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PreprintCC BYbioRxiv

A chromosome-scale genome and transcriptomic atlas of taro (Colocasia esculenta) corm development

  1. 1Guangxi Academy of Agricultural Sciences

Abstract

Aims: Taro corm development depends on carbohydrate metabolism, but cultivar-level annotation differences complicate the integration of genome comparisons and expression data. We assembled a GY2 reference genome and analysed developmental and tissue transcriptomes to characterise corm-associated transcription in a sequence-aware comparative framework. Data resources generated: The 2.309-Gb GY2 assembly contains 14 pseudomolecules and 20,063 primary gene models. Comparisons with LXY and Bun Long were integrated with six-stage corm and four-tissue RNA-seq datasets. Gene annotations, genomic comparisons, processed expression matrices and analysis scripts are supplied in Data S1, with figure source data in Data S2. Key results: The 14 GY2 pseudomolecules represent 98.83% of the assembly; contig and scaffold N50 values are 11.55 and 182.12 Mb, and liliopsid BUSCO completeness is 97.7%. Genome sequence searches reduced candidate assembly-specific orthogroups from 1,820 to 168. A total of 11,884 genes varied significantly across corm stages. Among 593 strictly corm-enriched genes, 522 were also development-responsive, including nine of 20 selected carbohydrate-associated genes. Utility of the resource: Consistent GY2 v3 gene identifiers link genomic homology, collinearity and gene-level expression, supporting cross-cultivar comparisons and prioritisation of corm-associated candidate genes.

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BibTeX
@misc{cai2026chromosomescale,
  title = {{A chromosome-scale genome and transcriptomic atlas of taro (Colocasia esculenta) corm development}},
  author = {X. Cai and F. He},
  howpublished = {bioRxiv},
  year = {2026},
  month = oct,
  doi = {10.64898/2026.10.11.758265},
  url = {https://www.biorxiv.org/content/10.64898/2026.10.11.758265v1},
  note = {CC BY},
}
RIS
TY  - UNPB
TI  - A chromosome-scale genome and transcriptomic atlas of taro (Colocasia esculenta) corm development
AU  - X. Cai
AU  - F. He
PY  - 2026
DA  - 2026/10/11
PB  - bioRxiv
DO  - 10.64898/2026.10.11.758265
UR  - https://www.biorxiv.org/content/10.64898/2026.10.11.758265v1
AB  - Aims: Taro corm development depends on carbohydrate metabolism, but cultivar-level annotation differences complicate the integration of genome comparisons and expression data. We assembled a GY2 reference genome and analysed developmental and tissue transcriptomes to characterise corm-associated transcription in a sequence-aware comparative framework. Data resources generated: The 2.309-Gb GY2 assembly contains 14 pseudomolecules and 20,063 primary gene models. Comparisons with LXY and Bun Long were integrated with six-stage corm and four-tissue RNA-seq datasets. Gene annotations, genomic comparisons, processed expression matrices and analysis scripts are supplied in Data S1, with figure source data in Data S2. Key results: The 14 GY2 pseudomolecules represent 98.83% of the assembly; contig and scaffold N50 values are 11.55 and 182.12 Mb, and liliopsid BUSCO completeness is 97.7%. Genome sequence searches reduced candidate assembly-specific orthogroups from 1,820 to 168. A total of 11,884 genes varied significantly across corm stages. Among 593 strictly corm-enriched genes, 522 were also development-responsive, including nine of 20 selected carbohydrate-associated genes. Utility of the resource: Consistent GY2 v3 gene identifiers link genomic homology, collinearity and gene-level expression, supporting cross-cultivar comparisons and prioritisation of corm-associated candidate genes.
ER  -