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日本赤松(Pinus densiflora)cDNA文库的从头转录组测序分析及大规模单基因组装

De Novo Transcriptome Sequencing Analysis of cDNA Library and Large-Scale Unigene Assembly in Japanese Red Pine (Pinus densiflora).

作者信息

Liu Le, Zhang Shijie, Lian Chunlan

机构信息

Asian Natural Environmental Science Center, The University of Tokyo, Midori-cho 1-1-8, Nishi Tokyo, Tokyo 188-0002, Japan.

出版信息

Int J Mol Sci. 2015 Dec 4;16(12):29047-59. doi: 10.3390/ijms161226139.

Abstract

Japanese red pine (Pinus densiflora) is extensively cultivated in Japan, Korea, China, and Russia and is harvested for timber, pulpwood, garden, and paper markets. However, genetic information and molecular markers were very scarce for this species. In this study, over 51 million sequencing clean reads from P. densiflora mRNA were produced using Illumina paired-end sequencing technology. It yielded 83,913 unigenes with a mean length of 751 bp, of which 54,530 (64.98%) unigenes showed similarity to sequences in the NCBI database. Among which the best matches in the NCBI Nr database were Picea sitchensis (41.60%), Amborella trichopoda (9.83%), and Pinus taeda (4.15%). A total of 1953 putative microsatellites were identified in 1784 unigenes using MISA (MicroSAtellite) software, of which the tri-nucleotide repeats were most abundant (50.18%) and 629 EST-SSR (expressed sequence tag- simple sequence repeats) primer pairs were successfully designed. Among 20 EST-SSR primer pairs randomly chosen, 17 markers yielded amplification products of the expected size in P. densiflora. Our results will provide a valuable resource for gene-function analysis, germplasm identification, molecular marker-assisted breeding and resistance-related gene(s) mapping for pine for P. densiflora.

摘要

日本赤松(Pinus densiflora)在日本、韩国、中国和俄罗斯广泛种植,其木材、纸浆材、园林和造纸市场都有采伐需求。然而,该物种的遗传信息和分子标记非常稀少。在本研究中,利用Illumina双末端测序技术从日本赤松mRNA中产生了超过5100万个测序纯净读段。共获得83,913个单基因,平均长度为751 bp,其中54,530个(64.98%)单基因与NCBI数据库中的序列相似。其中在NCBI Nr数据库中最佳匹配的是西加云杉(Picea sitchensis,41.60%)、无油樟(Amborella trichopoda,9.83%)和火炬松(Pinus taeda,4.15%)。使用MISA(微卫星)软件在1784个单基因中总共鉴定出1953个假定微卫星,其中三核苷酸重复最为丰富(50.18%),并成功设计了629对EST-SSR(表达序列标签-简单序列重复)引物对。在随机选择的20对EST-SSR引物对中,有17个标记在日本赤松中产生了预期大小的扩增产物。我们的结果将为日本赤松的基因功能分析、种质鉴定、分子标记辅助育种以及松树抗性相关基因定位提供宝贵资源。

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