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鉴定和验证二化螟有效 dsRNA 敲低分析的潜在内参基因。

Identification and validation of potential reference gene for effective dsRNA knockdown analysis in Chilo partellus.

机构信息

Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, 53700, Pakistan.

SAHARA Medical College, Narowal, Pakistan.

出版信息

Sci Rep. 2019 Sep 20;9(1):13629. doi: 10.1038/s41598-019-49810-w.

Abstract

Chilo partellus is an invasive polyphagous pest that has not been effectively managed with chemical pesticides. To select potential dsRNAs for use in an alternate control strategy, it is crucial to identify and evaluate stable reference genes for knockdown expression studies. This study evaluates the expression stability of seven candidate reference genes in C. partellus larvae fed on crude bacterially-expressed dsRNAs and purified dsRNAs at different time intervals, as well as the developmental stages and sexes. The expression stabilities of the reference genes were evaluated with different software programmes, such as BestKeeper, NormFinder, deltaCt, geNorm, and RefFinder. The overall results rank ELF as the most stably expressed reference gene when larvae were fed with crude bacteria-induced dsRNAs and purified dsRNA. However, Tubulin and HSP70 were more stable under different developmental stages and sexes. The expression levels of larvae that were fed crude bacteria-induced dsRNAs of Chitinase and Acetylcholinesterase were normalized with the four most stable reference genes (ELF, HSP70, V-ATPase and Tubulin) and the least stable reference gene (18S and HSP70) based on the geNorm algorithm. The least stable reference gene showed inconsistent knockdown expression, thereby confirming that the validation of a suitable reference gene is crucial to improve assay accuracy for dsRNA-targeted gene selection in C. partellus.

摘要

球孢白僵菌是一种具有广泛食性的入侵性害虫,目前尚未能通过化学农药进行有效防治。为了选择可能用于替代控制策略的潜在 dsRNA,鉴定和评估用于基因敲低表达研究的稳定内参基因至关重要。本研究评估了 7 种候选内参基因在取食粗菌诱导的 dsRNA 和纯化 dsRNA 的球孢白僵菌幼虫不同时间点,以及不同发育阶段和性别的表达稳定性。使用不同的软件程序,如 BestKeeper、NormFinder、deltaCt、geNorm 和 RefFinder,评估了参考基因的表达稳定性。总体结果表明,当幼虫取食粗菌诱导的 dsRNA 和纯化 dsRNA 时,ELF 是最稳定表达的参考基因。然而,在不同的发育阶段和性别下,Tubulin 和 HSP70 更为稳定。基于 geNorm 算法,用最稳定的 4 个参考基因(ELF、HSP70、V-ATPase 和 Tubulin)和最不稳定的参考基因(18S 和 HSP70)对取食几丁质酶和乙酰胆碱酯酶粗菌诱导 dsRNA 的幼虫进行归一化,最不稳定的参考基因显示出不一致的敲低表达,从而证实了验证合适的参考基因对于提高 dsRNA 靶向基因选择在球孢白僵菌中的实验准确性至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed31/6754392/85c08ab6ef96/41598_2019_49810_Fig1_HTML.jpg

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