Department of Biology, Baylor University, Waco, Texas, United States of America.
PLoS One. 2011;6(6):e21218. doi: 10.1371/journal.pone.0021218. Epub 2011 Jun 17.
Crumbs (Crb), a cell polarity gene, has been shown to provide a positional cue for the extension of the apical membrane domain, adherens junction (AJ), and rhabdomere along the growing proximal-distal axis during Drosophila photoreceptor morphogenesis. In developing Drosophila photoreceptors, a stabilized microtubule structure was discovered and its presence was linked to polarity protein localization. It was therefore hypothesized that the microtubules may provide trafficking routes for the polarity proteins during photoreceptor morphogenesis. This study has examined whether Kinesin heavy chain (Khc), a subunit of the microtubule-based motor Kinesin-1, is essential in polarity protein localization in developing photoreceptors.
METHODOLOGY/PRINCIPAL FINDINGS: Because a genetic interaction was found between crb and khc, Crb localization was examined in the developing photoreceptors of khc mutants. khc was dispensable during early eye differentiation and development. However, khc mutant photoreceptors showed a range of abnormalities in the apical membrane domain depending on the position along the proximal-distal axis in pupal photoreceptors. The khc mutant showed a progressive mislocalization in the apical domain along the distal-proximal axis during rhabdomere elongation. The khc mutation also led to a similar progressive defect in the stabilized microtubule structures, strongly suggesting that Khc is essential for microtubule structure and Crb localization during distal to proximal rhabdomere elongation in pupal morphogenesis. This role of Khc in apical domain control was further supported by khc's gain-of-function phenotype. Khc overexpression in photoreceptors caused disruption of the apical membrane domain and the stabilized microtubules in the developing photoreceptors.
CONCLUSIONS/SIGNIFICANCE: In summary, we examined the role of khc in the regulation of the apical Crb domain in developing photoreceptors. Since the rhabdomeres in developing pupal eyes grow along the distal-proximal axis, these phenotypes suggest that Khc is essential for the microtubule structures and apical membrane domains during the distal-proximal elongation of photoreceptors, but is dispensable for early eye development.
Crb(crumbs)是一个细胞极性基因,已被证明在果蝇光感受器形态发生过程中为顶膜域、黏着连接(AJ)和纤毛沿着生长的近-远轴延伸提供位置线索。在发育中的果蝇光感受器中,发现了一种稳定的微管结构,其存在与极性蛋白定位有关。因此,假设微管可能为极性蛋白在光感受器形态发生过程中提供运输途径。本研究探讨了微管基运动蛋白 Kinesin-1 的一个亚基 Kinesin 重链(Khc)是否对发育中的光感受器中极性蛋白的定位至关重要。
方法/主要发现:由于发现 crb 和 khc 之间存在遗传相互作用,因此在 khc 突变体的发育光感受器中检查了 Crb 的定位。khc 在早期眼分化和发育过程中是可有可无的。然而,在蛹期光感受器中,khc 突变体光感受器的顶膜域表现出一系列沿近-远轴的位置而异的异常。khc 突变体在纤毛伸长过程中沿着远-近轴表现出 Crb 定位的逐渐错误。khc 突变也导致稳定的微管结构出现类似的渐进缺陷,强烈表明 Khc 对于微管结构和 Crb 定位在蛹期形态发生过程中从远到近的纤毛伸长至关重要。Khc 在顶端域控制中的作用进一步得到了 khc 的功能获得表型的支持。在光感受器中过表达 Khc 会导致发育中的光感受器的顶端膜域和稳定的微管破坏。
结论/意义:总之,我们研究了 khc 在调节发育中的光感受器中顶端 Crb 域的作用。由于发育中的蛹眼的纤毛沿远-近轴生长,这些表型表明 Khc 在光感受器的远-近伸长过程中对于微管结构和顶膜域是必不可少的,但在早期眼发育中是可有可无的。