Evidence map›Paper›PMID 24814465›Full record

ArticleGenetics2014

Clinal variation at phenology-related genes in spruce: parallel evolution in FTL2 and Gigantea?

Jun Chen, Yoshiaki Tsuda, Michael Stocks, Thomas Källman, Nannan Xu, Katri Kärkkäinen, Tea Huotari, Vladimir L Semerikov, Giovanni G Vendramin, Martin Lascoux

Abstract read
In one paragraph

Article in Genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Molecular advances in bud dormancy in trees.Journal of experimental botany · 2024
    Review
  2. Article
  3. Article
  4. Article
  5. The long road to bloom in conifers.Forestry research · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. GIGANTEA - an emerging story.Frontiers in plant science · 2015
    Review
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

10 authors.

Jun ChenDepartment of Ecology and Genetics, Evolutionary Biology Centre, Uppsala University, 75236 Uppsala, Sweden.
Yoshiaki TsudaDepartment of Ecology and Genetics, Evolutionary Biology Centre, Uppsala University, 75236 Uppsala, Sweden.
Michael StocksDepartment of Ecology and Genetics, Evolutionary Biology Centre, Uppsala University, 75236 Uppsala, Sweden.
Thomas KällmanDepartment of Ecology and Genetics, Evolutionary Biology Centre, Uppsala University, 75236 Uppsala, Sweden.
Nannan XuDepartment of Ecology and Genetics, Evolutionary Biology Centre, Uppsala University, 75236 Uppsala, Sweden.
Katri KärkkäinenFinnish Forest Research Institute, 900014, Finland.
Tea HuotariFinnish Forest Research Institute, 900014, Finland.
Vladimir L SemerikovInstitute of Plant and Animal Ecology, Urals Division of the Russian Academy of Sciences, 620144 Ekaterinburg, Russia.
Giovanni G VendraminConsiglio Nazionale delle Ricerche, Institute of Biosciences and Bioresources, 50019 Sesto Fiorentino, Firenze, Italy.
Martin LascouxDepartment of Ecology and Genetics, Evolutionary Biology Centre and Science for Life Laboratory, Uppsala University, 75236 Uppsala, Sweden martin.lascoux@ebc.uu.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parallel clines in different species, or in different geographical regions of the same species, are an important source of information on the genetic basis of local adaptation. We recently detected latitudinal clines in SNPs frequencies and gene expression of candidate genes for growth cessation in Scandinavian populations of Norway spruce (Picea abies). Here we test whether the same clines are also present in Siberian spruce (P. obovata), a close relative of Norway spruce with a different Quaternary history. We sequenced nine candidate genes and 27 control loci and genotyped 14 SSR loci in six populations of P. obovata located along the Yenisei river from latitude 56°N to latitude 67°N. In contrast to Scandinavian Norway spruce that both departs from the standard neutral model (SNM) and shows a clear population structure, Siberian spruce populations along the Yenisei do not depart from the SNM and are genetically unstructured. Nonetheless, as in Norway spruce, growth cessation is significantly clinal. Polymorphisms in photoperiodic (FTL2) and circadian clock (Gigantea, GI, PRR3) genes also show significant clinal variation and/or evidence of local selection. In GI, one of the variants is the same as in Norway spruce. Finally, a strong cline in gene expression is observed for FTL2, but not for GI. These results, together with recent physiological studies, confirm the key role played by FTL2 and circadian clock genes in the control of growth cessation in spruce species and suggest the presence of parallel adaptation in these two species.

Indexed as

Evolution, MolecularGenes, PlantBayes TheoremCluster AnalysisComputer SimulationDemographyGene Expression Regulation, PlantGene FrequencyGenetic LociGenetics, PopulationGeographyLinear ModelsLinkage DisequilibriumNucleotidesPiceaPlant ProteinsNucleotidesPlant Proteinsclinal variationFTL2Giganteaparallel evolutionspruce

Identifiers

PMID24814465
PMCPMC4096357

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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.