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DDX6 解旋酶在人脂肪组织来源干细胞成脂和成骨早期的行为及其蛋白伴侣。

DDX6 Helicase Behavior and Protein Partners in Human Adipose Tissue-Derived Stem Cells during Early Adipogenesis and Osteogenesis.

机构信息

Laboratory of Basic Biology of Stem Cells, Carlos Chagas Institute, Fiocruz-Paraná, Curitiba 81350-010, Brazil.

Core for Cell Technology of Pontifical Catholic University of Paraná-PUCPR, Curitiba 80215-901, Brazil.

出版信息

Int J Mol Sci. 2020 Apr 9;21(7):2607. doi: 10.3390/ijms21072607.

Abstract

DDX6 helicase is an RNA-binding protein involved in different aspects of gene expression regulation. The roles played by DDX6 depend on the complexes associated with it. Here, for the first time, we characterize the protein complexes associated with DDX6 in human adipose tissue-derived stem cells (hASCs) and analyze the dynamics of this helicase under different conditions of translational activity and differentiation. The results obtained demonstrated that the DDX6 helicase is associated with proteins involved in the control of mRNA localization, translation and metabolism in hASCs. DDX6 complexes may also assemble into more complex structures, such as RNA-dependent granules, the abundance and composition of which change upon inhibited translational activity. This finding supports the supposition that DDX6 is possibly involved in the regulation of the mRNA life cycle in hASCs. Although there was no significant variation in the protein composition of these complexes during early adipogenic or osteogenic induction, there was a change in the distribution pattern of DDX6: the number of DDX6 granules per cell was reduced during adipogenesis and was enhanced during osteogenesis.

摘要

DDX6 解旋酶是一种 RNA 结合蛋白,参与基因表达调控的多个方面。DDX6 发挥的作用取决于与之相关的复合物。在这里,我们首次在人脂肪组织来源的干细胞(hASC)中对与 DDX6 相关的蛋白质复合物进行了表征,并分析了在不同翻译活性和分化条件下该解旋酶的动态变化。研究结果表明,DDX6 解旋酶与参与 hASC 中 mRNA 定位、翻译和代谢控制的蛋白有关。DDX6 复合物也可能组装成更复杂的结构,如 RNA 依赖性颗粒,其丰度和组成在翻译活性受到抑制时会发生变化。这一发现支持了 DDX6 可能参与 hASC 中 mRNA 生命周期调控的假设。尽管在早期成脂或成骨诱导过程中,这些复合物的蛋白质组成没有明显变化,但 DDX6 的分布模式发生了变化:细胞内 DDX6 颗粒的数量在成脂过程中减少,在成骨过程中增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e34/7177724/42a9302e0b7d/ijms-21-02607-g001.jpg

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