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

Jinmo Koo, S. R. Palli
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引用次数: 2

Abstract

RNA interference (RNAi) is inefficient in lepidopteran insects, including Spodoptera frugiperda. 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 S. frugiperda 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.
dsRNase1对Sf9细胞条件培养基中dsRNA降解活性的贡献
RNA干扰(RNAi)在鳞翅目昆虫中是低效的。众所周知,在这些昆虫中,管腔和血液中的RNAi活性导致了低RNAi效率。从frugiperda子房发育的Sf9细胞中提取的条件培养基显示出较高的dsRNA降解活性。但是负责这种活性的酶还没有被确定。鉴定出在Sf9细胞中高表达的核酸酶基因REase、RNaseT2和dsRNase1。Sf9细胞中dsRNase1的敲低导致Sf9细胞条件培养基中dsRNA降解活性降低。dsRNase1的敲低也提高了Sf9细胞的RNAi效率。这些研究的结果确定了Sf9细胞条件培养基中dsRNA降解活性的主要参与者。我们还描述了一个有效的系统,可用于鉴定Sf9细胞中负责dsRNA降解和RNAi效率的其他基因。
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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