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Pectin methylesterase inhibitors GhPMEI53 and AtPMEI19 improve seed germination by modulating cell wall plasticity in cotton and Arabidopsis
Yayue Pei, Yakong Wang, Zhenzhen Wei, Ji Liu, Yonghui Li, Shuya Ma, Ye Wang, Fuguang Li, Jun Peng, Zhi Wang
2024, 23 (10): 3487-3505.   DOI: 10.1016/j.jia.2024.03.036
Abstract77)      PDF in ScienceDirect      
The germination process of seeds is influenced by the interplay between two opposing factors, pectin methylesterase (PME) and pectin methylesterase inhibitor (PMEI), which collectively regulate patterns of pectin methylesterification.  Despite the recognized importance of pectin methylesterification in seed germination, the specific mechanisms that govern this process remain unclear.  In this study, we demonstrated that the overexpression of GhPMEI53 is associated with a decrease in PME activity and an increase in pectin methylesterification.  This leads to seed cell wall softening, which positively regulates cotton seed germination.  AtPMEI19, the homologue in Arabidopsis thaliana, plays a similar role in seed germination to GhPMEI53, indicating a conserved function and mechanism of PMEI in seed germination regulation.  Further studies revealed that GhPMEI53 and AtPMEI19 directly contribute to promoting radicle protrusion and seed germination by inducing cell wall softening and reducing mechanical strength.  Additionally, the pathways of abscicic acid (ABA) and gibberellin (GA) in the transgenic materials showed significant changes, suggesting that GhPMEI53/AtPMEI19-mediated pectin methylesterification serves as a regulatory signal for the related phytohormones involved in seed germination.  In summary, GhPMEI53 and its homologs alter the mechanical properties of cell walls, which influence the mechanical resistance of the endosperm or testa.  Moreover, they impact cellular phytohormone pathways (e.g., ABA and GA) to regulate seed germination.  These findings enhance our understanding of pectin methylesterification in cellular morphological dynamics and signaling transduction, and contribute to a more comprehensive understanding of the PME/PMEI gene superfamily in plants.


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EPSPS regulates cell elongation by disrupting the balance of lignin and flavonoid biosynthesis in cotton
Qingdi Yan, Wei Hu, Chenxu Gao, Lan Yang, Jiaxian Yang, Renju Liu, Masum Billah, Yongjun Lin, Ji Liu, Pengfei Miao, Zhaoen Yang, Fuguang Li, Wenqiang Qin
2024, 23 (10): 3437-3456.   DOI: 10.1016/j.jia.2023.11.002
Abstract97)      PDF in ScienceDirect      
EPSPS is a key gene in the shikimic acid synthesis pathway that has been widely used in breeding crops with herbicide resistance.  However, its role in regulating cell elongation is poorly understood.  Through the overexpression of EPSPS genes, we generated lines resistant to glyphosate that exhibit an unexpected dwarf phenotype.  A representative line, DHR1, exhibits a stable dwarf phenotype throughout its entire growth period.  Except for plant height, the other agronomic traits of DHR1 are similar to its transgenic explants ZM24.  Paraffin section observations showed that DHR1 internodes are shortened due to reduced elongation and division of the internode cells.  Exogenous hormones confirmed that DHR1 is not a classical brassinolide (BR)- or gibberellin (GA)-related dwarfing mutant.  Hybridization analysis and fine mapping confirmed that the EPSPS gene is the causal gene for dwarfism, and the phenotype can be inherited in different genotypes.  Transcriptome and metabolome analyses showed that genes associated with the phenylpropanoid synthesis pathway are enriched in DHR1 compared with ZM24.  Flavonoid metabolites are enriched in DHR1, whereas lignin metabolites are reduced.  The enhancement of flavonoids likely results in differential expression of auxin signal pathway genes and alters the auxin response, subsequently affecting cell elongation.  This study provides a new strategy for generating dwarfs and will accelerate advancements in light simplification in the cultivation and mechanized harvesting of cotton.


