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Late sowing enhances lodging resistance of wheat plants by improving the biosynthesis and accumulation of lignin and cellulose
DONG Xiu-chun, QIAN Tai-feng, CHU Jin-peng, ZHANG Xiu, LIU Yun-jing, DAI Xing-long, HE Ming-rong
2023, 22 (5): 1351-1365.   DOI: 10.1016/j.jia.2022.08.024
Abstract278)      PDF in ScienceDirect      

Delayed sowing mitigates lodging in wheat.  However, the mechanism underlying the enhanced lodging resistance in wheat has yet to be fully elucidated.  Field experiments were conducted to investigate the effects of sowing date on lignin and cellulose metabolism, stem morphological characteristics, lodging resistance, and grain yield.  Seeds of Tainong 18, a winter wheat variety, were sown on October 8 (normal sowing) and October 22 (late sowing) during both of the 2015–2016 and 2016–2017 growing seasons.  The results showed that late sowing enhanced the lodging resistance of wheat by improving the biosynthesis and accumulation of lignin and cellulose.  Under late sowing, the expression levels of key genes (TaPAL, TaCCR, TaCOMT, TaCAD, and TaCesA1, 3, 4, 7, and 8) and enzyme activities (TaPAL and  TaCAD) related to lignin and cellulose biosynthesis peaked 4–12 days earlier, and except for the TaPAL, TaCCR, and TaCesA1 genes and TaPAL, in most cases they were significantly higher than under normal sowing.  As a result, lignin and cellulose accumulated quickly during the stem elongation stage.  The mean and maximum accumulation rates of lignin and cellulose increased, the maximum accumulation contents of lignin and cellulose were higher, and the cellulose accumulation duration was prolonged.  Consequently, the lignin/cellulose ratio and lignin content were increased from 0 day and the cellulose content was increased from 11 days after jointing onward.  Our main finding is that the improved biosynthesis and accumulation of lignin and cellulose were responsible for increasing the stem-filling degree, breaking strength, and lodging resistance.  The major functional genes enhancing lodging resistance in wheat that are induced by delayed sowing need to be determined.

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TaABI19 positively regulates grain development in wheat
LIU Yun-chuan, WANG Xiao-lu, HAO Chen-yang, IRSHAD Ahsan, LI Tian, LIU Hong-xia, HOU Jian, ZHANG Xue-yong
2023, 22 (1): 41-51.   DOI: 10.1016/j.jia.2022.08.049
Abstract274)      PDF in ScienceDirect      
Starch is the most important component in endosperm, and its synthesis is regulated by multiple transcription factors (TFs) in cereals. However, whether the functions of these TFs are conserved or not among cereals unclear yet. Here, we cloned a B3 family TF, named as TaABI19 based on its orthologous in maize (Zea mays L.). Alignment of DNA and protein showed that ABI19 was conserved in maize and wheat (Triticum aestivum L.). We found that TaABI19 was highly expressed in young spike and developing grains and encoded a nucleus-localized transcriptional activator in wheat. The taabi19-b1 null mutants obtained by EMS performed down-regulation of starch synthesis, shorter grain length and lower thousand grain weight (TGW). Furthermore, we provided TaABI19 could bind to the promoters of TaPBF homology genes and enhance their expression. Haplotype association showed that TaABI19-B1 was significantly associated with TGW. We found that Hap2 and Hap3 were favored and underwent positive selection in China wheat breeding. Less than fifty percent in the modern cultivars conveying favored haplotypes indicates TaABI19 still can be considered as target loci for marker-assisted selection breeding to increase TGW in China.
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Image-based root phenotyping for field-grown crops: An example under maize/soybean intercropping
HUI Fang, XIE Zi-wen, LI Hai-gang, GUO Yan, LI Bao-guo, LIU Yun-ling, MA Yun-tao
2022, 21 (6): 1606-1619.   DOI: 10.1016/S2095-3119(20)63571-7
Abstract258)      PDF in ScienceDirect      
Root architecture, which determines the water and nutrient uptake ability of crops, is highly plastic in response to soil environmental changes and different cultivation patterns.  Root phenotyping for field-grown crops, especially topological trait extraction, is rarely performed.  In this study, an image-based semi-automatic root phenotyping method for field-grown crops was developed.  The method consisted of image acquisition, image denoising and segmentation, trait extraction and data analysis.  Five global traits and 40 local traits were extracted with this method.  A good consistency in 1st-order lateral root branching was observed between the visually counted values and the values extracted using the developed method, with R2=0.97.  Using the method, we found that the interspecific advantages for maize mainly occurred within 5 cm from the root base in the nodal roots of the 5th–7th nodes, and that the obvious inhibition of soybean was mostly reflected within 20 cm from the root base.  Our study provides a novel approach with high-throughput and high-accuracy for field research on root morphology and branching features.  It could be applied to the 3D reconstruction of field-grown root system architecture to improve the inputs to data-driven models (e.g., OpenSimRoot) that simulate root growth, solute transport and water uptake.
