4.7 Article

De novo Transcriptome Analysis and Molecular Marker Development of Two Hemarthria Species

期刊

FRONTIERS IN PLANT SCIENCE
卷 7, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fpls.2016.00496

关键词

de novo assembly; marker development; Hemarthria R. Br.; RNA-Seq; transcriptome

资金

  1. National Basic Research Program of China (973 Program) [2014CB138705]
  2. Strategic Planning and Management Innovation of Science and Technology Support Demonstration Project of Chongqing Modern Cattle and Sheep Industry [cstc2014zktjccxbx0021]
  3. Modern Agro-industry Technology Research System [CARS-35-05]
  4. Sichuan Agricultural University Excellent Master's Degree Papers Breeding [YS2014003]

向作者/读者索取更多资源

Hemarthria R. Br. is an important genus of perennial forage grasses that is widely used in subtropical and tropical regions. Hemarthria grasses have made remarkable contributions to the development of animal husbandry and agro-ecosystem maintenance; however, there is currently a lack of comprehensive genomic data available for these species. In this study, we used Illumina high-throughput deep sequencing to characterize of two agriculturally important Hemarthria materials, H. compressa Yaan and H. altissima 1110. Sequencing runs that used each of four normalized RNA samples from the leaves or roots of the two materials yielded more than 24 million high-quality reads. After de novo assembly, 137,142 and 77,150 unigenes were obtained for Yaan and 1110, respectively. In addition, a total of 86,731 Yawn and 48,645 1110 unigenes were successfully annotated. After consolidating the unigenes for both materials, 42,646 high-quality SNPs were identified in 10,880 unigenes and 10,888 SSRs were identified in 8330 unigenes. To validate the identified markers, high quality PCR primers were designed for both SNPs and SSRs. We randomly tested 16 of the SNP primers and 54 of the SSR primers and found that the majority of these primers successfully amplified the desired PCR product. In addition, high cross-species transferability (61.11-87.04%) of SSR markers was achieved for four other Poaceae species. The amount of RNA sequencing data that was generated for these two Hemarthria species greatly increases the amount of genomic information available for Hemarthria and the SSR and SNP markers identified in this study will facilitate further advancements in genetic and molecular studies of the Hemarthria genus.

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