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530 result(s) for "Qi, Chen-Hui"
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The R2R3 MYB transcription factor MdMYB30 modulates plant resistance against pathogens by regulating cuticular wax biosynthesis
Background The MYB transcription factor family is one of the largest transcriptional factor families in plants and plays a multifaceted role in plant growth and development. However, MYB transcription factors involved in pathogen resistance in apple remain poorly understood. Results We identified a new MYB family member from apple, and named it MdMYB30. MdMYB30 was localized to the nucleus, and was highly expressed in young apple leaves. Transcription of MdMYB30 was induced by abiotic stressors, such as polyethylene glycol and abscisic acid. Scanning electron microscopy and gas chromatograph–mass spectrometry analyses demonstrated that ectopically expressing MdMYB30 in Arabidopsis changed the wax content, the number of wax crystals, and the transcription of wax-related genes. MdMYB30 bound to the MdKCS1 promoter to activate its expression and regulate wax biosynthesis. MdMYB30 also contributed to plant surface properties and increased resistance to the bacterial strain Pst DC3000. Furthermore, a virus-based transformation in apple fruits and transgenic apple calli demonstrated that MdMYB30 increased resistance to Botryosphaeria dothidea . Our findings suggest that MdMYB30 plays a vital role in the accumulation of cuticular wax and enhances disease resistance in apple. Conclusions MdMYB30 bound to the MdKCS1 gene promoter to activate its transcription and regulate cuticular wax content and composition, which influenced the surface properties and expression of pathogenesis-related genes to resistance against pathogens. MdMYB30 appears to be a crucial element in the formation of the plant cuticle and confers apple with a tolerance to pathogens.
Apple AP2/EREBP transcription factor MdSHINE2 confers drought resistance by regulating wax biosynthesis
Plant cuticular wax plays crucial roles in protecting plants from environmental stresses, particularly drought stress. Many enzymes and transcription factors involved in wax biosynthesis have been identified in plant species. In this study, we identified an AP2/EREBP transcription factor, MdSHINE2 from apple, which is a homolog of AtSHINE2 in Arabidopsis. MdSHINE2 was constitutively expressed at different levels in various apple tissues, and the transcription level of MdSHINE2 was induced substantially by abiotic stress and hormone treatments. MdSHINE2-overexpressing Arabidopsis exhibited great change in cuticular wax crystal numbers and morphology and wax composition of leaves and stems. Moreover, MdSHINE2 heavily influenced cuticular permeability, sensitivity to abscisic acid, and drought resistance.
Progressive encephalomyelitis with rigidity and myoclonus: a pediatric case report and literature review
Background Progressive encephalomyelitis with rigidity and myoclonus (PERM) is a rare and life-threatening autoimmune disease of the central nervous system. So far, only ten cases of PERM have been reported in children worldwide, including the one in this study. Case presentation We report a case of an 11-year-old boy with PERM with an initial presentation of abdominal pain, skin itching, dysuria, urinary retention, truncal and limb rigidity, spasms of the trunk and limbs during sleep, deep and peripheral sensory disturbances, and dysphagia. A tissue-based assay using peripheral blood was positive, demonstrated by fluorescent staining of mouse cerebellar sections. He showed gradual and persistent clinical improvement after immunotherapy with intravenous immunoglobulin, steroids, plasmapheresis and rituximab. Conclusions We summarized the diagnosis and treatment of a patient with PERM and performed a literature review of pediatric PERM to raise awareness among pediatric neurologists. A better comprehension of this disease is required to improve its early diagnosis, treatment, and prognosis.
