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Butyrate Induced Cell Cycle Arrest in Bovine Cells through Targeting Gene Expression Relevant to DNA Replication Apparatus

机译: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中的细胞周期阻滞

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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 (p21waf1) 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 p21waf1 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.
机译:使用实时RT-PCR和Western印迹分析牛肾上皮细胞中,我们系统地研究了丁酸对DNA复制设备相关的基因表达模式的影响。实时PCR和Western印迹数据通常证实了先前报道的微阵列数据。在定量RT-PCR测试的五个基因中,CDKN1A(p21waf1)被上调,CDC2 / cdk1,MCM6,ORC1L被下调,而丁酸盐处理后ORC3L表达保持不变。 Western blot分析也与RT-PCR结果一致,证实丁酸酯以剂量依赖性方式上调了细胞周期蛋白激酶抑制剂p21waf1。相反,丁酸盐处理对ERK 1/2蛋白的表达没有影响。同样与mRNA结果一致的是,丁酸处理下调了ORC1和MCM3蛋白,而ORC2蛋白质则保持不变。目前的结果表明,ORC1,而不是ORC2或ORC3,以及MCM蛋白在调节MDBK细胞中DNA复制的起始和细胞周期进程中起着关键作用,并且是丁酸调节的靶标。

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