Evidence map›Paper›PMID 29268709›Full record

ArticleBMC plant biology2017

Negative correlation between rates of molecular evolution and flowering cycles in temperate woody bamboos revealed by plastid phylogenomics.

Peng-Fei Ma, Maria S Vorontsova, Olinirina Prisca Nanjarisoa, Jacqueline Razanatsoa, Zhen-Hua Guo, Thomas Haevermans, De-Zhu Li

Abstract read
In one paragraph

Article in BMC plant biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

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0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

28 citing papers in PubMed.

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  15. The complete chloroplast genome sequence ofMitochondrial DNA. Part B, Resources · 2023
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  16. PhytoKeys · 2023
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  17. PhytoKeys · 2022
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  18. The complete chloroplast genome and phylogenetic position ofMitochondrial DNA. Part B, Resources · 2022
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  19. The complete chloroplast genome ofMitochondrial DNA. Part B, Resources · 2022
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Peng-Fei MaPlant Germplasm and Genomics Center, Germplasm Bank of Wild Species, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan, 650201, China.ORCID 0000-0003-3061-1454
Maria S VorontsovaComparative Plant and Fungal Biology, Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AB, UK.
Olinirina Prisca NanjarisoaKew Madagascar Conservation Centre, Lot IIJ, 131B, Ambodivoanjo, Ivandry, Antananarivo 101, Madagascar.
Jacqueline RazanatsoaHerbier, Département Flore, Parc Botanique et Zoologique de Tsimbazaza, BP 4096, Antananarivo 101, Madagascar.
Zhen-Hua GuoPlant Germplasm and Genomics Center, Germplasm Bank of Wild Species, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan, 650201, China.
Thomas HaevermansInstitut de Systématique, Évolution, Biodiversité (ISYEB) UMR 7205 Centre national de la recherche scientifique - Muséum national d'histoire naturelle - École Pratique des Hautes Études - Université Pierre et Marie Curie, Sorbonne Universités, CP39, 57 rue Cuvier, 75231, Paris Cedex 05, France. thomas.haevermans@mnhn.fr.
De-Zhu LiPlant Germplasm and Genomics Center, Germplasm Bank of Wild Species, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan, 650201, China. dzl@mail.kib.ac.cn.

Funding

National Basic Research Program of China 2014CB954100National Natural Science Foundation of China 31300184National Natural Science Foundation of China 31430011Youth Innovation Promotion Association of the Chinese Academy of Sciences 2015321
6 · The paper itself

Abstract

backgroundHeterogeneous rates of molecular evolution are universal across the tree of life, posing challenges for phylogenetic inference. The temperate woody bamboos (tribe Arundinarieae, Poaceae) are noted for their extremely slow molecular evolutionary rates, supposedly caused by their mysterious monocarpic reproduction. However, the correlation between substitution rates and flowering cycles has not been formally tested.

resultsHere we present 15 newly sequenced plastid genomes of temperate woody bamboos, including the first genomes ever sequenced from Madagascar representatives. A data matrix of 46 plastid genomes representing all 12 lineages of Arundinarieae was assembled for phylogenetic and molecular evolutionary analyses. We conducted phylogenetic analyses using different sequences (e.g., coding and noncoding) combined with different data partitioning schemes, revealing conflicting relationships involving internodes among several lineages. A great difference in branch lengths were observed among the major lineages, and topological inconsistency could be attributed to long-branch attraction (LBA). Using clock model-fitting by maximum likelihood and Bayesian approaches, we furthermore demonstrated extensive rate variation among these major lineages. Rate accelerations mainly occurred for the isolated lineages with limited species diversification, totaling 11 rate shifts during the tribe's evolution. Using linear regression analysis, we found a negative correlation between rates of molecular evolution and flowering cycles for Arundinarieae, notwithstanding that the correlation maybe insignificant when taking the phylogenetic structure into account.

conclusionsUsing the temperate woody bamboos as an example, we found further evidence that rate heterogeneity is universal in plants, suggesting that this will pose a challenge for phylogenetic reconstruction of bamboos. The bamboos with longer flowering cycles tend to evolve more slowly than those with shorter flowering cycles, in accordance with a putative generation time effect.

Indexed as

Evolution, MolecularFlowersGenome, PlantGenome, PlastidPhylogenyPoaceaeReproductionSequence Analysis, DNAGeneration timeInfrequent floweringMolecular evolutionPlastid phylogenomicsRate heterogeneityTemperate woody bamboos

Identifiers

PMID29268709
PMCPMC5740905

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