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

BACKGROUND: Group 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 nu...

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Autores principales: Haugen, Peik, Bhattacharya, Debashish, Palmer, Jeffrey D, Turner, Seán, Lewis, Louise A, Pryer, Kathleen M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1995217/
https://www.ncbi.nlm.nih.gov/pubmed/17825109
http://dx.doi.org/10.1186/1471-2148-7-159
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author Haugen, Peik
Bhattacharya, Debashish
Palmer, Jeffrey D
Turner, Seán
Lewis, Louise A
Pryer, Kathleen M
author_facet Haugen, Peik
Bhattacharya, Debashish
Palmer, Jeffrey D
Turner, Seán
Lewis, Louise A
Pryer, Kathleen M
author_sort Haugen, Peik
collection PubMed
description BACKGROUND: Group 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. RESULTS: Here 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. CONCLUSION: We 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.
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spelling pubmed-19952172007-09-29 Cyanobacterial ribosomal RNA genes with multiple, endonuclease-encoding group I introns Haugen, Peik Bhattacharya, Debashish Palmer, Jeffrey D Turner, Seán Lewis, Louise A Pryer, Kathleen M BMC Evol Biol Research Article BACKGROUND: Group 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. RESULTS: Here 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. CONCLUSION: We 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. BioMed Central 2007-09-08 /pmc/articles/PMC1995217/ /pubmed/17825109 http://dx.doi.org/10.1186/1471-2148-7-159 Text en Copyright © 2007 Haugen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Haugen, Peik
Bhattacharya, Debashish
Palmer, Jeffrey D
Turner, Seán
Lewis, Louise A
Pryer, Kathleen M
Cyanobacterial ribosomal RNA genes with multiple, endonuclease-encoding group I introns
title Cyanobacterial ribosomal RNA genes with multiple, endonuclease-encoding group I introns
title_full Cyanobacterial ribosomal RNA genes with multiple, endonuclease-encoding group I introns
title_fullStr Cyanobacterial ribosomal RNA genes with multiple, endonuclease-encoding group I introns
title_full_unstemmed Cyanobacterial ribosomal RNA genes with multiple, endonuclease-encoding group I introns
title_short Cyanobacterial ribosomal RNA genes with multiple, endonuclease-encoding group I introns
title_sort cyanobacterial ribosomal rna genes with multiple, endonuclease-encoding group i introns
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1995217/
https://www.ncbi.nlm.nih.gov/pubmed/17825109
http://dx.doi.org/10.1186/1471-2148-7-159
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