Evidence map›Paper›PMID 32977771›Full record

ArticleBMC genomics2020

Role of diversity-generating retroelements for regulatory pathway tuning in cyanobacteria.

Alec Vallota-Eastman, Eleanor C Arrington, Siobhan Meeken, Simon Roux, Krishna Dasari, Sydney Rosen, Jeff F Miller, David L Valentine, Blair G Paul

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-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

12 citing papers in PubMed, 21 citations in OpenAlex.

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  5. Targeted hypermutation of putative antigen sensors in multicellular bacteria.Proceedings of the National Academy of Sciences of the United States of America · 2024
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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 4 institutions in 1 country.

Alec Vallota-EastmanInterdepartmental Graduate Program for Marine Science, University of California Santa Barbara, Santa Barbara, CA, 93106, USA.
Eleanor C ArringtonInterdepartmental Graduate Program for Marine Science, University of California Santa Barbara, Santa Barbara, CA, 93106, USA.
Siobhan MeekenJosephine Bay Paul Center, Marine Biological Laboratory, 7 MBL St, Woods Hole, MA, 02543, USA.
Simon RouxDOE Joint Genome Institute, Berkeley, CA, 94720, USA.
Krishna DasariResearch Mentorship Program (RMP), University of California, Santa Barbara, CA, 93106, USA.
Sydney RosenResearch Mentorship Program (RMP), University of California, Santa Barbara, CA, 93106, USA.
Jeff F MillerMicrobiology, Immunology and Molecular Genetics, University of California, Los Angeles, CA, 90095, USA.
David L ValentineMarine Science Institute, University of California Santa Barbara, Santa Barbara, CA, 93106, USA.
Blair G PaulJosephine Bay Paul Center, Marine Biological Laboratory, 7 MBL St, Woods Hole, MA, 02543, USA. bgpaul@mbl.edu.ORCID http://orcid.org/0000-0002-5738-5568
University of California, Santa Barbara · USMarine Biological Laboratory · USCalifornia NanoSystems Institute · USJoint Genome Institute · US

Funding

National Science Foundation 1650114National Science Foundation DEB170007National Science Foundation HRD-1701365U.S. Department of Energy DE-AC02-05CH11231
6 · The paper itself

Abstract

backgroundCyanobacteria maintain extensive repertoires of regulatory genes that are vital for adaptation to environmental stress. Some cyanobacterial genomes have been noted to encode diversity-generating retroelements (DGRs), which promote protein hypervariation through localized retrohoming and codon rewriting in target genes. Past research has shown DGRs to mainly diversify proteins involved in cell-cell attachment or viral-host attachment within viral, bacterial, and archaeal lineages. However, these elements may be critical in driving variation for proteins involved in other core cellular processes.

resultsMembers of 31 cyanobacterial genera encode at least one DGR, and together, their retroelements form a monophyletic clade of closely-related reverse transcriptases. This class of retroelements diversifies target proteins with unique domain architectures: modular ligand-binding domains often paired with a second domain that is linked to signal response or regulation. Comparative analysis indicates recent intragenomic duplication of DGR targets as paralogs, but also apparent intergenomic exchange of DGR components. The prevalence of DGRs and the paralogs of their targets is disproportionately high among colonial and filamentous strains of cyanobacteria.

conclusionWe find that colonial and filamentous cyanobacteria have recruited DGRs to optimize a ligand-binding module for apparent function in signal response or regulation. These represent a unique class of hypervariable proteins, which might offer cyanobacteria a form of plasticity to adapt to environmental stress. This analysis supports the hypothesis that DGR-driven mutation modulates signaling and regulatory networks in cyanobacteria, suggestive of a new framework for the utility of localized genetic hypervariation.

Indexed as

Genetic VariationRetroelementsBacterial ProteinsConserved SequenceCyanobacteriaMutagenesisProtein BindingProtein DomainsBacterial ProteinsRetroelements

Identifiers

PMID32977771
PMCPMC7517822
OpenAlexW3089045415

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.