Anderson Carrie, Bartlett Stephen J, Gansner John M, Wilson Duncan, He Ling, Gitlin Jonathan D, Kelsh Robert N, Dowden James
Centre for Regenerative Medicine, Department of Biology & Biochemistry, University of Bath, Bath, UKBA2 7AY.
Mol Biosyst. 2007 Jan;3(1):51-9. doi: 10.1039/b613673g. Epub 2006 Nov 14.
As a result of a chemical genetic screen for modulators of metalloprotease activity, we report that 2-mercaptopyridine-N-oxide induces a conspicuous undulating notochord defect in zebrafish embryos, a phenocopy of the leviathan mutant. The location of the chemically-induced wavy notochord correlated with the timing of application, thus defining a narrow chemical sensitivity window during segmentation stages. Microscopic observations revealed that notochord undulations appeared during the phase of notochord cell vacuolation and notochord elongation. Notochord cells become swollen as well as disorganized, while electron microscopy revealed disrupted organization of collagen fibrils in the surrounding sheath. We demonstrate by assay in zebrafish extracts that 2-mercaptopyridine-N-oxide inhibits lysyl oxidase. Thus, we provide insight into notochord morphogenesis and reveal novel compounds for lysyl oxidase inhibition. Taken together, these data underline the utility of small molecules for elucidating the dynamic mechanisms of early morphogenesis and provide a potential explanation for the recently established role of copper in zebrafish notochord formation.
通过对金属蛋白酶活性调节剂进行化学遗传筛选,我们发现2-巯基吡啶-N-氧化物可在斑马鱼胚胎中诱导出明显的波动脊索缺陷,这是leviathan突变体的表型模拟。化学诱导的波浪状脊索的位置与施用时间相关,从而确定了在体节形成阶段的一个狭窄的化学敏感性窗口。显微镜观察显示,脊索波动出现在脊索细胞空泡化和脊索伸长阶段。脊索细胞变得肿胀且排列紊乱,而电子显微镜显示周围鞘中的胶原纤维组织被破坏。我们通过在斑马鱼提取物中的测定证明,2-巯基吡啶-N-氧化物抑制赖氨酰氧化酶。因此,我们深入了解了脊索形态发生,并揭示了用于抑制赖氨酰氧化酶的新型化合物。综上所述,这些数据强调了小分子在阐明早期形态发生动态机制方面的效用,并为最近确定的铜在斑马鱼脊索形成中的作用提供了潜在解释。