Evidence map›Paper›PMID 38783209›Full record

ArticleBMC genomics2024

The modular architecture of sigma factors in cyanobacteria: a framework to assess their diversity and understand their evolution.

Marine Gevin, Amel Latifi, Emmanuel Talla

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Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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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

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Marine GevinAix Marseille Univ, CNRS, Laboratoire de Chimie Bactérienne, LCB, IMM, Marseille, France.
Amel LatifiAix Marseille Univ, CNRS, Laboratoire de Chimie Bactérienne, LCB, IMM, Marseille, France. latifi@imm.cnrs.fr.
Emmanuel TallaAix Marseille Univ, CNRS, Laboratoire de Chimie Bactérienne, LCB, IMM, Marseille, France. talla@imm.cnrs.fr.

Funding

Agence Nationale de la Recherche ANR-21-CE20-0025-01
6 · The paper itself

Abstract

backgroundBacterial RNA polymerase holoenzyme requires sigma70 factors to start transcription by identifying promoter elements. Cyanobacteria possess multiple sigma70 factors to adapt to a wide variety of ecological niches. These factors are grouped into two categories: primary sigma factor initiates transcription of housekeeping genes during normal growth conditions, while alternative sigma factors initiate transcription of specific genes under particular conditions. However, the present classification does not consider the modular organization of their structural domains, introducing therefore multiple functional and structural biases. A comprehensive analysis of this protein family in cyanobacteria is needed to address these limitations.

resultsWe investigated the structure and evolution of sigma70 factors in cyanobacteria, analyzing their modular architecture and variation among unicellular, filamentous, and heterocyst-forming morphotypes. 4,193 sigma70 homologs were found with 59 distinct modular patterns, including six essential and 29 accessory domains, such as DUF6596. 90% of cyanobacteria typically have 5 to 17 sigma70 homologs and this number likely depends on the strain morphotype, the taxonomic order and the genome size. We classified sigma70 factors into 12 clans and 36 families. According to taxonomic orders and phenotypic traits, the number of homologs within the 14 main families was variable, with the A.1 family including the primary sigma factor since this family was found in all cyanobacterial species. The A.1, A.5, C.1, E.1, J.1, and K.1 families were found to be key sigma families that distinguish heterocyst-forming strains. To explain the diversification and evolution of sigma70, we propose an evolutionary scenario rooted in the diversification of a common ancestor of the A1 family. This scenario is characterized by evolutionary events including domain losses, gains, insertions, and modifications. The high occurrence of the DUF6596 domain in bacterial sigma70 proteins, and its association with the highest prevalence observed in Actinobacteria, suggests that this domain might be important for sigma70 function. It also implies that the domain could have emerged in Actinobacteria and been transferred through horizontal gene transfer.

conclusionOur analysis provides detailed insights into the modular domain architecture of sigma70, introducing a novel robust classification. It also proposes an evolutionary scenario explaining their diversity across different taxonomical orders.

Indexed as

CyanobacteriaEvolution, MolecularPhylogenySigma FactorBacterial ProteinsGenetic VariationBacterial ProteinsSigma FactorCyanobacteriaGene transcriptionModular domainsSigma factors

Identifiers

PMID38783209
PMCPMC11119718

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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.