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Transcriptomic and proteomic analysis of Locusta migratoria eggs at different embryonic stages: Comparison for diapause and nondiapause regimes

机译:早熟禾卵在不同胚胎阶段的转录组学和蛋白质组学分析:滞育和非滞育方案的比较

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摘要

Temperate-zone insects typically survive winter by entering diapause.Although many aspects of insect diapause have been studied,the underlying molecular mechanism of insect diapause is not well understood.Here we report the results of the transcriptional and translational differences of migratory locust eggs at different emb~onic states using diapause (low temperature) and non-diapause (high temperature) regimes.Compared with non-diapause eggs at 100 degree-days (N2) treatment,29 671 transcripts and 296 proteins were differentially expressed at the diapause maintenance stage (D2).While compared with 150 degree-days (N3) treatment,45 922 transcripts and 404 proteins were differentially expressed in the post-diapause stage (D3).Among them,51 and 102 transcripts had concurrent transcription and translation profiles in D2 vs.N2 and D3 vs.N3 treatments,respectively.Analysis of Gene Ontology categorized these genes and proteins into three categories:biological processes,cellular components,and molecular functions.Biological pathway analysis indicated that three pathways:(1) insect hormone biosynthesis (KEGG:Map 00981),(2) the insulin signaling pathway (KEGG:Map 04910),and (3) the peroxisome proliferator-activated receptor (PPAR) signaling pathway (KEGG:Map 03320) play an important role in locust diapause regulation.Most of these transcripts and proteins were up-regulated in the diapause treatments,and were highly linked to juvenile hormone biosynthesis,insulin and PPAR signaling pathways,suggesting these three pathways may be involved in diapause and development regulation.This study demonstrates the applicability of high-throughput omics tools to identify biochemical pathways linked to diapause in locust egg development.In addition,it reveals that cellular metabolism in diapause eggs is more inactive than in non-diapause eggs,and most of the down-regulated enzymes and pathways are related to reduce energy loss.
机译:温带区昆虫通常通过进入滞育期而在冬季生存。尽管已经研究了昆虫滞育的许多方面,但对昆虫滞育的潜在分子机制尚不十分了解。在此,我们报道了不同蝗虫卵在转录和翻译方面的差异。使用滞育(低温)和非滞育(高温)模式的胚胎状态。与滞育100天(N2)下的非滞育卵相比,在滞育维持阶段差异表达了29671个转录本和296种蛋白质。 (D2)。与150度-日(N3)处理相比,在滞后后阶段(D3)有45 922个转录物和404蛋白差异表达。其中,D2中有51和102个转录物同时具有转录和翻译谱。分别比较N2和D3与N3的治疗。对基因本体的分析将这些基因和蛋白质分为三类:生物学过程,细胞成分,生物途径分析表明,存在以下三种途径:(1)昆虫激素的生物合成(KEGG:Map 00981),(2)胰岛素信号传导途径(KEGG:Map 04910)和(3)过氧化物酶体增殖物激活受体( PPAR)信号传导途径(KEGG:Map 03320)在蝗虫滞育调节中起着重要作用。在滞育过程中,大多数这些转录物和蛋白质均被上调,并且与幼年激素的生物合成,胰岛素和PPAR信号传导通路密切相关。这三个途径可能与滞育和发育调节有关。本研究表明高通量组学工具可用于鉴定与蝗虫卵滞育有关的生化途径。此外,它还表明滞育卵中的细胞代谢比无滞育卵更具活性。在无糖鸡蛋中,大多数被下调的酶和途径都与减少能量损失有关。

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  • 来源
    《农业科学学报(英文版)》 |2017年第8期|1777-1788|共12页
  • 作者单位

    State Key Laboratory for Biology of Plant Diseases and Insect Pests,Institute of Plant Protection,Chinese Academy of Agricultural Sciences,Beijing 100193,P.R.China;

    State Key Laboratory for Biology of Plant Diseases and Insect Pests,Institute of Plant Protection,Chinese Academy of Agricultural Sciences,Beijing 100193,P.R.China;

    State Key Laboratory for Biology of Plant Diseases and Insect Pests,Institute of Plant Protection,Chinese Academy of Agricultural Sciences,Beijing 100193,P.R.China;

    School of Biological Sciences,Illinois State University,Illinois 61761,USA;

    State Key Laboratory for Biology of Plant Diseases and Insect Pests,Institute of Plant Protection,Chinese Academy of Agricultural Sciences,Beijing 100193,P.R.China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 00:24:01
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