Evidence map›Paper›PMID 30761177›Full record

ArticleFrontiers in plant science2018

Genome-Wide Association Mapping and Genomic Prediction Analyses Reveal the Genetic Architecture of Grain Yield and Flowering Time Under Drought and Heat Stress Conditions in Maize.

Yibing Yuan, Jill E Cairns, Raman Babu, Manje Gowda, Dan Makumbi, Cosmos Magorokosho, Ao Zhang, Yubo Liu, Nan Wang, Zhuanfang Hao and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in plant science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
13.8field-weighted citation impact, top 1% 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

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3 · Its place in the literature

Who cites it

68 citing papers in PubMed, 153 citations in OpenAlex.

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8 more citing papers are in PubMed but not listed here.

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

15 authors at 5 institutions in 3 countries.

Yibing YuanMaize Research Institute, Sichuan Agricultural University, Wenjiang, China.
Jill E CairnsInternational Maize and Wheat Improvement Center, Harare, Zimbabwe.
Raman BabuInternational Maize and Wheat Improvement Center, Texcoco, Mexico.
Manje GowdaInternational Maize and Wheat Improvement Center, Nairobi, Kenya.
Dan MakumbiInternational Maize and Wheat Improvement Center, Nairobi, Kenya.
Cosmos MagorokoshoInternational Maize and Wheat Improvement Center, Harare, Zimbabwe.
Ao ZhangCollege of Bioscience and Biotechnology, Shenyang Agricultural University, Shenyang, China.
Yubo LiuCollege of Bioscience and Biotechnology, Shenyang Agricultural University, Shenyang, China.
Nan WangInternational Maize and Wheat Improvement Center, Texcoco, Mexico.
Zhuanfang HaoInstitute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing, China.
Felix San VicenteInternational Maize and Wheat Improvement Center, Texcoco, Mexico.
Michael S OlsenInternational Maize and Wheat Improvement Center, Nairobi, Kenya.
Boddupalli M PrasannaInternational Maize and Wheat Improvement Center, Nairobi, Kenya.
Yanli LuMaize Research Institute, Sichuan Agricultural University, Wenjiang, China.
Xuecai ZhangInternational Maize and Wheat Improvement Center, Texcoco, Mexico.
Centro Internacional de Mejoramiento de Maíz Y Trigo · MXInternational Maize and Wheat Improvement Center · KEChinese Academy of Agricultural Sciences · CNShenyang Agricultural University · CNSichuan Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drought stress (DS) is a major constraint to maize yield production. Heat stress (HS) alone and in combination with DS are likely to become the increasing constraints. Association mapping and genomic prediction (GP) analyses were conducted in a collection of 300 tropical and subtropical maize inbred lines to reveal the genetic architecture of grain yield and flowering time under well-watered (WW), DS, HS, and combined DS and HS conditions. Out of the 381,165 genotyping-by-sequencing SNPs, 1549 SNPs were significantly associated with all the 12 trait-environment combinations, the average PVE (phenotypic variation explained) by these SNPs was 4.33%, and 541 of them had a PVE value greater than 5%. These significant associations were clustered into 446 genomic regions with a window size of 20 Mb per region, and 673 candidate genes containing the significantly associated SNPs were identified. In addition, 33 hotspots were identified for 12 trait-environment combinations and most were located on chromosomes 1 and 8. Compared with single SNP-based association mapping, the haplotype-based associated mapping detected fewer number of significant associations and candidate genes with higher PVE values. All the 688 candidate genes were enriched into 15 gene ontology terms, and 46 candidate genes showed significant differential expression under the WW and DS conditions. Association mapping results identified few overlapped significant markers and candidate genes for the same traits evaluated under different managements, indicating the genetic divergence between the individual stress tolerance and the combined drought and HS tolerance. The GP accuracies obtained from the marker-trait associated SNPs were relatively higher than those obtained from the genome-wide SNPs for most of the target traits. The genetic architecture information of the grain yield and flowering time revealed in this study, and the genomic regions identified for the different trait-environment combinations are useful in accelerating the efforts on rapid development of the stress-tolerant maize germplasm through marker-assisted selection and/or genomic selection.

Indexed as

association mappingcombined drought and heat stressdrought stressgenomic predictionheat stressmaize

Identifiers

PMID30761177
PMCPMC6363715
OpenAlexW2913977798

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LicenceCC BY
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Registered trials

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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.