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1.
BMC Genomics ; 25(1): 182, 2024 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-38360569

RESUMEN

BACKGROUND: Homeodomain-leucine zipper (HD-Zip) transcription factors are plant-specific and play important roles in plant defense against environmental stresses. Identification and functional studies have been carried out in model plants such as rice, Arabidopsis thaliana, and poplar, but comprehensive analysis on the HD-Zip family of Salix suchowensis have not been reported. RESULTS: A total of 55 HD-Zip genes were identified in the willow genome, unevenly distributed on 18 chromosomes except for chromosome 19. And segmental duplication events containing SsHD-Zip were detected on all chromosomes except chromosomes 13 and 19. The SsHD-Zip were classified into 4 subfamilies subfamilies (I-IV) according to the evolutionary analysis, and members of each subfamily shared similar domain structure and gene structure. The combination of GO annotation and promoter analysis showed that SsHD-Zip genes responded to multiple abiotic stresses. Furthermore, the results of qPCR analysis showed that the SsHD-Zip I gene exhibited different degrees of expression under salt stress, PEG treatment and heat treatment. Moreover, there was a synergistic effect between SsHD-Zip I genes under stress conditions based on coregulatory networks analysis. CONCLUSIONS: In this study, HD-Zip transcription factors were systematically identified and analyzed at the whole genome level. These results preliminarily clarified the structural characteristics and related functions of willow HD-Zip family members, and it was found that SsHox34, SsHox36 and SsHox51 genes were significantly involved in the response to various stresses. Together, these findings laid the foundation for further research on the resistance functions of willow HD-Zip genes.


Asunto(s)
Arabidopsis , Salix , Leucina Zippers/genética , Salix/genética , Genoma de Planta , Factores de Transcripción/metabolismo , Arabidopsis/genética , Arabidopsis/metabolismo , Estrés Fisiológico/genética , Regulación de la Expresión Génica de las Plantas , Proteínas de Plantas/metabolismo , Proteínas de Homeodominio/química , Filogenia
2.
BMC Plant Biol ; 23(1): 327, 2023 Jun 20.
Artículo en Inglés | MEDLINE | ID: mdl-37340442

RESUMEN

BACKGROUND: Valine-glutamine (VQ) proteins are non-specific plant proteins that have a highly conserved motif: FxxhVQxhTG. These proteins are involved in the development of various plant organs such as seeds, hypocotyls, flowers, leaves and also play a role in response to salt, drought and cold stresses. Despite their importance, there is limited information available on the evolutionary and structural characteristics of VQ family genes in Coix lacryma-jobi. RESULTS: In this study, a total of 31 VQ genes were identified from the coix genome and classified into seven subgroups (I-VII) based on phylogenetic analysis. These genes were found to be unevenly distributed on 10 chromosomes. Gene structure analysis revealed that these genes had a similar type of structure within each subfamily. Moreover, 27 of ClVQ genes were found to have no introns. Conserved domain and multiple sequence alignment analysis revealed the presence of a highly conserved sequences in the ClVQ protein. This research utilized quantitative real-time PCR (qRT-PCR) and promoter analysis to investigate the expression of ClVQ genes under different stress conditions. Results showed that most ClVQ genes responded to polyethylene glycol, heat treatment, salt, abscisic acid and methyl jasmonate treatment with varying degrees of expression. Furthermore, some ClVQ genes exhibited significant correlation in expression changes under abiotic stress, indicating that these genes may act synergistically in response to adversarial stress. Additionally, yeast dihybrid verification revealed an interaction between ClVQ4, ClVQ12, and ClVQ26. CONCLUSIONS: This study conducted a genome-wide analysis of the VQ gene family in coix, including an examination of phylogenetic relationships, conserved domains, cis-elements and expression patterns. The goal of the study was to identify potential drought resistance candidate genes, providing a theoretical foundation for molecular resistance breeding.


Asunto(s)
Coix , Coix/genética , Filogenia , Genoma , Proteínas de Plantas/química , Estrés Fisiológico/genética
3.
Chem Commun (Camb) ; 55(3): 334-337, 2019 Jan 02.
Artículo en Inglés | MEDLINE | ID: mdl-30534687

RESUMEN

High-loading atomic cobalt (12.8 wt%) dispersed on nitrogen-doped graphene was successfully synthesized via considerably low temperature pyrolysis. The catalyst exhibits excellent electrocatalytic performance towards the oxygen reduction reaction with a large limiting diffusion current density of 5.60 mA cm-2 (10% higher than that of commercial Pt/C), and when acting as the air catalyst of Zn-air batteries, a high open-circuit voltage of >1.40 V and excellent power density are also achieved.

