Laboratory for Evolution and Development, National Research Centre for Growth and Development and Genetics Otago, Biochemistry Department, University of Otago, Dunedin 9054, New Zealand.
Development. 2011 Aug;138(16):3497-507. doi: 10.1242/dev.067926. Epub 2011 Jul 19.
Axis formation is a key step in development, but studies indicate that genes involved in insect axis formation are relatively fast evolving. Orthodenticle genes have conserved roles, often with hunchback, in maternal anterior patterning in several insect species. We show that two orthodenticle genes, otd1 and otd2, and hunchback act as maternal anterior patterning genes in the honeybee (Apis mellifera) but, unlike other insects, act to pattern the majority of the anteroposterior axis. These genes regulate the expression domains of anterior, central and posterior gap genes and may directly regulate the anterior gap gene giant. We show otd1 and hunchback also influence dorsoventral patterning by regulating zerknült (zen) as they do in Tribolium, but that zen does not regulate the expression of honeybee gap genes. This suggests that interactions between anteroposterior and dorsal-ventral patterning are ancestral in holometabolous insects. Honeybee axis formation, and the function of the conserved anterior patterning gene orthodenticle, displays unique characters that indicate that, even when conserved genes pattern the axis, their regulatory interactions differ within orders of insects, consistent with relatively fast evolution in axis formation pathways.
轴向形成是发育的关键步骤,但研究表明,参与昆虫轴向形成的基因进化速度相对较快。Orthodenticle 基因在几个昆虫物种的母体前体模式中具有保守作用,通常与 hunchback 一起发挥作用。我们表明,两个 Orthodenticle 基因,otd1 和 otd2,以及 hunchback,作为母本前体模式基因在蜜蜂(Apis mellifera)中发挥作用,但与其他昆虫不同,它们作用于大多数前后轴向的模式。这些基因调节前、中、后间隙基因的表达域,并可能直接调节前间隙基因 giant。我们表明,otd1 和 hunchback 也通过调节 Tribolium 中的 zen 来影响背腹模式,但是 zen 不调节蜜蜂间隙基因的表达。这表明,在完全变态昆虫中,前后和背腹模式之间的相互作用是祖先进化的。蜜蜂的轴向形成,以及保守的前体模式基因 Orthodenticle 的功能,表现出独特的特征,表明即使保守基因对轴进行模式化,它们在昆虫目中的调节相互作用也不同,这与轴向形成途径中的相对快速进化一致。