Suppr超能文献

基于 30K 基因芯片的平行多态性发现对辣椒遗传多样性和群体结构的分析

Characterization of Capsicum annuum genetic diversity and population structure based on parallel polymorphism discovery with a 30K unigene Pepper GeneChip.

机构信息

Seed Biotechnology Center, University of California Davis, Davis, California, United States of America.

出版信息

PLoS One. 2013;8(2):e56200. doi: 10.1371/journal.pone.0056200. Epub 2013 Feb 8.

Abstract

The widely cultivated pepper, Capsicum spp., important as a vegetable and spice crop world-wide, is one of the most diverse crops. To enhance breeding programs, a detailed characterization of Capsicum diversity including morphological, geographical and molecular data is required. Currently, molecular data characterizing Capsicum genetic diversity is limited. The development and application of high-throughput genome-wide markers in Capsicum will facilitate more detailed molecular characterization of germplasm collections, genetic relationships, and the generation of ultra-high density maps. We have developed the Pepper GeneChip® array from Affymetrix for polymorphism detection and expression analysis in Capsicum. Probes on the array were designed from 30,815 unigenes assembled from expressed sequence tags (ESTs). Our array design provides a maximum redundancy of 13 probes per base pair position allowing integration of multiple hybridization values per position to detect single position polymorphism (SPP). Hybridization of genomic DNA from 40 diverse C. annuum lines, used in breeding and research programs, and a representative from three additional cultivated species (C. frutescens, C. chinense and C. pubescens) detected 33,401 SPP markers within 13,323 unigenes. Among the C. annuum lines, 6,426 SPPs covering 3,818 unigenes were identified. An estimated three-fold reduction in diversity was detected in non-pungent compared with pungent lines, however, we were able to detect 251 highly informative markers across these C. annuum lines. In addition, an 8.7 cM region without polymorphism was detected around Pun1 in non-pungent C. annuum. An analysis of genetic relatedness and diversity using the software Structure revealed clustering of the germplasm which was confirmed with statistical support by principle components analysis (PCA) and phylogenetic analysis. This research demonstrates the effectiveness of parallel high-throughput discovery and application of genome-wide transcript-based markers to assess genetic and genomic features among Capsicum annuum.

摘要

广泛种植的辣椒,Capsicum spp.,作为一种蔬菜和香料作物在全球范围内都很重要,是最具多样性的作物之一。为了增强育种计划,需要对辣椒多样性进行详细的描述,包括形态学、地理和分子数据。目前,用于描述辣椒遗传多样性的分子数据有限。在辣椒中开发和应用高通量全基因组标记将有助于更详细地描述种质资源收集、遗传关系和生成超高密度图谱。我们已经从 Affymetrix 开发了用于辣椒多态性检测和表达分析的 Pepper GeneChip®阵列。该阵列上的探针是根据从表达序列标签 (EST) 组装的 30,815 个单基因设计的。我们的阵列设计提供了每个碱基位置最大 13 个探针的最大冗余度,允许每个位置的多个杂交值进行集成,以检测单个位置多态性 (SPP)。用来自 40 个不同的 C. annuum 品系的基因组 DNA 杂交,这些品系用于育种和研究计划,以及来自另外三个栽培种(C. frutescens、C. chinense 和 C. pubescens)的一个代表,在 13,323 个单基因中检测到 33,401 个 SPP 标记。在 C. annuum 品系中,鉴定了 3,818 个单基因中的 6,426 个 SPP。与辛辣品种相比,非辛辣品种的多样性估计降低了三倍,但我们能够在这些 C. annuum 品系中检测到 251 个高度信息丰富的标记。此外,在非辛辣的 C. annuum 中,在 Pun1 周围检测到一个没有多态性的 8.7 cM 区域。使用 Structure 软件进行的遗传关系和多样性分析显示,种质资源聚类,主成分分析 (PCA) 和系统发育分析的统计支持证实了这一点。这项研究证明了平行高通量发现和应用基于全基因组转录本标记来评估 Capsicum annuum 遗传和基因组特征的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3282/3568043/3e46eb462e86/pone.0056200.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