Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, 364 Plantation St./LRB815, Worcester, MA 01605-2324, USA.
Department of Biology, University of Massachusetts, Amherst, MA 01003, USA.
Dev Biol. 2014 Jun 15;390(2):247-60. doi: 10.1016/j.ydbio.2014.02.025. Epub 2014 Mar 11.
Proper functioning of the vertebrate central nervous system requires the precise positioning of many neuronal cell types. This positioning is established during early embryogenesis when gene regulatory networks pattern the neural tube along its anteroposterior and dorsoventral axes. Dorsoventral patterning of the embryonic neural tube gives rise to multiple progenitor cell domains that go on to differentiate unique classes of neurons and glia. While the genetic program is reasonably well understood for some lineages, such as ventrally derived motor neurons and glia, other lineages are much less characterized. Here we show that prdm12b, a member of the PR domain containing-family of transcriptional regulators, is expressed in the p1 progenitor domain of the zebrafish neural tube in response to Sonic Hedgehog signaling. We find that disruption of prdm12b function leads to dorsal expansion of nkx6.1 expression and loss of p1-derived eng1b-expressing V1 interneurons, while the adjacent p0 and p2 domains are unaffected. We also demonstrate that prdm12b-deficient fish exhibit an abnormal touch-evoked escape response with excessive body contractions and a prolonged response time, as well as an inability to coordinate swimming movements, thereby revealing a functional role for V1 interneurons in locomotor circuits. We conclude that prdm12b is required for V1 interneuron specification and that these neurons control swimming movements in zebrafish.
脊椎动物中枢神经系统的正常运作需要许多神经元细胞类型的精确定位。这种定位是在胚胎早期形成时建立的,当时基因调控网络沿着神经管的前后轴和背腹轴对神经管进行模式化。胚胎神经管的背腹模式化产生了多个祖细胞域,这些祖细胞域继续分化为独特的神经元和神经胶质细胞类群。虽然一些谱系(如腹侧衍生的运动神经元和神经胶质)的遗传程序已经得到了相当好的理解,但其他谱系的特征要少得多。在这里,我们表明 PR 结构域家族的转录调节因子成员 prdm12b 在斑马鱼神经管的 p1 祖细胞域中表达,响应 Sonic Hedgehog 信号。我们发现,prdm12b 功能的破坏导致 nkx6.1 表达的背侧扩展和 p1 衍生的 eng1b 表达的 V1 中间神经元的丧失,而相邻的 p0 和 p2 域不受影响。我们还证明,prdm12b 缺陷鱼表现出异常的触摸诱发逃避反应,伴有过度的身体收缩和延长的反应时间,以及无法协调游泳运动,从而揭示了 V1 中间神经元在运动回路中的功能作用。我们得出结论,prdm12b 是 V1 中间神经元特化所必需的,这些神经元控制着斑马鱼的游泳运动。