Fungal virulence and development is regulated by alternative pre-mRNA 3'end processing in Magnaporthe oryzae.

RNA-binding proteins play a central role in post-transcriptional mechanisms that control gene expression. Identification of novel RNA-binding proteins in fungi is essential to unravel post-transcriptional networks and cellular processes that confer identity to the fungal kingdom. Here, we carried ou...

Full description

Saved in:
Bibliographic Details
Main Authors: Marina Franceschetti, Emilio Bueno, Richard A Wilson, Sara L Tucker, Concepción Gómez-Mena, Grant Calder, Ane Sesma
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-12-01
Series:PLoS Pathogens
Online Access:https://journals.plos.org/plospathogens/article/file?id=10.1371/journal.ppat.1002441&type=printable
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849434128153313280
author Marina Franceschetti
Emilio Bueno
Richard A Wilson
Sara L Tucker
Concepción Gómez-Mena
Grant Calder
Ane Sesma
author_facet Marina Franceschetti
Emilio Bueno
Richard A Wilson
Sara L Tucker
Concepción Gómez-Mena
Grant Calder
Ane Sesma
author_sort Marina Franceschetti
collection DOAJ
description RNA-binding proteins play a central role in post-transcriptional mechanisms that control gene expression. Identification of novel RNA-binding proteins in fungi is essential to unravel post-transcriptional networks and cellular processes that confer identity to the fungal kingdom. Here, we carried out the functional characterisation of the filamentous fungus-specific RNA-binding protein RBP35 required for full virulence and development in the rice blast fungus. RBP35 contains an N-terminal RNA recognition motif (RRM) and six Arg-Gly-Gly tripeptide repeats. Immunoblots identified two RBP35 protein isoforms that show a steady-state nuclear localisation and bind RNA in vitro. RBP35 coimmunoprecipitates in vivo with Cleavage Factor I (CFI) 25 kDa, a highly conserved protein involved in polyA site recognition and cleavage of pre-mRNAs. Several targets of RBP35 have been identified using transcriptomics including 14-3-3 pre-mRNA, an important integrator of environmental signals. In Magnaporthe oryzae, RBP35 is not essential for viability but regulates the length of 3'UTRs of transcripts with developmental and virulence-associated functions. The Δrbp35 mutant is affected in the TOR (target of rapamycin) signaling pathway showing significant changes in nitrogen metabolism and protein secretion. The lack of clear RBP35 orthologues in yeast, plants and animals indicates that RBP35 is a novel auxiliary protein of the polyadenylation machinery of filamentous fungi. Our data demonstrate that RBP35 is the fungal equivalent of metazoan CFI 68 kDa and suggest the existence of 3'end processing mechanisms exclusive to the fungal kingdom.
format Article
id doaj-art-39694424c8fe4cf8978d300b437c6cf8
institution Kabale University
issn 1553-7366
1553-7374
language English
publishDate 2011-12-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Pathogens
spelling doaj-art-39694424c8fe4cf8978d300b437c6cf82025-08-20T03:26:47ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742011-12-01712e100244110.1371/journal.ppat.1002441Fungal virulence and development is regulated by alternative pre-mRNA 3'end processing in Magnaporthe oryzae.Marina FranceschettiEmilio BuenoRichard A WilsonSara L TuckerConcepción Gómez-MenaGrant CalderAne SesmaRNA-binding proteins play a central role in post-transcriptional mechanisms that control gene expression. Identification of novel RNA-binding proteins in fungi is essential to unravel post-transcriptional networks and cellular processes that confer identity to the fungal kingdom. Here, we carried out the functional characterisation of the filamentous fungus-specific RNA-binding protein RBP35 required for full virulence and development in the rice blast fungus. RBP35 contains an N-terminal RNA recognition motif (RRM) and six Arg-Gly-Gly tripeptide repeats. Immunoblots identified two RBP35 protein isoforms that show a steady-state nuclear localisation and bind RNA in vitro. RBP35 coimmunoprecipitates in vivo with Cleavage Factor I (CFI) 25 kDa, a highly conserved protein involved in polyA site recognition and cleavage of pre-mRNAs. Several targets of RBP35 have been identified using transcriptomics including 14-3-3 pre-mRNA, an important integrator of environmental signals. In Magnaporthe oryzae, RBP35 is not essential for viability but regulates the length of 3'UTRs of transcripts with developmental and virulence-associated functions. The Δrbp35 mutant is affected in the TOR (target of rapamycin) signaling pathway showing significant changes in nitrogen metabolism and protein secretion. The lack of clear RBP35 orthologues in yeast, plants and animals indicates that RBP35 is a novel auxiliary protein of the polyadenylation machinery of filamentous fungi. Our data demonstrate that RBP35 is the fungal equivalent of metazoan CFI 68 kDa and suggest the existence of 3'end processing mechanisms exclusive to the fungal kingdom.https://journals.plos.org/plospathogens/article/file?id=10.1371/journal.ppat.1002441&type=printable
spellingShingle Marina Franceschetti
Emilio Bueno
Richard A Wilson
Sara L Tucker
Concepción Gómez-Mena
Grant Calder
Ane Sesma
Fungal virulence and development is regulated by alternative pre-mRNA 3'end processing in Magnaporthe oryzae.
PLoS Pathogens
title Fungal virulence and development is regulated by alternative pre-mRNA 3'end processing in Magnaporthe oryzae.
title_full Fungal virulence and development is regulated by alternative pre-mRNA 3'end processing in Magnaporthe oryzae.
title_fullStr Fungal virulence and development is regulated by alternative pre-mRNA 3'end processing in Magnaporthe oryzae.
title_full_unstemmed Fungal virulence and development is regulated by alternative pre-mRNA 3'end processing in Magnaporthe oryzae.
title_short Fungal virulence and development is regulated by alternative pre-mRNA 3'end processing in Magnaporthe oryzae.
title_sort fungal virulence and development is regulated by alternative pre mrna 3 end processing in magnaporthe oryzae
url https://journals.plos.org/plospathogens/article/file?id=10.1371/journal.ppat.1002441&type=printable
work_keys_str_mv AT marinafranceschetti fungalvirulenceanddevelopmentisregulatedbyalternativepremrna3endprocessinginmagnaportheoryzae
AT emiliobueno fungalvirulenceanddevelopmentisregulatedbyalternativepremrna3endprocessinginmagnaportheoryzae
AT richardawilson fungalvirulenceanddevelopmentisregulatedbyalternativepremrna3endprocessinginmagnaportheoryzae
AT saraltucker fungalvirulenceanddevelopmentisregulatedbyalternativepremrna3endprocessinginmagnaportheoryzae
AT concepciongomezmena fungalvirulenceanddevelopmentisregulatedbyalternativepremrna3endprocessinginmagnaportheoryzae
AT grantcalder fungalvirulenceanddevelopmentisregulatedbyalternativepremrna3endprocessinginmagnaportheoryzae
AT anesesma fungalvirulenceanddevelopmentisregulatedbyalternativepremrna3endprocessinginmagnaportheoryzae