Evidence map›Paper›PMID 28957460›Full record

ArticleGenome biology and evolution2017

The Huperzia selago Shoot Tip Transcriptome Sheds New Light on the Evolution of Leaves.

Anastasiia I Evkaikina, Lidija Berke, Marina A Romanova, Estelle Proux-Wéra, Alexandra N Ivanova, Catarina Rydin, Katharina Pawlowski, Olga V Voitsekhovskaja

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
28.9field-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

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

14 citing papers in PubMed, 74 citations in OpenAlex.

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  13. Characterization of chloroplast iridescence inJournal of the Royal Society, Interface · 2018
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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

8 authors at 4 institutions in 3 countries.

Anastasiia I EvkaikinaLaboratory of Molecular and Ecological Physiology, Komarov Botanical Institute, Russian Academy of Sciences, St. Petersburg, Russia.
Lidija BerkeDepartment of Plant Sciences, Wageningen University, The Netherlands.
Marina A RomanovaDepartment of Botany, St. Petersburg State University, St. Petersburg, Russia.
Estelle Proux-WéraDepartment of Plant Protection Biology, Swedish University of Agricultural Sciences, Alnarp, Sweden.
Alexandra N IvanovaLaboratory of Anatomy and Morphology, Komarov Botanical Institute, Russian Academy of Sciences, St. Petersburg, Russia.
Catarina RydinDepartment of Ecology, Environment and Plant Sciences, Stockholm University, Stockholm, Sweden.
Katharina PawlowskiDepartment of Ecology, Environment and Plant Sciences, Stockholm University, Stockholm, Sweden.
Olga V VoitsekhovskajaLaboratory of Molecular and Ecological Physiology, Komarov Botanical Institute, Russian Academy of Sciences, St. Petersburg, Russia.
Russian Academy of Sciences · RUStockholm University · SEGraduate School Experimental Plant Sciences · NLSt Petersburg University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lycopodiophyta-consisting of three orders, Lycopodiales, Isoetales and Selaginellales, with different types of shoot apical meristems (SAMs)-form the earliest branch among the extant vascular plants. They represent a sister group to all other vascular plants, from which they differ in that their leaves are microphylls-that is, leaves with a single, unbranched vein, emerging from the protostele without a leaf gap-not megaphylls. All leaves represent determinate organs originating on the flanks of indeterminate SAMs. Thus, leaf formation requires the suppression of indeterminacy, that is, of KNOX transcription factors. In seed plants, this is mediated by different groups of transcription factors including ARP and YABBY.We generated a shoot tip transcriptome of Huperzia selago (Lycopodiales) to examine the genes involved in leaf formation. Our H. selago transcriptome does not contain any ARP homolog, although transcriptomes of Selaginella spp. do. Surprisingly, we discovered a YABBY homolog, although these transcription factors were assumed to have evolved only in seed plants.The existence of a YABBY homolog in H. selago suggests that YABBY evolved already in the common ancestor of the vascular plants, and subsequently was lost in some lineages like Selaginellales, whereas ARP may have been lost in Lycopodiales. The presence of YABBY in the common ancestor of vascular plants would also support the hypothesis that this common ancestor had a simplex SAM. Furthermore, a comparison of the expression patterns of ARP in shoot tips of Selaginella kraussiana (Harrison CJ, etal. 2005. Independent recruitment of a conserved developmental mechanism during leaf evolution. Nature 434(7032):509-514.) and YABBY in shoot tips of H. selago implies that the development of microphylls, unlike megaphylls, does not seem to depend on the combined activities of ARP and YABBY. Altogether, our data show that Lycopodiophyta are a diverse group; so, in order to understand the role of Lycopodiophyta in evolution, representatives of Lycopodiales, Selaginellales, as well as of Isoetales, have to be examined.

Indexed as

Evolution, MolecularTranscriptomeGene Expression Regulation, DevelopmentalGene Expression Regulation, PlantHuperziaPlant LeavesPlant ProteinsPlant ShootsTranscription FactorsPlant ProteinsTranscription FactorsARPHuperziaKNOXleaf developmentLycopodiophytashoot apexYABBY

Identifiers

PMID28957460
PMCPMC5622374
OpenAlexW2753734032

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.