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Extracellular superoxide dismutase VdSOD5 is required for virulence in Verticillium dahliae
TIAN Li, HUANG Cai-min, ZHANG Dan-dan, LI Ran, CHEN Jie-yin, SUN Wei-xia, QIU Nian-wei, DAI Xiao-feng
2021, 20 (7): 1858-1870.   DOI: 10.1016/S2095-3119(20)63353-6
Abstract135)      PDF in ScienceDirect      
Plants produce reactive oxygen species (ROS) to defend pathogens.  To counteract this attack, certain pathogens express superoxide dismutases (SODs) to scavenge host-derived ROS.  However, the roles of SODs in Verticillium dahliae, an important vascular pathogen, are not clear.  Our previous study has shown that a putative extracellular SOD (VdSOD5) of V. dahliae is significantly induced by culturing in cotton tissues, suggesting that VdSOD5 may play an important role in host–pathogen interactions and virulence.  Here, we showed that VdSOD5 encoded a superoxide dismutase with a co-factor copper-binding site and a functional signal peptide that can conduct protein secretion in an invertase-mutated yeast strain.  The mutations in VdSOD5 (ΔVdSOD5) did not change the normal vegetative growth and conidial production but reduced the virulence of V. dahliae on susceptible host cotton.  Further studies showed that the transcription of VdSOD5 was significantly up-regulated during the early stage of infection, and the loss-of-function of VdSOD5 decreased culture filtrate and fungal tissue SOD activities of V. dahliae by 74 and 28%, respectively.  Compared to the wild-type strain Vd991, the ΔVdSOD5 showed the same sensitivity to the intracellular ROS generator menadione.  Furthermore, nitroblue tetrazolium (NBT) staining demonstrated that VdSOD5 functioned in the detoxification of superoxides generated by host roots during infection.  These results suggest that VdSOD5 of V. dahliae is an important virulence factor, secreted out of cells to combat host-derived ROS. 
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Yield-related agronomic traits evaluation for hybrid wheat and relations of ethylene and polyamines biosynthesis to filling at the mid-grain filling stage
YANG Wei-bing, QIN Zhi-lie, SUN Hui, LIAO Xiang-zheng, GAO Jian-gang, WANG Yong-bo, HOU Qi-ling, CHEN Xian-chao, TIAN Li-ping, ZHANG li-ping, MA Jin-xiu, CHEN Zhao-bo, ZHANG Feng-ting, ZHAO Chang-ping
2020, 19 (10): 2407-2418.   DOI: 10.1016/S2095-3119(19)62873-X
Abstract106)      PDF in ScienceDirect      
Because of the yield increase of 3.5–15% compared to conventional wheat, hybrid wheat is considered to be one of the main ways to greatly improve the wheat yield in the future.  In this study, we performed a principal component analysis (PCA) on two-line hybrids wheat and their parents using the grain weight (GW), the length of spike (LS), the kernel number of spike (KSN), and spike number (SPN) as variables.  The results showed that the variables could be classified into three main factors, the weight factor (factor 1), the quantity factor 1 (factor 2) and the quantity factor 2 (factor 3), which accounted for 37.1, 22.6 and 18.5%, respectively of the total variance in different agronomic variables, suggesting that the GW is an important indicator for evaluating hybrid combinations, and the grain weight of restorer line (RGW) could be used as a reference for parents selection.  The hybrid combination with a higher score in factor 1 direction and larger mid-parent heterosis (MPH) of the GW and its parents were used to carry out the analysis of grain filling, 1-aminocylopropane-1-carboxylicacid (ACC) and polyamine synthesis related genes.  The results suggested that the GW of superior grain was significantly higher than that of inferior grains in BS1453×JS1 (H) and its parents.  Both grain types showed a weight of H between BS1453 (M) and JS1(R), and a larger MPH, which may be caused by their differences in the active filling stage and the grain filling rate.  The ADP-glucose pyrophosphorylase (AGPase), granule bound starch synthase I (GBSSI), starch synthase III (SSS), and starch branching enzyme-I (SBE-I) expression levels of H were intermediated between M and R, which might be closely related to MPH formation of the GW.  Compared with R and H, the GW of M at maturity was the lowest.  The expression levels of spermidine synthase 2 (Spd2), ornithine decarboxylase (ODC) and S-adenosylmethionine decarboxylase (SAMDC) had significantly positive correlations with the grain filling rate (r=0.77*, 0.51*, 0.59*), suggesting their major roles in the grain filling and heterosis formation.  These provide a theoretical basis for improving the GW of photo-thermo-sensitive male sterile lines (PTSMSL) by changing the endogenous polyamine synthesis in commercial applications.
  
