Department of Cell and Developmental Biology, University of Pennsylvania Perelman School of Medicine, 1157 BRB II/III, 421 Curie Blvd., Philadelphia, PA 19104, USA; Department of Biological Sciences, W.M. Keck Center for Behavioral Biology, North Carolina State University, 127 David Clark Labs, 100 Brooks Ave., Raleigh, NC 27607, USA.
Department of Cell and Developmental Biology, University of Pennsylvania Perelman School of Medicine, 1157 BRB II/III, 421 Curie Blvd., Philadelphia, PA 19104, USA; Department of Biology, Haverford College, S108 Sharpless Hall, 370 Lancaster Ave., Haverford, PA 19041, USA.
Cell Rep. 2018 Apr 17;23(3):878-887. doi: 10.1016/j.celrep.2018.03.095.
Sensory experiences dynamically modify whether animals respond to a given stimulus, but it is unclear how innate behavioral thresholds are established. Here, we identify molecular and circuit-level mechanisms underlying the innate threshold of the zebrafish startle response. From a forward genetic screen, we isolated five mutant lines with reduced innate startle thresholds. Using whole-genome sequencing, we identify the causative mutation for one line to be in the fragile X mental retardation protein (FMRP)-interacting protein cyfip2. We show that cyfip2 acts independently of FMRP and that reactivation of cyfip2 restores the baseline threshold after phenotype onset. Finally, we show that cyfip2 regulates the innate startle threshold by reducing neural activity in a small group of excitatory hindbrain interneurons. Thus, we identify a selective set of genes critical to establishing an innate behavioral threshold and uncover a circuit-level role for cyfip2 in this process.
感觉体验可以动态地改变动物对特定刺激的反应,但目前尚不清楚先天行为阈值是如何建立的。在这里,我们确定了斑马鱼惊跳反应先天阈值的分子和电路水平机制。通过正向遗传筛选,我们分离出五个先天惊跳阈值降低的突变系。通过全基因组测序,我们确定了其中一个系的致病突变位于脆性 X 智力低下蛋白 (FMRP)-相互作用蛋白 cyfip2 中。我们表明 cyfip2 独立于 FMRP 起作用,并且在表型出现后,cyfip2 的重新激活可以恢复基线阈值。最后,我们表明 cyfip2 通过减少一小群兴奋性后脑神经中的神经活动来调节先天惊跳阈值。因此,我们确定了一组对建立先天行为阈值至关重要的选择性基因,并揭示了 cyfip2 在该过程中的电路水平作用。