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丁酸盐通过靶向与DNA复制装置相关的基因表达,诱导牛细胞的细胞周期停滞。

Butyrate induced cell cycle arrest in bovine cells through targeting gene expression relevant to DNA replication apparatus.

作者信息

Li Cong-jun, Li Robert W

机构信息

Bovine Functional Genomics Laboratory, Animal and Natural Resources Institute, ARS, USDA, USA.

出版信息

Gene Regul Syst Bio. 2008 Mar 17;2:113-23. doi: 10.4137/grsb.s465.

Abstract

Using real-time RT-PCR and Western blot analysis in bovine kidney epithelial cells, we systematically investigated the effects of butyrate on patterns of gene expression relevant to DNA replication apparatus. The real-time PCR and Western blot data generally confirmed previously reported microarray data. Of the five genes tested by quantitative RT-PCR, CDKN1A (p21(waf1)) was up regulated, CDC2/cdk1, MCM6, ORC1L were down regulated, while ORC3L expression remained unchanged following butyrate treatment. Also consistent with RT-PCR results, Western blot analysis confirmed that butyrate up-regulated cyclin-kinase inhibitor p21(waf1) in a does-dependent manner. In contrast, butyrate treatment had no effect on the expression of ERK 1/2 proteins. Also consistent with mRNA results, ORC1 and MCM3 proteins were down-regulated by butyrate treatment, while ORC2 protein remained unchanged. The present results suggest that ORC1, not ORC2 or ORC3, along with MCM proteins play a critical role in regulating the initiation of DNA replication and cell cycle progression in MDBK cells and are targets of butyrate regulation.

摘要

在牛肾上皮细胞中运用实时逆转录聚合酶链反应(RT-PCR)和蛋白质免疫印迹分析,我们系统地研究了丁酸盐对与DNA复制装置相关的基因表达模式的影响。实时PCR和蛋白质免疫印迹数据总体上证实了先前报道的微阵列数据。在通过定量RT-PCR检测的五个基因中,CDKN1A(p21(waf1))上调,CDC2/cdk1、MCM6、ORC1L下调,而丁酸盐处理后ORC3L表达保持不变。同样与RT-PCR结果一致,蛋白质免疫印迹分析证实丁酸盐以剂量依赖的方式上调细胞周期蛋白激酶抑制剂p21(waf1)。相反,丁酸盐处理对ERK 1/2蛋白的表达没有影响。同样与mRNA结果一致,丁酸盐处理使ORC1和MCM3蛋白下调,而ORC2蛋白保持不变。目前的结果表明,ORC1而非ORC2或ORC3,与MCM蛋白一起在调节MDBK细胞中DNA复制的起始和细胞周期进程中起关键作用,并且是丁酸盐调节的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2302/2733093/cba283184c24/grsb-2008-113f1a.jpg

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