Comparative reconstruction of the predatory feeding structures of the polyphenic nematode Pristionchus pacificus

IF 2.6 3区 生物学 Q2 DEVELOPMENTAL BIOLOGY
Clayton J. Harry, Sonia M. Messar, Erik J. Ragsdale
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引用次数: 5

Abstract

Pristionchus pacificus is a nematode model for the developmental genetics of morphological polyphenism, especially at the level of individual cells. Morphological polyphenism in this species includes an evolutionary novelty, moveable teeth, which have enabled predatory feeding in this species and others in its family (Diplogastridae). From transmission electron micrographs of serial thin sections through an adult hermaphrodite of P. pacificus, we three-dimensionally reconstructed all epithelial and myoepithelial cells and syncytia, corresponding to 74 nuclei, of its face, mouth, and pharynx. We found that the epithelia that produce the predatory morphology of P. pacificus are identical to Caenorhabditis elegans in the number of cell classes and nuclei. However, differences in cell form, spatial relationships, and nucleus position correlate with gross morphological differences from C. elegans and outgroups. Moreover, we identified fine-structural features, especially in the anteriormost pharyngeal muscles, that underlie the conspicuous, left-right asymmetry that characterizes the P. pacificus feeding apparatus. Our reconstruction provides an anatomical map for studying the genetics of polyphenism, feeding behavior, and the development of novel form in a satellite model to C. elegans.

Abstract Image

多食线虫捕食结构的比较重建
太平洋竖纹线虫是形态多表型的发育遗传学模型,特别是在单个细胞水平上。该物种的形态多表型包括一种进化上的新颖性,即可移动的牙齿,这使得该物种及其家族(双腹蝗科)的其他物种能够捕食。通过对太平洋p.p pacificus成年雌雄同体的一系列薄片的透射电子显微照片,我们三维重建了其面部、口腔和咽部的所有上皮细胞和肌上皮细胞以及合胞体,对应74个细胞核。我们发现产生捕食形态的太平洋p.a ificus的上皮细胞在细胞类别和细胞核数量上与秀丽隐杆线虫相同。然而,细胞形态、空间关系和细胞核位置的差异与秀丽隐杆线虫和外群的总体形态差异有关。此外,我们还发现了精细的结构特征,特别是在最前面的咽肌中,这是太平洋p.p . pacificus进食装置明显的左右不对称的基础。我们的重建为研究秀丽隐杆线虫的多表型遗传学、摄食行为和新形态发展的卫星模型提供了解剖图谱。
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来源期刊
Evolution & Development
Evolution & Development 生物-发育生物学
CiteScore
6.30
自引率
3.40%
发文量
26
审稿时长
>12 weeks
期刊介绍: Evolution & Development serves as a voice for the rapidly growing research community at the interface of evolutionary and developmental biology. The exciting re-integration of these two fields, after almost a century''s separation, holds much promise as the focus of a broader synthesis of biological thought. Evolution & Development publishes works that address the evolution/development interface from a diversity of angles. The journal welcomes papers from paleontologists, population biologists, developmental biologists, and molecular biologists, but also encourages submissions from professionals in other fields where relevant research is being carried out, from mathematics to the history and philosophy of science.
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