Feitosa Natália Martins, Pechmann Matthias, Schwager Evelyn E, Tobias-Santos Vitória, McGregor Alistair P, Damen Wim G M, Nunes da Fonseca Rodrigo
Laboratório Integrado de Ciências Morfofuncionais, Núcleo em Ecologia e Desenvolvimento Socio-Ambiental de Macaé (NUPEM), Campus Macaé, Universidade Federal do Rio de Janeiro (UFRJ), Macaé, Rio de Janeiro, 27920-560, Brazil.
Institute for Developmental Biology, University of Cologne, Cologne, North-Rhine Westphalia, 50674, Germany.
Genesis. 2017 May;55(5). doi: 10.1002/dvg.23033. Epub 2017 Apr 22.
The development of a digestive system is an essential feature of bilaterians. Studies of the molecular control of gut formation in arthropods have been studied in detail in the fruit fly Drosophila melanogaster. However, little is known in other arthropods, especially in noninsect arthropods. To better understand the evolution of arthropod alimentary system, we investigate the molecular control of gut development in the spider Parasteatoda tepidariorum (Pt), the primary chelicerate model species for developmental studies. Orthologs of the ectodermal genes Pt-wingless (Pt-wg) and Pt-hedgehog (Pt-hh), of the endodermal genes, Pt-serpent (Pt-srp) and Pt-hepatocyte-nuclear factor-4 (Pt-hnf4) and of the mesodermal gene Pt-twist (Pt-twi) are expressed in the same germ layers during spider gut development as in D. melanogaster. Thus, our expression data suggest that the downstream molecular components involved in gut development in arthropods are conserved. However, Pt-forkhead (Pt-fkh) expression and function in spiders is considerably different from its D. melanogaster ortholog. Pt-fkh is expressed before gastrulation in a cell population that gives rise to endodermal and mesodermal precursors, suggesting a possible role for this factor in specification of both germ layers. To test this hypothesis, we knocked down Pt-fkh via RNA interference. Pt-fkh RNAi embryos not only fail to develop a proper gut, but also lack the mesodermal Pt-twi expressing cells. Thus, in spiders Pt-fkh specifies endodermal and mesodermal germ layers. We discuss the implications of these findings for the evolution and development of gut formation in Ecdysozoans.
消化系统的发育是两侧对称动物的一个基本特征。在果蝇黑腹果蝇中,对节肢动物肠道形成的分子控制进行了详细研究。然而,在其他节肢动物中,尤其是非昆虫节肢动物中,人们了解甚少。为了更好地理解节肢动物消化系统的进化,我们研究了蜘蛛温驯拟壁钱(Pt)肠道发育的分子控制,Pt是发育研究的主要螯肢动物模式物种。外胚层基因Pt-无翅(Pt-wg)和Pt-刺猬(Pt-hh)、内胚层基因Pt-蛇形(Pt-srp)和Pt-肝细胞核因子-4(Pt-hnf4)以及中胚层基因Pt-扭曲(Pt-twi)的直系同源基因,在蜘蛛肠道发育过程中与在黑腹果蝇中一样,在相同的胚层中表达。因此,我们的表达数据表明,节肢动物肠道发育中涉及的下游分子成分是保守的。然而,Pt-叉头(Pt-fkh)在蜘蛛中的表达和功能与其黑腹果蝇直系同源基因有很大不同。Pt-fkh在原肠胚形成之前在一个产生内胚层和中胚层前体的细胞群体中表达,这表明该因子在两个胚层的特化中可能发挥作用。为了验证这一假设,我们通过RNA干扰敲低了Pt-fkh。Pt-fkh RNAi胚胎不仅无法发育出正常的肠道,而且还缺乏表达中胚层Pt-twi的细胞。因此,在蜘蛛中,Pt-fkh决定了内胚层和中胚层胚层。我们讨论了这些发现对蜕皮动物肠道形成的进化和发育的意义。