LZLijie Zhang

Lijie Zhang

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Lijie Zhang has a total of 14 co-authors. Here are the top co-authors by number of shared publications:

  • Lingqiang Wang

    Guangxi Sugarcane Bio-breeding Laboratory, State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, College of Agriculture, Guangxi University, China

    2 shared publications
  • Yuxin Wu

    College of Life Sciences and Technology, Huazhong University of Sciences and Technology, Wuhan 430074, China

    2 shared publications
  • Chongjian Ma

    Guangdong Provincial Key Laboratory of Utilization and Conservation of Food and Medicinal Resources in Northern Region, School of Biology and Agriculture, Shaoguan University, Shaoguan 512005, China

    1 shared publication
  • Haiyu Zhou

    State Key Laboratory of Conservation and Utilization of Subtropical Agricultural Biological Resources, Guangxi University, Nanning 530004, China

    1 shared publication
  • Jingzheng Wang

    College of Plant Science and Technology, Huazhong Agricultural University, Wuhan 430070, China

    1 shared publication
  • Lihua Hu

    State Key Laboratory of Conservation and Utilization of Subtropical Agricultural Biological Resources, Guangxi University, Nanning, China

    1 shared publication

Latest Publications

  • Open Access

    Evolution and Functional Dynamics of the BAG Gene Family in Passion Fruit (Passiflora edulis)

    by Munsif Ali Shad, Songguo Wu, Yuxin Wu, Lijie Zhang, Yuhong Zhou, Jingzheng Wang, Lingqiang Wang, Chongjian Ma, Lihua Hu

    B-cell lymphoma 2 (Bcl-2)-associated athanogene (BAG) family proteins are co-chaperones that regulate growth, development, and cell death and are evolutionarily conserved across eukaryotes. The BAG gene family has attracted intense interest in human health research, but its plant counterparts have received little attention. In this study, we conducted a genome-wide scan of the BAG family in passion fruit, a crop of great economic importance. Fifteen PeBAG genes were identified, with all but PeBAG5 having multiple copies. PeBAG members, each characterized by a BAG domain, were categorized into two groups: Group 1 (PeBAG1/2/3/4) with extra ubiquitin domains, and Group 2 (PeBAG5/6-1/6-2) with additional plant-specific calmodulin-binding domains. The transcriptome data suggest that PeBAGs exhibit high gene expression in stems, flowers, and fruit, while PeBAG4-3 and 6-1 upregulated under hormonal and abiotic stresses. qRT-PCR further confirmed the heat stress activation of PeBAG4-3 and 6-1. Subcellular localization in planta revealed varied compartmentalization, with members in the nucleus, cytoplasm, and plastids demonstrating functional divergence. This study provides a guide for investigating and employing PeBAG genes to improve heat resistance in passion fruit.


  • Open Access

    Determining the Role of OsAGP6P in Anther Development Within the Arabinogalactan Peptide Family of Rice (Oryza sativa)

    by Shuai Shao, Yuxin Wu, Lijie Zhang, Zhiyuan Zhao, Xianlong Li, Mingchong Yang, Haiyu Zhou, Songguo Wu, Lingqiang Wang

    Arabinogalactan proteins (AGPs) are complex proteoglycans present in plant cell walls across the kingdom. They play crucial roles in biological functions throughout the plant life cycle. In this study, we identified 43 gene members of the AG peptide (an AGP subfamily) within the rice genome, detailing their structure, protein-conserved domains, and motif compositions for the first time. We also examined the expression patterns of these genes across 18 tissues and organs, especially the different parts of the flower (anthers, pollen, pistil, sperm cells, and egg cells). Interestingly, the expression of some AG peptides is mainly present in the pollen grain. Transcription data and GUS staining confirmed that OsAGP6P—a member of the AG peptide gene family—is expressed in the stamen during pollen development stages 11–14, which are critical for maturation as microspores form after meiosis of pollen mother cells. It became noticeable from stage 11, when exine formation occurred—specifically at stage 12, when the intine began to develop. The overexpression of this gene in rice decreased the seed-setting rate (from 91.5% to 30.5%) and plant height (by 21.9%) but increased the tillering number (by 34.1%). These results indicate that AGP6P contributes to the development and fertility of pollen, making it a valuable gene target for future genetic manipulation of plant sterility through gene overexpression or editing.