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柚的从头转录组组装与分子标记开发

De novo transcriptome assembly of pummelo and molecular marker development.

作者信息

Liang Mei, Yang Xiaoming, Li Hang, Su Shiying, Yi Hualin, Chai Lijun, Deng Xiuxin

机构信息

Key Laboratory of Horticultural Plant Biology, Ministry of Education, Key Laboratory of Horticultural Crop Biology and Genetic improvement (Central Region), MOA, Huazhong Agricultural University, Wuhan, Hubei, 430070, China.

出版信息

PLoS One. 2015 Mar 23;10(3):e0120615. doi: 10.1371/journal.pone.0120615. eCollection 2015.

Abstract

Pummelo (Citrus grandis) is an important fruit crop worldwide because of its nutritional value. To accelerate the pummelo breeding program, it is essential to obtain extensive genetic information and develop relative molecular markers. Here, we obtained a 12-Gb transcriptome dataset of pummelo through a mixture of RNA from seven tissues using Illumina pair-end sequencing, assembled into 57,212 unigenes with an average length of 1010 bp. The annotation and classification results showed that a total of 39,584 unigenes had similar hits to the known proteins of four public databases, and 31,501 were classified into 55 Gene Ontology (GO) functional sub-categories. The search for putative molecular markers among 57,212 unigenes identified 10,276 simple sequence repeats (SSRs) and 64,720 single nucleotide polymorphisms (SNPs). High-quality primers of 1174 SSR loci were designed, of which 88.16% were localized to nine chromosomes of sweet orange. Of 100 SSR primers that were randomly selected for testing, 87 successfully amplified clear banding patterns. Of these primers, 29 with a mean PIC (polymorphic information content) value of 0.52 were effectively applied for phylogenetic analysis. Of the 20 SNP primers, 14 primers, including 54 potential SNPs, yielded target amplifications, and 46 loci were verified via Sanger sequencing. This new dataset will be a valuable resource for molecular biology studies of pummelo and provides reliable information regarding SNP and SSR marker development, thus expediting the breeding program of pummelo.

摘要

柚子(Citrus grandis)因其营养价值而成为全球重要的水果作物。为加速柚子育种计划,获取广泛的遗传信息并开发相关分子标记至关重要。在此,我们通过对来自七个组织的RNA混合物进行Illumina双末端测序,获得了一个12-Gb的柚子转录组数据集,组装成57,212个单基因,平均长度为1010 bp。注释和分类结果表明,共有39,584个单基因与四个公共数据库中的已知蛋白质有相似匹配,31,501个被分类到55个基因本体(GO)功能亚类中。在57,212个单基因中搜索假定的分子标记,鉴定出10,276个简单序列重复(SSR)和64,720个单核苷酸多态性(SNP)。设计了1174个SSR位点的高质量引物,其中88.16%定位到甜橙的九条染色体上。随机选择100个SSR引物进行测试,87个成功扩增出清晰的条带模式。其中,29个平均多态信息含量(PIC)值为0.52的引物有效地用于系统发育分析。在20个SNP引物中,14个引物(包括54个潜在SNP)产生了目标扩增,46个位点通过Sanger测序得到验证。这个新数据集将成为柚子分子生物学研究的宝贵资源,并为SNP和SSR标记开发提供可靠信息,从而加速柚子的育种计划。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/563d/4370633/7bdf63119d63/pone.0120615.g001.jpg

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