4.7 Article

Gap-free genome assembly and comparative analysis reveal the evolution and anthocyanin accumulation mechanism of Rhodomyrtus tomentosa

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HORTICULTURE RESEARCH
卷 10, 期 3, 页码 -

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OXFORD UNIV PRESS INC
DOI: 10.1093/hr/uhad005

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This study presented a chromosome-level, gap-free T2T genome assembly of Rhodomyrtus tomentosa using PacBio and ONT long read sequencing. The assembled genome size was 470.35 Mb with 11 pseudochromosomes, and it contained 33,382 genes and 239.31 Mb of repetitive sequences. Phylogenetic analysis revealed the independent evolution of R. tomentosa and a recent whole-genome duplication event. The study also identified the major compounds of anthocyanins and their synthetic pathways in R. tomentosa and suggested that the coloring and high anthocyanin accumulation in R. tomentosa were determined by the activation of anthocyanin synthesis pathway.
Rhodomyrtus tomentosa is an important fleshy-fruited tree and a well-known medicinal plant of the Myrtaceae family that is widely cultivated in tropical and subtropical areas of the world. However, studies on the evolution and genomic breeding of R. tomentosa were hindered by the lack of a reference genome. Here, we presented a chromosome-level gap-free T2T genome assembly of R. tomentosa using PacBio and ONT long read sequencing. We assembled the genome with size of 470.35 Mb and contig N50 of similar to 43.80 Mb with 11 pseudochromosomes. A total of 33 382 genes and 239.31 Mb of repetitive sequences were annotated in this genome. Phylogenetic analysis elucidated the independent evolution of R. tomentosa starting from 14.37MYA and shared a recent WGD event with other Myrtaceae species. We identified four major compounds of anthocyanins and their synthetic pathways in R. tomentosa. Comparative genomic and gene expression analysis suggested the coloring and high anthocyanin accumulation in R. tomentosa tends to be determined by the activation of anthocyanin synthesis pathway. The positive selection and up-regulation of MYB transcription factors were the implicit factors in this process. The copy number increase of downstream anthocyanin transport-related OMT and GST gene were also detected in R. tomentosa. Expression analysis and pathway identification enriched the importance of starch degradation, response to stimuli, effect of hormones, and cell wall metabolism during the fleshy fruit development in Myrtaceae. Our genome assembly provided a foundation for investigating the origins and differentiation of Myrtaceae species and accelerated the genetic improvement of R. tomentosa.

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