Department of Clinical and Experimental Medicine, Linkoping University, Linkoping, SE-58185, Sweden.
Dev Biol. 2011 May 1;353(1):72-80. doi: 10.1016/j.ydbio.2011.02.015. Epub 2011 Feb 23.
In the Drosophila ventral nerve cord, the three pairs of Capability neuropeptide-expressing Va neurons are exclusively found in the second, third and fourth abdominal segments (A2-A4). To address the underlying mechanisms behind such segment-specific cell specification, we followed the developmental specification of these neurons. We find that Va neurons are initially generated in all ventral nerve cord segments and progress along a common differentiation path. However, their terminal differentiation only manifests itself in A2-A4, due to two distinct mechanisms: segment-specific programmed cell death (PCD) in posterior segments, and differentiation to an alternative identity in segments anterior to A2. Genetic analyses reveal that the Hox homeotic genes are involved in the segment-specific appearance of Va neurons. In posterior segments, the Hox gene Abdominal-B exerts a pro-apoptotic role on Va neurons, which involves the function of several RHG genes. Strikingly, this role of Abd-B is completely opposite to its role in the segment-specific apoptosis of other classes of neuropeptide neurons, the dMP2 and MP1 neurons, where Abd-B acts in an anti-apoptotic manner. In segments A2-A4 we find that abdominal A is important for the terminal differentiation of Va cell fate. In the A1 segment, Ultrabithorax acts to specify an alternate Va neuron fate. In contrast, in thoracic segments, Antennapedia suppresses the Va cell fate. Thus, Hox genes act in a multi-faceted manner to control the segment-specific appearance of the Va neuropeptide neurons in the ventral nerve cord.
在果蝇的腹神经索中,三对表达 Capability 神经肽的 Va 神经元仅存在于第二、三、四个腹节(A2-A4)中。为了解决这些细胞特异性存在的潜在机制,我们对这些神经元的发育特异性进行了研究。我们发现,Va 神经元最初在所有腹神经索节段中产生,并沿着共同的分化途径进行。然而,由于两种不同的机制,它们的终末分化仅在 A2-A4 中表现出来:后节段的特异性程序性细胞死亡(PCD)和在 A2 之前的节段分化为替代身份。遗传分析表明,Hox 同源基因参与 Va 神经元的节段特异性出现。在后节段,Hox 基因 Abdominal-B 对 Va 神经元发挥促凋亡作用,涉及几个 RHG 基因的功能。引人注目的是,Abd-B 的这种作用与其在其他类神经肽神经元(dMP2 和 MP1 神经元)的节段特异性凋亡中的作用完全相反,Abd-B 在后者中发挥抗凋亡作用。在 A2-A4 节段中,我们发现腹部 A 对 Va 细胞命运的终末分化很重要。在 A1 节段,Ultrabithorax 作用于指定替代 Va 神经元命运。相比之下,在胸段,Antennapedia 抑制 Va 细胞命运。因此,Hox 基因以多方面的方式控制腹神经索中 Va 神经肽神经元的节段特异性出现。