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Involvement of histone deacetylation in MORC2-mediated down-regulation of carbonic anhydrase IX

机译:组蛋白脱乙酰基参与MORC2介导的碳酸酐酶IX的下调

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Carbonic anhydrase IX (CAIX) plays an important role in the growth and survival of tumor cells. MORC2 is a member of the MORC protein family. The MORC proteins contain a CW-type zinc finger domain and are predicted to have the function of regulating transcription, but no MORC2 target genes have been identified. Here we performed a DNA microarray hybridization and found CAIX mRNA to be down-regulated 8-fold when MORC2 was overexpressed. This result was further confirmed by northern and western blot analysis. Our results also showed that the protected region 4 (PR4) was important for the repression function of MORC2. Moreover, MORC2 decreased the acetylation level of histone H3 at the CAIX promoter. Meanwhile, trichostatin A (TSA) had an increasing effect on CAIX promoter activity. Among the six HDACs tested, histone deacetylase 4 (HDAC4) had a much more prominent effect on CAIX repression. ChIP and ChIP Re-IP assays showed that MORC2 and HDAC4 were assembled on the same region of the CAIX promoter. Importantly, we further confirmed that both proteins are simultaneously present in the PR4-binding complex. These results may contribute to understanding the molecular mechanisms of CAIX regulation.
机译:碳酸酐酶IX(CAIX)在肿瘤细胞的生长和存活中起重要作用。 MORC2是MORC蛋白家族的成员。 MORC蛋白包含CW型锌指结构域,并被预测具有调节转录的功能,但尚未鉴定MORC2靶基因。在这里,我们进行了DNA微阵列杂交,并发现当MORC2过表达时,CAIX mRNA被下调了8倍。通过Northern和Western印迹分析进一步证实了该结果。我们的结果还表明,保护区4(PR4)对于MORC2的抑制功能很重要。此外,MORC2降低了CAIX启动子上组蛋白H3的乙酰化水平。同时,曲古抑菌素A(TSA)对CAIX启动子活性的作用增加。在所测试的六个HDAC中,组蛋白脱乙酰基酶4(HDAC4)对CAIX的抑制作用更为显着。 ChIP和ChIP Re-IP分析表明MORC2和HDAC4组装在CAIX启动子的同一区域。重要的是,我们进一步证实了两种蛋白质同时存在于PR4结合复合物中。这些结果可能有助于理解CAIX调节的分子机制。

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