Suppr超能文献

利用抑制性消减杂交技术鉴定抗性香蕉种质‘加尔各答-4’中响应香蕉黑叶条斑病菌的差异表达基因

Identification of Differentially-Expressed Genes in Response to Mycosphaerella fijiensis in the Resistant Musa Accession 'Calcutta-4' Using Suppression Subtractive Hybridization.

作者信息

Sánchez Timm Eduardo, Hidalgo Pardo Lisette, Pacheco Coello Ricardo, Chávez Navarrete Tatiana, Navarrete Villegas Oscar, Santos Ordóñez Efrén

机构信息

Escuela Superior Politécnica del Litoral, ESPOL, Centro de Investigaciones Biotecnológicas del Ecuador, Campus Gustavo Galindo Km 30.5 Vía Perimetral, P.O. Box 09-01-5863, Guayaquil, Ecuador.

Escuela Superior Politécnica del Litoral, ESPOL, Facultad de Ciencias de la Vida, Campus Gustavo Galindo Km 30.5 Vía Perimetral, P.O. Box 09-01-5863, Guayaquil, Ecuador.

出版信息

PLoS One. 2016 Aug 3;11(8):e0160083. doi: 10.1371/journal.pone.0160083. eCollection 2016.

Abstract

Bananas and plantains are considered an important crop around the world. Banana production is affected by several constraints, of which Black Sigatoka Disease, caused by the fungus Mycosphaerella fijiensis, is considered one of the most important diseases in banana plantations. The banana accession 'Calcutta-4' has a natural resistance to Black Sigatoka; however, the fruit is not valuable for commercialization. Gene identification and expression studies in 'Calcutta-4' might reveal possible gene candidates for resistant to the disease and elucidate mechanisms for resistance. A subtracted cDNA library was generated from leaves after 6, 9 and 12 days inoculated with M. fijiensis conidia on greenhouse banana plants of the accession 'Calcutta-4'. Bioinformatic analysis revealed 99 good quality sequences. Blast2go analysis revealed that 31% of the sequences could not be categorized and, according to the Biological Process Category, 32 and 28 ESTs are related to general metabolic and cellular processes, respectively; while 10 ESTs response to stimulus. Seven sequences were redundant and one was similar to genes that may be involved in pathogen resistance including the putative disease resistance protein RGA1. Genes encoding zinc finger domains were identified and may play an important role in pathogen resistance by inducing the expression of downstream genes. Expression analysis of four selected genes was performed using RT-qPCR during the early stage of the disease development at 6, 9, 12 and 15 days post inoculation showing a peak of up regulation at 9 or 12 days post inoculation. Three of the four genes showed an up-regulation of expression in 'Calcutta-4' when compared to 'Williams' after inoculation with M. fijiensis, suggesting a fine regulation of specific gene candidates that may lead to a resistance response. The genes identified in early responses in a plant-pathogen interaction may be relevant for the resistance response of 'Calcutta-4' to Black Sigatoka. Genes with different functions may play a role in plant response to the disease. The present study suggests a fine up regulation of these genes that might be needed to perform an incompatible interaction. Further gene functional studies need to be performed to validate their use as candidate resistance genes in susceptible banana cultivars.

摘要

香蕉和大蕉被认为是全球一种重要的作物。香蕉生产受到多种限制因素的影响,其中由斐济球腔菌引起的香蕉黑叶斑病被认为是香蕉种植园中最重要的病害之一。香蕉品种“加尔各答 - 4”对香蕉黑叶斑病具有天然抗性;然而,其果实对于商业化来说没有价值。对“加尔各答 - 4”进行基因鉴定和表达研究可能会揭示出对该病具有抗性的潜在基因候选物,并阐明抗性机制。在温室中,对接种了斐济球腔菌分生孢子6天、9天和12天后的“加尔各答 - 4”香蕉植株的叶片构建了一个扣除cDNA文库。生物信息学分析揭示了99条高质量序列。Blast2go分析表明,31%的序列无法分类,根据生物过程类别,分别有32条和28条EST与一般代谢和细胞过程相关;而有10条EST对刺激有反应。7条序列是冗余的,1条与可能参与病原体抗性的基因相似,包括假定的抗病蛋白RGA1。鉴定出了编码锌指结构域的基因,它们可能通过诱导下游基因的表达在病原体抗性中发挥重要作用。在接种后6天、9天、12天和15天疾病发展的早期阶段,使用RT - qPCR对四个选定基因进行表达分析,结果显示在接种后9天或12天出现上调峰值。与接种斐济球腔菌后的“威廉姆斯”相比,这四个基因中的三个在“加尔各答 - 4”中表现出表达上调,表明特定基因候选物的精细调控可能导致抗性反应。在植物 - 病原体相互作用早期反应中鉴定出的这些基因可能与“加尔各答 - 4”对香蕉黑叶斑病的抗性反应相关。具有不同功能的基因可能在植物对该病的反应中发挥作用。本研究表明可能需要对这些基因进行精细上调,以实现不亲和相互作用。需要进一步进行基因功能研究,以验证它们作为易感香蕉品种抗性候选基因的用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ba/4972352/331893c105b9/pone.0160083.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验