Ipomoea trifida strain:Y601
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ABSTRACT:
PROVIDER: PRJNA376216 | ENA |
REPOSITORIES: ENA
Similar Datasets
Project description:Hexaploid I.trifida Transcriptome Assembly
| PRJNA378859 | ENA
Project description:Drought transcriptome of hexaploid Ipomoea trifida
| PRJNA384302 | ENA
Project description:QTL-seq for root thickness in wild sweetpotato
| PRJDB10778 | ENA
Project description:I. trifida NCNSP0306 biotic and abiotic stress RNA-Seq
| PRJNA491290 | ENA
Project description:Diploid Ipomoea trifida Genome sequencing and assembly
| PRJNA362521 | ENA
Project description:Ipomoea trifida cultivar:NCNSP0306 Genome sequencing and assembly
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Project description:Ipomoea trifida cultivar:Y601 Transcriptome or Gene expression
| PRJNA384881 | ENA
Project description:BACKGROUND:Sweetpotato (Ipomoea batatas (L.) Lam.) is the seventh most important crop in the world and is mainly cultivated for its underground storage root (SR). The genetic studies of this species have been hindered by a lack of high-quality reference sequence due to its complex genome structure. Diploid Ipomoea trifida is the closest relative and putative progenitor of sweetpotato, which is considered a model species for sweetpotato, including genetic, cytological, and physiological analyses. RESULTS:Here, we generated the chromosome-scale genome sequence of SR-forming diploid I. trifida var. Y22 with high heterozygosity (2.20%). Although the chromosome-based synteny analysis revealed that the I. trifida shared conserved karyotype with Ipomoea nil after the separation, I. trifida had a much smaller genome than I. nil due to more efficient eliminations of LTR-retrotransposons and lack of species-specific amplification bursts of LTR-RTs. A comparison with four non-SR-forming species showed that the evolution of the beta-amylase gene family may be related to SR formation. We further investigated the relationship of the key gene BMY11 (with identity 47.12% to beta-amylase 1) with this important agronomic trait by both gene expression profiling and quantitative trait locus (QTL) mapping. And combining SR morphology and structure, gene expression profiling and qPCR results, we deduced that the products of the activity of BMY11 in splitting starch granules and be recycled to synthesize larger granules, contributing to starch accumulation and SR swelling. Moreover, we found the expression pattern of BMY11, sporamin proteins and the key genes involved in carbohydrate metabolism and stele lignification were similar to that of sweetpotato during the SR development. CONCLUSIONS:We constructed the high-quality genome reference of the highly heterozygous I. trifida through a combined approach and this genome enables a better resolution of the genomics feature and genome evolutions of this species. Sweetpotato SR development genes can be identified in I. trifida and these genes perform similar functions and patterns, showed that the diploid I. trifida var. Y22 with typical SR could be considered an ideal model for the studies of sweetpotato SR development.
| S-EPMC6444543 | biostudies-literature