J Integr Plant Biol.

• Resources •    

Gap-free genome and efficient transcript purification system reveals the genomes diversity and chlorophyll degradation mechanism in pitaya

Jiaxuan Chen1†, Fangping Li1,2†*, Jieying Liu2, Yuchen Mao1, Zhenpeng Gan2, Haifei Hu2, Irfan Ali Sabir1, Imran Khan1, Jiayi Chen1, Canbin Chen1, Zhike Zhang1, Jietang Zhao1, Guibing Hu1, Shaokui Wang2 and Yonghua Qin1*   

  1. 1. Guangdong Provincial Key Laboratory of Postharvest Science of Fruits and Vegetables and Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (South China), Ministry of Agriculture and Rural Affairs, College of Horticulture, South China Agricultural University, Guangzhou 510642, China
    2. Guangdong Provincial Key Laboratory of Plant Molecular Breeding, State Key Laboratory for Conservation and Utilization of Subtropical Agro‐Bioresources, South China Agricultural University, Guangzhou 510642, China

    These authors contributed equally in this work.
    *Correspondences: Fangping Li (fangping.li@scau.edu.cn); Yonghua Qin (qinyh@scau.edu.cn, Dr. Qin is fully responsible for the distribution of all materials associated with this article)
  • Received:2024-12-03 Accepted:2025-04-02 Online:2025-06-05
  • Supported by:
    This work was supported by the Natural Science Foundation of Guangdong Province (2025A1515012561 and 2024A1515013152), National Natural Science Foundation of China (W2433071 and 31972367), and Provincial Rural Revitalization Strategy Special Project of Guangdong in 2024 (2024‐NPY‐00‐030).

Abstract: Pitaya is an important perennial herbaceous fruit tree. The color of fruit determines pitaya nutritive (and attractive) value, which is considered as an important objective in breeding improvement. In this study, we reported the first telomere-to-telomere (T2T) gap-free genome of “Shuangse No. 1” pitaya (Hylocereus polyrhizus; red peel). Two high-quality genomes for “Dahong” (H. polyrhizus; red peel) and “Honghuaqinglong” (H. stenopterus; stay-green) were further assembled, aiming to explore the genetic diversity of pitaya genomes. In further analysis, we noticed a high proportion of viral contamination in pitaya tissues, which hindered the efficient utilization of transcriptomic data. To address this issue, we analyzed 111 pitaya transcriptome data from different geographic regions to characterize and separate viral components. Then we developed an efficient, novel, and universal transcript purification system for pitaya transcriptomes by applying it to 27 samples from different tissues and species, thereby enhancing the utility for transcriptomic and broader biological research. Combining the purified transcriptomic data with comparative genomic analyses, we identified HuERF72, a transcription factor (TF) that potentially regulates chlorophyll degradation in pitaya. Interaction assays and plant transformation elucidated that HuERF72 acts as a repressive TF by directly binding to the promoter of HuSGR1, a key structural gene in the chlorophyll degradation pathway. This study provides high-quality genomic resources and novel methodologies for molecular investigations in pitaya. Additionally, the proposed regulatory network advances our understanding of the transcriptional regulatory mechanisms underlying chlorophyll degradation, offering valuable insights into the genetic improvement of pitaya.

Key words: chlorophyll degradation, gap‐free genome,  HuERF72,  pitaya, transcript purification system

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