Literature DB >> 31053830

Methylamine-specific methyltransferase paralogs in Methanosarcina are functionally distinct despite frequent gene conversion.

Dipti D Nayak1, William W Metcalf2.   

Abstract

Sequenced archaeal genomes are mostly smaller and more streamlined than typical bacterial genomes; however, members of the Methanosarcina genus within the Euryarchaeaota are a significant exception, with M. acetivorans being the largest archaeal genome (5.8 Mbp) sequenced thus far. This finding is partially explained by extensive gene duplication within Methanosarcina spp. Significantly, the evolutionary pressures leading to gene duplication and subsequent genome expansion have not been well investigated, especially with respect to biological methane production (methanogenesis), which is the key biological trait of these environmentally important organisms. In this study, we address this question by specifically probing the functional evolution of two methylamine-specific methyltransferase paralogs in members of the Methanosarcina genus. Using the genetically tractable strain, M. acetivorans, we first show that the two paralogs have distinct cellular functions: one being required for methanogenesis from methylamine, the other for use of methylamine as a nitrogen source. Subsequently, through comparative sequence analyses, we show that functional divergence of paralogs is primarily mediated by divergent evolution of the 5' regulatory region, despite frequent gene conversion within the coding sequence. This unique evolutionary paradigm for functional divergence of genes post-duplication underscores a divergent role for an enzyme singularly associated with methanogenic metabolism in other aspects of cell physiology.

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Year:  2019        PMID: 31053830      PMCID: PMC6776008          DOI: 10.1038/s41396-019-0428-6

Source DB:  PubMed          Journal:  ISME J        ISSN: 1751-7362            Impact factor:   10.302


  5 in total

1.  Effect of Sulfur-Containing Compounds on Growth of Methanosarcina barkeri in Defined Medium.

Authors:  T K Mazumder; N Nishio; S Fukuzaki; S Nagai
Journal:  Appl Environ Microbiol       Date:  1986-10       Impact factor: 4.792

2.  Disaggregation of Methanosarcina spp. and Growth as Single Cells at Elevated Osmolarity.

Authors:  K R Sowers; J E Boone; R P Gunsalus
Journal:  Appl Environ Microbiol       Date:  1993-11       Impact factor: 4.792

3.  An anaerobic, intrachamber incubator for growth of Methanosarcina spp. on methanol-containing solid media.

Authors:  W W Metcalf; J K Zhang; R S Wolfe
Journal:  Appl Environ Microbiol       Date:  1998-02       Impact factor: 4.792

4.  Multiple recombination events maintain sequence identity among members of the nitrogenase multigene family in Rhizobium etli.

Authors:  C Rodríguez; D Romero
Journal:  Genetics       Date:  1998-06       Impact factor: 4.562

5.  Clustered genes encoding the methyltransferases of methanogenesis from monomethylamine.

Authors:  S A Burke; S L Lo; J A Krzycki
Journal:  J Bacteriol       Date:  1998-07       Impact factor: 3.490

  5 in total
  2 in total

1.  A CRISPRi-dCas9 System for Archaea and Its Use To Examine Gene Function during Nitrogen Fixation by Methanosarcina acetivorans.

Authors:  Ahmed E Dhamad; Daniel J Lessner
Journal:  Appl Environ Microbiol       Date:  2020-10-15       Impact factor: 4.792

2.  Soil Metabolomics Predict Microbial Taxa as Biomarkers of Moisture Status in Soils from a Tidal Wetland.

Authors:  Taniya RoyChowdhury; Lisa M Bramer; Joseph Brown; Young-Mo Kim; Erika Zink; Thomas O Metz; Lee Ann McCue; Heida L Diefenderfer; Vanessa Bailey
Journal:  Microorganisms       Date:  2022-08-16
  2 in total

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