Evidence map›Paper›PMID 17825109›Full record

ArticleBMC evolutionary biology2007

Cyanobacterial ribosomal RNA genes with multiple, endonuclease-encoding group I introns.

Peik Haugen, Debashish Bhattacharya, Jeffrey D Palmer, Seán Turner, Louise A Lewis, Kathleen M Pryer

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

16 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  12. Multiple self-splicing introns in the 16S rRNA genes of giant sulfur bacteria.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
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  14. Review
  15. Review
  16. 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

6 authors at 5 institutions in 2 countries.

Peik HaugenDepartment of Biological Sciences and Roy J, Carver Center for Comparative Genomics, University of Iowa, 446 Biology Building, Iowa City, IA 52242, USA. peik.haugen@fagmed.uit.no
Debashish Bhattacharya
Jeffrey D Palmer
Seán Turner
Louise A Lewis
Kathleen M Pryer
University of Iowa · USDuke University · USIndiana University Bloomington · USNational Institutes of Health · USUniversity of Connecticut · US

Funding

Horizontal Gene Transfer in Multicellular EukaryotesR01GM070612 · NIGMS · TRUSTEES OF INDIANA UNIVERSITY · PI PALMER, JEFFREY D · 2005 to 2008
$1.6M
Intramural NIH HHSNIGMS NIH HHS GM-70612NIGMS NIH HHS R01 GM070612
6 · The paper itself

Abstract

backgroundGroup I introns are one of the four major classes of introns as defined by their distinct splicing mechanisms. Because they catalyze their own removal from precursor transcripts, group I introns are referred to as autocatalytic introns. Group I introns are common in fungal and protist nuclear ribosomal RNA genes and in organellar genomes. In contrast, they are rare in all other organisms and genomes, including bacteria.

resultsHere we report five group I introns, each containing a LAGLIDADG homing endonuclease gene (HEG), in large subunit (LSU) rRNA genes of cyanobacteria. Three of the introns are located in the LSU gene of Synechococcus sp. C9, and the other two are in the LSU gene of Synechococcus lividus strain C1. Phylogenetic analyses show that these introns and their HEGs are closely related to introns and HEGs located at homologous insertion sites in organellar and bacterial rDNA genes. We also present a compilation of group I introns with homing endonuclease genes in bacteria.

conclusionWe have discovered multiple HEG-containing group I introns in a single bacterial gene. To our knowledge, these are the first cases of multiple group I introns in the same bacterial gene (multiple group I introns have been reported in at least one phage gene and one prophage gene). The HEGs each contain one copy of the LAGLIDADG motif and presumably function as homodimers. Phylogenetic analysis, in conjunction with their patchy taxonomic distribution, suggests that these intron-HEG elements have been transferred horizontally among organelles and bacteria. However, the mode of transfer and the nature of the biological connections among the intron-containing organisms are unknown.

Indexed as

Genes, BacterialIntronsPhylogenyCyanobacteriaDNA, BacterialDNA, RibosomalEndonucleasesNucleic Acid ConformationPolymerase Chain ReactionRNA, BacterialRNA, RibosomalSequence Analysis, DNASynechococcusDNA, BacterialDNA, RibosomalEndonucleasesRNA, BacterialRNA, Ribosomal

Identifiers

PMID17825109
PMCPMC1995217
OpenAlexW2130842423

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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.