Recent Developments and Perspectives of Cobalt Sulfide-Based Composite Materials in Photocatalysis
Photocatalysis, as an inexpensive and safe technology to convert solar energy, is essential for the efficient utilization of sustainable renewable energy sources. Earth-abundant cobalt sulfide-based composites have generated great interest in the field of solar fuel conversion because of their cheap, diverse structures and facile preparation. Over the past 10 years, the number of reports on cobalt sulfide-based photocatalysts has increased year by year, and more than 500 publications on the application of cobalt sulfide groups in photocatalysis can be found in the last three years. In this review, we initially summarize the four common strategies for preparing cobalt sulfide-based composite materials. Then, the multiple roles of cobalt sulfide-based cocatalysts in photocatalysis have been discussed. After that, we present the latest progress of cobalt sulfide in four fields of photocatalysis application, including photocatalytic hydrogen production, carbon dioxide reduction, nitrogen fixation, and photocatalytic degradation of pollutants. Finally, the development prospects and challenges of cobalt sulfide-based photocatalysts are discussed. This review is expected to provide useful reference for the construction of high-performance cobalt sulfide-based composite photocatalytic materials for sustainable solar-chemical energy conversion.
MdHIR4 transcription and translation levels associated with disease in apple are regulated by MdWRKY31
Key messageHere we describe that the regulation of MdWRKY31 on MdHIR4 in transcription and translation levels associated with disease in apple.The phytohormone salicylic acid (SA) is a main factor in apple (Malus domestica) production due to its function in disease resistance. WRKY transcription factors play a vital role in response to stress. An RNA-seq analysis was conducted with ‘Royal Gala’ seedlings treated with SA to identify the WRKY regulatory mechanism of disease resistance in apple. The analysis indicated that MdWRKY31 was induced. A quantitative real-time polymerase chain reaction (qPCR) analysis demonstrated that the expression of MdWRKY31 was induced by SA and flg22. Ectopic expression of MdWRKY31 in Arabidopsis and Nicotiana benthamiana increased the resistance to flg22 and Pseudomonas syringae tomato (Pst DC3000). A yeast two-hybrid screen was conducted to further analyze the function of MdWRKY31. As a result, hypersensitive-induced reaction (HIR) protein MdHIR4 interacted with MdWRKY31. Biomolecular fluorescence complementation, yeast two-hybrid, and pull-down assays demonstrated the interaction. In our previous study, MdHIR4 conferred decreased resistance to Botryosphaeria dothidea (B. dothidea). A viral vector-based transformation assay indicated that MdWRKY31 evaluated the transcription of SA-related genes, including MdPR1, MdPR5, and MdNPR1 in an MdHIR4-dependent way. A GUS analysis demonstrated that the w-box, particularly w-box2, of the MdHIR4 promoter played a major role in the responses to SA and B. dothidea. Electrophoretic mobility shift assays, yeast one-hybrid assay, and chromatin immunoprecipitation-qPCR demonstrated that MdWRKY31 directly bound to the w-box2 motif in the MdHIR4 promoter. GUS staining activity and a protein intensity analysis further showed that MdWRKY31 repressed MdHIR4 expression. Taken together, our findings reveal that MdWRKY31 regulated plant resistance to B. dothidea through the SA signaling pathway by interacting with MdHIR4.
Isolation and functional identification of an apple MdCER1 gene
The outermost layer of the plant epidermis is covered by cuticular wax, which resists UV radiation, insects, and pathogens, and protects the plant from various environmental stressors. We cloned MdCER1 to further study the molecular regulatory pathway of cuticular wax in apple (Malus × domestica Borkh.). The results showed that MdCER1 is a homolog of Arabidopsis CER1, which is essential for wax synthesis. A subcellular localization study revealed that MdCER1 was localized on the endoplasmic reticulum. We examined the expression pattern of MdCER1 in different tissues and found that it was constitutively expressed in roots, stems, leaves, flowers, and fruits, with the highest expression in leaves. Ectopic expression of MdCER1 promoted the accumulation of cuticular wax by changing the permeability of the epidermis and the response to abscisic acid, as well as by improving drought resistance in Arabidopsis.
