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1.
Plant Cell Physiol ; 59(11): 2366-2380, 2018 Nov 01.
Article in English | MEDLINE | ID: mdl-30101323

ABSTRACT

Auxin homeostasis is a highly regulated process that must be maintained to allow auxin to exert critical growth and developmental controls. Auxin conjugase and hydrolase family proteins play important roles in auxin homeostasis through means of storage, activation, inactivation, response inhibition and degradation of auxins in plants. We systematically evaluated 60 GRETCHEN HAGEN3 (GH3) proteins from diverse plant species for amino acid conjugation activity with the known substrates jasmonic acid (JA), IAA and 4-hydroxybenzoate (4-HBA). While our results largely confirm that Group II conjugases prefer IAA, we observed no clear substrate preference among Group III proteins, and only three of 11 Group I proteins showed the expected preference for JA, indicating that sequence similarity does not always predict substrate specificity. Such a sequence-substrate relationship held true when sequence similarity at the acyl acid-binding site was used for grouping. Several GH3 proteins could catalyze formation of the potentially degradation-destined aspartate (Asp) and glutamate (Glu) conjugates of IAA and the synthetic auxins 2,4-D and dicamba. We found that 2,4-D-Asp/Glu conjugates, but not dicamba and IAA conjugates, were hydrolyzed in Arabidopsis and soybean by AtILL5- and AtIAR3-like amidohydrolases, releasing free 2,4-D in plant cells when conjugates were exogenously applied to seedlings. Dicamba-Asp or dicamba-Glu conjugates were not hydrolyzed in vivo in infiltrated plants nor in vitro with recombinant amidohydrolases. These findings could open the door for exploration of a dicamba herbicide tolerance strategy through conjugation.


Subject(s)
2,4-Dichlorophenoxyacetic Acid/metabolism , Aspartic Acid/metabolism , Dicamba/metabolism , Glutamic Acid/metabolism , Plant Proteins/metabolism , Arabidopsis/metabolism , Arabidopsis Proteins/metabolism , Benzoates/metabolism , Cyclopentanes/metabolism , Indoleacetic Acids/metabolism , Oxylipins/metabolism , Phylogeny , Plant Growth Regulators/metabolism , Plant Proteins/genetics , Glycine max/metabolism , Substrate Specificity
2.
Planta ; 236(4): 1153-64, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22644767

ABSTRACT

Purple cauliflower (Brassica oleracea L. var. botrytis) Graffiti represents a unique mutant in conferring ectopic anthocyanin biosynthesis, which is caused by the tissue-specific activation of BoMYB2, an ortholog of Arabidopsis PAP2 or MYB113. To gain a better understanding of the regulatory network of anthocyanin biosynthesis, we investigated the interaction among cauliflower MYB-bHLH-WD40 network proteins and examined the interplay of BoMYB2 with various bHLH transcription factors in planta. Yeast two-hybrid studies revealed that cauliflower BoMYBs along with the other regulators formed the MYB-bHLH-WD40 complexes and BobHLH1 acted as a bridge between BoMYB and BoWD40-1 proteins. Different BoMYBs exhibited different binding activity to BobHLH1. Examination of the BoMYB2 transgenic lines in Arabidopsis bHLH mutant backgrounds demonstrated that TT8, EGL3, and GL3 were all involved in the BoMYB2-mediated anthocyanin biosynthesis. Expression of BoMYB2 in Arabidopsis caused up-regulation of AtTT8 and AtEGL3 as well as a subset of anthocyanin structural genes encoding flavonoid 3'-hydroxylase, dihydroflavonol 4-reductase, and leucoanthocyanidin dioxygenase. Taken together, our results show that MYB-bHLH-WD40 network transcription factors regulated the bHLH gene expression, which may represent a critical feature in the control of anthocyanin biosynthesis. BoMYB2 together with various BobHLHs specifically regulated the late anthocyanin biosynthetic pathway genes for anthocyanin biosynthesis. Our findings provide additional information for the complicated regulatory network of anthocyanin biosynthesis and the transcriptional regulation of transcription factors in vegetable crops.


