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MCRIP1 promotes the expression of lung-surfactant proteins in mice by disrupting CtBP-mediated epigenetic gene silencing

机译:MCRIP1通过破坏CtBP介导的表观遗传基因沉默来促进小鼠肺表面活性蛋白的表达

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摘要

Proper regulation of epigenetic states of chromatin is crucial to achieve tissue-specific gene expression during embryogenesis. The lung-specific gene products, surfactant proteins B (SP-B) and C (SP-C), are synthesized in alveolar epithelial cells and prevent alveolar collapse. Epigenetic regulation of these surfactant proteins, however, remains unknown. Here we report that MCRIP1, a regulator of the CtBP transcriptional co-repressor, promotes the expression of SP-B and SP-C by preventing CtBP-mediated epigenetic gene silencing. Homozygous deficiency of Mcrip1 in mice causes fatal respiratory distress due to abnormal transcriptional repression of these surfactant proteins. We found that MCRIP1 interferes with interactions of CtBP with the lung-enriched transcriptional repressors, Foxp1 and Foxp2, thereby preventing the recruitment of the CtBP co-repressor complex to the SP-B and SP-C promoters and maintaining them in an active chromatin state. Our findings reveal a molecular mechanism by which cells prevent inadvertent gene silencing to ensure tissue-specific gene expression during organogenesis.
机译:染色质的表观遗传状态的正确调节对于在胚胎发生过程中实现组织特异性基因表达至关重要。肺特异性基因产物表面活性剂蛋白B(SP-B)和C(SP-C)在肺泡上皮细胞中合成,可防止肺泡塌陷。然而,这些表面活性剂蛋白的表观遗传调控仍然未知。在这里,我们报告说,MCRIP1,CtBP转录共阻遏物的调节剂,通过防止CtBP介导的表观遗传基因沉默来促进SP-B和SP-C的表达。由于这些表面活性剂蛋白的异常转录抑制,小鼠Mcrip1的纯合子缺乏会导致致命的呼吸窘迫。我们发现MCRIP1干扰了CtBP与富含肺的转录阻遏物Foxp1和Foxp2的相互作用,从而阻止了CtBP协同阻遏物复合物向SP-B和SP-C启动子的募集并将它们保持在活跃的染色质状态。我们的发现揭示了一种分子机制,细胞可通过这种分子机制防止无意的基因沉默,从而确保器官发生过程中组织特异性基因的表达。

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