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Creation of purple leaf peanut germplasm through metabolic engineering of the betalain biosynthesis pathway
Dongxin Huai, Jie Wu, Xiaomeng Xue, Hao Liu, Nian Liu, Li Huang, Liying Yan, Yuning Chen, Xin Wang, Qianqian Wang, Yanping Kang, Zhihui Wang, Yanbin Hong, Huifang Jiang, Boshou Liao, Yong Lei
2025, 24 (4): 1606-1609.   DOI: 10.1016/j.jia.2024.09.034
Abstract106)      PDF in ScienceDirect      
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Upregulation of the glycine-rich protein-encoding gene GhGRPL enhances plant tolerance to abiotic and biotic stressors by promoting secondary cell wall development
Wanting Yu, Yonglu Dai, Junmin Chen, Aimin Liang, Yiping Wu, Qingwei Suo, Zhong Chen, Xingying Yan, Chuannan Wang, Hanyan Lai, Fanlong Wang, Jingyi Zhang, Qinzhao Liu, Yi Wang, Yaohua Li, Lingfang Ran, Jie Xiang, Zhiwu Pei, Yuehua Xiao, Jianyan Zeng
2024, 23 (10): 3311-3327.   DOI: 10.1016/j.jia.2024.05.025
Abstract93)      PDF in ScienceDirect      
Abiotic and biotic stressors adversely affect plant survival, biomass generation, and crop yields.  As the global availability of arable land declines and the impacts of global warming intensify, such stressors may have increasingly pronounced effects on agricultural productivity.  Currently, researchers face the overarching challenge of comprehensively enhancing plant resilience to abiotic and biotic stressors.  The secondary cell wall plays a crucial role in bolstering the stress resistance of plants.  To increase plant resistance to stress through genetic manipulation of the secondary cell wall, we cloned a cell wall protein designated glycine-rich protein-like (GhGRPL) from cotton fibers, and found that it is specifically expressed during the period of secondary cell wall biosynthesis.  Notably, this protein differs from its Arabidopsis homolog, AtGRP, since its glycine-rich domain is deficient in glycine residues.  GhGRPL is involved in secondary cell wall deposition.  Upregulation of GhGRPL enhances lignin accumulation and, consequently, the thickness of the secondary cell walls, thereby increasing the plant’s resistance to abiotic stressors, such as drought and salinity, and biotic threats, including Verticillium dahliae infection.  Conversely, interference with GhGRPL expression in cotton reduces lignin accumulation and compromises that resistance.  Taken together, our findings elucidate the role of GhGRPL in regulating secondary cell wall development through its influence on lignin deposition, which, in turn, reinforces cell wall robustness and impermeability.  These findings highlight the promising near-future prospect of adopting GhGRPL as a viable, effective approach for enhancing plant resilience to abiotic and biotic stress factors.


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CRISPR-based genetic control strategies for insect pests
Ying YAN, Roswitha A. AUMANN, Irina HÄCKER, Marc F. SCHETELIG
2023, 22 (3): 651-668.   DOI: 10.1016/j.jia.2022.11.003
Abstract265)      PDF in ScienceDirect      

Genetic control strategies such as the sterile insect technique have successfully fought insect pests worldwide.  The CRISPR (clustered regularly interspaced short palindromic repeats) technology, together with high-quality genomic resources obtained in more and more species, greatly facilitates the development of novel genetic control insect strains that can be used in area-wide and species-specific pest control programs.  Here, we review the research progress towards state-of-art CRISPR-based genetic control strategies, including gene drive, sex ratio distortion, CRISPR-engineered genetic sexing strains, and precision-guided sterile insect technique.  These strategies’ working mechanisms, potential resistance development mechanisms, and regulations are illustrated and discussed.  In addition, recent developments such as stacked and conditional systems are introduced.  We envision that the advances in genetic technology will continue to be one of the driving forces for developing the next generation of pest control strategies.  

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Cytogenetic characterization and molecular marker development of a novel wheat-Thinopyrum ponticum 5E (5D) disomic substitution line with resistance to powdery mildew and stripe rust 
Xiaofang Cheng, Yi Xiao, Luhui Wang, Xiaoying Yang, Pingchuan Deng, Jixin Zhao, Changyou Wang, Chunhuan Chen, Tingdong Li, Wanquan Ji
DOI: 10.1016/j.jia.2024.04.012 Online: 10 May 2024
Abstract30)      PDF in ScienceDirect      
Thinopyrum ponticum (2n=10x=70), a wild relative of common wheat (Triticum aestivum L.), is considered an invaluable genetic resource for wheat improvement due to its abundance of genes that confer resistance to biotic and abiotic stresses.  This study focused on the CH97 line, derived from the BC1F7 progeny of a cross between wheat cv. 7182 and Th. ponticum.  Cytological evidence showed that CH97 has 42 chromosomes, forming 21 bivalents at meiotic metaphase I, with the bivalents subsequently separating and moving to opposite poles during meiotic anaphase I.  Through a combination of FISH (fluorescence in situ hybridization), GISH (genomic in situ hybridization), mc-GISH (multicolor genomic in situ hybridization), and liquid array analysis, it was determined that CH97 comprises 40 wheat chromosomes and two alien chromosomes from the Ee genome of Th. ponticum, featuring the absence of a pair of 5D chromosomes and variations in 1B, 6B, and 7B chromosomes.  These findings confirm that CH97 is a stable wheat-Th. ponticum 5E (5D) alien disomic substitution line.  Inoculation experiments revealed that CH97 exhibits high resistance to wheat powdery mildew and stripe rust throughout the growth period, in contrast to the highly susceptible common wheat parent 7182.  Compared to 7182, CH97 displayed improvements in spikelets per spike, thousand-kernel weight, and kernel length.  Additionally, utilizing SLAF-seq technology, chromosome 5E-specific molecular markers were developed and validated, achieving a 33.3% success rate, which facilitates marker-assisted selection to enhance disease resistance in wheat.  Overall, the CH97 substitution line, with its resistance to diseases and improved agronomic traits represents valuable new germplasm for wheat chromosome engineering and breeding.
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