HSP gene superfamily in Aspongopus chinensis Dallas: unravelling identification, characterisation and expression patterns during diapause and non-diapause stages.

IF 1.6 3区 农林科学 Q2 ENTOMOLOGY Bulletin of Entomological Research Pub Date : 2024-04-01 Epub Date: 2024-03-01 DOI:10.1017/S0007485324000075
Xinyi Ma, Zhiyong Yin, Haiyin Li, Jianjun Guo
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Abstract

Aspongopus chinensis Dallas 1851, an insect of important economic value, faces challenges in artificial breeding due to mandatory diapause and limited access to wild resources. Heat shock proteins (Hsps) are thought to influence diapause in insects, but little is known about their role in A. chinensis during diapause. This study used genomic methods to identify 25 Hsp genes in A. chinensis, including two Hsp90, 14 Hsp70, four Hsp60 and five small Hsp genes, were located on seven chromosomes, respectively. The gene structures among the same families are relatively conserved. Meanwhile, the motif compositions and secondary structures of A. chinensis Hsps (AcHsps) were predicted. RNA-seq data and fluorescence quantitative PCR analysis showed that there were differences in the expression patterns of AcHsps in diapause and non-diapause stages, and AcHsp70-5 was significantly differentially expressed in both analysis, which was enriched in the pathway of response to hormone. All the results showed that Hsps play an important role in the diapause mechanism of A. chinensis. Our observations highlight the molecular evolution of the Hsp gene and their effect on diapause in A. chinensis.

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金龙鱼中的HSP基因超家族▄■▓:揭示休眠期和非休眠期的识别、特征和表达模式。
Aspongopus chinensis Dallas 1851 是一种具有重要经济价值的昆虫,由于强制休眠和野生资源有限,其人工繁育面临挑战。热休克蛋白(Hsps)被认为会影响昆虫的休眠,但人们对其在秦艽休眠期的作用知之甚少。本研究利用基因组学方法鉴定了25个Hsp基因,包括2个Hsp90、14个Hsp70、4个Hsp60和5个小Hsp基因,分别位于7条染色体上。同一家族的基因结构相对保守。同时,预测了A. chinensis Hsps(AcHsps)的基序组成和二级结构。RNA-seq数据和荧光定量PCR分析表明,AcHps在休眠期和非休眠期的表达模式存在差异,AcHsp70-5在两种分析中均有显著差异表达,且富集在对激素的响应通路中。所有这些结果都表明,Hsps在中秋菊的休眠机制中起着重要作用。我们的观察结果突显了Hsp基因的分子进化及其对秦艽休眠的影响。
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来源期刊
CiteScore
4.00
自引率
0.00%
发文量
160
审稿时长
6-12 weeks
期刊介绍: Established in 1910, the internationally recognised Bulletin of Entomological Research aims to further global knowledge of entomology through the generalisation of research findings rather than providing more entomological exceptions. The Bulletin publishes high quality and original research papers, ''critiques'' and review articles concerning insects or other arthropods of economic importance in agriculture, forestry, stored products, biological control, medicine, animal health and natural resource management. The scope of papers addresses the biology, ecology, behaviour, physiology and systematics of individuals and populations, with a particular emphasis upon the major current and emerging pests of agriculture, horticulture and forestry, and vectors of human and animal diseases. This includes the interactions between species (plants, hosts for parasites, natural enemies and whole communities), novel methodological developments, including molecular biology, in an applied context. The Bulletin does not publish the results of pesticide testing or traditional taxonomic revisions.
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