期刊导航

论文摘要

T细胞蛋白p80调控c-Myc表达的机理

The mechanism of c-Myc expression regulated by T cell protein p80

作者:王巧(四川大学生命科学学院 生长代谢与衰老研究中心);张渝君(四川大学生命科学学院 生长代谢与衰老研究中心);蒋贤杰(四川大学生命科学学院 生长代谢与衰老研究中心)

Author:WANG Qiao(Center for Growth, Metabolism and Aging, College of Life Sciences, Sichuan University);ZHANG Yu-Jun(Center for Growth, Metabolism and Aging, College of Life Sciences, Sichuan University);JIANG Xian-Jie(Center for Growth, Metabolism and Aging, College of Life Sciences, Sichuan University)

收稿日期:2018-07-28          年卷(期)页码:2019,56(4):771-778

期刊名称:四川大学学报: 自然科学版

Journal Name:Journal of Sichuan University (Natural Science Edition)

关键字:白介素16前体蛋白; 组蛋白去乙酰化酶; 细胞周期; T细胞淋巴瘤

Key words:p80; HDAC; Cell cycle; T cell lymphoma

基金项目:国家自然科学基金(31170729)

中文摘要

为了解p80在正常T细胞以及T细胞癌变过程中的作用,在缺失p80的T淋巴瘤细胞中重新表达p80,其结果显示:原癌基因c-Myc的表达受到显著抑制,且细胞周期在G1期出现了停滞.定量PCR的结果表明:p80 对c-Myc表达的抑制是转录水平的抑制.双荧光素酶报告基因试验表明:p80对c-Myc的抑制作用定位于c-Myc启动子上相对于转录起始位点的-1042bp~-630bp区域.运用TFSEARCH软件对这一区域的分析发现存在多个c-Myb结合位点.在稳定表达p80的T淋巴癌细胞中敲低c-Myb,表明p80对c-Myc的转录抑制是通过c Myb来实现的.免疫共沉淀实验表明p80和c-Myb在细胞中存在相互作用.进一步的研究显示p80对c-Myc的转录抑制依赖于组蛋白去乙酰化酶的活性.研究结果表明p80有可能通过与c-Myb的相互作用将组蛋白去乙酰化酶募集至c-Myc启动子区域,并通过组蛋白的去乙酰化抑制c-Myc的表达.

英文摘要

Our experimental data indicate that overexpression of p80 in p80 null T cell leukemia cells significantly down regulates c-Myc oncoprotein and blocks cell cycle progression from G1 to S phase. The qPCR examination and protein stability test found that p80 regulates expression of c-Myc at the transcriptional level. The analysis of c-Myc promoter activity at the presence of p80 by Dual Luciferase Reporter Assay indicated that the transcriptional repression of p80 on c-Myc promoter is located at -1042bp~-630bp above the transcription start site of c Myc gene. The transcription factor binding sites search of this region by software TFSEARCH revealed multiple binding sequences of c-Myb, another oncoprotein and transcription factor which plays an important role in the proliferation and differentiation of blood cells during hematopoiesis. Knockdown c-Myb in MOLT-4 cells stably expressing p80 indicate that p80 suppresses the transcription of c-Myc gene through c-Myb. Co-immunoprecipitation experiment demonstrated that p80 interacts with c-Myb inside cells. The further experiment has shown that transcriptional repression of c-Myc by p80 is dependent on the enzymatic activity of histone deacetylase. Taken together, our results suggest that p80 recruits histone deacetylase to the c-Myc promoter through interaction with transcription factor c-Myb, and p80 suppresses c-Myc expression by histone deacetylation.

关闭

Copyright © 2020四川大学期刊社 版权所有.

地址:成都市一环路南一段24号

邮编:610065