Evidence map›Paper›PMID 25566271›Full record

ArticleFrontiers in plant science2014

Evidence for lateral gene transfer (LGT) in the evolution of eubacteria-derived small GTPases in plant organelles.

I Nengah Suwastika, Masatsugu Denawa, Saki Yomogihara, Chak Han Im, Woo Young Bang, Ryosuke L Ohniwa, Jeong Dong Bahk, Kunio Takeyasu, Takashi Shiina

Open access · goldAbstract read
In one paragraph

Article in Frontiers in plant science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

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  12. Root Endophytes andFrontiers in plant science · 2021
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  14. A Natural Variation inThe Plant cell · 2020
    Article
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  16. Disassembly of theProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  17. Article
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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 at 5 institutions in 3 countries.

I Nengah SuwastikaGraduate School of Biostudies, Kyoto University Kyoto, Japan ; Department of Biology, Faculty of Science, Tadulako University Palu, Indonesia.
Masatsugu DenawaGraduate School of Biostudies, Kyoto University Kyoto, Japan ; Graduate School of Medicine, Kyoto University Kyoto, Japan.
Saki YomogiharaGraduate School of Life and Environmental Sciences, Kyoto Prefectural University Kyoto, Japan.
Chak Han ImDivision of Life Science (BK21 plus program), Graduate School of Gyeongsang National University Jinju, South Korea.
Woo Young BangDivision of Life Science (BK21 plus program), Graduate School of Gyeongsang National University Jinju, South Korea.
Ryosuke L OhniwaDivision of Biomedical Science, Faculty of Medicine, University of Tsukuba Tsukuba, Japan.
Jeong Dong BahkDivision of Life Science (BK21 plus program), Graduate School of Gyeongsang National University Jinju, South Korea.
Kunio TakeyasuGraduate School of Biostudies, Kyoto University Kyoto, Japan.
Takashi ShiinaGraduate School of Life and Environmental Sciences, Kyoto Prefectural University Kyoto, Japan.
Gyeongsang National University · KRKyoto Prefectural University · JPKyoto University · JPTadulako University · IDUniversity of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The genomes of free-living bacteria frequently exchange genes via lateral gene transfer (LGT), which has played a major role in bacterial evolution. LGT also played a significant role in the acquisition of genes from non-cyanobacterial bacteria to the lineage of "primary" algae and land plants. Small GTPases are widely distributed among prokaryotes and eukaryotes. In this study, we inferred the evolutionary history of organelle-targeted small GTPases in plants. Arabidopsis thaliana contains at least one ortholog in seven subfamilies of OBG-HflX-like and TrmE-Era-EngA-YihA-Septin-like GTPase superfamilies (together referred to as Era-like GTPases). Subcellular localization analysis of all Era-like GTPases in Arabidopsis revealed that all 30 eubacteria-related GTPases are localized to chloroplasts and/or mitochondria, whereas archaea-related DRG and NOG1 are localized to the cytoplasm and nucleus, respectively, suggesting that chloroplast- and mitochondrion-localized GTPases are derived from the ancestral cyanobacterium and α-proteobacterium, respectively, through endosymbiotic gene transfer (EGT). However, phylogenetic analyses revealed that plant organelle GTPase evolution is rather complex. Among the eubacterium-related GTPases, only four localized to chloroplasts (including one dual targeting GTPase) and two localized to mitochondria were derived from cyanobacteria and α-proteobacteria, respectively. Three other chloroplast-targeted GTPases were related to α-proteobacterial proteins, rather than to cyanobacterial GTPases. Furthermore, we found that four other GTPases showed neither cyanobacterial nor α-proteobacterial affiliation. Instead, these GTPases were closely related to clades from other eubacteria, such as Bacteroides (Era1, EngB-1, and EngB-2) and green non-sulfur bacteria (HflX). This study thus provides novel evidence that LGT significantly contributed to the evolution of organelle-targeted Era-like GTPases in plants.

Indexed as

endosymbiotic gene transferevolution of organellegenomic analysislateral gene transfersmall GTPase

Identifiers

PMID25566271
PMCPMC4263083
OpenAlexW2044769177

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.