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Effects of dietary amylose to amylopectin ratio on growth performance, carcass quality characteristics and meat fatty acids in Chinese Qinchuan cattle
PIAO Min-yu, HU Feng-ming, KONG Fan-lin, LIU Yun-long, WANG Shuo, CUI Kai, SUN Tao, DIAO Qi-yu, TU Yan
2021, 20 (12): 3256-2169.   DOI: 10.1016/S2095-3119(20)63576-6
Abstract181)      PDF in ScienceDirect      
This study evaluated the effects of the dietary starch amylose/amylopectin ratio on growth performance, rumen fermentation and blood parameters, carcass characteristics and marbling score, and meat fatty acid profiles and transcriptional changes in the genes involved in the gluconeogenesis pathway in Chinese Qinchuan cattle.  Forty-five cattle were randomly divided into three groups.  The bulls were fed a control diet (middle amylose/amylopectin ratio=0.47) or diets with either waxy corn starch (WS) inclusion (low amylose/amylopectin ratio=0.23) or pea starch (PS) inclusion (high amylose/amylopectin ratio=0.60) for 90 days.  The bulls were individually allowed to receive the diets at the daily amount of at least 2.1% of their individual BW twice daily.  The bulls were weighed at 45-day intervals, and blood and rumen fluid samples were also collected at 45-day intervals.  The bulls were slaughtered and longissimus thoracis (LT) samples were collected for meat quality measurements.  Compared with PS, the average daily gain (ADG) and feed efficiency in control and WS were increased (P<0.05) during d 0 to 45.  However, the feed efficiency in PS was increased (P<0.05) compared with the control and WS during d 46 to 90.  During the whole feeding trial, the ADG in control and WS showed trends that were higher (0.05<P<0.1) than that of PS, while other growth performance measures and feed intake did not differ (P>0.05) among the three groups.  Compared with PS, the serum insulin concentration in WS was increased (P<0.05) at d 45, but not at d 90.  Compared with control and WS, the serum SOD and T-AOC concentrations in PS were increased (P<0.05) at d 45, but not at d 90.  Compared with control, the rumen microbial crude protein contents in WS and PS were increased (P<0.05) at d 0, while those of control and WS were higher (P<0.05) than that of PS at d 45, but not at d 90.  Compared with PS, the backfat thickness in control and WS were increased (P<0.05), however, the marbling score and expression of genes related to the gluconeogenesis pathway in liver of the three groups did not differ (P>0.05).  Chemical and physio-chemical compositions of LT did not differ (P>0.05) among the three groups.  In conclusion, diets with low or middle amylose/amylopectin ratios increased the backfat thickness, and tended to improve ADG, but had no effect on other carcass characteristics, fat content in the LT, or the expression of hepatic genes related to the gluconeogenesis pathway in Chinese Qinchuan cattle. 
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Alphaherpesvirus-vectored vaccines against animal diseases: Current progress
HU Yang, WANG Ming-shu, CHENG An-chun, JIA Ren-yong, YANG Qiao, WU Ying, LIU Ma-feng, ZHAO Xin-xin, ZHU De-kang, CHEN Shun, ZHANG Sha-qiu, WANG Yin, GAO Qun, OU Xu-min, MAO Sai, WEN Xing-jian, XU Zhi-wen, CHEN Zheng-li, ZHU Ling, LUO Qi-hui, TIAN Bin, PAN Lei-chang, Mujeeb Ur REHMAN, LIU Yun-ya, YU Yan-ling, ZHANG Ling, CHEN Xiao-yue
2020, 19 (8): 1928-1940.   DOI: 10.1016/S2095-3119(20)63175-6
Abstract242)      PDF in ScienceDirect      
Recombinant virus-vectored vaccines are novel agents that can effectively activate specific and nonspecific immunity, are multivalent and multieffective, and have high safety ratings.  Animal alphaherpesviruses have a large genome, contain multiple nonessential regions that do not affect viral replication and are capable of accepting the insertion of an exogenous gene and expressing the antigen protein.  Furthermore, animal alphaherpesviruses have a wide host spectrum, can replicate in the host and continuously stimulate the animal to produce immunity to the corresponding pathogen, thus making them ideal carriers for recombinant virus-vectored vaccines.  With the development of gene-editing technology, recombinant viruses capable of expressing foreign genes can be constructed by various methods.  Currently, studies on recombinant virus-vectored vaccines constructed based on animal alphaherpesviruses have involved poultry, pigs, cattle, sheep, and companion animals.  Studies have shown that the construction of recombinant animal alphaherpesviruses enables the acquisition of immunity to multiple diseases.  This article mainly summarizes the current progress on animal alphaherpesvirus-vectored vaccines, aiming to provide reference for the development of new animal alphaherpesvirus-vectored vaccines.
