A Novel Allele in the Promoter of Wx Decreases Gene Expression and Confers Lower Apparent Amylose Contents in Japonica Rice (Oryza sativa L.).

Wx is the key gene that controls amylose content (AC), and various alleles have been found in rice populations. Wxb is the major allele in japonica and produces moderate AC (15~18%). It was recently found that editing the promoter of Wx could produce a series of alleles that have different Wx activities. Although some studies have edited the promoter, few studies have focused on the natural variations in Wx. Here, we used the Rice3K database to investigate variations in the Wx promoter and found that the allele Wx1764178 (A/G) has a higher LD (linkage disequilibrium) with the two key SNPs (1765751, T/G; 1768006, A/C), which could produce different Wx alleles and influence AC, as reported previously. Further study showed that the Wx1764178 allele (A/G) is functional and influences the expression of Wx positively. Editing the A allele using CRISPR‒Cas9 produced 36 and 3 bp deletions and caused a decrease in the expression of Wx. The apparent amylose content (AAC) in the edited lines was decreased by 7.09% and 11.50% compared with that of the wild type, which was the japonica variety Nipponbare with Wxb and the A allele at 1764178, while a complementary line with the G allele showed a lower AAC than the A allele with no effect on other agronomic traits. The AAC of the edited lines showed a higher increase than that of the wild type (Nipponbare, Wxb) in low-nitrogen conditions relative to high-nitrogen conditions. We also developed a dCAPS marker to identify the allele and found that the G allele has widely been used (82.95%) in japonica-bred varieties from Jiangsu Province, China. Overall, we found a functional allele (Wx1764178, A/G) in the Wx promoter that could affect AAC in japonica cultivars and be developed as markers for quality improvement in rice breeding programs.

Rice transcriptional repressor OsTIE1 controls anther dehiscence and male sterility by regulating JA biosynthesis.

Proper anther dehiscence is essential for successful pollination and reproduction in angiosperms, and jasmonic acid (JA) is crucial for the process. However, the mechanisms underlying the tight regulation of JA biosynthesis during anther development remain largely unknown. Here, we demonstrate that the rice (Oryza sativa L.) ethylene-response factor-associated amphiphilic repression (EAR) motif-containing protein TEOSINTE BRANCHED1/CYCLOIDEA/PROLIFERATING CELL FACTORS (TCP) INTERACTOR CONTAINING EAR MOTIF PROTEIN1 (OsTIE1) tightly regulates JA biosynthesis by repressing TCP transcription factor OsTCP1/PCF5 during anther development. The loss of OsTIE1 function in Ostie1 mutants causes male sterility. The Ostie1 mutants display inviable pollen, early stamen filament elongation, and precocious anther dehiscence. In addition, JA biosynthesis is activated earlier and JA abundance is precociously increased in Ostie1 anthers. OsTIE1 is expressed during anther development, and OsTIE1 is localized in nuclei and has transcriptional repression activity. OsTIE1 directly interacts with OsTCP1, and overexpression of OsTCP1 caused early anther dehiscence resembling that of Ostie1. JA biosynthesis genes including rice LIPOXYGENASE are regulated by the OsTIE1-OsTCP1 complex. Our findings reveal that the OsTIE1-OsTCP1 module plays a critical role in anther development by finely tuning JA biosynthesis and provide a foundation for the generation of male sterile plants for hybrid seed production.

Selection and Validation of 48 KASP Markers for Variety Identification and Breeding Guidance in Conventional and Hybrid Rice (Oryza sativa L.).

BACKGROUND: Breeding of conventional and hybrid rice (Oryza sativa L.) have solved hunger problems and increased farmers' income in the world. Molecular markers have been widely used in marker-assisted breeding and identification of larger numbers of different bred varieties in the past decades. The recently developed SNP markers are applied for more stable and detectable compared with other markers. But the cost of genotyping lots SNPs is high. So, it is essential to select less representative SNPs and inexpensive detecting methods to lower the cost and accelerate variety identification and breeding process. KASP (Kompetitive Allele-Specific PCR) is a flexible method to detect the SNPs, and large number of KASP markers have been widely used in variety identification and breeding. However, the ability of less KASP markers on massive variety identification and breeding remains unknown. RESULTS: Here, 48 KASP markers were selected from 378 markers to classify and analyze 518 varieties including conventional and hybrid rice. Through analyzing the population structure, the 48 markers could almost represent the 378 markers. In terms of variety identification, the 48 KASP markers had a 100% discrimination rate in 53 conventional indica varieties and 193 hybrid varieties, while they could distinguish 89.1% conventional japonica rice from different breeding institutes. Two more markers added would increase the ratio from 68.38 to 77.94%. Additionally, the 48 markers could be used for classification of subpopulations in the bred variety. Also, 8 markers had almost completely different genotypes between japonica and indica, and 3 markers were found to be very important for japonica hybrid rice. In hybrid varieties, the heterozygosity of chromosomes 3, 6 and 11 was relatively higher than others. CONCLUSIONS: Our results showed that 48 KASP markers could be used to identify rice varieties, and the panel we tested could provide a database for breeders to identify new breeding lines. Also, the specific markers we found were useful for marker-assisted breeding in rice, including conventional and hybrid.

