Evidence map›Paper›PMID 32513104›Full record

ArticleBMC plant biology2020

SH1-dependent maize seed development and starch synthesis via modulating carbohydrate flow and osmotic potential balance.

Ke Zhang, Li Guo, Wen Cheng, Baiyu Liu, Wendi Li, Fei Wang, Changzheng Xu, Xiangyu Zhao, Zhaohua Ding, Kewei Zhang and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

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  15. A Novel Banana Mutant "Frontiers in plant science · 2021
    Article
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

11 authors at 5 institutions in 2 countries.

Ke ZhangThe Key Laboratory of Plant Development and Environment Adaptation Biology, Ministry of Education, School of Life Science, Shandong University, Qingdao, 266237, China.
Li GuoThe Key Laboratory of Plant Development and Environment Adaptation Biology, Ministry of Education, School of Life Science, Shandong University, Qingdao, 266237, China.
Wen ChengMaize Institute of Shandong Academy of Agricultural Sciences, Jinan, Shandong, China.
Baiyu LiuThe Key Laboratory of Plant Development and Environment Adaptation Biology, Ministry of Education, School of Life Science, Shandong University, Qingdao, 266237, China.
Wendi LiThe Key Laboratory of Plant Development and Environment Adaptation Biology, Ministry of Education, School of Life Science, Shandong University, Qingdao, 266237, China.
Fei WangNational Key Laboratory of Plant Molecular Genetics, CAS Center for Excellence in Molecular Plant Sciences, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, 200032, China.
Changzheng XuSchool of Life Sciences, Southwest University, Chongqing, 400715, China.
Xiangyu ZhaoState Key Laboratory of Crop Biology, College of Life Sciences, Shandong Agricultural University, Taian, 271018, Shandong, China.
Zhaohua DingMaize Institute of Shandong Academy of Agricultural Sciences, Jinan, Shandong, China.
Kewei ZhangThe Key Laboratory of Plant Development and Environment Adaptation Biology, Ministry of Education, School of Life Science, Shandong University, Qingdao, 266237, China.
Kunpeng LiThe Key Laboratory of Plant Development and Environment Adaptation Biology, Ministry of Education, School of Life Science, Shandong University, Qingdao, 266237, China. likp@sdu.edu.cn.ORCID http://orcid.org/0000-0003-1807-4545
Shandong University · CNShandong Academy of Agricultural Sciences · CNChinese Academy of Sciences · CNShandong Agricultural University · CNSouthwest University · CN

Funding

National Key R&D Program of China 2016YFD0102104National Key R&D Program of China 2016YFE0200300Shandong Provincial key research and development program, China 2017GSF21107Shandong Provincial Natural Science Foundation, China ZR2016CM05Shandong Provincial Natural Science Foundation, China ZR2017YL011
6 · The paper itself

Abstract

backgroundAs the main form of photoassimilates transported from vegetative tissues to the reproductive organs, sucrose and its degradation products are crucial for cell fate determination and development of maize kernels. Despite the relevance of sucrose synthase SH1 (shrunken 1)-mediated release of hexoses for kernel development, the underlying physiological and molecular mechanisms are not yet well understood in maize (Zea mays).

resultsHere, we identified a new allelic mutant of SH1 generated by EMS mutagenesis, designated as sh1*. The mutation of SH1 caused more than 90% loss of sucrose synthase activity in sh1* endosperm, which resulted in a significant reduction in starch contents while a dramatic increase in soluble sugars. As a result, an extremely high osmolality in endosperm cells of sh1* was generated, which caused kernel swelling and affected the seed development. Quantitative measurement of phosphorylated sugars showed that Glc-1-P in endosperm of sh1* (17 μg g

conclusionsOur results demonstrated that SH1-mediated sucrose degradation is critical for maize kernel development and starch synthesis by regulating the flow of carbohydrates and maintaining the balance of osmotic potential.

Indexed as

Carbohydrate MetabolismGene Expression Regulation, PlantGlucosyltransferasesOsmotic PressurePhylogenyPlant ProteinsSeedsStarchZea maysGlucosyltransferasesPlant ProteinsStarchsucrose synthaseGlucose-1-phosphateSeed developmentSH1Soluble sugarsStarch synthesisZea mays

Identifiers

PMID32513104
PMCPMC7282075
OpenAlexW3034149277

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.