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TaRLK-1B: A novel wheat gene conferring resistance to leaf rust revealed by a genome-wide association study
Shujuan Liu, Li Zhao, Chenyang Hao, Yuxue Pan, Mengjiao Guo, Yilin Huang, Haixia Liu, Jian Hou, Zaifeng Li, Tian Li, Xinhong Chen, Xueyong Zhang
DOI: 10.1016/j.jia.2025.02.028 Online: 19 February 2025
Abstract5)      PDF in ScienceDirect      

Leaf rust is a highly destructive foliar disease in wheat, causing major constraints in wheat production worldwide.  In this study, we conducted a comprehensive assessment of adult plant resistance to leaf rust in 590 accessions from the advanced backcross-nested association mapping plus inter-crossed (AB-NAMIC) population. We used 660K genotype data to perform a genome-wide association study (GWAS), identifying significant quantitative trait loci (QTLs) on chromosomes 1B, 2A, 2B, and 7D, with particular emphasis on the candidate gene TaRLK-1B on chromosome 1B.  A cleaved amplified polymorphic sequence (CAPS) marker was developed based on TaRLK-1B haplotypes and effectively differentiated between resistant and susceptible varieties.  This gene encodes a membrane-localized leucine-rich repeat receptor-like kinase (LRR-RLK) that is upregulated in response to the fungal infection that causes leaf rust.  Targeted knockout of TaRLK-1B in wheat led to reduced resistance to leaf rust, underscoring its essential role as a positive regulator in defense against this disease.  Additionally, we propose that TaRLK-1B interacts with the receptor-like cytoplasmic kinase TaRLCK1B, potentially facilitating immune signal transduction.  Our findings also demonstrate that pyramiding minor effect QTLs significantly increases resistance to leaf rust.  This study provides novel insights into resistance genes and valuable QTL information, which could improve marker-assisted wheat breeding efforts.

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An integrate methods to improve the high efficiency of embryo rescue breeding in seedless grapes
Xi Chen, Khalid Ayesha, Xue Wen, Yanan Zhang, Mengru Dou, Kexuan Jia, Yong Wang, Yuling Li, Feng Sun, Guotian Liu, Yan Xu
DOI: 10.1016/j.jia.2025.02.042 Online: 21 February 2025
Abstract1)      PDF in ScienceDirect      

The embryo rescue technique plays an essential part in developing new varieties of seedless grapes. To enhance the efficiency of seedless grape embryo rescue breeding, this study evaluated 22 hybrid combinations, It systematically probed into the impacts of diverse parental genotypes and plant hormones on both embryo development and germination. In addition, an in-depth exploration was carried out regarding the transformation of abnormal plantlets. Results indicate that ‘Ruby Seedless’, ‘Delight’, ‘Huozhouheiyu’, ‘Zitian Seedless’, and ‘Zhengyan Seedless’ are suitable as maternal parents, while ‘Zitian Seedless’, ‘Shennongxiangfeng’, ‘Hongqitezao’, and ‘Guibao’ are optimal as paternal parents. Among these combinations, ‘Ruby Seedless × Shennongxiangfeng’ and ‘Ruby Seedless × Zitian Seedless’ demonstrated the highest embryo rescue efficiency. Their embryo development rates were 55.05% and 59.76%, yielding 1,348 and 2,235 viable plantlets, respectively. When 1.0 mg L-1 ZT(Zeatin) was added to the MM3 + 0.2 mg L-1 IAA (Indole - 3 - Acetic Acid) embryo development medium, the development rate of the ‘Ruby Seedless × Zitian Seedless’ embryos went up by a huge 64.73%. In the germination medium WPM, the supplementation of 0.2 mg L-1 ZT + 0.2 mg L-1 IAA resulted in the highest germination rate of 85.71% for the hybrid combination ‘Huozhouheiyu × Shine Muscat’. Furthermore, we successfully recovered a total of 3,365 abnormal plantlets and regenerated 1,234 normal plantlets through direct transformation and cotyledon induction. After hybridization, we successfully transplanted 4,287 plants. This study offers theoretical insights that can enhance the efficiency of embryo rescue breeding for seedless grapes, offering valuable resources for future breeding programs.

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