Variation in arsenic accumulation and translocation among 74 main rice cultivars in Jiangsu Province, China.

Arsenic (As) is a ubiquitous carcinogen and environmental toxin. In China, rice consumption is a major dietary source of inorganic As. Thus, the development of strategies to decrease As accumulation in rice is of considerable importance. In this study, we investigated variation in As accumulation and translocation among 74 hydroponically grown rice cultivars in Jiangsu Province, China. We also examined the relationships between As accumulation and translocation, and the uptake of elements such as silicon (Si), phosphorus (P), iron (Fe), and manganese (Mn). Our results showed 3.43-, 2.7-, and 6.34-fold variations in shoot As concentration, root As concentration, and root-to-shoot As translocation factors (TFs), respectively, among 74 cultivars, indicating that cultivar genotype significantly affected As accumulation and translocation. Redundancy analysis revealed that As uptake and transport were more closely related to P and Mn uptake than to Si and Fe uptake, for all 74 rice genotypes. In addition, the 20 cultivars that accumulated the least shoot As (low-As), and those that accumulated the most shoot As (high-As), exhibited different strategies in response to As exposure. The As TFs were key factors influencing shoot As concentrations in high-As cultivars, but this was not the case in low-As cultivars. In the latter, more accumulated As were sequestered in roots, which restricted As translocation to shoots, thus leading to lower shoot As concentrations. In addition, the shoot As concentrations of various rice cultivars and their parents differed. The low-As rice cultivar YJ2 exhibited a significantly lower shoot As concentration than its parents, suggesting that it is possible to breed low-As rice cultivars from parents that also exhibit low-As characteristics.

Genotypic Variation in Nickel Accumulation and Translocation and Its Relationships with Silicon, Phosphorus, Iron, and Manganese among 72 Major Rice Cultivars from Jiangsu Province, China.

Nickel (Ni) is a ubiquitous environmental toxicant and carcinogen, and rice is a major dietary source of Ni for the Chinese population. Recently, strategies to decrease Ni accumulation in rice have received considerable attention. This study investigated the variation in Ni accumulation and translocation, and also multi-element (silicon (Si), phosphorus (P), iron (Fe), and manganese (Mn)) uptake and transport among 72 rice cultivars from Jiangsu Province, China, that were grown under hydroponic conditions. Our results showed a 2.2-, 4.2-, and 5.3-fold variation in shoot Ni concentrations, root Ni concentrations, and translocation factors (TFs) among cultivars, respectively. This suggests that Ni accumulation and translocation are significantly influenced by the genotypes of the different rice cultivars. Redundancy analysis of the 72 cultivars revealed that the uptake and transport of Ni were more similar to those of Si and Fe than to those of P and Mn. The Ni TFs of high-Ni cultivars were significantly greater than those of low-Ni cultivars (p < 0.001). However, there were no significant differences in root Ni concentrations of low-Ni and high-Ni cultivars, suggesting that high-Ni cultivars could translocate Ni to shoots more effectively than low-Ni cultivars. In addition, the cultivars HD8 and YD8 exhibited significantly lower levels of Ni accumulation than their parents (p < 0.05). Our results suggest that breeding can be an effective strategy for mitigating excessive Ni accumulation in rice grown in Ni-contaminated environments.

Rice tocopherol deficiency 1 encodes a homogentisate phytyltransferase essential for tocopherol biosynthesis and plant development in rice.

KEY MESSAGE: RTD1 encodes a homogentisate phytyltransferase catalyzing a key step in rice tocopherol biosynthesis, confers cold tolerance and regulates rice development by affecting the accumulation of DELLA protein SLENDER RICE1. Tocopherols are one of the most important lipid-soluble antioxidants having indispensable roles in living organisms. The physiological functions of tocopherols have been comprehensively characterized in animals and artificial membranes. However, genetic and molecular functions of tocopherols in plants are less understood. This study aimed to isolate a tocopherol-deficient mutant rtd1 in rice. The rtd1 mutant showed overall growth retardation throughout the growth period. Most of the agronomic traits were impaired in rtd1. Map-based cloning revealed that the RTD1 gene encoded a homogentisate phytyltransferase, a key enzyme catalyzing the committed step in tocopherol biosynthesis. RTD1 was preferentially expressed in green leafy tissues, and the protein was located in chloroplasts. Cold tolerance was found to be reduced in rtd1. The cold-related C-repeat-binding factor (CBF)/dehydration-responsive element-binding protein 1 (DREB1) genes were significantly upregulated in rtd1 under natural growth conditions. Moreover, rtd1 exhibited a reduced response to gibberellin (GA).The transcript and protein levels of DELLA protein-coding gene SLENDER RICE 1 (SLR1) in rice was increased in rtd1. However, the GA content was not changed, suggesting a transcriptional, not posttranslational, regulation of SLR1. These findings implied that tocopherols play important roles in regulating rice growth and development.

Finite-time synchronization for recurrent neural networks with discontinuous activations and time-varying delays.

