Cargando…

Purriato is a conserved small open reading frame gene that interacts with the CASA pathway to regulate muscle homeostasis and epithelial tissue growth in Drosophila

Recent advances in proteogenomic techniques and bioinformatic pipelines have permitted the detection of thousands of translated small Open Reading Frames (smORFs), which contain less than 100 codons, in eukaryotic genomes. Hundreds of these actively translated smORFs display conserved sequence, stru...

Descripción completa

Detalles Bibliográficos
Autores principales: Pueyo, Jose I., Salazar, Jorge, Grincho, Carolina, Berni, Jimena, Towler, Benjamin P., Newbury, Sarah F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036370/
https://www.ncbi.nlm.nih.gov/pubmed/36968202
http://dx.doi.org/10.3389/fcell.2023.1117454
_version_ 1784911638063742976
author Pueyo, Jose I.
Salazar, Jorge
Grincho, Carolina
Berni, Jimena
Towler, Benjamin P.
Newbury, Sarah F.
author_facet Pueyo, Jose I.
Salazar, Jorge
Grincho, Carolina
Berni, Jimena
Towler, Benjamin P.
Newbury, Sarah F.
author_sort Pueyo, Jose I.
collection PubMed
description Recent advances in proteogenomic techniques and bioinformatic pipelines have permitted the detection of thousands of translated small Open Reading Frames (smORFs), which contain less than 100 codons, in eukaryotic genomes. Hundreds of these actively translated smORFs display conserved sequence, structure and evolutionary signatures indicating that the translated peptides could fulfil important biological roles. Despite their abundance, only tens of smORF genes have been fully characterised; these act mainly as regulators of canonical proteins involved in essential cellular processes. Importantly, some of these smORFs display conserved functions with their mutations being associated with pathogenesis. Thus, investigating smORF roles in Drosophila will not only expand our understanding of their functions but it may have an impact in human health. Here we describe the function of a novel and essential Drosophila smORF gene named purriato (prto). prto belongs to an ancient gene family whose members have expanded throughout the Protostomia clade. prto encodes a transmembrane peptide which is localized in endo-lysosomes and perinuclear and plasma membranes. prto is dynamically expressed in mesodermal tissues and imaginal discs. Targeted prto knockdown (KD) in these organs results in changes in nuclear morphology and endo-lysosomal distributions correlating with the loss of sarcomeric homeostasis in muscles and reduction of mitosis in wing discs. Consequently, prto KD mutants display severe reduction of motility, and shorter wings. Finally, our genetic interaction experiments show that prto function is closely associated to the CASA pathway, a conserved mechanism involved in turnover of mis-folded proteins and linked to muscle dystrophies and neurodegenerative diseases. Thus, this study shows the relevance of smORFs in regulating important cellular functions and supports the systematic characterisation of this class of genes to understand their functions and evolution.
format Online
Article
Text
id pubmed-10036370
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-100363702023-03-25 Purriato is a conserved small open reading frame gene that interacts with the CASA pathway to regulate muscle homeostasis and epithelial tissue growth in Drosophila Pueyo, Jose I. Salazar, Jorge Grincho, Carolina Berni, Jimena Towler, Benjamin P. Newbury, Sarah F. Front Cell Dev Biol Cell and Developmental Biology Recent advances in proteogenomic techniques and bioinformatic pipelines have permitted the detection of thousands of translated small Open Reading Frames (smORFs), which contain less than 100 codons, in eukaryotic genomes. Hundreds of these actively translated smORFs display conserved sequence, structure and evolutionary signatures indicating that the translated peptides could fulfil important biological roles. Despite their abundance, only tens of smORF genes have been fully characterised; these act mainly as regulators of canonical proteins involved in essential cellular processes. Importantly, some of these smORFs display conserved functions with their mutations being associated with pathogenesis. Thus, investigating smORF roles in Drosophila will not only expand our understanding of their functions but it may have an impact in human health. Here we describe the function of a novel and essential Drosophila smORF gene named purriato (prto). prto belongs to an ancient gene family whose members have expanded throughout the Protostomia clade. prto encodes a transmembrane peptide which is localized in endo-lysosomes and perinuclear and plasma membranes. prto is dynamically expressed in mesodermal tissues and imaginal discs. Targeted prto knockdown (KD) in these organs results in changes in nuclear morphology and endo-lysosomal distributions correlating with the loss of sarcomeric homeostasis in muscles and reduction of mitosis in wing discs. Consequently, prto KD mutants display severe reduction of motility, and shorter wings. Finally, our genetic interaction experiments show that prto function is closely associated to the CASA pathway, a conserved mechanism involved in turnover of mis-folded proteins and linked to muscle dystrophies and neurodegenerative diseases. Thus, this study shows the relevance of smORFs in regulating important cellular functions and supports the systematic characterisation of this class of genes to understand their functions and evolution. Frontiers Media S.A. 2023-03-10 /pmc/articles/PMC10036370/ /pubmed/36968202 http://dx.doi.org/10.3389/fcell.2023.1117454 Text en Copyright © 2023 Pueyo, Salazar, Grincho, Berni, Towler and Newbury. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Pueyo, Jose I.
Salazar, Jorge
Grincho, Carolina
Berni, Jimena
Towler, Benjamin P.
Newbury, Sarah F.
Purriato is a conserved small open reading frame gene that interacts with the CASA pathway to regulate muscle homeostasis and epithelial tissue growth in Drosophila
title Purriato is a conserved small open reading frame gene that interacts with the CASA pathway to regulate muscle homeostasis and epithelial tissue growth in Drosophila
title_full Purriato is a conserved small open reading frame gene that interacts with the CASA pathway to regulate muscle homeostasis and epithelial tissue growth in Drosophila
title_fullStr Purriato is a conserved small open reading frame gene that interacts with the CASA pathway to regulate muscle homeostasis and epithelial tissue growth in Drosophila
title_full_unstemmed Purriato is a conserved small open reading frame gene that interacts with the CASA pathway to regulate muscle homeostasis and epithelial tissue growth in Drosophila
title_short Purriato is a conserved small open reading frame gene that interacts with the CASA pathway to regulate muscle homeostasis and epithelial tissue growth in Drosophila
title_sort purriato is a conserved small open reading frame gene that interacts with the casa pathway to regulate muscle homeostasis and epithelial tissue growth in drosophila
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036370/
https://www.ncbi.nlm.nih.gov/pubmed/36968202
http://dx.doi.org/10.3389/fcell.2023.1117454
work_keys_str_mv AT pueyojosei purriatoisaconservedsmallopenreadingframegenethatinteractswiththecasapathwaytoregulatemusclehomeostasisandepithelialtissuegrowthindrosophila
AT salazarjorge purriatoisaconservedsmallopenreadingframegenethatinteractswiththecasapathwaytoregulatemusclehomeostasisandepithelialtissuegrowthindrosophila
AT grinchocarolina purriatoisaconservedsmallopenreadingframegenethatinteractswiththecasapathwaytoregulatemusclehomeostasisandepithelialtissuegrowthindrosophila
AT bernijimena purriatoisaconservedsmallopenreadingframegenethatinteractswiththecasapathwaytoregulatemusclehomeostasisandepithelialtissuegrowthindrosophila
AT towlerbenjaminp purriatoisaconservedsmallopenreadingframegenethatinteractswiththecasapathwaytoregulatemusclehomeostasisandepithelialtissuegrowthindrosophila
AT newburysarahf purriatoisaconservedsmallopenreadingframegenethatinteractswiththecasapathwaytoregulatemusclehomeostasisandepithelialtissuegrowthindrosophila