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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Differential roles of engrailed paralogs in determining sensory axon guidance and synaptic target recognition.
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Differential roles of engrailed paralogs in determining sensory axon guidance and synaptic target recognition.

机译:参与的旁系同源物在确定感觉轴突指导和突触目标识别中的不同作用。

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摘要

The transcription factor Engrailed (En) controls axon pathfinding and synaptic target choice in an identified neuron (6m) of the cockroach cercal sensory system. Knock-out of En using double-stranded RNA interference (dsRNAi) transforms 6m so that it resembles a neighboring neuron that normally does not express the en gene, has a different arbor anatomy, and makes different connections. Like many animals, the cockroach has two En paralogs, Pa-En1 and Pa-En2. In this study we tested the hypothesis that the paralogs have different effects on axon guidance and synaptic target recognition, using RNAi to knock out each one individually. Using dye injections into 6m and intracellular recordings from target interneurons, we obtained evidence that both Pa-En1 and Pa-En2 determine the axonal arborization, but only Pa-En1 controls synaptic connections. However, because immunocytochemical quantification of En protein in 6m after RNAi showed that Pa-En1 represents 65% of the total En activity and Pa-En2 only 35%, our results could be caused by dosage effects. We measured the effects of diluting the mixture of both dsRNAs on the amounts of En protein. From this dose-response curve, we calculated the appropriate dilutions of the dsRNA mixture that would titrate total En protein to levels equivalent to knock-out of either paralog. RNAi using these dilutions showed that Pa-En1 and Pa-En2 both contribute toward the control of axonal guidance and confirmed that Pa-En1 has the paralog-specific function of controlling synaptic target recognition.
机译:转录因子Engrailed(En)控制着蟑螂盲肠感觉系统神经元(6m)中的轴突寻路和突触靶点选择。使用双链RNA干扰(dsRNAi)敲除En可以转化6m,因此它类似于通常不表达en基因的相邻神经元,具有不同的乔木解剖结构,并且具有不同的连接。像许多动物一样,蟑螂有两个En旁系同源物Pa-En1和Pa-En2。在这项研究中,我们检验了使用RNAi单独敲除每个旁系同源物对轴突导向和突触靶标识别具有不同影响的假设。使用染料注射到6m和目标内部神经元的细胞内记录,我们获得了证据,即Pa-En1和Pa-En2均可确定轴突的轴突,但只有Pa-En1控制突触连接。但是,由于RNAi后6m内En蛋白的免疫细胞化学定量显示Pa-En1代表总En活性的65%,而Pa-En2仅代表总En活性的35%,因此我们的结果可能是剂量效应引起的。我们测量了稀释两种dsRNA混合物对En蛋白含量的影响。根据该剂量反应曲线,我们计算了dsRNA混合物的适当稀释度,该稀释度会将总En蛋白滴定至等同于任一旁系同源物敲除的水平。使用这些稀释液的RNAi显示Pa-En1和Pa-En2均有助于控制轴突导向,并证实Pa-En1具有控制突触目标识别的特定旁系同源功能。

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