Evidence map›Paper›PMID 39522159›Full record

ArticlePlant biotechnology journal2025

ZmCCD8 regulates sugar and amino acid accumulation in maize kernels via strigolactone signalling.

Yanting Zhong, Yongqi Wang, Xiaoying Pan, Ruifeng Wang, Dongdong Li, Wei Ren, Ziyi Hao, Xionggao Shi, Jingyu Guo, Elia Ramarojaona and 13 more

Abstract read
In one paragraph

Article in Plant biotechnology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

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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

23 authors.

Yanting ZhongState Key Laboratory of Nutrient Use and Management, College of Resources and Environmental Sciences, China Agricultural University, Beijing, China.
Yongqi WangState Key Laboratory of Nutrient Use and Management, College of Resources and Environmental Sciences, China Agricultural University, Beijing, China.
Xiaoying PanState Key Laboratory of Nutrient Use and Management, College of Resources and Environmental Sciences, China Agricultural University, Beijing, China.
Ruifeng WangState Key Laboratory of Nutrient Use and Management, College of Resources and Environmental Sciences, China Agricultural University, Beijing, China.
Dongdong LiCollege of Agronomy and Biotechnology, China Agricultural University, Beijing, China.
Wei RenCollege of Grassland Science and Technology, China Agricultural University, Beijing, China.ORCID https://orcid.org/0000-0001-6050-660X
Ziyi HaoDepartment of Ecology and Ecological Engineering, China Agricultural University, Beijing, China.
Xionggao ShiState Key Laboratory of Nutrient Use and Management, College of Resources and Environmental Sciences, China Agricultural University, Beijing, China.
Jingyu GuoBeijing Key Laboratory of Growth and Developmental Regulation for Protected Vegetable Crops, Department of Vegetable Sciences, China Agricultural University, Beijing, China.
Elia RamarojaonaPlant Hormone Biology Group, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, The Netherlands.
Mario SchilderPlant Hormone Biology Group, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, The Netherlands.
Harro BouwmeesterPlant Hormone Biology Group, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, The Netherlands.
Limei ChenState Key Laboratory of Plant Environmental Resilience, Center for crop functional genomics and molecular breeding, College of Biological Science, China Agricultural University, Beijing, China.ORCID https://orcid.org/0000-0001-8734-3820
Peng YuEmmy Noether Group Root Functional Biology, Institute of Crop Science and Resource Conservation, University of Bonn, Bonn, Germany.
Jijun YanNational Centre for Plant Gene Research (Beijing), Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Jinfang ChuNational Centre for Plant Gene Research (Beijing), Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Yanjun XuDepartment of Applied Chemistry, China Agricultural University, Beijing, China.
Wenxin LiuCollege of Agronomy and Biotechnology, China Agricultural University, Beijing, China.
Zhaobin DongCollege of Agronomy and Biotechnology, China Agricultural University, Beijing, China.
Yi WangState Key Laboratory of Plant Environmental Resilience, Center for crop functional genomics and molecular breeding, College of Biological Science, China Agricultural University, Beijing, China.ORCID https://orcid.org/0000-0002-3660-5859
Xiaolan ZhangBeijing Key Laboratory of Growth and Developmental Regulation for Protected Vegetable Crops, Department of Vegetable Sciences, China Agricultural University, Beijing, China.ORCID https://orcid.org/0000-0002-6343-3116
Fusuo ZhangState Key Laboratory of Nutrient Use and Management, College of Resources and Environmental Sciences, China Agricultural University, Beijing, China.
Xuexian LiState Key Laboratory of Nutrient Use and Management, College of Resources and Environmental Sciences, China Agricultural University, Beijing, China.ORCID https://orcid.org/0000-0002-0863-9250

Funding

China Postdoctoral Science Foundation 2022M713396National Key Research and Development Program of China 2021YFF1000500National Natural Science Foundation of China 31972491
6 · The paper itself

Abstract

How carbon (sucrose) and nitrogen (amino acid) accumulation is coordinatively controlled in cereal grains remains largely enigmatic. We found that overexpression of the strigolactone (SL) biosynthesis gene CAROTENOID CLEAVAGE DIOXYGENASE 8 (CCD8) resulted in greater ear diameter and enhanced sucrose and amino acid accumulation in maize kernels. Loss of ZmCCD8 function reduced kernel growth with lower sugar and amino acid concentrations. Transcriptomic analysis showed down-regulation of the transcription factors ZmMYB42 and ZmMYB63 in ZmCCD8 overexpression alleles and up-regulation in zmccd8 null alleles. Importantly, ZmMYB42 and ZmMYB63 were negatively regulated by the SL signalling component UNBRANCHED 3, and repressed expression of the sucrose transporters ZmSWEET10 and ZmSWEET13c and the lysine/histidine transporter ZmLHT14. Consequently, null alleles of ZmMYB42 or ZmMYB63 promoted accumulation of soluble sugars and free amino acids in maize kernels, whereas ZmLHT14 overexpression enhanced amino acid accumulation in kernels. Moreover, overexpression of the SL receptor DWARF 14B resulted in more sucrose and amino acid accumulation in kernels, down-regulation of ZmMYB42 and ZmMYB63 expression, and up-regulation of ZmSWEETs and ZmLHT14 transcription. Together, we uncover a distinct SL signalling pathway that regulates sucrose and amino acid accumulation in kernels. Significant association of two SNPs in the 5' upstream region of ZmCCD8 with ear and cob diameter implicates its potential in breeding toward higher yield and nitrogen efficiency.

Indexed as

Amino AcidsLactonesPlant ProteinsSugarsZea maysGene Expression Regulation, PlantSeedsSignal TransductionSucroseTranscription FactorsAmino AcidsLactonesPlant ProteinsSucroseSugarsTranscription Factorsamino acid transporterCCD8maizestrigolactonesugar transporter

Identifiers

PMID39522159
PMCPMC11772326

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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.