Evidence map›Paper›PMID 29433444›Full record

ArticleBMC evolutionary biology2018

A novel short L-arginine responsive protein-coding gene (laoB) antiparallel overlapping to a CadC-like transcriptional regulator in Escherichia coli O157:H7 Sakai originated by overprinting.

Sarah M Hücker, Sonja Vanderhaeghen, Isabel Abellan-Schneyder, Romy Wecko, Svenja Simon, Siegfried Scherer, Klaus Neuhaus

Abstract read
In one paragraph

Article in BMC evolutionary biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. EcoSal Plus · 2020
    Review
  8. Are Antisense Proteins in Prokaryotes Functional?Frontiers in molecular biosciences · 2020
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Sarah M HückerChair for Microbial Ecology, Wissenschaftszentrum Weihenstephan, Technische Universität München, Weihenstephaner Berg 3, 85354, Freising, Germany.
Sonja VanderhaeghenChair for Microbial Ecology, Wissenschaftszentrum Weihenstephan, Technische Universität München, Weihenstephaner Berg 3, 85354, Freising, Germany.
Isabel Abellan-SchneyderChair for Microbial Ecology, Wissenschaftszentrum Weihenstephan, Technische Universität München, Weihenstephaner Berg 3, 85354, Freising, Germany.
Romy WeckoChair for Microbial Ecology, Wissenschaftszentrum Weihenstephan, Technische Universität München, Weihenstephaner Berg 3, 85354, Freising, Germany.
Svenja SimonDepartment of Computer and Information Science, University of Konstanz, Box 78, 78457, Konstanz, Germany.
Siegfried SchererChair for Microbial Ecology, Wissenschaftszentrum Weihenstephan, Technische Universität München, Weihenstephaner Berg 3, 85354, Freising, Germany.
Klaus NeuhausChair for Microbial Ecology, Wissenschaftszentrum Weihenstephan, Technische Universität München, Weihenstephaner Berg 3, 85354, Freising, Germany. neuhaus@tum.de.ORCID 0000-0002-6020-2814

Funding

Deutsche Forschungsgemeinschaft KE740/13-1,2,3Deutsche Forschungsgemeinschaft SCHE316/3-1,2,3
6 · The paper itself

Abstract

backgroundDue to the DNA triplet code, it is possible that the sequences of two or more protein-coding genes overlap to a large degree. However, such non-trivial overlaps are usually excluded by genome annotation pipelines and, thus, only a few overlapping gene pairs have been described in bacteria. In contrast, transcriptome and translatome sequencing reveals many signals originated from the antisense strand of annotated genes, of which we analyzed an example gene pair in more detail.

resultsA small open reading frame of Escherichia coli O157:H7 strain Sakai (EHEC), designated laoB (L-arginine responsive overlapping gene), is embedded in reading frame -2 in the antisense strand of ECs5115, encoding a CadC-like transcriptional regulator. This overlapping gene shows evidence of transcription and translation in Luria-Bertani (LB) and brain-heart infusion (BHI) medium based on RNA sequencing (RNAseq) and ribosomal-footprint sequencing (RIBOseq). The transcriptional start site is 289 base pairs (bp) upstream of the start codon and transcription termination is 155 bp downstream of the stop codon. Overexpression of LaoB fused to an enhanced green fluorescent protein (EGFP) reporter was possible. The sequence upstream of the transcriptional start site displayed strong promoter activity under different conditions, whereas promoter activity was significantly decreased in the presence of L-arginine. A strand-specific translationally arrested mutant of laoB provided a significant growth advantage in competitive growth experiments in the presence of L-arginine compared to the wild type, which returned to wild type level after complementation of laoB in trans. A phylostratigraphic analysis indicated that the novel gene is restricted to the Escherichia/Shigella clade and might have originated recently by overprinting leading to the expression of part of the antisense strand of ECs5115.

conclusionsHere, we present evidence of a novel small protein-coding gene laoB encoded in the antisense frame -2 of the annotated gene ECs5115. Clearly, laoB is evolutionarily young and it originated in the Escherichia/Shigella clade by overprinting, a process which may cause the de novo evolution of bacterial genes like laoB.

Indexed as

Genes, OverlappingTranscription, GeneticArginineBase SequenceEscherichia coli O157Escherichia coli ProteinsGenes, BacterialGreen Fluorescent ProteinsMutationOpen Reading FramesPhylogenyPromoter Regions, GeneticProtein BiosynthesisRecombinant Fusion ProteinsTrans-ActivatorsTranscriptomeArginineCadC protein, E colienhanced green fluorescent proteinEscherichia coli ProteinsGreen Fluorescent ProteinsRecombinant Fusion ProteinsTrans-ActivatorsDe novo geneEHECOverlapping geneOverprintingSmall protein

Identifiers

PMID29433444
PMCPMC5810103

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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.