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利用从头转录组组装开发 SSR 标记在 (Thunb.)Koidz. 中

Development of SSR markers via de novo transcriptome assembly in (Thunb.) Koidz.

机构信息

Institute of Bast Fiber Crops, Chinese Academy of Agricultural Sciences/Key Laboratory of Stem-Fiber Biomass and Engineering Microbiology, Ministry of Agriculture, Changsha 410205, P.R. China.

Jiangxi Academy of Forestry of China, Nanchang 330033, P.R. China.

出版信息

Genome. 2019 Dec;62(12):817-831. doi: 10.1139/gen-2019-0068. Epub 2019 Sep 6.

Abstract

Owing to its high nutritive, economic, and medicinal values, has received increased attention, making worthy of being used as a new fruit crop for further domestication and commercialization in China. However, molecular research of has lagged as investigations of its genomic resources and molecular markers are rare. In this study, a cDNA library of leaves was sequenced using the Illumina NovaSeq. 6000 sequencing system. In total, 101 417 transcripts, 63 757 unigenes, and 9494 simple sequence repeats were assembled and identified from the transcriptome datasets. The majority of the SSRs were di- and trinucleotide repeats. Length and number of SSR motifs ranged from 15 to 66, and 5 to 48 bp, respectively. Of which, the A/T mononucleotide motif and AG/TC and CT/GA dinucleotide motifs were the most abundant. Furthermore, 100 SSR primers were randomly selected to validate amplification and polymorphism, and 88 accessions were definitively distinguished by 49 primers. With the Qinling mountains and Huaihe River line as the boundaries, the northern and southern accessions were clustered into different groups, but no clear geographical patterns (city or origin) were observed in the southern accessions. These newly identified molecular markers may provide a foundation for the genetic identification and diversity analysis and marker-assisted selection breeding in species of .

摘要

由于其具有较高的营养价值、经济价值和药用价值,受到了越来越多的关注,有望成为中国进一步驯化和商业化的新型水果作物。然而, 的分子研究相对滞后,对其基因组资源和分子标记的研究很少。本研究利用 Illumina NovaSeq. 6000 测序系统对 叶片 cDNA 文库进行了测序。从转录组数据集中共组装和鉴定了 101417 条转录本、63757 条 unigenes 和 9494 个简单序列重复。大多数 SSR 是二核苷酸和三核苷酸重复。SSR 基元的长度和数量范围分别为 15-66bp 和 5-48bp,其中 A/T 单核苷酸基元以及 AG/TC 和 CT/GA 二核苷酸基元最为丰富。此外,随机选择了 100 个 SSR 引物进行扩增和多态性验证,其中 49 个引物可明确区分 88 个品种。以秦岭-淮河线为界,北方和南方品种聚为不同的组,但南方品种没有明显的地理模式(城市或起源)。这些新鉴定的分子标记可为 种的遗传鉴定、多样性分析和标记辅助选择育种提供基础。

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