Cargando…

Operons Are a Conserved Feature of Nematode Genomes

The organization of genes into operons, clusters of genes that are co-transcribed to produce polycistronic pre-mRNAs, is a trait found in a wide range of eukaryotic groups, including multiple animal phyla. Operons are present in the class Chromadorea, one of the two main nematode classes, but their...

Descripción completa

Detalles Bibliográficos
Autores principales: Pettitt, Jonathan, Philippe, Lucas, Sarkar, Debjani, Johnston, Christopher, Gothe, Henrike Johanna, Massie, Diane, Connolly, Bernadette, Müller, Berndt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4125394/
https://www.ncbi.nlm.nih.gov/pubmed/24931407
http://dx.doi.org/10.1534/genetics.114.162875
_version_ 1782329772992364544
author Pettitt, Jonathan
Philippe, Lucas
Sarkar, Debjani
Johnston, Christopher
Gothe, Henrike Johanna
Massie, Diane
Connolly, Bernadette
Müller, Berndt
author_facet Pettitt, Jonathan
Philippe, Lucas
Sarkar, Debjani
Johnston, Christopher
Gothe, Henrike Johanna
Massie, Diane
Connolly, Bernadette
Müller, Berndt
author_sort Pettitt, Jonathan
collection PubMed
description The organization of genes into operons, clusters of genes that are co-transcribed to produce polycistronic pre-mRNAs, is a trait found in a wide range of eukaryotic groups, including multiple animal phyla. Operons are present in the class Chromadorea, one of the two main nematode classes, but their distribution in the other class, the Enoplea, is not known. We have surveyed the genomes of Trichinella spiralis, Trichuris muris, and Romanomermis culicivorax and identified the first putative operons in members of the Enoplea. Consistent with the mechanism of polycistronic RNA resolution in other nematodes, the mRNAs produced by genes downstream of the first gene in the T. spiralis and T. muris operons are trans-spliced to spliced leader RNAs, and we are able to detect polycistronic RNAs derived from these operons. Importantly, a putative intercistronic region from one of these potential enoplean operons confers polycistronic processing activity when expressed as part of a chimeric operon in Caenorhabditis elegans. We find that T. spiralis genes located in operons have an increased likelihood of having operonic C. elegans homologs. However, operon structure in terms of synteny and gene content is not tightly conserved between the two taxa, consistent with models of operon evolution. We have nevertheless identified putative operons conserved between Enoplea and Chromadorea. Our data suggest that operons and “spliced leader” (SL) trans-splicing predate the radiation of the nematode phylum, an inference which is supported by the phylogenetic profile of proteins known to be involved in nematode SL trans-splicing.
format Online
Article
Text
id pubmed-4125394
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Genetics Society of America
record_format MEDLINE/PubMed
spelling pubmed-41253942014-08-11 Operons Are a Conserved Feature of Nematode Genomes Pettitt, Jonathan Philippe, Lucas Sarkar, Debjani Johnston, Christopher Gothe, Henrike Johanna Massie, Diane Connolly, Bernadette Müller, Berndt Genetics Investigations The organization of genes into operons, clusters of genes that are co-transcribed to produce polycistronic pre-mRNAs, is a trait found in a wide range of eukaryotic groups, including multiple animal phyla. Operons are present in the class Chromadorea, one of the two main nematode classes, but their distribution in the other class, the Enoplea, is not known. We have surveyed the genomes of Trichinella spiralis, Trichuris muris, and Romanomermis culicivorax and identified the first putative operons in members of the Enoplea. Consistent with the mechanism of polycistronic RNA resolution in other nematodes, the mRNAs produced by genes downstream of the first gene in the T. spiralis and T. muris operons are trans-spliced to spliced leader RNAs, and we are able to detect polycistronic RNAs derived from these operons. Importantly, a putative intercistronic region from one of these potential enoplean operons confers polycistronic processing activity when expressed as part of a chimeric operon in Caenorhabditis elegans. We find that T. spiralis genes located in operons have an increased likelihood of having operonic C. elegans homologs. However, operon structure in terms of synteny and gene content is not tightly conserved between the two taxa, consistent with models of operon evolution. We have nevertheless identified putative operons conserved between Enoplea and Chromadorea. Our data suggest that operons and “spliced leader” (SL) trans-splicing predate the radiation of the nematode phylum, an inference which is supported by the phylogenetic profile of proteins known to be involved in nematode SL trans-splicing. Genetics Society of America 2014-08 2014-06-13 /pmc/articles/PMC4125394/ /pubmed/24931407 http://dx.doi.org/10.1534/genetics.114.162875 Text en Copyright © 2014 by the Genetics Society of America Available freely online through the author-supported open access option.
spellingShingle Investigations
Pettitt, Jonathan
Philippe, Lucas
Sarkar, Debjani
Johnston, Christopher
Gothe, Henrike Johanna
Massie, Diane
Connolly, Bernadette
Müller, Berndt
Operons Are a Conserved Feature of Nematode Genomes
title Operons Are a Conserved Feature of Nematode Genomes
title_full Operons Are a Conserved Feature of Nematode Genomes
title_fullStr Operons Are a Conserved Feature of Nematode Genomes
title_full_unstemmed Operons Are a Conserved Feature of Nematode Genomes
title_short Operons Are a Conserved Feature of Nematode Genomes
title_sort operons are a conserved feature of nematode genomes
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4125394/
https://www.ncbi.nlm.nih.gov/pubmed/24931407
http://dx.doi.org/10.1534/genetics.114.162875
work_keys_str_mv AT pettittjonathan operonsareaconservedfeatureofnematodegenomes
AT philippelucas operonsareaconservedfeatureofnematodegenomes
AT sarkardebjani operonsareaconservedfeatureofnematodegenomes
AT johnstonchristopher operonsareaconservedfeatureofnematodegenomes
AT gothehenrikejohanna operonsareaconservedfeatureofnematodegenomes
AT massiediane operonsareaconservedfeatureofnematodegenomes
AT connollybernadette operonsareaconservedfeatureofnematodegenomes
AT mullerberndt operonsareaconservedfeatureofnematodegenomes