Subject(s)
Anthocyanins/genetics , Brassica/genetics , Gene Regulatory Networks/genetics , Plant Proteins/genetics , Alcohol Oxidoreductases/genetics , Anthocyanins/biosynthesis , Arabidopsis/genetics , Arabidopsis/metabolism , Basic Helix-Loop-Helix Transcription Factors/genetics , Basic Helix-Loop-Helix Transcription Factors/metabolism , Biosynthetic Pathways/genetics , Brassica/metabolism , Cytochrome P-450 Enzyme System/genetics , Flowers/genetics , Flowers/metabolism , Gene Expression Regulation, Plant/genetics , Meristem/genetics , Meristem/metabolism , Mutation , Organ Specificity , Oxygenases/genetics , Plant Leaves/genetics , Plant Leaves/metabolism , Plant Proteins/metabolism , Plants, Genetically Modified , Protein Binding , Protein Interaction Mapping , Seedlings/genetics , Seedlings/metabolism , Seeds/genetics , Seeds/metabolism , Transcription Factors/genetics , Transcription Factors/metabolism , Up-Regulation
3.
Plant Physiol ; 154(3): 1470-80, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20855520

ABSTRACT

Anthocyanins are responsible for the color of many flowers, fruits, and vegetables. An interesting and unique Purple (Pr) gene mutation in cauliflower (Brassica oleracea var botrytis) confers an abnormal pattern of anthocyanin accumulation, giving the striking mutant phenotype of intense purple color in curds and a few other tissues. To unravel the nature of the Pr mutation in cauliflower, we isolated the Pr gene via a combination of candidate gene analysis and fine mapping. Pr encoded a R2R3 MYB transcription factor that exhibited tissue-specific expression, consistent with an abnormal anthocyanin accumulation pattern in the mutant. Transgenic Arabidopsis (Arabidopsis thaliana) and cauliflower plants expressing the Pr-D allele recapitulated the mutant phenotype, confirming the isolation of the Pr gene. Up-regulation of Pr specifically activated a basic helix-loop-helix transcription factor and a subset of anthocyanin structural genes encoding flavonoid 3'-hydroxylase, dihydroflavonol 4-reductase, and leucoanthocyanidin dioxygenase to confer ectopic accumulation of pigments in the purple cauliflower. Our results indicate that the genetic variation including a Harbinger DNA transposon insertion in the upstream regulatory region of the Pr-D allele is responsible for the up-regulation of the Pr gene in inducing phenotypic change in the plant. The successful isolation of Pr provides important information on the regulatory control of anthocyanin biosynthesis in Brassica vegetables, and offers a genetic resource for development of new varieties with enhanced health-promoting properties and visual appeal.


Subject(s)
Anthocyanins/biosynthesis , Basic Helix-Loop-Helix Transcription Factors/metabolism , Brassica/genetics , Plant Proteins/metabolism , Amino Acid Sequence , Arabidopsis/genetics , Basic Helix-Loop-Helix Transcription Factors/genetics , Brassica/metabolism , Chromosome Mapping , DNA, Plant/genetics , Gene Expression Regulation, Plant , Molecular Sequence Data , Phenotype , Plant Proteins/genetics , Plants, Genetically Modified/genetics , Sequence Analysis, DNA
4.
Medicine (Baltimore) ; 100(42): e27548, 2021 Oct 22.
Article in English | MEDLINE | ID: mdl-34678889

ABSTRACT

RATIONALE: Progressive encephalopathy with brain edema and/or leukoencephalopathy-1 is an infantile, lethal neurometabolic disorder caused by a NAD(P)HX epimerase (NAXE) gene mutation. It is characterized by a fluctuating disease course with repeated episodes of improvement and regression. In this report, we present a rare case of NAXE gene mutation-related encephalopathy with unexpected neurological recovery and long survival time. PATIENT CONCERNS: A 20-month-old girl presented with progressively unsteady gait and bilateral hand tremors after a trivial febrile illness. Her disease rapidly progressed to consciousness disturbance, 4-limb weakness (muscle power: 1/5 on the Medical Research Council scale), and respiratory failure. The patient gradually recovered 2 months later. However, another episode of severe fever-induced encephalopathy developed 2 years after the initial presentation. DIAGNOSES: Results of laboratory investigations, including complete blood count, blood chemistry, inflammatory markers, and cerebral spinal fluid analysis were unremarkable. Electroencephalography and nerve conduction velocity studies yielded normal results. Brain magnetic resonance imaging on diffusion-weighted imaging revealed abnormal sysmmetric hyperintensity in the bilateral middle cerebellar peduncles. A genetic study using whole exome sequencing confirmed the diagnosis of NAXE gene mutation-related encephalopathy. INTERVENTIONS: Pulse therapy with methylprednisolone, intravenous immunoglobulin, coenzyme Q10, and carnitine were initially introduced. After a NAXE gene defect was detected, the vitamin B complex and coenzyme Q10 were administered. A continuous rehabilitation program was also implemented. OUTCOMES: NAXE gene mutation-related encephalopathy is usually regarded as a lethal neurometabolic disorder. However, the outcome in this case is better than that in the previous cases. She showed progressive neurological recovery and a longer survival time. The muscle power of the 4 limbs recovered to grade 4. At present (age of 5.5 years old), she can walk with an unsteady gait and go to school. LESSONS: Although NAXE gene mutation-related encephalopathy is rare, it should be considered as a differential diagnosis of early onset progressive encephalopathy.


