2018
DOI: 10.1101/278432
|View full text |Cite
Preprint
|
Sign up to set email alerts
|

Comparative Transcriptomic and Metabolomic Analyses in Response to Cold in Tartary Buckwheat (Fagopyrum tataricum)

Abstract: Highlight: 22Using the RNA-sequencing data and the metabolic profiling analysis, we identified the (which was not peer-reviewed) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. showed that all the phenylpropanoid biosynthetic transcripts were upregulated in cold-

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2019
2019
2021
2021

Publication Types

Select...
2

Relationship

1
1

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 47 publications
0
2
0
Order By: Relevance
“…The cDNA was mixed with 2X Real-Time PCR Master Mix (BIOFACT Co., Daejeon, Korea) and run on a qRT-PCR device, CFX96 Real-Time System (Bio-Rad Laboratories, Hercules, CA, USA) for gene expression analysis. Phenylpropanoid pathway gene sequences were obtained from the transcriptomic data of F. tataricum in our laboratory, where DNA sequences were determined by the Illumina NextSeq500 sequencer [ 29 ]. The conditions for qRT-PCR were as follows: 95 °C for 10 min, 40 cycles with two steps: denaturation at 95 °C for 15 s, annealing and elongation at 58 °C ( FtC3H , FtHQT , FtANR , and FtACT ), 60 °C ( FtC4H ), 61 °C ( FtPAL , FtCHI , FtF3H , and FtANS ), 62 °C ( Ft4CL , FtCHS , FtDFR , and FtFLS2 ) for 65 s, and 95 °C for 10 s; the temperature was increased by 0.5 °C per minute from 60 °C to 95 °C for detection of the melting curve.…”
Section: Methodsmentioning
confidence: 99%
“…The cDNA was mixed with 2X Real-Time PCR Master Mix (BIOFACT Co., Daejeon, Korea) and run on a qRT-PCR device, CFX96 Real-Time System (Bio-Rad Laboratories, Hercules, CA, USA) for gene expression analysis. Phenylpropanoid pathway gene sequences were obtained from the transcriptomic data of F. tataricum in our laboratory, where DNA sequences were determined by the Illumina NextSeq500 sequencer [ 29 ]. The conditions for qRT-PCR were as follows: 95 °C for 10 min, 40 cycles with two steps: denaturation at 95 °C for 15 s, annealing and elongation at 58 °C ( FtC3H , FtHQT , FtANR , and FtACT ), 60 °C ( FtC4H ), 61 °C ( FtPAL , FtCHI , FtF3H , and FtANS ), 62 °C ( Ft4CL , FtCHS , FtDFR , and FtFLS2 ) for 65 s, and 95 °C for 10 s; the temperature was increased by 0.5 °C per minute from 60 °C to 95 °C for detection of the melting curve.…”
Section: Methodsmentioning
confidence: 99%
“…Buckwheat is an annual eudicot plant belonging to the family Polygonaceae, genus Fagopyrum [1]. Tartary buckwheat ( Fagopyrum tataricum (L.) Gaertn) and common buckwheat ( Fagopyrum esculentum Moench) are the two main species of buckwheat [2], which are considered as alternative crops or minor cereals and are popular food in Asia and Europe [3,4]. Tartary buckwheat and common buckwheat are traditionally regarded as medicinal and food homologous crops, because their grains are characterized by high contents of starch and dietary fibre, and protein with an advantageous amino acid composition.…”
Section: Introductionmentioning
confidence: 99%