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Nkx6.2 synergizes with Cdx-2 in stimulating proglucagon gene expression

机译:Nkx6.2与Cdx-2协同刺激胰高血糖素原基因的表达

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摘要

AIM: To investigate whether the transactivator of the proglucagon gene (Gcg), Cdx-2, synergizes with other transcription factors in stimulating Gcg expression and the trans-differentiation of Gcg-expressing cells.METHODS: We conducted affinity chromatography to identify proteins that interact with Cdx-2, using GST-tagged Cdx-2 against cell lysates from pancreatic InR1-G9 and intestinal GLUTag cell lines. This was followed by a mass-spectrometry analysis. From a potential Cdx-2 interaction protein identified, we examined its expression in pancreatic and gut endocrine cells, confirmed its interaction with Cdx-2 by GST-pull down and determined its effect in provoking Gcg expression in cell lines that do not express endogenous Gcg.RESULTS: We identified 18 potential Cdx-2 interacting proteins. One of them is Nkx6.2. This homeodomain (HD) protein is expressed in pancreatic α and intestinal endocrine L cells but not in insulin producing cell lines, including In111. Nkx6.2, but not Nkx6.1, was shown to interact with Cdx-2, detected by GST-pull down. Furthermore, Nkx6.2 was found to synergize with Cdx-2 in provoking Gcg expression when they were ectopically expressed in the In111 cell line. Finally, when Cdx-2 and Nkx6.2 were co-transfected into the undifferentiated rat intestinal IEC-6 cell line, it produced detectable amount of Gcg mRNA.CONCLUSION: Cdx-2 recruits Nkx6.2 in exerting its effect in stimulating Gcg expression. Our observations further support the notion that multiple HD proteins, including Cdx-2 and Nkx6.2, are involved in the regulation of Gcg expression and the genesis of Gcg-producing cells.
机译:目的:研究前胰高血糖素基因(Gcg)的反式激活子Cdx-2是否与其他转录因子协同刺激表达Gcg的细胞和表达Gcg的细胞的分化。方法:我们进行了亲和层析以鉴定相互作用的蛋白质使用Cdx-2,使用GST标签的Cdx-2对抗来自胰腺InR1-G9和肠道GLUTag细胞系的细胞裂解液。随后进行质谱分析。从鉴定出的潜在Cdx-2相互作用蛋白中,我们检查了其在胰腺和肠道内分泌细胞中的表达,通过GST-pull down证实了其与Cdx-2的相互作用,并确定了其在不表达内源性Gcg的细胞系中引起Gcg表达的作用。结果:我们鉴定了18种潜在的Cdx-2相互作用蛋白。其中之一是Nkx6.2。该同源域(HD)蛋白在胰腺α和肠内分泌L细胞中表达,但在包括In111在内的胰岛素生产细胞系中不表达。 Nkx6.2,但不是Nkx6.1,显示与Gd-pull down检测到的Cdx-2相互作用。此外,当它们在In111细胞系中异位表达时,发现Nkx6.2在Cgx表达中与Cdx-2协同作用。最后,当将Cdx-2和Nkx6.2共转染到未分化的大鼠肠IEC-6细胞系中时,它产生了可检测量的Gcg mRNA。结论:Cdx-2募集Nkx6.2在刺激Gcg表达中发挥作用。我们的观察结果进一步支持了这样的观点,即多种HD蛋白,包括Cdx-2和Nkx6.2,都参与了Gcg表达的调控和Gcg产生细胞的起源。

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