Department of Physiology, Anatomy and Microbiology, La Trobe University, Bundoora, VIC, 3086, Australia.
The Victorian Comprehensive Cancer Centre, Peter MacCallum Cancer Centre, Parkville, VIC, 3050, Australia.
Sci Rep. 2017 Dec 14;7(1):17607. doi: 10.1038/s41598-017-17898-7.
The grainyhead-like (grhl) transcription factors play crucial roles in craniofacial development, epithelial morphogenesis, neural tube closure, and dorso-ventral patterning. By utilising the zebrafish to differentially regulate expression of family members grhl2b and grhl3, we show that both genes regulate epithelial migration, particularly convergence-extension (CE) type movements, during embryogenesis. Genetic deletion of grhl3 via CRISPR/Cas9 results in failure to complete epiboly and pre-gastrulation embryonic rupture, whereas morpholino (MO)-mediated knockdown of grhl3 signalling leads to aberrant neural tube morphogenesis at the midbrain-hindbrain boundary (MHB), a phenotype likely due to a compromised overlying enveloping layer (EVL). Further disruptions of grhl3-dependent pathways (through co-knockdown of grhl3 with target genes spec1 and arhgef19) confirm significant MHB morphogenesis and neural tube closure defects. Concomitant MO-mediated disruption of both grhl2b and grhl3 results in further extensive CE-like defects in body patterning, notochord and somite morphogenesis. Interestingly, over-expression of either grhl2b or grhl3 also leads to numerous phenotypes consistent with disrupted cellular migration during gastrulation, including embryo dorsalisation, axial duplication and impaired neural tube migration leading to cyclopia. Taken together, our study ascribes novel roles to the Grhl family in the context of embryonic development and morphogenesis.
粒头样(grhl)转录因子在颅面发育、上皮形态发生、神经管闭合和背腹模式形成中发挥着关键作用。通过利用斑马鱼来差异调控家族成员 grhl2b 和 grhl3 的表达,我们表明这两个基因都调节上皮细胞迁移,特别是在胚胎发生过程中的会聚-延伸(CE)类型运动。通过 CRISPR/Cas9 对 grhl3 进行基因缺失会导致胚胎不能完成外包和原肠胚破裂,而通过 MO 介导的 grhl3 信号通路敲低会导致中脑-后脑边界(MHB)处的神经管形态发生异常,这一表型可能是由于覆盖层(EVL)受损。进一步破坏 grhl3 依赖的途径(通过 grhl3 与靶基因 spec1 和 arhgef19 的共敲低)证实了 MHB 形态发生和神经管闭合缺陷。同时敲低 grhl2b 和 grhl3 的 MO 会导致体模式形成和脊索及体节形态发生的进一步广泛的 CE 样缺陷。有趣的是,grhl2b 或 grhl3 的过表达也会导致许多与原肠胚迁移过程中断相关的表型,包括胚胎背侧化、轴重复和神经管迁移受损导致独眼畸形。总之,我们的研究在胚胎发育和形态发生的背景下赋予了 Grhl 家族新的角色。