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Genetic identification and characterization of a novel locus for wheat kernel length
Qian Liu, Qijing Xuan, Yuxin Lan, Xinlin Xie, Bin Chen, Jianing You, Longxing Su, Md Nahibuzzaman Lohani, Lei Wu, Xinrong Hu, Li Yin, Yanlin Liu, Tongzhu Wang, Qiantao Jiang, Yuming Wei, Youliang Zheng, Chunji Liu, Hongwei Geng, Jian Ma
DOI: 10.1016/j.jia.2024.10.005 Online: 25 October 2024
Abstract26)      PDF in ScienceDirect      

Kernel length (KL) is one of the components determining grain weight (GW) in wheat.  In this study, we firstly detected a putative locus on chromosome arm 2BL from a mutant BLS2 with long kernels using a Bulked Segregant Analysis (BSA) combined with a 60 K SNP array.  This putative locus was then confirmed as a major and stable QTL based on linkage mapping.  The locus, Qkl.sau-BC-2B.1, was mapped in an interval of 0.4 cM, and phenotypic variance explained by it varied from 17.01 to 30.53% across different environments.  Effects of this locus was further verified in a second population.  The positive allele of the locus could significantly increase hundred-kernel weight and prolong anthesis date, but it did not affect plant height, tiller number, spike length, and spikelet number per spike.  Expression and sequencing analyses identified TraesCS2B02G478100, possessing a G to C transition variation leading to an amino acid change, as the likely candidate gene underlying the locus.  Further, a new model for analyzing the genetic basis of yield-related traits was proposed. Taken together, our results provide a foundation for subsequent gene mining and breeding utilization of this promising QTL for KL.

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Major and stably expressed QTL for grain cadmium, copper, and magnesium concentrations independent of main agronomic traits in tetraploid wheat
Zhaoyong Zeng, Jian Ma, Ying Wang, Yuxin Lan, Longxing Su, Bin Chen, Huaping Tang, Deyi Hu, Bingjie Chen, Yinggang Xu, Yang Li, Xuesong Gao, Chunji Liu, Guangdeng Chen
DOI: 10.1016/j.jia.2024.12.019 Online: 17 December 2024
Abstract9)      PDF in ScienceDirect      

Excessive cadmium (GrCdc) and deficiencies of copper (GrCuc) and magnesium (GrMgc) in grains pose serious human health risks.  Common wheat breeding has reduced genetic diversity within elite germplasm resources, negatively impacting future wheat production.  Thus, identifying loci controlling GrCdc, GrCuc, and GrMgc from tetraploid wheat and introducing them into common wheat is essential for genetic improvement.  In this study, we identified quantitative trait loci (QTL) for GrCdc, GrCuc, and GrMgc using the Wheat 55K single nucleotide polymorphism (SNP) array-based linkage map and phenotypic data across multiple environments in recombinant inbred lines derived from a cross between a wild emmer accession (LM001) and an endemic tetraploid wheat in Sichuan (Ailanmai).  Four major, stably expressed QTL were identified.  Three of these, including QGrCdc.sau-AM-5A for GrCdc, QGrCuc.sau-AM-4A for GrCuc, and QGrMgc.sau-AM-4A for GrMgc, were novel. These loci were validated using tightly linked Kompetitive Allele Specific PCR (KASP) markers in various genetic backgrounds. Several candidate genes (TRIDC5AG052690, TRIDC5BG060070, and TRIDC4AG008520) with sequence variations were predicted to influence Cd, Cu, or Mg absorption and transport within these QTL intervals.  Correlation analysis revealed that GrCdc was not correlated with GrCuc or GrMgc, although GrCuc was significantly correlated with GrMgc.  Furthermore, no significant effects of GrCdc, GrCuc, or GrMgc on agronomic traits were detected, as no correlation between them and any of the eleven agronomic traits investigated was observed.  Additionally, QGrCuc.sau-AM-4A colocalized with QGrMgc.sau-AM-4A, suggesting potential shared physiological and/or genetic control.  Altogether, these stably expressed QTL across environments provide theoretical guidance for further germplasm improvement and fine mapping.

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