In this paper, we study the finite-time synchronization problem for recurrent neural networks with discontinuous activations and time-varying delays. Based on the finite-time convergence theory and by using the nonsmooth analysis technique, some finite-time synchronization criteria for the considered neural network model are established, which are new and complement some existing ones. The feasibility and effectiveness of the proposed synchronization method are supported by two examples with numerical simulations.

Trapped spoof surface plasmons with structured defects in textured closed surfaces.

We demonstrate that a defect unit in periodic textured closed surfaces is able to trap spoof surface plasmons (SPs) into a deep subwavelength scale. The resonant frequency of a trapped spoof SP can be tuned freely by properly tailoring the dimension of the defect unit. By introducing multiple defect units with different dimensions at different positions of the textured closed surfaces, the spoof SPs with different frequencies trapped effectively at desired places are also demonstrated. In addition, we further design a graded defect structure with continuously variable dimensions to trap the spoof SPs over an ultrawide spectral band. The interval between the trapped waves on the closed surfaces can be tuned conveniently by changing the grade of the defect dimensions. The designer structures may indicate potential applications in the optical switch and storage in the microwave and terahertz frequencies.

Robust signatures detection of Majorana fermions in superconducting iron chains.

We theoretically propose an optical means to detect Majorana fermions in superconducting iron (Fe) chains with a hybrid quantum dot-nanomechanical resonator system driven by two-tone fields, which is very different from the current tunneling spectroscopy experiments with electrical means. Based on the scheme, the phenomenon of Majorana modes induced transparency is demonstrated and a straightforward method to determine the quantum dot-Majorana fermions coupling strength is also presented. We further investigate the role of the nanomechanical resonator, and the resonator behaving as a phonon cavity enhances the exciton resonance spectrum, which is robust for detecting of Majorana fermions. The coherent optical spectrum affords a potential supplement to detecte Majorana fermions and supports Majorana fermions-based topological quantum computation in superconducting iron chains.

Loss of GltB Inhibits Biofilm Formation and Biocontrol Efficiency of Bacillus subtilis Bs916 by Altering the Production of γ-Polyglutamate and Three Lipopeptides.

AIMS: This study examined the contribution of GltB on biofilm formation and biocontrol efficiency of B. subtilis Bs916. METHODS AND RESULTS: The gltB gene was identified through a biofilm phenotype screen and a bioinformatics analysis of serious biofilm formation defects, and then a gltB single knockout mutant was constructed using homologous recombination. This mutant demonstrated severe deficits in biofilm formation and colonisation along with significantly altered production ofγ-polyglutamate (γ-PGA) and three lipopeptide antibiotics (LPs) as measured by a transcriptional analysis of both the wild type B. subtilis Bs916 and the gltB mutant. Consequently, the mutant strain retained almost no antifungal activity against Rhizoctonia solani and exhibited decreased biocontrol efficiency against rice sheath blight. Very few gltB mutant cells colonised the rice stem, and they exhibited no significant nutrient chemotaxis compared to the wild type B. subtilis Bs916. The mechanism underlying these deficits in the gltB mutant appears to be decreased significantly in production of γ-PGA and a reduction in the production of both bacillomycin L and fengycin. Biofilm restoration of gltB mutant by additionγ-PGA in the EM medium demonstrated that biofilm formation was able to restore significantly at 20 g/L. CONCLUSIONS: GltB regulates biofilm formation by altering the production ofγ-PGA, the LPs bacillomycin L and fengcin and influences bacterial colonisation on the rice stem, which consequently leads to poor biocontrol efficiency against rice sheath blight. SIGNIFICANCE AND IMPACT OF STUDY: This is the first report of a key regulatory protein (GltB) that is involved in biofilm regulation and its regulation mechanism and biocontrol efficiency by B. subtilis.

Synthesis and antitumor activity of novel nitrogen mustard-linked chalcones.

A series of nitrogen mustard-linked chalcones were synthesized and evaluated for their antitumor activity in vitro against the K562 and HepG2 cell lines. The aldol condensation of [N,N-bis(chloroethyl)-3-amino]-acetophenone (2) with aromatic aldehydes afforded the nitrogen mustard-linked chalcones. Among the analogs tested, compounds 5e and 5k exhibited significant anti-proliferation activities against K562 cells with IC50 values of 2.55 and 0.61 µM, respectively, which revealed higher cell toxicity than the standard drugs cisplatin (IC50>200 µM) and adriamycin (IC50=14.88 µM). The methoxyl and N,N-dimethyl groups on the B-ring of the chalcone frame enhanced the inhibitory activities against both the K562 and HepG2 cell lines. The structure-activity relationship study indicated that the inhibitory activities significantly varied with the position(s) and species of the substituted group(s).

4-Methyl-2,7-dioxo-3,6-dioxa-1(1,1')-ferrocenacyclo-hepta-phane.

In the title compound, [Fe(C(15)H(14)O(4))], the two cyclo-penta-dienyl (Cp) rings are nearly parallel, making a dihedral angle of 2.6 (1)°. The distance between the centroids of the Cp rings is 3.309 (8) Å. The relative orientation of the two Cp rings is characterized by a torsion angle of -43.99 (6)° defined by the two centroids and the two substituted C atoms.