Walters Edgar T, Moroz Leonid L
Department of Integrative Biology and Pharmacology, University of Texas Medical School at Houston, Houston, Tex. 77030, USA.
Brain Behav Evol. 2009;74(3):206-18. doi: 10.1159/000258667. Epub 2009 Dec 21.
Molluscan preparations have yielded seminal discoveries in neuroscience, but the experimental advantages of this group have not, until now, been complemented by adequate molecular or genomic information for comparisons to genetically defined model organisms in other phyla. The recent sequencing of the transcriptome and genome of Aplysia californica, however, will enable extensive comparative studies at the molecular level. Among other benefits, this will bring the power of individually identifiable and manipulable neurons to bear upon questions of cellular function for evolutionarily conserved genes associated with clinically important neural dysfunction. Because of the slower rate of gene evolution in this molluscan lineage, more homologs of genes associated with human disease are present in Aplysia than in leading model organisms from Arthropoda (Drosophila) or Nematoda (Caenorhabditis elegans). Research has hardly begun in molluscs on the cellular functions of gene products that in humans are associated with neurological diseases. On the other hand, much is known about molecular and cellular mechanisms of long-term neuronal plasticity. Persistent nociceptive sensitization of nociceptors in Aplysia displays many functional similarities to alterations in mammalian nociceptors associated with the clinical problem of chronic pain. Moreover, in Aplysia and mammals the same cell signaling pathways trigger persistent enhancement of excitability and synaptic transmission following noxious stimulation, and these highly conserved pathways are also used to induce memory traces in neural circuits of diverse species. This functional and molecular overlap in distantly related lineages and neuronal types supports the proposal that fundamental plasticity mechanisms important for memory, chronic pain, and other lasting alterations evolved from adaptive responses to peripheral injury in the earliest neurons. Molluscan preparations should become increasingly useful for comparative studies across phyla that can provide insight into cellular functions of clinically important genes.
软体动物标本在神经科学领域取得了开创性的发现,但迄今为止,该类动物的实验优势尚未得到足够的分子或基因组信息的补充,以便与其他门中基因定义明确的模式生物进行比较。然而,最近加州海兔的转录组和基因组测序将使分子水平上的广泛比较研究成为可能。除其他益处外,这将使个体可识别和可操纵的神经元的力量用于解决与临床重要神经功能障碍相关的进化保守基因的细胞功能问题。由于该软体动物谱系中基因进化速度较慢,与人类疾病相关的基因在海兔中的同源物比节肢动物(果蝇)或线虫(秀丽隐杆线虫)等主要模式生物中更多。关于在人类中与神经疾病相关的基因产物的细胞功能,在软体动物中的研究几乎尚未开始。另一方面,人们对长期神经元可塑性的分子和细胞机制了解很多。海兔中伤害感受器的持续性伤害性敏感化与哺乳动物伤害感受器中与慢性疼痛临床问题相关的改变表现出许多功能相似性。此外,在海兔和哺乳动物中,相同的细胞信号通路在有害刺激后触发兴奋性和突触传递的持续增强,并且这些高度保守的通路也用于在不同物种的神经回路中诱导记忆痕迹。这种在远缘谱系和神经元类型中的功能和分子重叠支持了这样一种观点,即对记忆、慢性疼痛和其他持久改变重要的基本可塑性机制是从最早神经元对外周损伤的适应性反应进化而来的。软体动物标本对于跨门比较研究将变得越来越有用,这些研究可以深入了解临床重要基因的细胞功能。