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The effect of MRN complex and ATM kinase inhibitors on Zebrafish embryonic development

机译:MRN复合物和ATM激酶抑制剂对斑马胚发育的影响

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Zebrafish is an ideal animal model to study developmental biology due to its transparent embryos and rapid development stages of embryogenesis. Here we investigate the role of DNA damage proteins, specifically Mre11/Rad50/NBN (MRN) complex and ataxia-telangiectasia mutated (ATM) kinase during embryogenesis by inhibiting its function using specific MRN complex (Mirin) and ATM Kinase inhibitors (Ku60019 and Ku55933). Zebrafish embryos at midblastula transition (MBT) stage are treated with Mirin, Ku60019 and Ku55933. The embryonic development of the embryos was monitored at 24 hours-post fertilisation (hpf), 48 hpf and 72 hpf. We observed that at the lowest concentrations (3 μM of Mirin, 1.5 nM of Ku60019 and 3 nM of Ku55933), the inhibitors treated embryos have 100% survivability. However, with increasing inhibitor concentration, the survivability drops. Control or mock treatment of all embryos shows 100 % survivability rate. This study suggests that DNA damage repair proteins may be crucial for normal zebrafish embryo development and survival.
机译:斑马鱼是一种理想的动物模型,用于研究其透明胚胎和胚胎发生的快速发展阶段的发展生物学。在这里,我们通过使用特异性MRN综合体(Mirin)和ATM激酶抑制剂(Ku60019和Ku55933,探讨DNA损伤蛋白质,特别是MRE11 / RAD50 / NBN(MRN)复合物和Ataxia-Telanciectasia突变(ATM)激酶在胚胎发生过程中的作用(Ku60019和Ku55933 )。 MIRIN,KU60019和KU55933治疗MIDLASTULA过渡(MBT)阶段的斑马鱼胚胎。在24小时后施肥(HPF),48 HPF和72 HPF时监测胚胎的胚胎发育。我们观察到,在最低浓度(3μm的米林,1.5nm的Ku60019和3nm的Ku55933),抑制剂处理的胚胎具有100%的生存性。然而,随着抑制剂浓度的增加,存活性下降。所有胚胎的控制或模拟处理显示出100%的生存能力率。该研究表明,DNA损伤修复蛋白可能对正常斑马鱼胚胎发育和生存至关重要。

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