Evidence map›Paper›PMID 20195500›Full record

ArticlePLoS genetics2010

Bacterial genes in the aphid genome: absence of functional gene transfer from Buchnera to its host.

Naruo Nikoh, John P McCutcheon, Toshiaki Kudo, Shin-ya Miyagishima, Nancy A Moran, Atsushi Nakabachi

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
21.7field-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

96 citing papers in PubMed, 198 citations in OpenAlex.

  1. Evolutionary innovation through fusion of sequences from across the tree of life.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  2. Uncovering thousands of endosymbiont DNA transfer events within single cockroach genomes.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  13. Assembly-free quantification of vagrant DNA inserts.Molecular ecology resources · 2023
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36 more citing papers are in PubMed but not listed here.

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

6 authors at 4 institutions in 2 countries.

Naruo NikohDepartment of Liberal Arts, The Open University of Japan, Chiba, Japan.
John P McCutcheon
Toshiaki Kudo
Shin-ya Miyagishima
Nancy A Moran
Atsushi Nakabachi
RIKEN Advanced Science Institute · JPUniversity of Arizona · USRIKEN · JPThe Open University of Japan · JP

Funding

POST DOCTORAL EXCELLENCE IN RESEARCH AND TEACHINGK12GM000708 · NIGMS · UNIVERSITY OF ARIZONA · PI STRAUSFELD, NICHOLAS J · 2000 to 2018
$21.5M
NIGMS NIH HHS 1K 12 GM00708NIGMS NIH HHS K12 GM000708
6 · The paper itself

Abstract

Genome reduction is typical of obligate symbionts. In cellular organelles, this reduction partly reflects transfer of ancestral bacterial genes to the host genome, but little is known about gene transfer in other obligate symbioses. Aphids harbor anciently acquired obligate mutualists, Buchnera aphidicola (Gammaproteobacteria), which have highly reduced genomes (420-650 kb), raising the possibility of gene transfer from ancestral Buchnera to the aphid genome. In addition, aphids often harbor other bacteria that also are potential sources of transferred genes. Previous limited sampling of genes expressed in bacteriocytes, the specialized cells that harbor Buchnera, revealed that aphids acquired at least two genes from bacteria. The newly sequenced genome of the pea aphid, Acyrthosiphon pisum, presents the first opportunity for a complete inventory of genes transferred from bacteria to the host genome in the context of an ancient obligate symbiosis. Computational screening of the entire A. pisum genome, followed by phylogenetic and experimental analyses, provided strong support for the transfer of 12 genes or gene fragments from bacteria to the aphid genome: three LD-carboxypeptidases (LdcA1, LdcA2,psiLdcA), five rare lipoprotein As (RlpA1-5), N-acetylmuramoyl-L-alanine amidase (AmiD), 1,4-beta-N-acetylmuramidase (bLys), DNA polymerase III alpha chain (psiDnaE), and ATP synthase delta chain (psiAtpH). Buchnera was the apparent source of two highly truncated pseudogenes (psiDnaE and psiAtpH). Most other transferred genes were closely related to genes from relatives of Wolbachia (Alphaproteobacteria). At least eight of the transferred genes (LdcA1, AmiD, RlpA1-5, bLys) appear to be functional, and expression of seven (LdcA1, AmiD, RlpA1-5) are highly upregulated in bacteriocytes. The LdcAs and RlpAs appear to have been duplicated after transfer. Our results excluded the hypothesis that genome reduction in Buchnera has been accompanied by gene transfer to the host nuclear genome, but suggest that aphids utilize a set of duplicated genes acquired from other bacteria in the context of the Buchnera-aphid mutualism.

Indexed as

Amino Acid SequenceAnimalsAphidsBacterial ProteinsBuchneraCarboxypeptidasesDNA Polymerase IIIEukaryotic CellsGene DuplicationGene FusionGenes, BacterialGene Transfer, HorizontalGenomeGlycoside HydrolasesHost-Pathogen InteractionsMolecular Sequence DataBacterial ProteinsCarboxypeptidasesDNA Polymerase IIIDNA polymerase III, alpha subunitendo-N-acetylmuramidaseGlycoside HydrolasesLD-carboxypeptidaseMuramidaseN-Acetylmuramoyl-L-alanine Amidase

Identifiers

PMID20195500
PMCPMC2829048
OpenAlexW2016664568

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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.