 
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Effects of different molecular weights of chitosan on methane production and bacterial community structure in vitro
TONG Jin-jin, ZHANG Hua, WANG Jia, LIU Yun, MAO Sheng-yong, XIONG Ben-hai, JIANG Lin-shu
2020, 19 (6): 1644-1655.   DOI: 10.1016/S2095-3119(20)63174-4
Abstract89)      PDF in ScienceDirect      
As a new feed additive, chitosan has been shown in recent years to have a certain role in reducing methane emissions from the gastrointestinal tracts of ruminants.  However, the effects of chitosan with different molecular weights on rumen fermentation, methane production and bacterial community structure are not yet clear.  A basal diet without chitosan served as the control (CTL), and the treatment diets were supplemented with chitosan with different molecular weights: 1 000 (1K), 3 000 (3K), 5 000 (5K), 50 000 (5W) and 200 000 (20W) dry matter (DM).  Six fermentation units per treatment were established.  Gas chromatography was used to measure the concentrations of methane, H2 and volatile fatty acids (VFAs).  The bacterial 16S rRNA genes were sequenced with an Illumina MiSeq platform and analysed to reveal the relative abundances of bacterial community taxa.  The results showed that the propionate proportion was significantly increased by the addition of chitosan with different molecular weights (P<0.05), while methane production and the acetate proportion were significantly decreased (P<0.05).  The relative abundances of Rikenellaceae_RC9_gut_group and Prevotellaceae_UCG_003 were significantly increased in the 3K chitosan group compared with the CTL group, whereas the relative abundance of Ruminococcaceae_NK4A214_group was significantly decreased (P<0.05).  Correlation analyses of the relative abundances of the bacterial genera showed that Prevotella was positively related to propionate production (P<0.05).  In conclusion, 3K chitosan could reduce methane production by replacing fibrolytic bacteria (Firmicutes and Fibrobacteres) with amylolytic bacteria (Bacteroidetes and Proteobacteria) in the bacterial community structure.
 
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Overexpression of a modified AM79 aroA gene in transgenic maize confers high tolerance to glyphosate
REN Zhen-jing, CAO Gao-yi, ZHANG Yu-wen, LIU Yan, LIU Yun-jun
2015, 14 (3): 414-422.   DOI: 10.1016/S2095-3119(14)60920-5
Abstract2025)      PDF in ScienceDirect      
It has previously been shown that a bacterial 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) encoding gene AM79 aroA can be a candidate gene to develop glyphosate-tolerant transgenic crops (Cao et al. 2012). In this study, AM79 aroA was redesigned using the plant biased codons and eliminating the motifs which would lead to the instability of mRNA, to create a synthetic gene that would be expressed highly in plant cells. The redesigned and artificially synthesized gene, named as mAM79, was cloned into plant expression vector pM3301UbiSpAM79, where mAM79 is fused with signal peptide sequence of pea rib-1,5-bisphospate carboxylase (rbcS) small subunit and controlled by ubiquitin promoter. The plasmid was transformed into maize (Zea mays) immature embryos using Agrobacterium-mediated transformation method. Total 74 regenerated plants were obtained and PCR analysis showed that these transgenic plants had the integration of mAM79. Southern blot analysis was performed on the genomic DNA from four transgenic lines, and the result showed that one or two copies of mAM79 were integrated into maize genome. RT-PCR analysis result indicated that mAM79 was highly transcribed in transgenic maize plants. When sprayed with glyphosate, transgenic maize line AM85 and AM72 could tolerate 4-fold of commercial usage of glyphosate; however, all the non-transgenic maize plants were killed by glyphosate. The results in this study confirmed that mAM79 could be used to develop glyphosate-tolerant maize, and the obtained transgenic maize lines could be used for the breeding of glyphosate-tolerant maize.
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