Garcia-Padilla Carlos, Dueñas Angel, Franco Diego, Garcia-Lopez Virginio, Aranega Amelia, Garcia-Martinez Virginio, Lopez-Sanchez Carmen
Department of Human Anatomy and Embryology, Faculty of Medicine, Institute of Molecular Pathology Biomarkers, University of Extremadura, Badajoz, Spain.
Department of Experimental Biology, University of Jaen, Jaen, Spain.
Front Cell Dev Biol. 2022 Jan 11;9:767954. doi: 10.3389/fcell.2021.767954. eCollection 2021.
MicroRNAs have been explored in different organisms and are involved as molecular switches modulating cellular specification and differentiation during the embryonic development, including the cardiovascular system. In this study, we analyze the expression profiles of different microRNAs during early cardiac development. By using whole mount hybridization in developing chick embryos, with microRNA-specific LNA probes, we carried out a detailed study of miR-23b, miR-130a, miR-106a, and miR-100 expression during early stages of embryogenesis (HH3 to HH17). We also correlated those findings with putative microRNA target genes by means of mirWalk and TargetScan analyses. Our results demonstrate a dynamic expression pattern in cardiac precursor cells from the primitive streak to the cardiac looping stages for miR-23b, miR-130a, and miR-106a. Additionally, miR-100 is later detectable during cardiac looping stages (HH15-17). Interestingly, the /inflow tract was shown to be the most representative cardiac area for the convergent expression of the four microRNAs. Through analysis we revealed that distinct Hox family members are predicted to be targeted by the above microRNAs. We also identified expression of several Hox genes in the at stages HH11 and HH15. In addition, by means of gain-of-function experiments both in cardiomyoblasts and explants, we demonstrated the modulation of the different Hox clusters, Hoxa, Hoxb, Hoxc, and Hoxd genes, by these microRNAs. Furthermore, we correlated the negative modulation of several Hox genes, such as Hoxa3, Hoxa4, Hoxa5, Hoxc6, or Hoxd4. Finally, we demonstrated through a dual luciferase assay that Hoxa1 is targeted by miR-130a and Hoxa4 is targeted by both miR-23b and miR-106a, supporting a possible role of these microRNAs in Hox gene modulation during differentiation and compartmentalization of the posterior structures of the developing venous pole of the heart.
微小RNA已在不同生物体中得到研究,并作为分子开关参与胚胎发育过程中的细胞特化和分化调控,包括心血管系统的发育。在本研究中,我们分析了早期心脏发育过程中不同微小RNA的表达谱。通过使用针对微小RNA的锁核酸(LNA)探针,对发育中的鸡胚进行全胚胎原位杂交,我们详细研究了胚胎发育早期阶段(HH3至HH17)miR-23b、miR-130a、miR-106a和miR-100的表达情况。我们还通过mirWalk和TargetScan分析,将这些结果与推测的微小RNA靶基因进行了关联。我们的结果表明,miR-23b、miR-130a和miR-106a在从原条到心脏环化阶段的心脏前体细胞中呈现动态表达模式。此外,miR-100在心脏环化阶段(HH15 - 17)后期可检测到。有趣的是,流入道被证明是这四种微小RNA汇聚表达最具代表性的心脏区域。通过分析我们发现,上述微小RNA预计靶向不同的Hox家族成员。我们还在HH11和HH15阶段鉴定了几种Hox基因的表达。此外,通过在心肌成纤维细胞和外植体中进行功能获得实验,我们证明了这些微小RNA对不同Hox簇(Hoxa、Hoxb、Hoxc和Hoxd基因)的调控作用。此外,我们还关联了几种Hox基因(如Hoxa3、Hoxa4,、Hoxa5、Hoxc6或Hoxd4)的负调控。最后,我们通过双荧光素酶测定法证明,Hoxa1被miR-130a靶向,Hoxa4被miR-23b和miR-106a靶向,这支持了这些微小RNA在心脏发育静脉极后部结构分化和分区过程中对Hox基因调控可能发挥的作用。