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转染领鞭毛原生动物揭示了它们的细胞生物学和动物 septin 的祖先。

Transfection of choanoflagellates illuminates their cell biology and the ancestry of animal septins.

机构信息

Howard Hughes Medical Institute and Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720.

出版信息

Mol Biol Cell. 2018 Dec 1;29(25):3026-3038. doi: 10.1091/mbc.E18-08-0514. Epub 2018 Oct 3.

Abstract

As the closest living relatives of animals, choanoflagellates offer unique insights into animal origins and core mechanisms underlying animal cell biology. However, unlike traditional model organisms, such as yeast, flies, and worms, choanoflagellates have been refractory to DNA delivery methods for expressing foreign genes. Here we report a robust method for expressing transgenes in the choanoflagellate , overcoming barriers that have previously hampered DNA delivery and expression. To demonstrate how this method accelerates the study of cell biology, we engineered a panel of fluorescent protein markers that illuminate key features of choanoflagellate cells. We then investigated the localization of choanoflagellate septins, a family of GTP-binding cytoskeletal proteins that are hypothesized to regulate multicellular rosette development in Fluorescently tagged septins localized to the basal poles of single cells and rosettes in a pattern resembling septin localization in animal epithelia. The establishment of transfection in and its application to the study of septins represent critical advances in the use of as an experimental model for investigating choanoflagellate cell biology, core mechanisms underlying animal cell biology, and the origin of animals.

摘要

作为动物最亲近的现存亲属,领鞭毛虫为动物起源和动物细胞生物学的核心机制提供了独特的见解。然而,与传统的模式生物(如酵母、苍蝇和蠕虫)不同,领鞭毛虫一直难以通过表达外源基因的 DNA 传递方法进行改造。在这里,我们报告了一种在领鞭毛虫中表达转基因的有效方法,克服了以前阻碍 DNA 传递和表达的障碍。为了展示这种方法如何加速细胞生物学的研究,我们设计了一组荧光蛋白标记物,可照亮领鞭毛虫细胞的关键特征。然后,我们研究了领鞭毛虫隔膜蛋白的定位,隔膜蛋白是一类 GTP 结合细胞骨架蛋白,据推测它们调节多细胞玫瑰结的发育。荧光标记的隔膜蛋白定位于单细胞和玫瑰结的基底极,其定位模式类似于动物上皮细胞中隔膜蛋白的定位。在 中建立转染及其在隔膜蛋白研究中的应用代表了使用 作为实验模型研究领鞭毛虫细胞生物学、动物细胞生物学核心机制和动物起源的重要进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a48a/6333174/e4cba1ca9fab/mbc-29-3026-g001.jpg

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