Evidence map›Paper›PMID 38509491›Full record

ArticleBMC plant biology2024

Integrated transcriptomic and metabolomic analyses reveals anthocyanin biosynthesis in leaf coloration of quinoa (Chenopodium quinoa Willd.).

Min Zhang, Yueyou Li, Junling Wang, Shaopu Shang, Hongxia Wang, Xinlei Yang, Chuan Lu, Mei Wang, Xinbo Sun, Xiaoqing Liu and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 4 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

Min ZhangNorth China Key Laboratory for Crop Germplasm Resources of Education Ministry, The Key Laboratory of Germplasm Resources of Hebei Province, Hebei Agricultural University, Baoding, Hebei Province, 071000, P. R. China.
Yueyou LiThe S&T Innovation Service Center of Hebei Province, Shijiazhuang, Hebei Province, 050000, P. R. China.
Junling WangNorth China Key Laboratory for Crop Germplasm Resources of Education Ministry, The Key Laboratory of Germplasm Resources of Hebei Province, Hebei Agricultural University, Baoding, Hebei Province, 071000, P. R. China.
Shaopu ShangThe S&T Innovation Service Center of Hebei Province, Shijiazhuang, Hebei Province, 050000, P. R. China.
Hongxia WangNorth China Key Laboratory for Crop Germplasm Resources of Education Ministry, The Key Laboratory of Germplasm Resources of Hebei Province, Hebei Agricultural University, Baoding, Hebei Province, 071000, P. R. China.
Xinlei YangNorth China Key Laboratory for Crop Germplasm Resources of Education Ministry, The Key Laboratory of Germplasm Resources of Hebei Province, Hebei Agricultural University, Baoding, Hebei Province, 071000, P. R. China.
Chuan LuThe S&T Innovation Service Center of Hebei Province, Shijiazhuang, Hebei Province, 050000, P. R. China.
Mei WangNorth China Key Laboratory for Crop Germplasm Resources of Education Ministry, The Key Laboratory of Germplasm Resources of Hebei Province, Hebei Agricultural University, Baoding, Hebei Province, 071000, P. R. China.
Xinbo SunNorth China Key Laboratory for Crop Germplasm Resources of Education Ministry, The Key Laboratory of Germplasm Resources of Hebei Province, Hebei Agricultural University, Baoding, Hebei Province, 071000, P. R. China.
Xiaoqing LiuNorth China Key Laboratory for Crop Germplasm Resources of Education Ministry, The Key Laboratory of Germplasm Resources of Hebei Province, Hebei Agricultural University, Baoding, Hebei Province, 071000, P. R. China.
Xiaoxia WangNorth China Key Laboratory for Crop Germplasm Resources of Education Ministry, The Key Laboratory of Germplasm Resources of Hebei Province, Hebei Agricultural University, Baoding, Hebei Province, 071000, P. R. China.
Boxiang WeiNorth China Key Laboratory for Crop Germplasm Resources of Education Ministry, The Key Laboratory of Germplasm Resources of Hebei Province, Hebei Agricultural University, Baoding, Hebei Province, 071000, P. R. China.
Wei LvThe S&T Innovation Service Center of Hebei Province, Shijiazhuang, Hebei Province, 050000, P. R. China. lvwei91@126.com.
Guojun MuNorth China Key Laboratory for Crop Germplasm Resources of Education Ministry, The Key Laboratory of Germplasm Resources of Hebei Province, Hebei Agricultural University, Baoding, Hebei Province, 071000, P. R. China. mgj99999@126.com.
Zhangjiakou Academy of Agricultural Sciences · CNHebei Agricultural University · CN

Funding

the key research and development project of science and technology department of Hebei Province: Key Project of Technologies for Industrialization of Quinoa in Bashang Region 19227527D
6 · The paper itself

Abstract

backgroundQuinoa leaves demonstrate a diverse array of colors, offering a potential enhancement to landscape aesthetics and the development of leisure-oriented sightseeing agriculture in semi-arid regions. This study utilized integrated transcriptomic and metabolomic analyses to investigate the mechanisms underlying anthocyanin synthesis in both emerald green and pink quinoa leaves.

resultsIntegrated transcriptomic and metabolomic analyses indicated that both flavonoid biosynthesis pathway (ko00941) and anthocyanin biosynthesis pathway (ko00942) were significantly associated with anthocyanin biosynthesis. Differentially expressed genes (DEGs) and differentially accumulated metabolites (DAMs) were analyzed between the two germplasms during different developmental periods. Ten DEGs were verified using qRT-PCR, and the results were consistent with those of the transcriptomic sequencing. The elevated expression of phenylalanine ammonia-lyase (PAL), chalcone synthase (CHS), 4-coumarate CoA ligase (4CL) and Hydroxycinnamoyltransferase (HCT), as well as the reduced expression of flavanone 3-hydroxylase (F3H) and Flavonol synthase (FLS), likely cause pink leaf formation. In addition, bHLH14, WRKY46, and TGA indirectly affected the activities of CHS and 4CL, collectively regulating the levels of cyanidin 3-O-(3'', 6''-O-dimalonyl) glucoside and naringenin. The diminished expression of PAL, 4CL, and HCT decreased the formation of cyanidin-3-O-(6"-O-malonyl-2"-O-glucuronyl) glucoside, leading to the emergence of emerald green leaves. Moreover, the lowered expression of TGA and WRKY46 indirectly regulated 4CL activity, serving as another important factor in maintaining the emerald green hue in leaves N1, N2, and N3.

conclusionThese findings establish a foundation for elucidating the molecular regulatory mechanisms governing anthocyanin biosynthesis in quinoa leaves, and also provide some theoretical basis for the development of leisure and sightseeing agriculture.

Indexed as

AnthocyaninsChenopodium quinoaGene Expression ProfilingGene Expression Regulation, PlantGlucosidesPlant LeavesTranscriptomeAnthocyaninsGlucosidesDAMsDEGsIntegrated transcriptomic and metabolomic analysesqRT-PCRTFs

Identifiers

PMID38509491
PMCPMC10953167
OpenAlexW4393011320

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.