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甲虫中持续的亲本RNA干扰涉及长双链RNA的母系传递。

Persistent Parental RNAi in the Beetle Involves Maternal Transmission of Long Double-Stranded RNA.

作者信息

Horn Thorsten, Narov Kalin D, Panfilio Kristen A

机构信息

Institute for Zoology: Developmental Biology University of Cologne Zülpicher Straße 47b 50674 Cologne Germany.

School of Life Sciences University of Warwick Gibbet Hill Campus Coventry CV4 7AL UK.

出版信息

Adv Genet (Hoboken). 2022 Mar 20;3(3):2100064. doi: 10.1002/ggn2.202100064. eCollection 2022 Sep.

DOI:10.1002/ggn2.202100064
PMID:36620196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9744488/
Abstract

Parental RNA interference (pRNAi) is a powerful and widely used method for gene-specific knockdown. Yet in insects its efficacy varies between species, and how the systemic response is transmitted from mother to offspring remains elusive. Using the beetle , an RT-qPCR strategy to distinguish the presence of double-stranded RNA (dsRNA) from endogenous mRNA is reported. It is found that injected dsRNA is directly transmitted into the egg and persists throughout embryogenesis. Despite this depletion of dsRNA from the mother, it is shown that strong pRNAi can persist for months before waning at strain-specific rates. In seeking the receptor proteins for cellular uptake of long dsRNA into the egg, a phylogenomics profiling approach of candidate proteins is also presented. A visualization strategy based on taxonomically hierarchical assessment of orthology clustering data to rapidly assess gene age and copy number changes, refined by sequence-based evidence, is demonstrated. Repeated losses of SID-1-like channel proteins in the arthropods, including wholesale loss in the Heteroptera (true bugs), which are nonetheless highly sensitive to pRNAi, are thereby documented. Overall, practical considerations for insect pRNAi against a backdrop of outstanding questions on the molecular mechanism of dsRNA transmission for long-term, systemic knockdown are elucidated.

摘要

亲代RNA干扰(pRNAi)是一种强大且广泛应用的基因特异性敲低方法。然而在昆虫中,其效果因物种而异,并且系统性反应如何从母体传递给后代仍不清楚。利用甲虫,报道了一种通过RT-qPCR策略来区分双链RNA(dsRNA)与内源性mRNA的方法。研究发现,注射的dsRNA直接进入卵中,并在整个胚胎发育过程中持续存在。尽管母体中的dsRNA会减少,但研究表明,强烈的pRNAi可以持续数月,然后以菌株特异性速率减弱。在寻找长dsRNA细胞摄取进入卵中的受体蛋白时,还提出了一种候选蛋白的系统发育组学分析方法。展示了一种基于直系同源聚类数据分类层次评估的可视化策略,用于快速评估基因年龄和拷贝数变化,并通过基于序列的证据进行完善。由此记录了节肢动物中SID-1样通道蛋白的反复丢失,包括异翅亚目(真蝽)中的完全丢失,而这些昆虫对pRNAi却高度敏感。总体而言,在关于dsRNA长期系统性敲低的分子机制存在诸多突出问题的背景下,阐明了昆虫pRNAi的实际考虑因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c828/9744488/483946c782d9/GGN2-3-2100064-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c828/9744488/42fa4dfe8b28/GGN2-3-2100064-g004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c828/9744488/722c93d35fab/GGN2-3-2100064-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c828/9744488/c84b96e858e6/GGN2-3-2100064-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c828/9744488/483946c782d9/GGN2-3-2100064-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c828/9744488/42fa4dfe8b28/GGN2-3-2100064-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c828/9744488/2a465a37a2e8/GGN2-3-2100064-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c828/9744488/699306e02571/GGN2-3-2100064-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c828/9744488/388a8f92b3d2/GGN2-3-2100064-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c828/9744488/722c93d35fab/GGN2-3-2100064-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c828/9744488/c84b96e858e6/GGN2-3-2100064-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c828/9744488/483946c782d9/GGN2-3-2100064-g007.jpg

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