LncRNA FLAIL affects alternative splicing and represses flowering in Arabidopsis

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How the noncoding genome affects cellular functions is a key biological question. A particular challenge is to distinguish the effects of noncoding DNA elements from long noncoding RNAs (lncRNAs) that coincide at the same loci. Here, we identified the flowering-associated intergenic lncRNA (FLAIL) in Arabidopsis through early flowering flail mutants. Expression of FLAIL RNA from a different chromosomal location in combination with strand-specific RNA knockdown characterized FLAIL as a trans-acting RNA molecule. FLAIL directly binds to differentially expressed target genes that control flowering via RNA–DNA interactions through conserved sequence motifs. FLAIL interacts with protein and RNA components of the spliceosome to affect target mRNA expression through co-transcriptional alternative splicing (AS) and linked chromatin regulation. In the absence of FLAIL, splicing defects at the direct FLAIL target flowering gene LACCASE 8 (LAC8) correlated with reduced mRNA expression. Double mutant analyses support a model where FLAIL-mediated splicing of LAC8 promotes its mRNA expression and represses flowering. Our study suggests lncRNAs as accessory components of the spliceosome that regulate AS and gene expression to impact organismal development.

OriginalsprogEngelsk
Artikelnummere110921
TidsskriftEMBO Journal
Vol/bind42
Udgave nummer11
Antal sider21
ISSN0261-4189
DOI
StatusUdgivet - 2023

Bibliografisk note

Funding Information:
We thank Prof. Anders H. Lund for kindly providing Luc probes. We thank Prof. Peter Brodersen for sharing amiRNA vectors. We thank Dr. Pan Zhu and Dr. Marta Montes for assistance with ChIRP, Prof. Egle Kudirkiene and Dr. Quentin Thomas for sequencing. We thank Jasmin Dilgen, Evangelia Lakita, Ida Damholt Richardt, Lei Li for technical assistance, Jan Høstrup for excellent plant care, Prof. Staffan Persson, Alessandro Giannetti, Dr. Deyong Zhu, and the members of Marquardt lab for discussions and manuscript feedback. SM acknowledges the funding from the Novo Nordisk Foundation (NNF15OC0014202, NNF19OC0057485, NNF21OC0066776), Carlsberg Foundation infrastructure support (CF18‐1075), a Copenhagen Plant Science Centre Young Investigator Starting grant and EMBO YIP. This project receives support from the European Research Council (ERC) under the European Union's Horizon 2020 Research and Innovation Programme (StG2017‐757411 to SM). ADLN would like to acknowledge funding from NSF‐IOS 1758532 and NSF‐IOS 2023310.

Publisher Copyright:
© 2023 The Authors. Published under the terms of the CC BY NC ND 4.0 license.

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