Evidence map›Paper›PMID 32005164›Full record

ArticleBMC plant biology2020

Sequential Paleotetraploidization shaped the carrot genome.

Jinpeng Wang, Jigao Yu, Yuxian Li, Chendan Wei, He Guo, Ying Liu, Jin Zhang, Xiuqing Li, Xiyin Wang

Abstract 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 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

9 authors.

Jinpeng WangCenter for Genomics and Computational Biology, School of Life Sciences, North China University of Science and Technology, Tangshan, 063200, Hebei, China.
Jigao YuCenter for Genomics and Computational Biology, School of Life Sciences, North China University of Science and Technology, Tangshan, 063200, Hebei, China.
Yuxian LiCenter for Genomics and Computational Biology, School of Life Sciences, North China University of Science and Technology, Tangshan, 063200, Hebei, China.
Chendan WeiCenter for Genomics and Computational Biology, School of Life Sciences, North China University of Science and Technology, Tangshan, 063200, Hebei, China.
He GuoCenter for Genomics and Computational Biology, School of Life Sciences, North China University of Science and Technology, Tangshan, 063200, Hebei, China.
Ying LiuCenter for Genomics and Computational Biology, School of Life Sciences, North China University of Science and Technology, Tangshan, 063200, Hebei, China.
Jin ZhangCenter for Genomics and Computational Biology, School of Life Sciences, North China University of Science and Technology, Tangshan, 063200, Hebei, China.
Xiuqing LiFredericton Research and Development Centre, Agriculture and Agri-Food Canada, Fredericton, Frederiction, New Brunswick, E3B 4Z7, Canada.
Xiyin WangCenter for Genomics and Computational Biology, School of Life Sciences, North China University of Science and Technology, Tangshan, 063200, Hebei, China. wangxiyin@vip.sina.com.ORCID http://orcid.org/0000-0003-3454-0374

Funding

Chinese national key clinical specialty construction programs and the natural science foundation of Fujian province, China 2017Y91030022Startup Fund for scientific research, Fujian Medical University 2017XQ1035
6 · The paper itself

Abstract

backgroundCarrot (Daucus carota subsp. carota L.) is an important root crop with an available high-quality genome. The carrot genome is thought to have undergone recursive paleo-polyploidization, but the extent, occurrences, and nature of these events are not clearly defined.

resultsUsing a previously published comparative genomics pipeline, we reanalysed the carrot genome and characterized genomic fractionation, as well as gene loss and retention, after each of the two tetraploidization events and inferred a dominant and sensitive subgenome for each event. In particular, we found strong evidence of two sequential tetraploidization events, with one (Dc-α) approximately 46-52 million years ago (Mya) and the other (Dc-β) approximately 77-87 Mya, both likely allotetraploidization in nature. The Dc-β event was likely common to all Apiales plants, occurring around the divergence of Apiales-Bruniales and after the divergence of Apiales-Asterales, likely playing an important role in the derivation and divergence of Apiales species. Furthermore, we found that rounds of polyploidy events contributed to the expansion of gene families responsible for plastidial methylerythritol phosphate (MEP), the precursor of carotenoid accumulation, and shaped underlying regulatory pathways. The alignment of orthologous and paralogous genes related to different events of polyploidization and speciation constitutes a comparative genomics platform for studying Apiales, Asterales, and many other related species.

conclusionsHierarchical inference of homology revealed two tetraploidization events that shaped the carrot genome, which likely contributed to the successful establishment of Apiales plants and the expansion of MEP, upstream of the carotenoid accumulation pathway.

Indexed as

Genome, PlantTetraploidyBiological EvolutionDaucus carotaCarotenoidsCarrotCoffeeGene collinearityGenomic fractionationLettucePolyploidization

Identifiers

PMID32005164
PMCPMC6995200

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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.