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Transcriptome analysis of Gossypium hirsutum flower buds infested by cotton boll weevil (Anthonomus grandis) larvae

机译:棉铃象鼻虫(Anthonomus grandis)幼虫侵染的陆地棉花蕾的转录组分析

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摘要

Background Cotton is a major fibre crop grown worldwide that suffers extensive damage from chewing insects, including the cotton boll weevil larvae (Anthonomus grandis). Transcriptome analysis was performed to understand the molecular interactions between Gossypium hirsutum L. and cotton boll weevil larvae. The Illumina HiSeq 2000 platform was used to sequence the transcriptome of cotton flower buds infested with boll weevil larvae. Results The analysis generated a total of 327,489,418 sequence reads that were aligned to the G. hirsutum reference transcriptome. The total number of expressed genes was over 21,697 per sample with an average length of 1,063 bp. The DEGseq analysis identified 443 differentially expressed genes (DEG) in cotton flower buds infected with boll weevil larvae. Among them, 402 (90.7%) were up-regulated, 41 (9.3%) were down-regulated and 432 (97.5%) were identified as orthologues of A. thaliana genes using Blastx. Mapman analysis of DEG indicated that many genes were involved in the biotic stress response spanning a range of functions, from a gene encoding a receptor-like kinase to genes involved in triggering defensive responses such as MAPK, transcription factors (WRKY and ERF) and signalling by ethylene (ET) and jasmonic acid (JA) hormones. Furthermore, the spatial expression pattern of 32 of the genes responsive to boll weevil larvae feeding was determined by “in situ” qPCR analysis from RNA isolated from two flower structures, the stamen and the carpel, by laser microdissection (LMD). Conclusion A large number of cotton transcripts were significantly altered upon infestation by larvae. Among the changes in gene expression, we highlighted the transcription of receptors/sensors that recognise chitin or insect oral secretions; the altered regulation of transcripts encoding enzymes related to kinase cascades, transcription factors, Ca2+ influxes, and reactive oxygen species; and the modulation of transcripts encoding enzymes from phytohormone signalling pathways. These data will aid in the selection of target genes to genetically engineer cotton to control the cotton boll weevil.
机译:背景技术棉花是世界范围内种植的主要纤维作物,其遭受咀嚼昆虫(包括棉铃象鼻虫幼虫(Anthonomus grandis))的广泛破坏。进行了转录组分析以了解陆地棉和棉铃象鼻虫幼虫之间的分子相互作用。 Illumina HiSeq 2000平台用于对棉铃象鼻虫幼虫侵染的棉花花蕾的转录组进行测序。结果该分析产生了总计327,489,418条序列读数,这些读数与G. hirsutum参考转录组对齐。每个样品中表达的基因总数超过21,697,平均长度为1,063 bp。 DEGseq分析在感染了铃象鼻虫幼虫的棉花花蕾中鉴定出443个差异表达基因(DEG)。其中,使用Blastx鉴定出402个(90.7%)上调,41个(9.3%)下调并且432个(97.5%)被鉴定为拟南芥基因的直向同源物。 Mapman对DEG的分析表明,许多基因都参与了生物应激反应,涉及多种功能,从编码受体样激酶的基因到涉及触发防御反应的基因,例如MAPK,转录因子(WRKY和ERF)和信号转导。由乙烯(ET)和茉莉酸(JA)激素组成。此外,通过“原位” qPCR分析,通过激光显微切割(LMD)从从两个花结构(雄蕊和心皮)中分离的RNA进行“原位” qPCR分析,确定了对铃象鼻虫幼虫摄食有响应的32个基因的空间表达模式。结论幼虫侵染后大量棉花转录本发生明显变化。在基因表达的变化中,我们强调了识别几丁质或昆虫口腔分泌物的受体/传感器的转录;编码与激酶级联反应,转录因子,Ca2 +涌入和活性氧有关的酶的转录物的调控改变;以及编码来自植物激素信号通路的酶的转录物的调控。这些数据将有助于选择靶基因以对棉花进行基因工程改造,从而控制棉铃象鼻虫。

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