Transcription of lncRNA ACoS-AS1 is essential to trans-splicing between SlPsy1 and ACoS-AS1 that causes yellow fruit in tomato. Issue 4 (2nd April 2020)

• Record Type: Journal Article
• Authors: Xiao, Yao; Kang, Baoshan; Li, Meng; Xiao, Liangjun; Xiao, Han; Shen, Huolin; Yang, Wencai
• Is Part Of: RNA biology. Volume 17:Issue 4(2020)
• Page Start: 596
• Page End: 607
• Publication Date: 2020-04-02
• Subjects: Trans-splicing -- SlPsy1 -- lncRNA -- carotenoids -- yellow fruit -- tomato; RNA -- Periodicals; Molecular biology -- Periodicals; Molecular biology; RNA; Periodicals; 572.8805
• DOI: 10.1080/15476286.2020.1721095
• Languages: English
• ISSNs: 1547-6286

Abstract

ABSTRACT: Phytoene synthase (PSY) has been considered as an important regulatory enzyme in carotenoids biosynthesis pathway. Previous study finds that the yellow fruit in Solanum lycopersicum var. cerasiforme accession PI 114490 is caused by loss-of-function of SlPSY1 due to trans -splicing between SlPsy1 and an unknown gene transcribed from neighbour opposite strand DNA of SlPsy1 . The genomic DNA sequences of SlPsy1 between red and yellow-fruited tomato lines have one single-nucleotide polymorphism (SNP) in the fourth intron and one SSR in the intergenic region. In the current study, the cause of trans -splicing event was further investigated. The data showed that the previously defined unknown gene was a putative long non-coding RNA ACoS-AS1 with three variants in many yellow-fruited tomato lines. The intronic SNP and intergenic SSR were tightly associated with trans -splicing event SlPsy1-ACoS-AS1 . However, transgenic tomato lines carrying the genomic DNA of SlPsy1 from PI 114490 did not generate transcripts of ACoS-AS1 and SlPsy1-ACoS-AS1 suggesting that only the intronic SNP could not cause the trans -splicing event. Over-expression of SlPsy1-ACoS-AS1 in red-fruited tomato line M82 did not have any phenotype change while over-expression of wild type SlPsy1 resulted in altered leaf colour. Sub-cellular localization analysis showed that SlPSY1-ACoS-AS1 could not enter plastids where SlPSY1 has its enzyme activity. Mutation of ACoS-AS1 in PI 114490 generated by CRISPR/Cas9 techniques resulted in red fruits implying that ACoS-AS1 was essential to trans -splicing event SlPsy1-ACoS-AS1 . The results obtained here will extend knowledge to understand the mechanism of trans -splicing event SlPsy1-ACoS-AS1 and provide additional information for the regulation of carotenoids biosynthesis.