Enteric infection induces Lark-mediated intron retention at the 5′ end of Drosophila genes
Abstract Background RNA splicing is a key post-transcriptional mechanism that generates protein diversity and contributes to the fine-tuning of gene expression, which may facilitate adaptation to environmental challenges. Here, we employ a systems approach to study alternative splicing changes upon...
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doaj-3d9ca418408842eca65439d8d29521d42021-01-17T12:56:37ZengBMCGenome Biology1474-760X2020-01-0121111910.1186/s13059-019-1918-6Enteric infection induces Lark-mediated intron retention at the 5′ end of Drosophila genesMaroun Bou Sleiman0Michael Vincent Frochaux1Tommaso Andreani2Dani Osman3Roderic Guigo4Bart Deplancke5Laboratory of Integrative Systems Physiology, Institue of Bioengineering, Ecole Polytechnique Fédérale de Lausanne (EPFL)Laboratory of System Biology and Genetics and Swiss Institute of Bioinformatics, Institute of Bioengineering, Ecole Polytechnique Fédérale de Lausanne (EPFL)Computational Biology and Data Mining Group, Institute of Molecular BiologyFaculty of Sciences III and Azm Center for Research in Biotechnology and its Applications, LBA3B, EDST, Lebanese UniversityCentre for Genomic Regulation (CRG), The Barcelona Institute of Science and TechnologyLaboratory of Integrative Systems Physiology, Institue of Bioengineering, Ecole Polytechnique Fédérale de Lausanne (EPFL)Abstract Background RNA splicing is a key post-transcriptional mechanism that generates protein diversity and contributes to the fine-tuning of gene expression, which may facilitate adaptation to environmental challenges. Here, we employ a systems approach to study alternative splicing changes upon enteric infection in females from classical Drosophila melanogaster strains as well as 38 inbred lines. Results We find that infection leads to extensive differences in isoform ratios, which results in a more diverse transcriptome with longer 5′ untranslated regions (5′UTRs). We establish a role for genetic variation in mediating inter-individual splicing differences, with local splicing quantitative trait loci (local-sQTLs) being preferentially located at the 5′ end of transcripts and directly upstream of splice donor sites. Moreover, local-sQTLs are more numerous in the infected state, indicating that acute stress unmasks a substantial number of silent genetic variants. We observe a general increase in intron retention concentrated at the 5′ end of transcripts across multiple strains, whose prevalence scales with the degree of pathogen virulence. The length, GC content, and RNA polymerase II occupancy of these introns with increased retention suggest that they have exon-like characteristics. We further uncover that retained intron sequences are enriched for the Lark/RBM4 RNA binding motif. Interestingly, we find that lark is induced by infection in wild-type flies, its overexpression and knockdown alter survival, and tissue-specific overexpression mimics infection-induced intron retention. Conclusion Our collective findings point to pervasive and consistent RNA splicing changes, partly mediated by Lark/RBM4, as being an important aspect of the gut response to infection.https://doi.org/10.1186/s13059-019-1918-6InfectionGutSplicingIntron retentionDrosophila melanogasterDGRP |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Maroun Bou Sleiman Michael Vincent Frochaux Tommaso Andreani Dani Osman Roderic Guigo Bart Deplancke |
spellingShingle |
Maroun Bou Sleiman Michael Vincent Frochaux Tommaso Andreani Dani Osman Roderic Guigo Bart Deplancke Enteric infection induces Lark-mediated intron retention at the 5′ end of Drosophila genes Genome Biology Infection Gut Splicing Intron retention Drosophila melanogaster DGRP |
author_facet |
Maroun Bou Sleiman Michael Vincent Frochaux Tommaso Andreani Dani Osman Roderic Guigo Bart Deplancke |
author_sort |
Maroun Bou Sleiman |
title |
Enteric infection induces Lark-mediated intron retention at the 5′ end of Drosophila genes |
title_short |
Enteric infection induces Lark-mediated intron retention at the 5′ end of Drosophila genes |
title_full |
Enteric infection induces Lark-mediated intron retention at the 5′ end of Drosophila genes |
title_fullStr |
Enteric infection induces Lark-mediated intron retention at the 5′ end of Drosophila genes |
title_full_unstemmed |
Enteric infection induces Lark-mediated intron retention at the 5′ end of Drosophila genes |
title_sort |
enteric infection induces lark-mediated intron retention at the 5′ end of drosophila genes |
publisher |
BMC |
series |
Genome Biology |
issn |
1474-760X |
publishDate |
2020-01-01 |
description |
Abstract Background RNA splicing is a key post-transcriptional mechanism that generates protein diversity and contributes to the fine-tuning of gene expression, which may facilitate adaptation to environmental challenges. Here, we employ a systems approach to study alternative splicing changes upon enteric infection in females from classical Drosophila melanogaster strains as well as 38 inbred lines. Results We find that infection leads to extensive differences in isoform ratios, which results in a more diverse transcriptome with longer 5′ untranslated regions (5′UTRs). We establish a role for genetic variation in mediating inter-individual splicing differences, with local splicing quantitative trait loci (local-sQTLs) being preferentially located at the 5′ end of transcripts and directly upstream of splice donor sites. Moreover, local-sQTLs are more numerous in the infected state, indicating that acute stress unmasks a substantial number of silent genetic variants. We observe a general increase in intron retention concentrated at the 5′ end of transcripts across multiple strains, whose prevalence scales with the degree of pathogen virulence. The length, GC content, and RNA polymerase II occupancy of these introns with increased retention suggest that they have exon-like characteristics. We further uncover that retained intron sequences are enriched for the Lark/RBM4 RNA binding motif. Interestingly, we find that lark is induced by infection in wild-type flies, its overexpression and knockdown alter survival, and tissue-specific overexpression mimics infection-induced intron retention. Conclusion Our collective findings point to pervasive and consistent RNA splicing changes, partly mediated by Lark/RBM4, as being an important aspect of the gut response to infection. |
topic |
Infection Gut Splicing Intron retention Drosophila melanogaster DGRP |
url |
https://doi.org/10.1186/s13059-019-1918-6 |
work_keys_str_mv |
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