Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, 421 Curie Boulevard, Philadelphia, PA 19104, USA.
Department of Cancer Biology, Perelman School of Medicine, University of Pennsylvania, 421 Curie Boulevard, Philadelphia, PA 19104, USA.
Curr Biol. 2020 Jul 20;30(14):2729-2738.e4. doi: 10.1016/j.cub.2020.05.016. Epub 2020 Jun 4.
Habituation is an adaptive learning process that enables animals to adjust innate behaviors to changes in their environment. Despite its well-documented implications for a wide diversity of behaviors, the molecular and cellular basis of habituation learning is not well understood. Using whole-genome sequencing of zebrafish mutants isolated in an unbiased genetic screen, we identified the palmitoyltransferase Huntingtin interacting protein 14 (Hip14) as a critical regulator of habituation learning. We demonstrate that Hip14 regulates depression of sensory inputs onto an identified hindbrain neuron and provide evidence that Hip14 palmitoylates the Shaker-like K voltage-gated channel subunit (Kv1.1), thereby regulating Kv1.1 subcellular localization. Furthermore, we show that, like for Hip14, loss of Kv1.1 leads to habituation deficits and that Hip14 is dispensable in development and instead acts acutely to promote habituation. Combined, these results uncover a previously unappreciated role for acute posttranslational palmitoylation at defined circuit components to regulate learning.
习惯化是一种适应性学习过程,使动物能够根据环境变化调整先天行为。尽管习惯化学习对广泛的行为具有很好的记录意义,但习惯化学习的分子和细胞基础还不是很清楚。我们使用在无偏遗传筛选中分离出的斑马鱼突变体的全基因组测序,鉴定出棕榈酰转移酶亨廷顿相互作用蛋白 14(Hip14)是习惯化学习的关键调节因子。我们证明 Hip14 调节感觉输入到已鉴定的后脑神经元的抑制,并提供证据表明 Hip14 棕榈酰化 Shaker 样 K 电压门控通道亚基(Kv1.1),从而调节 Kv1.1 亚细胞定位。此外,我们还表明,与 Hip14 一样,Kv1.1 的缺失导致习惯化缺陷,而 Hip14 在发育过程中是可有可无的,而是急性起作用以促进习惯化。综上所述,这些结果揭示了以前未被重视的在特定回路成分上进行急性翻译后棕榈酰化以调节学习的作用。