Marie Bruno, Blagburn Jonathan M
Institute of Neurobiology, University of Puerto Rico, San Juan, Puerto Rico 00901, USA.
J Neurosci. 2003 Aug 27;23(21):7854-62. doi: 10.1523/JNEUROSCI.23-21-07854.2003.
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.
转录因子Engrailed(En)控制蟑螂尾须感觉系统中一个已确定的神经元(6m)的轴突导向和突触靶标选择。使用双链RNA干扰(dsRNAi)敲除En会使6m发生转变,使其类似于一个通常不表达en基因的相邻神经元,具有不同的树突解剖结构,并形成不同的连接。与许多动物一样,蟑螂有两个En旁系同源物,Pa-En1和Pa-En2。在本研究中,我们测试了以下假设:利用RNAi分别敲除每个旁系同源物,它们对轴突导向和突触靶标识别具有不同的影响。通过向6m注射染料并从靶中间神经元进行细胞内记录,我们获得的证据表明,Pa-En1和Pa-En2都决定轴突分支,但只有Pa-En1控制突触连接。然而,由于RNAi后对6m中En蛋白进行免疫细胞化学定量显示,Pa-En1占总En活性的65%,而Pa-En2仅占35%,我们的结果可能是由剂量效应引起的。我们测量了稀释两种dsRNA混合物对En蛋白量的影响。根据该剂量反应曲线,我们计算出了dsRNA混合物的合适稀释度,该稀释度可将总En蛋白滴定至与敲除任一旁系同源物相当的水平。使用这些稀释度进行RNAi表明,Pa-En1和Pa-En2都有助于控制轴突导向,并证实Pa-En1具有控制突触靶标识别的旁系同源物特异性功能。