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A noncanonical function of histidyl‐tRNA synthetase: inhibition of vascular hyperbranching during zebrafish development

机译:组氨酸tRNA合成酶的非规范功能:斑马鱼发育过程中血管过度分支的抑制

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摘要

Histidyl‐tRNA synthetase (Hars) catalyzes the ligation of histidine residues to cognate tRNA. Here, we demonstrate a noncanonical function of Hars in vascular development in zebrafish. We obtained a novel zebrafish cq34 mutant which exhibited hyperbranching of cranial and intersegmental blood vessels 48 h after fertilization. The gene responsible for this phenotype was identified as hars. We found the increased expression of cdh5 and vegfa in the harscq34 mutant. Knockdown of cdh5 in the mutant reduced disordered connections of the hindbrain capillaries. Inhibition of vascular endothelial growth factor signaling suppressed the abnormal vascular branching observed in the mutant. Moreover, the human HARSmRNA rescued the vascular defects in the cq34 mutant. Thus, the noncanonical function of Hars regulates vascular development, mainly by modulating expression of cdh5 and vegfa.
机译:Histidyl-tRNA合成酶(Hars)催化组氨酸残基与同源tRNA的连接。在这里,我们证明了Hars在斑马鱼血管发育中的非经典功能。我们获得了一个新的斑马鱼cq34突变体,在受精后48小时,该突变体表现出颅和节间血管的超支化。负责该表型的基因被鉴定为hars。我们发现harscq34突变体中cdh5和vegfa的表达增加。击倒突变体中的cdh5可以减少后脑毛细血管的无序连接。抑制血管内皮生长因子信号转导抑制了突变体中观察到的异常血管分支。此外,人类HARSmRNA拯救了cq34突变体中的血管缺陷。因此,Hars的非规范功能主要通过调节cdh5和vegfa的表达来调节血管发育。

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