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躯体依赖的调节作用有助于果蝇卵壳形态进化过程中菱形蛋白表达的差异。

Soma-dependent modulations contribute to divergence of rhomboid expression during evolution of Drosophila eggshell morphology.

作者信息

Nakamura Yukio, Kagesawa Tatsuo, Nishikawa Minori, Hayashi Yoshiki, Kobayashi Satoru, Niimi Teruyuki, Matsuno Kenji

机构信息

Department of Biological Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan.

出版信息

Development. 2007 Apr;134(8):1529-37. doi: 10.1242/dev.001578. Epub 2007 Mar 14.

Abstract

Patterning of the respiratory dorsal appendages (DAs) on the Drosophila melanogaster eggshell is tightly regulated by epidermal growth factor receptor (EGFR) signaling. Variation in the DA number is observed among Drosophila species; D. melanogaster has two DAs and D. virilis has four. Diversification in the expression pattern of rhomboid (rho), which activates EGFR signaling in somatic follicle cells, could cause the evolutionary divergence of DA numbers. Here we identified a cis-regulatory element of D. virilis rho. A comparison with D. melanogaster rho enhancer and activity studies in homologous and heterologous species suggested that these rho enhancers did not functionally diverge significantly during the evolution of these species. Experiments using chimeric eggs composed of a D. virilis oocyte and D. melanogaster follicle cells showed the evolution of DA number was not attributable to germline Gurken (Grk) signaling, but to divergence in events downstream of Grk signaling affecting the rho enhancer activity in somatic follicle cells. We found that a transcription factor, Mirror, which activates rho, could be one of these downstream factors. Thus, evolution of the trans-regulatory environment that controls rho expression in somatic follicle cells could be a major contributor to the evolutionary changes in DA number.

摘要

果蝇黑腹果蝇卵壳上呼吸背附肢(DAs)的模式由表皮生长因子受体(EGFR)信号通路严格调控。在果蝇物种中观察到DA数量的变化;黑腹果蝇有两个DA,而粗壮果蝇有四个。菱形蛋白(rho)在体细胞滤泡细胞中激活EGFR信号通路,其表达模式的多样化可能导致DA数量的进化差异。在这里,我们鉴定了粗壮果蝇rho的一个顺式调控元件。与黑腹果蝇rho增强子的比较以及在同源和异源物种中的活性研究表明,在这些物种的进化过程中,这些rho增强子在功能上没有显著分化。使用由粗壮果蝇卵母细胞和黑腹果蝇滤泡细胞组成的嵌合卵进行的实验表明,DA数量的进化不归因于种系Gurken(Grk)信号通路,而是归因于Grk信号通路下游影响体细胞滤泡细胞中rho增强子活性的事件的差异。我们发现,一种激活rho的转录因子Mirror可能是这些下游因子之一。因此,控制体细胞滤泡细胞中rho表达的反式调控环境的进化可能是DA数量进化变化的主要因素。

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