来自螳螂的神经肽:焦激肽和色激肽的缺失对这些肽的内分泌功能有何启示

Jan Adrianus Veenstra
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引用次数: 0

摘要

背景。神经肽在昆虫中发挥着重要作用,但在许多情况下,它们的功能仍不明确。神经肽组的比较分析可为了解这些功能提供线索。螳螂是捕食者,也是蟑螂的近亲。蟑螂的神经肽组已经非常成熟,但对螳螂的神经肽却知之甚少。最近公布的中华螳螂(Tenodera sinensis)基因组组装结果有可能改变这一现状。研究方法对中华螳螂的基因组进行分析,以确定是否存在编码神经肽的基因。为了进行比较,还研究了该螳螂和其他螳螂物种的公开短读取档案,以确定神经肽的存在和表达。一般来说,螳螂科和蜚蠊科的神经肽群几乎完全相同;螳螂和蜚蠊使用的神经肽非常相似。然而,有一个令人惊讶的例外。螳螂缺乏热激肽受体,包括色激肽受体。没有发现典型的热激肽基因,但有些物种确实有一个色激肽基因,在其他物种中,这个基因也已经丢失,在一个物种中,它是一个矛基因。大多数螳螂没有关于色激肽在哪里表达的信息,但在 Deroplatys truncata 中,色激肽在胸部表达,因此不像其他昆虫那样在食管下神经节中表达。在两个物种的基因组短读数档案中,共发现了 52 个物种的色激肽特异性受体序列。这两个物种的系统发育位置意味着该受体基因曾多次独立丢失。色激肽基因的丢失也不止一次。螳螂体内热激肽受体的多次独立丢失表明,这些受体与螳螂无关。这是非常令人惊讶的,因为在卵磷脂下神经节的两个神经内分泌细胞中,色激肽的表达是非常保守的。在已知的物种中,其受体在唾液腺中表达。作为一种神经内分泌物质,色激肽不太可能对唾液分泌进行急性调节,在其他昆虫中,唾液分泌是由特征明显的神经元调节的。如果色激肽的作用是为唾液腺随后的分泌唾液做准备,那么螳螂失去这种能力就完全说得通了,因为它们无法预测何时才能捕捉到下一个猎物。在真正需要唾液腺分泌唾液的几小时前就对其进行引流,会耗费大量能量。众所周知,其他的焦激肽能促进进食,并能以类似的方式刺激肌肉,使它们移动到食物来源处并消化食物。这一假说很好地解释了为什么螳螂不需要焦激肽,以及这些无处不在的节肢动物神经肽的功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuropeptides from a praying mantis: What the loss of pyrokinins and tryptopyrokinins suggests about the endocrine functions of these peptides
Background. Neuropeptides play important roles in insects, but in many cases their functions remain obscure. Comparative neuropeptidome analyses may provide clues to what these functions might be. Praying mantises are predators and close relatives of cockroaches that are scavengers. Cockroach neuropeptidomes are well established, but little is known about mantis neuropeptides. The recently published genome assembly of the praying mantis Tenodera sinensis makes it possble to change that. Methods. The genome assembly from T. sinensis was analyzed for the presence of genes coding neuropeptides. For comparison publicly available short read archives from this and other mantis species were also examined for the presence and expression of neuropeptides. Results. As a rule the neuropeptidomes of the Mantodea and Blattodea are almost identical; praying mantises and cockroaches use very similar neuropeptides. However, there is one surprising exception. Praying mantises lack the receptors for pyrokinins, including those for the tryptopyrokinins. No typical pyrokinin genes were found, but some species do have a tryptopyrokinin gene, in others this has also been lost and in one species it is a speudogene. For most praying mantises there is no information where tryptopyrokinin is expressed, but in Deroplatys truncata it is in the thorax and thus not in the suboesophageal ganglion as in other insects. In the genomic short read archives of two species, out 52, sequences were found for a tryptopyrokinin specific receptor. The phylogenetic position of those two species implies that the receptor gene was independently lost on multiple occasions. The loss of the tryptopyrokinin gene also happened more than once. Discussion. The multiple independent losses of the pyrokinin receptors in mantises suggests that these receptors are irrelevant in praying mantises. This is very surprising, since expression of tryptopyrokinin is very strongly conserved in two neuroendocrine cells in the suboeosphageal ganglion. In those species for which this is known, the expression of its receptor is in the salivary gland. As a neuroendocrine. tryptopyrokinin is unlikely to acutely regulate salivation, which in other insects is regulated by well characterized neurons. If the action of tryptopyrokinin were to prime the salivary gland for subsequent salivation, it would make perfect sense for a praying mantis to loose this capacity, as they can not anticipate when they will catch their next prey. Priming the salivary gland hours before it is actually needed would be energetically costly. The other pyrokinins are known to facilitate feeding and may in a similar fashion prime muscles needed for moving to the food source and digesting it. This hypothesis provides a good explanation as to why praying mantises do not need pyrokinins and also what the function of these ubiquitous arthropod neuropeptides may be.
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