Evidence map›Paper›PMID 23633572›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Surface display of a massively variable lipoprotein by a Legionella diversity-generating retroelement.

Diego Arambula, Wenge Wong, Bob A Medhekar, Huatao Guo, Mari Gingery, Elizabeth Czornyj, Minghsun Liu, Sanghamitra Dey, Partho Ghosh, Jeff F Miller

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Targeted hypermutation of putative antigen sensors in multicellular bacteria.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. NovelMicroorganisms · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Core Concepts: How diversity-generating retroelements promote mutation and adaptation in myriad microbes.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Review
  20. Article
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.

Diego ArambulaDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095, USA.
Wenge Wong
Bob A Medhekar
Huatao Guo
Mari Gingery
Elizabeth Czornyj
Minghsun Liu
Sanghamitra Dey
Partho Ghosh
Jeff F Miller

Funding

MULTIDISCIPLINARY TRAINING IN MICROBIAL PATHOGENESIST32AI007323 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Peter John Bradley · 1988 to 2026
$8.6M
Diversity-Generation and Variable Protein Displays in Pathogens and PhageR01AI096838 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GHOSH, PARTHO, MILLER, JEFFERY F. · 2012 to 2016
$2.7M
Variable-Protein Surface Display in Treponema denticolaR21DE021528 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MILLER, JEFFERY F. · 2011 to 2012
$412k
NIAID NIH HHS R01 AI069838NIAID NIH HHS R01 AI096838NIAID NIH HHS T32 AI007323NIDCR NIH HHS R21 DE021528
6 · The paper itself

Abstract

Diversity-generating retroelements (DGRs) are a unique family of retroelements that confer selective advantages to their hosts by facilitating localized DNA sequence evolution through a specialized error-prone reverse transcription process. We characterized a DGR in Legionella pneumophila, an opportunistic human pathogen that causes Legionnaires disease. The L. pneumophila DGR is found within a horizontally acquired genomic island, and it can theoretically generate 10(26) unique nucleotide sequences in its target gene, legionella determinent target A (ldtA), creating a repertoire of 10(19) distinct proteins. Expression of the L. pneumophila DGR resulted in transfer of DNA sequence information from a template repeat to a variable repeat (VR) accompanied by adenine-specific mutagenesis of progeny VRs at the 3'end of ldtA. ldtA encodes a twin-arginine translocated lipoprotein that is anchored in the outer leaflet of the outer membrane, with its C-terminal variable region surface exposed. Related DGRs were identified in L. pneumophila clinical isolates that encode unique target proteins with homologous VRs, demonstrating the adaptability of DGR components. This work characterizes a DGR that diversifies a bacterial protein and confirms the hypothesis that DGR-mediated mutagenic homing occurs through a conserved mechanism. Comparative bioinformatics predicts that surface display of massively variable proteins is a defining feature of a subset of bacterial DGRs.

Indexed as

RetroelementsBacterial ProteinsBase SequenceCell MembraneGenomic IslandsLegionella pneumophilaLipoproteinsMolecular Sequence DataMutagenesisOpen Reading FramesProtein Structure, TertiarySequence Analysis, DNASurface PropertiesVirulenceBacterial ProteinsLipoproteinsRetroelementsaccelerated evolutionbacterial surface displayTAT

Identifiers

PMID23633572
PMCPMC3657778

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.