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Feedback regulation of BMP signaling by Caenorhabditis elegans cuticle collagens

机译:Caenorhabditise秀丽隐角Cuclics Collagens的BMP信号传导的反馈调节

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Cellular responsiveness to environment, including changes in extracellular matrix (ECM), is critical for normal processes such as development and wound healing, but can go awry, as in oncogenesis and fibrosis. One type of molecular pathway contributing to this responsiveness is the BMP signaling pathway. Owing to their broad and potent functions, BMPs and their pathways are regulated at multiple levels. In Caenorhabditis elegans , the BMP ligand DBL-1 is a regulator of body size. We previously showed that DBL-1/BMP signaling determines body size through transcriptional regulation of cuticle collagen genes. We now identify feedback regulation of DBL-1/BMP through analysis of four DBL-1–regulated collagen genes. Inactivation of any of these genes reduces DBL-1/BMP signaling, measured by a pathway activity reporter. Furthermore, depletion of these collagens reduces GFP::DBL-1 fluorescence and acts unexpectedly at the level of dbl-1 transcription. We conclude that cuticle, a specialized ECM, impinges on DBL-1/BMP expression and signaling. Interestingly, the feedback regulation of DBL-1/BMP signaling by collagens is likely to be contact independent due to physical separation of the cuticle from DBL-1–expressing cells in the ventral nerve cord. Our results provide an entry point into a novel regulatory mechanism for BMP signaling, with broader implications for mechanical regulation of gene expression.
机译:对环境的细胞响应性,包括细胞外基质(ECM)的变化,对于正常过程至关重要,例如发育和伤口愈合,但可以致以血管生成和纤维化。有助于这种反应性的一种分子途径是BMP信号通路。由于其宽泛且有效的功能,BMP和其途径受到多个层面的管制。在CaenorhabditiseDeltans中,BMP配体DBL-1是体尺寸的调节器。我们以前表明DBL-1 / BMP信号传导通过角质层胶原基因的转录调节来确定体尺寸。现在,我们通过分析四种DBL-1调节的胶原基因识别DBL-1 / BMP的反馈调节。任何这些基因的失活减少DBL-1 / BMP信号,通过途径活动报告者测量。此外,这些胶原蛋白的耗竭降低了GFP :: DBL-1荧光,并且在DBL-1转录的水平下意外起作用。我们得出结论,一种专门的ECM,撞击DBL-1 / BMP表达和信号传导。有趣的是,由于角膜脊髓中的DBL-1表达的细胞,胶原蛋白的DBL-1 / BMP信号传导的反馈调节可能与腹侧神经帘线中的DBL-1表达细胞的物理分离无关。我们的结果为BMP信号传导的新型调节机制提供了一个进入点,对基因表达的机械调节更广泛影响。

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