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dsRNase1对Sf9细胞条件培养基中dsRNA降解活性的贡献。

dsRNase1 contribution to dsRNA degradation activity in the Sf9 cells conditioned medium.

作者信息

Koo Jinmo, Palli Subba Reddy

机构信息

Department of Entomology, College of Agriculture, University of Kentucky, Lexington, KY, United States.

出版信息

Front Insect Sci. 2023 Jan 24;3:1118775. doi: 10.3389/finsc.2023.1118775. eCollection 2023.

Abstract

RNA interference (RNAi) is inefficient in lepidopteran insects, including . RNase activity in the lumen and hemocoel is known to contribute to low RNAi efficiency in these insects. Conditioned medium from Sf9 cells developed from ovaries of shows high dsRNA degradation activity. But the enzymes responsible for this activity have not been identified. The nuclease genes that are highly expressed in Sf9 cells, REase, RNaseT2, and dsRNase1, were identified. Knockdown of dsRNase1 in Sf9 cells resulted in a reduction of dsRNA degradation activity in the Sf9 cells conditioned medium. Knockdown of dsRNase1 also increased RNAi efficiency in Sf9 cells. The results from these studies identified a major player in dsRNA degradation activity in the Sf9 cells conditioned medium. We also describe an efficient system that can be used to identify other genes responsible for dsRNA degradation and RNAi efficiency in Sf9 cells.

摘要

RNA干扰(RNAi)在包括鳞翅目昆虫在内的昆虫中效率低下。已知中肠腔和血腔中的核糖核酸酶活性会导致这些昆虫的RNAi效率低下。从卵巢发育而来的Sf9细胞的条件培养基显示出高双链RNA降解活性。但负责这种活性的酶尚未确定。已鉴定出在Sf9细胞中高表达的核酸酶基因,即REase、RNaseT2和dsRNase1。在Sf9细胞中敲低dsRNase1导致Sf9细胞条件培养基中双链RNA降解活性降低。敲低dsRNase1也提高了Sf9细胞中的RNAi效率。这些研究结果确定了Sf9细胞条件培养基中双链RNA降解活性的一个主要作用因子。我们还描述了一个高效的系统,可用于鉴定Sf9细胞中其他负责双链RNA降解和RNAi效率的基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca1a/10926405/e31d4f09fbd7/finsc-03-1118775-g001.jpg

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