Evidence map›Paper›PMID 25886949›Full record

ArticleGenome biology2015

A haplotype map of allohexaploid wheat reveals distinct patterns of selection on homoeologous genomes.

Katherine W Jordan, Shichen Wang, Yanni Lun, Laura-Jayne Gardiner, Ron MacLachlan, Pierre Hucl, Krysta Wiebe, Debbie Wong, Kerrie L Forrest, IWGS Consortium and 15 more

Abstract read
In one paragraph

Article in Genome biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 131 papers.

0numbers the graph read from it
0cells of the map it votes in
131citing 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

131 citing papers in PubMed.

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  10. GWAS elucidated grain yield genetics in Indian spring wheat under diverse water conditions.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Wheat bZIPC1 interacts with FT2 and contributes to the regulation of spikelet number per spike.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2023
    Article
  15. Review
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  18. Triticeae crop genome biology: an endless frontier.Frontiers in plant science · 2023
    Review
  19. Article
  20. Article

71 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

25 authors.

Katherine W JordanDepartment Plant Pathology, Kansas State University, Manhattan, KS, 66506, USA. kwjordan@k-state.edu.
Shichen WangDepartment Plant Pathology, Kansas State University, Manhattan, KS, 66506, USA. shichen.wang@gmail.com.
Yanni LunDepartment Plant Pathology, Kansas State University, Manhattan, KS, 66506, USA. yanni@k-state.edu.
Laura-Jayne GardinerInstitute of Integrative Biology, University of Liverpool, Liverpool, L69 7ZB, UK. L.Gardiner@liverpool.ac.uk.
Ron MacLachlanDepartment Plant Sciences, University of Saskatchewan, Saskatoon, SK, S7N 5A8, Canada. ron.maclachlan@usask.ca.
Pierre HuclDepartment Plant Sciences, University of Saskatchewan, Saskatoon, SK, S7N 5A8, Canada. pierre.hucl@usask.ca.
Krysta WiebeDepartment Plant Sciences, University of Saskatchewan, Saskatoon, SK, S7N 5A8, Canada. krysta.wiebe@usask.ca.
Debbie WongDepartment Environment and Primary Industries, Bundoora, VIC, 3083, Australia. debbie.wong@depi.vic.gov.au.
Kerrie L ForrestDepartment Environment and Primary Industries, Bundoora, VIC, 3083, Australia. kerrie.forrest@dpi.vic.gov.au.
IWGS Consortium
Andrew G SharpeNational Research Council Canada, 110 Gymnasium Place, Saskatoon, SK, S7N 0 W9, Canada. Andrew.Sharpe@nrc-cnrc.gc.ca.
Christine Hd SidebottomNational Research Council Canada, 110 Gymnasium Place, Saskatoon, SK, S7N 0 W9, Canada. Christine.Sidebottom@nrc-cnrc.gc.ca.
Neil HallInstitute of Integrative Biology, University of Liverpool, Liverpool, L69 7ZB, UK. Neil.Hall@liverpool.ac.uk.
Christopher ToomajianDepartment Plant Pathology, Kansas State University, Manhattan, KS, 66506, USA. toomajia@ksu.edu.
Timothy CloseDepartment Botany & Plant Sciences, University of California, Riverside, CA, 92521, USA. timothy.close@ucr.edu.
Jorge DubcovskyDepartment Plant Sciences, University of California, Davis, CA, 95616, USA. jdubcovsky@ucdavis.edu.
Alina AkhunovaDepartment Plant Pathology, Kansas State University, Manhattan, KS, 66506, USA. akhunova@ksu.edu.
Luther TalbertDepartment Plant Sciences & Plant Pathology, Montana State University, Bozeman, MT, 59717, USA. ltalbert@montana.edu.
Urmil K BansalPlant Breeding Institute-Cobbitty, The University of Sydney, PMB4011, Narellan, NSW, 2567, Australia. urmil.bansal@sydney.edu.au.
Harbans S BarianaPlant Breeding Institute-Cobbitty, The University of Sydney, PMB4011, Narellan, NSW, 2567, Australia. harbans.bariana@sydney.edu.au.
Matthew J HaydenDepartment Environment and Primary Industries, Bundoora, VIC, 3083, Australia. matthew.hayden@depi.vic.gov.au.
Curtis PozniakDepartment Plant Sciences, University of Saskatchewan, Saskatoon, SK, S7N 5A8, Canada. curtis.pozniak@usask.ca.
Jeffrey A JeddelohRoche NimbleGen, Inc, Madison, WI, 53719, USA. jeffrey.jeddeloh@roche.com.
Anthony HallInstitute of Integrative Biology, University of Liverpool, Liverpool, L69 7ZB, UK. Anthony.Hall@liverpool.ac.uk.
Eduard AkhunovDepartment Plant Pathology, Kansas State University, Manhattan, KS, 66506, USA. eakhunov@ksu.edu.

Funding

Biotechnology and Biological Sciences Research Council BB/G013004/1Biotechnology and Biological Sciences Research Council BB/H022333/1Howard Hughes Medical Institute
6 · The paper itself

Abstract

backgroundBread wheat is an allopolyploid species with a large, highly repetitive genome. To investigate the impact of selection on variants distributed among homoeologous wheat genomes and to build a foundation for understanding genotype-phenotype relationships, we performed population-scale re-sequencing of a diverse panel of wheat lines.

resultsA sample of 62 diverse lines was re-sequenced using the whole exome capture and genotyping-by-sequencing approaches. We describe the allele frequency, functional significance, and chromosomal distribution of 1.57 million single nucleotide polymorphisms and 161,719 small indels. Our results suggest that duplicated homoeologous genes are under purifying selection. We find contrasting patterns of variation and inter-variant associations among wheat genomes; this, in addition to demographic factors, could be explained by differences in the effect of directional selection on duplicated homoeologs. Only a small fraction of the homoeologous regions harboring selected variants overlapped among the wheat genomes in any given wheat line. These selected regions are enriched for loci associated with agronomic traits detected in genome-wide association studies.

conclusionsEvidence suggests that directional selection in allopolyploids rarely acted on multiple parallel advantageous mutations across homoeologous regions, likely indicating that a fitness benefit could be obtained by a mutation at any one of the homoeologs. Additional advantageous variants in other homoelogs probably either contributed little benefit, or were unavailable in populations subjected to directional selection. We hypothesize that allopolyploidy may have increased the likelihood of beneficial allele recovery by broadening the set of possible selection targets.

Indexed as

Genome, PlantPolyploidyChromosome MappingChromosomes, PlantExomeGene FrequencyGenotypeHaplotypesPolymorphism, Single NucleotideSelection, GeneticTriticum

Identifiers

PMID25886949
PMCPMC4389885

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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.