The MdWRKY31 transcription factor binds to the MdRAV1 promoter to mediate ABA sensitivity
The phytohormone abscisic acid (ABA) is a major element involved in apple ( Malus domestica ) production because of its role in seed germination and early seedling development. The WRKY family, which is one of the largest families of transcription factors, plays an important role in ABA signaling in plants. However, the underlying molecular mechanisms of WRKY-mediated ABA sensitivity in apple are poorly understood. A genome-wide transcriptome analysis indicated that MdWRKY31 is a key factor induced by ABA. Quantitative real-time PCR showed that MdWRKY31 is induced by ABA in response to PEG4000, which is used to simulate drought. As a transcription factor, MdWRKY31 is localized in the nucleus. Ectopic expression of MdWRKY31 in Arabidopsis and Nicotiana benthamiana enhanced plant sensitivity to ABA. Overexpression of MdWRKY31 in apple roots and apple calli increased sensitivity to ABA, whereas repression of MdWRKY31 reduced sensitivity to ABA in the roots of ‘Royal Gala’. Electrophoretic mobility shift assays, chromatin immunoprecipitation PCR, and yeast one-hybrid assays indicated that MdWRKY31 directly binds to the promoter of MdRAV1 . Expression analyses of transgenic apple calli containing MdWRKY31 and pMdRAV1::GUS implied that MdWRKY31 represses the expression of MdRAV1 . We also found that MdRAV1 binds directly to the promoters of MdABI3 and MdABI4 and repressed their expression. Our findings reveal a new important regulatory mechanism of MdWRKY31-MdRAV1-MdABIs in the ABA signaling pathway in apple.
Molecular states from B¯(∗)N interactions
In 2019, two new structures Λ b ( 6146 ) and Λ b ( 6152 ) were observed by the LHCb Collaboration at the invariant mass spectrum of Λ b 0 π + π - , which aroused a hot discussion about their inner structures. The Λ b ( 6146 ) and Λ b ( 6152 ) might still be molecular states because their masses are close to threshold of a B ¯ meson and a nucleon. In this work, we perform a systematical investigation of possible heavy baryonic molecular states from the B ¯ N interaction. Since the B ¯ N channel strongly couples to the B ¯ ∗ N channel, the possible B ¯ N - B ¯ ∗ N bound states are also studied. The interaction of the system considered is described by the t -channel σ , π , η , ω , and ρ mesons exchanges. By solving the non-relativistic Schrödinger equation with the obtained one-boson-exchange potentials, the B ¯ ( ∗ ) N bound states with different quantum numbers are searched. The calculation suggests that recently observed Λ b ( 6146 ) can be assigned as a P -wave B ¯ N molecular state with spin parity J P = 3 / 2 + or a B ¯ N - B ¯ ∗ N bound state. However, assignment of Λ b ( 6152 ) as an F -wave B ¯ N molecular is disfavored. The Λ b ( 6152 ) can be explained as meson–baryon molecular state with a small B ¯ N component. The calculation also predict the existence of two B ¯ N - B ¯ ∗ N bound states with J P = 1 / 2 - and J P = 3 / 2 - .
MdBT2 regulates nitrogen-mediated cuticular wax biosynthesis via a MdMYB106-MdCER2L1 signalling pathway in apple
Cuticular waxes play important roles in plant development and the interaction between plants and their environment. Researches on wax biosynthetic pathways have been reported in several plant species. Also, wax formation is closely related to environmental condition. However, the regulatory mechanism between wax and environmental factors, especially essential mineral elements, is less studied. Here we found that nitrogen (N) played a negative role in the regulation of wax synthesis in apple. We therefore analysed wax content, composition and crystals in BTB-TAZ domain protein 2 (MdBT2) overexpressing and antisense transgenic apple seedlings and found that MdBT2 could downregulate wax biosynthesis. Furthermore, R2R3-MYB transcription factor 16-like protein (MdMYB106) interacted with MdBT2, and MdBT2 mediated its ubiquitination and degradation through the 26S proteasome pathway. Finally, HXXXD-type acyl-transferase ECERIFERUM 2-like1 (MdCER2L1) was confirmed as a downstream target gene of MdMYB106. Our findings reveal an N-mediated apple wax biosynthesis pathway and lay a foundation for further study of the environmental factors associated with wax regulatory networks in apple.Cuticular wax is crucial for plant development and environmental interaction. This study reveals the negative impact of nitrogen on cuticular wax via MdBT2–MdMYB106–MdCER2L1, thus uncovering a novel pathway for N-mediated wax biosynthesis in apple.