University of Notre Dame, Notre Dame, Eck Institute for Global Health and Department of Biological Sciences, Notre Dame, IN 46556, USA.
Evodevo. 2013 Mar 6;4(1):9. doi: 10.1186/2041-9139-4-9.
Despite the devastating global impact of mosquito-borne illnesses on human health, very little is known about mosquito developmental biology. In this investigation, functional genetic analysis of embryonic salivary gland development was performed in Aedes aegypti, the dengue and yellow fever vector and an emerging model for vector mosquito development. Although embryonic salivary gland development has been well studied in Drosophila melanogaster, little is known about this process in mosquitoes or other arthropods.
Mosquitoes possess orthologs of many genes that regulate Drosophila melanogaster embryonic salivary gland development. The expression patterns of a large subset of these genes were assessed during Ae. aegypti development. These studies identified a set of molecular genetic markers for the developing mosquito salivary gland. Analysis of marker expression allowed for tracking of the progression of Ae. aegypti salivary gland development in embryos. In Drosophila, the salivary glands develop from placodes located in the ventral neuroectoderm. However, in Ae. aegypti, salivary marker genes are not expressed in placode-like patterns in the ventral neuroectoderm. Instead, marker gene expression is detected in salivary gland rudiments adjacent to the proventriculus. These observations highlighted the need for functional genetic characterization of mosquito salivary gland development. An siRNA- mediated knockdown strategy was therefore employed to investigate the role of one of the marker genes, cyclic-AMP response element binding protein A (Aae crebA), during Ae. aegypti salivary gland development. These experiments revealed that Aae crebA encodes a key transcriptional regulator of the secretory pathway in the developing Ae. aegypti salivary gland.
The results of this investigation indicated that the initiation of salivary gland development in Ae. aegypti significantly differs from that of D. melanogaster. Despite these differences, some elements of salivary gland development, including the ability of CrebA to regulate secretory gene expression, are conserved between the two species. These studies underscore the need for further analysis of mosquito developmental genetics and may foster comparative studies of salivary gland development in additional insect species.
尽管蚊媒疾病对人类健康造成了毁灭性的全球影响,但我们对蚊子的发育生物学知之甚少。在这项研究中,对埃及伊蚊(登革热和黄热病的载体,也是新兴的蚊子发育模型)的胚胎唾液腺发育进行了功能遗传分析。尽管在黑腹果蝇中已经对胚胎唾液腺发育进行了很好的研究,但我们对蚊子或其他节肢动物的这一过程知之甚少。
蚊子拥有许多调控黑腹果蝇胚胎唾液腺发育的同源基因。在埃及伊蚊发育过程中,评估了这些基因的一个大子集的表达模式。这些研究确定了一组蚊子唾液腺发育的分子遗传标记。标记物表达的分析允许跟踪埃及伊蚊唾液腺的发育进展。在果蝇中,唾液腺从位于腹侧神经外胚层的侧板中发育而来。然而,在埃及伊蚊中,唾液标记基因在腹侧神经外胚层中没有以侧板样的模式表达。相反,标记基因的表达在靠近前胃的唾液腺原基中检测到。这些观察结果强调了对蚊子唾液腺发育进行功能遗传表征的必要性。因此,采用了 siRNA 介导的敲低策略来研究标记基因之一,即环腺苷酸反应元件结合蛋白 A(Aae crebA),在埃及伊蚊唾液腺发育中的作用。这些实验表明,Aae crebA 编码了埃及伊蚊发育中的唾液腺分泌途径的关键转录调节因子。
本研究的结果表明,埃及伊蚊唾液腺发育的起始与黑腹果蝇有很大的不同。尽管存在这些差异,但唾液腺发育的一些元素,包括 CrebA 调节分泌基因表达的能力,在这两个物种中是保守的。这些研究强调了进一步分析蚊子发育遗传学的必要性,并可能促进对其他昆虫物种唾液腺发育的比较研究。