David Aldana P, Margarit Ezequiel, Domizi Pablo, Banchio Claudia, Armas Pablo, Calcaterra Nora B
Instituto de Biología Molecular y Celular de Rosario (IBR), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) - Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario (UNR), Ocampo y Esmeralda, (S2000EZP) Rosario, Argentina.
Instituto de Biología Molecular y Celular de Rosario (IBR), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) - Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario (UNR), Ocampo y Esmeralda, (S2000EZP) Rosario, Argentina
Nucleic Acids Res. 2016 May 19;44(9):4163-73. doi: 10.1093/nar/gkw011. Epub 2016 Jan 14.
G-quadruplexes are dynamic structures folded in G-rich single-stranded DNA regions. These structures have been recognized as a potential nucleic acid based mechanism for regulating multiple cellular processes such as replication, transcription and genomic maintenance. So far, their transcriptional role in vivo during vertebrate embryonic development has not yet been addressed. Here, we performed an in silico search to find conserved putative G-quadruplex sequences (PQSs) within proximal promoter regions of human, mouse and zebrafish developmental genes. Among the PQSs able to fold in vitro as G-quadruplex, those present in nog3, col2a1 and fzd5 promoters were selected for further studies. In cellulo studies revealed that the selected G-quadruplexes affected the transcription of luciferase controlled by the SV40 nonrelated promoter. G-quadruplex disruption in vivo by microinjection in zebrafish embryos of either small ligands or DNA oligonucleotides complementary to the selected PQSs resulted in lower transcription of the targeted genes. Moreover, zebrafish embryos and larvae phenotypes caused by the presence of complementary oligonucleotides fully resembled those ones reported for nog3, col2a1 and fzd5 morphants. To our knowledge, this is the first work revealing in vivo the role of conserved G-quadruplexes in the embryonic development, one of the most regulated processes of the vertebrates biology.
G-四链体是在富含鸟嘌呤的单链DNA区域折叠形成的动态结构。这些结构已被认为是一种潜在的基于核酸的机制,可调节多种细胞过程,如复制、转录和基因组维持。到目前为止,它们在脊椎动物胚胎发育过程中的体内转录作用尚未得到研究。在这里,我们进行了一项计算机搜索,以在人类、小鼠和斑马鱼发育基因的近端启动子区域内寻找保守的假定G-四链体序列(PQSs)。在能够在体外折叠成G-四链体的PQSs中,选择了存在于nog3、col2a1和fzd5启动子中的序列进行进一步研究。细胞内研究表明,所选的G-四链体影响由SV40无关启动子控制的荧光素酶的转录。通过向斑马鱼胚胎显微注射与所选PQSs互补的小分子配体或DNA寡核苷酸,在体内破坏G-四链体,导致靶向基因的转录降低。此外,由互补寡核苷酸的存在引起的斑马鱼胚胎和幼虫表型与报道的nog3、col2a1和fzd5基因敲降表型完全相似。据我们所知,这是第一项在体内揭示保守G-四链体在胚胎发育中作用的研究,胚胎发育是脊椎动物生物学中调控最为严格的过程之一。