Subject(s)
Brain Diseases/genetics , Brain Diseases/physiopathology , Racemases and Epimerases/genetics , Dietary Supplements , Female , Humans , Infant , Ubiquinone/analogs & derivatives , Ubiquinone/therapeutic use , Vitamin B Complex/therapeutic use , Exome Sequencing
5.
J Psychosom Obstet Gynaecol ; 41(2): 137-143, 2020 06.
Article in English | MEDLINE | ID: mdl-31462149

ABSTRACT

Objective: To evaluate the suicide rate among patients oophorectomized for benign conditions and its association with confounding comorbidities.Method: We conducted a population-based, retrospective cohort study of women aged ≥20 years that underwent oophorectomy including unilateral or bilateral in laparotomy or laparoscopy for benign conditions during 2000-2013. A total of 145,588 oophorectomized and 582,352 non-oophorectomized women were included with an average follow-up time of 7 years. The comorbidities assessed were hypertension (HTN), diabetes mellitus, hyperlipidemia, stroke, chronic obstructive pulmonary disease (COPD), chronic liver disease and cirrhosis, chronic kidney disease and anxiety disorder.Result: The overall suicide rate was significantly higher in the oophorectomized group. The rate among oophorectomized patients of 20-49 years was significantly greater than in non-oophorectomized patients of the same age group. Hypertension, COPD, anxiety disorder and chronic liver disease and cirrhosis were associated with a significantly higher suicide rate in oophorectomized women. A significant increase in suicide incidence was observed in patients with <6 years' follow-up.Conclusion: A significant increase in suicide rate among oophorectomized women aged 20-49 years was found. The decision to perform oophorectomy should be made cautiously, especially in patients with hypertension, COPD, chronic liver disease and cirrhosis or anxiety disorder. Patients should be followed for at least 6 years postoperatively since the suicide rate is significantly higher in this period.


Subject(s)
Ovariectomy/psychology , Suicide/statistics & numerical data , Adult , Aged , Anxiety Disorders/epidemiology , Cohort Studies , Comorbidity , Female , Humans , Hypertension/epidemiology , Incidence , Liver Diseases/epidemiology , Middle Aged , Ovariectomy/statistics & numerical data , Pulmonary Disease, Chronic Obstructive/epidemiology , Retrospective Studies , Risk Factors , Taiwan/epidemiology , Young Adult
6.
Planta ; 230(6): 1141-53, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19756724

ABSTRACT

The color of red cabbage (Brassica oleracea var. capitata) is due to anthocyanin accumulation. To investigate the regulatory control of anthocyanin production in red cabbage, the expression of anthocyanin biosynthetic and regulatory genes from eight commercial cultivars was examined. While the four green varieties had negligible amount of anthocyanins under normal growth condition, the four red cultivars contained up to 1.60 mg g(-1) fresh weight. HPLC analysis of the four red cultivars revealed that they produced similar composition of various forms of cyanidin glucosides but at different concentrations. Molecular analysis indicated that all the red cabbage shared common mechanism of regulatory control for anthocyanin biosynthesis. Except CHI which showed similar expression levels between green and red cultivars, the other structural genes, CHS, F3H, F3'H, DFR, LDOX, and GST, were constitutively up-regulated during all stages of vegetative growth in red varieties. The expression of these structural genes was also dramatically increased in green and red cabbage under nutrient stresses. The increased expression of the structural genes coincided with a coordinated increase in transcript levels of a bHLH gene, BoTT8, and a MYB transcription factor, BoMYB2. These results indicate that activation of these two regulatory factors by unknown mechanisms constitutively up-regulates nearly the entire pathway genes for the onset of anthocyanin biosynthesis in red cabbage. Moreover, the amount of total anthocyanins in red cabbage was found to be positively correlated with total antioxidant power, implicating the potential health benefit of red cabbage to human health.


Subject(s)
Anthocyanins/biosynthesis , Brassica/genetics , Brassica/metabolism , Gene Expression Profiling , Acyltransferases/genetics , Acyltransferases/metabolism , Anthocyanins/analysis , Antioxidants/metabolism , Brassica/growth & development , Chromatography, High Pressure Liquid , Gene Expression Regulation, Developmental , Gene Expression Regulation, Plant , Glutathione Transferase/genetics , Glutathione Transferase/metabolism , Oxygenases/genetics , Oxygenases/metabolism , Plant Proteins/genetics , Plant Proteins/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Species Specificity , Time Factors
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