Garcia-Riart Beatriz, Lorda-Diez Carlos I, Marin-Llera Jessica C, Garcia-Porrero Juan A, Hurle Juan M, Montero Juan A
Departamento de Anatomía y Biología Celular and IDIVAL, Universidad de Cantabria, Santander, Spain.
J Anat. 2017 Aug;231(2):275-286. doi: 10.1111/joa.12629. Epub 2017 May 24.
Next-generation sequencing in combination with quantitative polymerase chain reaction analysis revealed a dynamic miRNA signature in the interdigital mesoderm of the chick embryonic hinlimb in the course of interdigit remodelling. During this period, 612 previously known chicken miRNAs (gga-miRNAs) and 401 non-identified sequences were expressed in the interdigital mesoderm. Thirty-six microRNAs, represented by more than 750 reads per million, displayed differential expression between stages HH29 (6 id) and HH32 (7.5 id), which correspond to the onset and the peak of interdigital cell death. Twenty miRNAs were upregulated by at least 1.5-fold, and sixteen were downregulated by at least 0.5-fold. Upregulated miRNAs included miRNAs with recognized proapoptotic functions in other systems (miR-181 family, miR-451 and miR-148a), miRNAs associated with inflammation and cell senescence (miR-21 and miR-146) and miRNAs able to induce changes in the extracellular matrix (miR-30c). In contrast, miRNAs with known antiapoptotic effects in other systems, such as miR-222 and miR-205, became downregulated. In addition, miR-92, an important positive regulator of cell proliferation, was also downregulated. Together, these findings indicate a role for miRNAs in the control of tissue regression and cell death in a characteristic morphogenetic embryonic process based on massive apoptosis.
下一代测序结合定量聚合酶链反应分析揭示了鸡胚后肢趾间中胚层在趾间重塑过程中的动态miRNA特征。在此期间,612个先前已知的鸡miRNA(gga-miRNA)和401个未鉴定序列在趾间中胚层中表达。以每百万超过750条读数为代表的36个微小RNA在HH29(6期趾间)和HH32(7.5期趾间)阶段之间表现出差异表达,这两个阶段分别对应趾间细胞死亡的开始和峰值。20个miRNA上调至少1.5倍,16个miRNA下调至少0.5倍。上调的miRNA包括在其他系统中具有公认促凋亡功能的miRNA(miR-181家族、miR-451和miR-148a)、与炎症和细胞衰老相关的miRNA(miR-21和miR-146)以及能够诱导细胞外基质变化的miRNA(miR-30c)。相比之下,在其他系统中具有已知抗凋亡作用的miRNA,如miR-222和miR-205,则下调。此外,细胞增殖的重要正调节因子miR-92也下调。总之,这些发现表明miRNA在基于大量凋亡的特征性胚胎形态发生过程中对组织消退和细胞死亡的控制中发挥作用。