2016
DOI: 10.1155/2016/5781412
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De NovoSequencing and Characterization of the Transcriptome of Dwarf Polish Wheat (Triticum polonicumL.)

Abstract: Construction as well as characterization of a polish wheat transcriptome is a crucial step to study useful traits of polish wheat. In this study, a transcriptome, including 76,014 unigenes, was assembled from dwarf polish wheat (DPW) roots, stems, and leaves using the software of Trinity. Among these unigenes, 61,748 (81.23%) unigenes were functionally annotated in public databases and classified into differentially functional types. Aligning this transcriptome against draft wheat genome released by the Intern… Show more

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Cited by 8 publications
(6 citation statements)
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“…While mining the public transcriptome database for the discovery of novel viral sequences [ 32 ], we discovered the presence of an unannotated TSA sequence related to WhCV1 (accession no. GEDL01038361, 15,366 nt in length) in the transcriptomic data of Polish wheat ( Triticum polonicum L.) from a Chinese research group [ 33 ]. During the preparation and submission of this paper, another research group mined the same TSA sequence for the same virus as we discovered and tentatively named it Triticum polonicum closterovirus (TriPCV; TPA no.…”
Section: Resultsmentioning
confidence: 99%
“…While mining the public transcriptome database for the discovery of novel viral sequences [ 32 ], we discovered the presence of an unannotated TSA sequence related to WhCV1 (accession no. GEDL01038361, 15,366 nt in length) in the transcriptomic data of Polish wheat ( Triticum polonicum L.) from a Chinese research group [ 33 ]. During the preparation and submission of this paper, another research group mined the same TSA sequence for the same virus as we discovered and tentatively named it Triticum polonicum closterovirus (TriPCV; TPA no.…”
Section: Resultsmentioning
confidence: 99%
“…PCR primers (F: 5′-TCATTGGGAGAGAGTGAGCAT-3′; R: 5′-ACATATCTAGTTT CCTCGCTGC-3′) for the full-length cDNA of TpNRAMP3 were designed according to DPW transcript ( Wang et al, 2016 ). PCR volume included 2.5 μl 10× buffer, 2.0 μl MgCl 2 (25 mM), 2.0 μl dNTP mixture (2.5 Mm each), 2.0 μl forward primer (4 pM), 2.0 μl reverse primer (4 pM), 3.0 μl cDNA, 0.5 μl ExTaq, and added sterilized distilled water up to 25 μl.…”
Section: Methodsmentioning
confidence: 99%
“…The full-length cDNAs of TpIRT1A and TpIRT1B were ampli ed from leaves. PCR primers were selected based on the reference sequence of the wheat genome (Wang et al 2016) were designed using Beacon Designer v7.0 (PREMIER Biosoft International, California, USA) (Table S1). Ten tetraploid wheat and two diploid ancestral species were used to investigate IRT1 homoeologs with the same primers (Table S2).…”
Section: Gene Cloning Bioinformatics and Phylogenetic Analysismentioning
confidence: 99%
“…Here, we thought to characterize IRT1 homoeologous from wheat. We speci cally focused on Dwarf Polish Wheat (DPW) because it can accumulate high concentrations of Cd, Zn, and Fe in its seedlings without showing toxicity symptoms (Wang et al 2016). DPW (Triticum polonicum L., 2n = 4x = 28, AABB) was originally collected from Tulufan, Xinjiang province, China, by Prof. Chi Yen of the Sichuan Agricultural University, China.…”
Section: Introductionmentioning
confidence: 99%