (DAOY). Results:Quantitative PCR and Western blot experiments found that Sufu missense mutant(H87R)expression level of endogenous Gli1 showed wild type inhibition level, three nonsense mutants(R146X, R299X, W430X)of endogenous Gli1 expression level increased obviously;Under normal conditions, WT-Sufu can be combined with Gli1 protein, The CO-IP experiment found that the mutants of Sufu had different degrees of damage to the combination of Gli1 protein. The protein turnover rate experiment showed that Sufu mutants could be degraded by proteasome pathway and MTT assay showed that Sufu mutants lost their ability to inhibit the growth and proliferation of human medulloblastom DAOY cells. Conclusion:Clinically observed mutations in Sufu can drive tumor growth and further elucidates Sufu's role in binding to and suppressing Gli function.

关键词

Sonic Hedgehog信号通路/髓母细胞瘤/supressor of fused/Gli

Key words

Sonic Hedgehog signaling pathway/medulloblastom/suppressor of fused/Gli

分类

医药卫生

引用本文复制引用

王美,程雁..Sufu的突变位点对Sonic Hedgehog信号通路调控机制的研究[J].南京医科大学学报(自然科学版),2018,38(4):429-434,6.

基金项目

国家重点基础研究发展(973)计划(2009CB918403) (973)

南京医科大学学报(自然科学版)

OA北大核心CSCDCSTPCD

1007-4368

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