Transgenerational Sterility of a Transgenic C. elegans : A Cautionary Tale.

microPublication biology Pub Date : 2024-11-08 eCollection Date: 2024-01-01 DOI:10.17912/micropub.biology.001343
Zachary Leydig, Judith Yanowitz
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Abstract

The integration of fluorescent protein tags (GFP, mScarlet, mNeon, etc) by CRISPR is often inefficient due to the size of the tags (hundreds of base pairs). To facilitate fluorescent tagging, the split-GFP and split-Scarlet systems have been optimized for use in C. elegans (Goudeau et al., 2021). In C. elegans , glh-1 ::T2A::wrmScarlet(1-10) allows germline gene expression of red fusion proteins. While initial studies reported wild-type broods at both permissive and non-permissive temperatures, we report here that at least one such transgene confers sterility after continuous culturing at 25.5 °C. This serves as a cautionary tale for use of the glh-1 driver and/or T2A::mScarlet fusions to this protein.

转基因 elegans 的跨代不育:一个警世故事。
由于标签的大小(数百个碱基对),CRISPR 整合荧光蛋白标签(GFP、mScarlet、mNeon 等)的效率往往不高。为方便荧光标记,已优化了用于 elegans 的 split-GFP 和 split-Scarlet 系统(Goudeau 等人,2021 年)。在 elegans 中,glh-1 ::T2A::wrmScarlet(1-10) 允许生殖系基因表达红色融合蛋白。最初的研究报告称,在允许温度和非允许温度下,野生型幼虫都能繁殖,但我们在此报告称,至少有一种此类转基因在 25.5 °C下连续培养后会导致不育。这对使用 glh-1 驱动程序和/或与该蛋白融合的 T2A::mScarlet 是一个警示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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