4.
Med Sci Monit ; 20: 639-43, 2014 Apr 18.
Artículo en Inglés | MEDLINE | ID: mdl-24743332

RESUMEN

Graves' ophthalmopathy is an inflammatory autoimmune disease of the orbit, characterized by inflammation and proliferation of the orbital tissue caused by CD4+T cells and orbital fibroblasts. Despite recent substantial findings regarding its cellular and molecular foundations, the pathogenesis of Graves' ophthalmopathy remains unclear. Accumulating data suggest that microRNAs play important roles in the pathophysiology of autoimmunity and proliferation. Specifically, microRNA-155 (miR-155) can promote autoimmune inflammation by enhancing inflammatory T cell development. In contrast to miR-155, microRNA-146a (miR-146a) can inhibit the immune response by suppressing T cell activation. Furthermore, miR-155 and miR-146a are involved in cell proliferation, differentiation, and many other life processes. Thus, miR-155 and miR-146a, with opposite impacts on inflammatory responses carried out by T lymphocytes, appear to have multiple targets in the pathogenesis of Graves' ophthalmopathy. Our previous work showed that the expression of miR-146a was significantly decreased in peripheral blood mononuclear cells from Graves' ophthalmopathy patients compared with normal subjects. Accordingly, we proposed that the expression of miR-155 increased and the expression of miR-146a decreased in the target cells (CD4+T cells and orbital fibroblasts), thus promoting ocular inflammation and proliferation in Graves' ophthalmopathy. The proposed hypothesis warrants further investigation of the function of the differentially expressed microRNAs, which may shed new light on the pathogenesis of Graves' ophthalmopathy and lead to new strategies for its management.


Asunto(s)
Ojo/patología , Oftalmopatía de Graves/genética , Oftalmopatía de Graves/patología , Inflamación/genética , MicroARNs/metabolismo , Proliferación Celular , Oftalmopatía de Graves/complicaciones , Oftalmopatía de Graves/inmunología , Humanos , Inmunomodulación , Inflamación/complicaciones , Inflamación/patología , MicroARNs/genética , Modelos Biológicos
5.
Eye Sci ; 28(1): 48-50, 2013 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-24404670

RESUMEN

PURPOSE: To report a case of Leber hereditary optic neuropathy combined with fibrous boney dysplasia. METHODS: Case report. RESULTS: A 16-year-old boy presented with painless vision loss in both eyes. He had a history of a right humerus fracture and right femoral fracture surgery after an uncomplicated fall. On examination in our clinic, his visual acuity was counting fingers at 20 cm OD and counting fingers at 40 cm OS. Both pupils reacted sluggishly to light. The findings on slit-lamp examination and funduscopy after pupillary dilation were all unremarkable. Computed tomography scans demonstrated fibrous dysplasia involving the right frontal, temporal, parietal, and occipital bones but no stenosis of either optic canal. His serum alkaline phosphatase was 522 U/L (reference range: 40-150 U/L). His vision showed no improvement after intravenous methylprednisolone pulse therapy. Finally, a 11778 mitochondrial DNA mutation was detected. He still had no visual recovery after treatment with oral coenzyme Q10, vitamin B1, and citicoline. CONCLUSION: Fibrous dysplasia of bone may be associated with Leber hereditary optic neuropathy, possibly due to the fact that it increases local oxygen consumption.


Asunto(s)
ADN Mitocondrial/genética , Displasia Fibrosa Ósea/complicaciones , Mutación , Atrofia Óptica Hereditaria de Leber/complicaciones , Adolescente , Ceguera/etiología , Displasia Fibrosa Ósea/diagnóstico por imagen , Humanos , Masculino , Tomografía Computarizada por Rayos X , Agudeza Visual
6.
J Clin Neurosci ; 19(10): 1380-2, 2012 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-22819060

RESUMEN

Bilateral acute optic neuritis (AON) is rare in adults in Western countries, but is relatively common in Asian populations. We aimed to document clinical features in Chinese patients with bilateral AON, and to identify factors that are predictive of visual acuity outcome. We reviewed 41 patients (23 males, 18 females; age 18-74 years) diagnosed with bilateral AON from three centers between 2003 and 2009. Demographic and clinical data were compared to a group of patients with unilateral AON. Univariate analysis and multivariate linear regression were used to identify prognostic factors. We found that the median visual acuity (expressed as the logarithm of the minimal angle of resolution [LogMAR] scores) in our patients was 1.55 at presentation and 0.72 at discharge (p<0.001). There was a higher proportion of males (56% compared to 34%, p=0.015), a higher percentage with disc swelling (71% compared to 48%, p=0.014), and poorer visual acuity at presentation (median LogMAR scores: 1.55 compared to 1.70, p=0.001) in patients with bilateral AON than in those with unilateral AON. Both disc swelling (p=0.036) and visual acuity at presentation (p=0.023) were significantly associated with visual acuity at discharge. Our study suggests that bilateral AON has some clinical differences to unilateral AON, and that disc swelling and initial visual acuity may predict a short-term visual acuity outcome in bilateral AON.


Asunto(s)
Edema/etiología , Enfermedades del Nervio Óptico/etiología , Neuritis Óptica/complicaciones , Neuritis Óptica/diagnóstico , Trastornos de la Percepción/etiología , Agudeza Visual/fisiología , Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Análisis Multivariante , Estudios Retrospectivos
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