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tailup(一种LIM-HD基因)与Iro-C在果蝇中胸背板特化过程中协同作用。

tailup, a LIM-HD gene, and Iro-C cooperate in Drosophila dorsal mesothorax specification.

作者信息

de Navascués Joaquín, Modolell Juan

机构信息

Centro de Biología Molecular Severo Ochoa, CSIC and UAM, Cantoblanco, Madrid, Spain.

出版信息

Development. 2007 May;134(9):1779-88. doi: 10.1242/dev.02844. Epub 2007 Apr 4.

Abstract

The LIM-HD gene tailup (tup; also known as islet) has been categorised as a prepattern gene that antagonises the formation of sensory bristles on the notum of Drosophila by downregulating the expression of the proneural achaete-scute genes. Here we show that tup has an earlier function in the development of the imaginal wing disc; namely, the specification of the notum territory. Absence of tup function causes cells of this anlage to upregulate different wing-hinge genes and to lose expression of some notum genes. Consistently, these cells differentiate hinge structures or modified notum cuticle. The LIM-HD co-factors Chip and Ssdp are also necessary for notum specification. This suggests that Tup acts in this process in a complex with Chip and Ssdp. Overexpression of tup, together with araucan, a 'pronotum' gene of the iroquois complex (Iro-C), synergistically reinforces the weak capacity of either gene, when overexpressed singly, to induce ectopic notum-like development. Whereas the Iro-C genes are activated in the notum anlage by EGFR signalling, tup is positively regulated by Dpp signalling. Our data support a model in which the EGFR and Dpp signalling pathways, with their respective downstream Iro-C and tup genes, converge and cooperate to commit cells to the notum developmental fate.

摘要

LIM-HD基因tailup(tup;也称为islet)已被归类为一种前模式基因,它通过下调原神经achaete-scute基因的表达来拮抗果蝇背板上感觉刚毛的形成。在此我们表明,tup在成虫翅盘发育中具有早期功能;即背板区域的特化。tup功能的缺失会导致该原基的细胞上调不同的翅铰链基因,并失去一些背板基因的表达。相应地,这些细胞分化为铰链结构或经过修饰的背板表皮。LIM-HD辅助因子Chip和Ssdp对于背板特化也是必需的。这表明Tup在这个过程中与Chip和Ssdp形成复合物发挥作用。tup与伊洛魁族复合体(Iro-C)的一个“前胸背板”基因araucan一起过表达,当单独过表达时,这两个基因诱导异位背板样发育的能力较弱,但二者协同作用时会增强这种能力。虽然Iro-C基因在背板原基中通过EGFR信号通路被激活,但tup受Dpp信号通路的正向调控。我们的数据支持一种模型,即EGFR和Dpp信号通路及其各自下游的Iro-C和tup基因汇聚并协同作用,使细胞确定为背板发育命运。

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