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一个古老且重要的微小RNA家族控制着……中的细胞相互作用途径。

An ancient and essential miRNA family controls cellular interaction pathways in .

作者信息

Santillan Emilio M, Cormack Eric D, Wang Jingkui, Rodriguez-Steube Micaela, Cochella Luisa

机构信息

School of Medicine, Johns Hopkins University, Baltimore, MD, USA.

Research Institute of Molecular Pathology (IMP), Vienna BioCenter (VBC), Vienna, Austria.

出版信息

Sci Adv. 2025 Sep 5;11(36):eadz1934. doi: 10.1126/sciadv.adz1934. Epub 2025 Sep 3.

Abstract

The transition from unicellular to multicellular life required the acquisition of coordinated and regulated cellular behaviors, including adhesion and migration. In metazoans, this involves adhesion proteins, signaling systems, and an elaborate extracellular matrix (ECM) that contributes to adhesion and signaling interactions. Innovations that enabled complex multicellularity occurred through new genes in these pathways, novel functions for existing genes, and regulatory changes. Gene regulation by microRNAs (miRNAs) expanded with multicellularity. A single miRNA, miR-100, arose in the last common eumetazoan ancestor and is widely conserved across animals. We reveal the molecular function of its homolog, the miR-51 family. This family acts in a dose-dependent manner to control morphogenesis by regulating several genes involved in cell signaling, adhesion, and migration, including ECM modifiers-specifically heparan sulfate sulfotransferases (HSTs). Some of these targets are also predicted to be conserved targets across vertebrates. Our work suggests that this miRNA provided an innovation in the regulation of cellular interactions early in metazoan evolution.

摘要

从单细胞生命向多细胞生命的转变需要获得协调且受调控的细胞行为,包括黏附和迁移。在多细胞动物中,这涉及黏附蛋白、信号系统以及一个有助于黏附和信号相互作用的复杂细胞外基质(ECM)。实现复杂多细胞性的创新是通过这些途径中的新基因、现有基因的新功能以及调控变化而发生的。微小RNA(miRNA)介导的基因调控随着多细胞性的出现而扩展。单个miRNA,即miR-100,出现在最后的共同真后生动物祖先中,并在动物界广泛保守。我们揭示了其同源物miR-51家族的分子功能。这个家族以剂量依赖的方式发挥作用,通过调控几个参与细胞信号传导、黏附和迁移的基因来控制形态发生,这些基因包括细胞外基质修饰因子——特别是硫酸乙酰肝素磺基转移酶(HSTs)。其中一些靶标也被预测为脊椎动物中的保守靶标。我们的研究表明,这种miRNA在多细胞动物进化早期为细胞相互作用的调控提供了一项创新。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16cf/12407057/7c3c8da0cb3b/sciadv.adz1934-f1.jpg

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