4.7 Article

The novel activity of Argonautes in intron splicing: A transcriptome-wide survey in plants

Journal

JOURNAL OF PLANT PHYSIOLOGY
Volume 270, Issue -, Pages -

Publisher

ELSEVIER GMBH
DOI: 10.1016/j.jplph.2022.153632

Keywords

Argonaute (AGO); Alternative splicing (AS); Intron splicing; Organ-specific; Arabidopsis(Arabidopsisthaliana); Rice (Oryza sativa)

Categories

Funding

  1. National Natural Science Foundation of China [31970637, 32070655, 31771457]

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This study reveals the novel role of plant AGO proteins in intron splicing by demonstrating their involvement in the RNA interference pathway. The research shows that AGOs can either positively or negatively regulate intron excision in Arabidopsis. Furthermore, organ-specific regulation of AGO-dependent introns was observed. RIP-seq data supports the high intron binding affinities of AGOs. Identifying protein interactors involved in mRNA binding provides insight into the mechanisms underlying AGO-mediated RNA splicing. The study also highlights the importance of AGO18 in intron expression in rice.
The importance of the evolutionarily conserved Argonaute (AGO) proteins has been well recognized for their involvement in the RNA interference pathways. Recent discoveries in animals demonstrated that AGOs also participate in alternative splicing (AS). Motivated by the question whether the AGO proteins are also functional in RNA splicing in plants, we searched for the introns excised through an AGO-dependent manner in Arabidopsis (Arabidopsis thaliana). RNA sequencing (RNA-seq) data analysis uncovered hundreds of the introns up-or down-regulated in the ago1 and ago4 mutants, respectively. For different genes, AGOs might play either a positive or a negative role in intron excision, which was further validated by reverse transcription-polymerase chain reaction (RT-PCR). Some introns were specifically regulated by one of the AGO proteins, while some were regulated by both AGOs. Besides, a large portion of the AGO-dependent introns were organ-specifically regulated. RNA immunoprecipitation combined with high-throughput sequencing (RIP-seq) revealed that both AGOs preferen-tially bound to the intronic regions, supporting their high intron binding affinities. Immunoprecipitation fol-lowed by mass spectrometry (IP-MS) was performed to identify the proteins potentially interacting with the two AGOs. Six novel interactors (two interacting with AGO1 and four with both AGOs) involved in mRNA binding were uncovered, which might facilitate AGO-intron recognition. Analysis of the RNA-seq data from the rice (Oryza sativa) ago18 mutants revealed that hundreds of the introns were expressed in an AGO18-dependent manner. In summary, our results point to the novel role of the plant AGOs in intron splicing, paving a way for further studies on the mechanisms underlying AGO-mediated RNA splicing.

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