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1.
Int J Mol Sci ; 20(14)2019 Jul 17.
Article in English | MEDLINE | ID: mdl-31319494

ABSTRACT

Pongamia (Millettia pinnata syn. Pongamia pinnata) is a multipurpose biofuel tree which can withstand a variety of abiotic stresses. Commercial applications of Pongamia trees may substantially benefit from improvements in their oil-seed productivity, which is governed by complex regulatory mechanisms underlying seed development. MicroRNAs (miRNAs) are important molecular regulators of plant development, while relatively little is known about their roles in seed development, especially for woody plants. In this study, we identified 236 conserved miRNAs within 49 families and 143 novel miRNAs via deep sequencing of Pongamia seeds sampled at three developmental phases. For these miRNAs, 1327 target genes were computationally predicted. Furthermore, 115 differentially expressed miRNAs (DEmiRs) between successive developmental phases were sorted out. The DEmiR-targeted genes were preferentially enriched in the functional categories associated with DNA damage repair and photosynthesis. The combined analyses of expression profiles for DEmiRs and functional annotations for their target genes revealed the involvements of both conserved and novel miRNA-target modules in Pongamia seed development. Quantitative Real-Time PCR validated the expression changes of 15 DEmiRs as well as the opposite expression changes of six targets. These results provide valuable miRNA candidates for further functional characterization and breeding practice in Pongamia and other oilseed plants.


Subject(s)
Gene Expression Regulation, Plant , MicroRNAs/genetics , Pongamia/genetics , RNA, Plant/genetics , Seeds/genetics , Gene Expression Profiling , MicroRNAs/biosynthesis , Pongamia/growth & development , RNA, Plant/biosynthesis , Seeds/growth & development
2.
BMC Plant Biol ; 18(1): 140, 2018 Jul 09.
Article in English | MEDLINE | ID: mdl-29986660

ABSTRACT

BACKGROUND: Pongamia (Millettia pinnata syn. Pongamia pinnata), an oilseed legume species, is emerging as potential feedstock for sustainable biodiesel production. Breeding Pongamia for favorable traits in commercial application will rely on a comprehensive understanding of molecular mechanism regulating oil accumulation during its seed development. To date, only limited genomic or transcript sequences are available for Pongamia, while a temporal transcriptome profiling of developing seeds is still lacking in this species. RESULTS: In this work, we conducted a time-series analysis of morphological and physiological characters, oil contents and compositions, as well as global gene expression profiles in developing Pongamia seeds. Firstly, three major developmental phases were characterized based on the combined evidences from embryonic shape, seed weight, seed moisture content, and seed color. Then, the gene expression levels at these three phases were quantified by RNA-Seq analyses with three biological replicates from each phase. Nearly 94% of unigenes were expressed at all three phases, whereas only less than 2% of unigenes were exclusively expressed at one of these phases. A total of 8881 differentially expressed genes (DEGs) were identified between phases. Furthermore, the qRT-PCR analyses for 10 DEGs involved in lipid metabolism demonstrated a good reliability of our RNA-Seq data in temporal gene expression profiling. We observed a dramatic increase in seed oil content from the embryogenesis phase to the early seed-filling phase, followed by a steady and moderate increase towards the maximum at the desiccation phase. We proposed that a highly active expression of most genes related to fatty acid (FA) and triacylglycerol (TAG) biosynthesis at the embryogenesis phase might trigger both the substantial oil accumulation and the membrane lipid synthesis for rapid cell proliferation at this phase, while a concerted reactivation of TAG synthesis-related genes at the desiccation phase might further promote storage lipid synthesis to achieve the maximum content of seed oils. CONCLUSIONS: This study not only built a bridge between gene expression profiles and oil accumulation in developing seeds, but also laid a foundation for future attempts on genetic engineering of Pongamia varieties to acquire higher oil yield or improved oil properties for biofuel applications.


Subject(s)
Gene Expression Regulation, Plant/genetics , Millettia/metabolism , Plant Oils/metabolism , Seeds/metabolism , Fatty Acids/analysis , Fatty Acids/metabolism , Gene Expression Profiling , Gene Expression Regulation, Developmental , Genes, Plant/genetics , Metabolic Networks and Pathways/genetics , Millettia/genetics , Plant Oils/analysis , Seeds/chemistry , Seeds/growth & development , Transcriptome
3.
Proc Natl Acad Sci U S A ; 107(6): 2699-704, 2010 Feb 09.
Article in English | MEDLINE | ID: mdl-20133658

ABSTRACT

Hemoproteins, hemoglobin and myoglobin, once released from cells can cause severe oxidative damage as a consequence of heme redox cycling between ferric and ferryl states that generates radical species that induce lipid peroxidation. We demonstrate in vitro that acetaminophen inhibits hemoprotein-induced lipid peroxidation by reducing ferryl heme to its ferric state and quenching globin radicals. Severe muscle injury (rhabdomyolysis) is accompanied by the release of myoglobin that becomes deposited in the kidney, causing renal injury. We previously showed in a rat model of rhabdomyolysis that redox cycling between ferric and ferryl myoglobin yields radical species that cause severe oxidative damage to the kidney. In this model, acetaminophen at therapeutic plasma concentrations significantly decreased oxidant injury in the kidney, improved renal function, and reduced renal damage. These findings also provide a hypothesis for potential therapeutic applications for acetaminophen in diseases involving hemoprotein-mediated oxidative injury.


Subject(s)
Acetaminophen/pharmacology , Hemeproteins/metabolism , Lipid Peroxidation/drug effects , Renal Insufficiency/prevention & control , Rhabdomyolysis/complications , Animals , Arachidonic Acids/chemistry , Arachidonic Acids/metabolism , Catalysis/drug effects , Dose-Response Relationship, Drug , Hemeproteins/chemistry , Hemoglobins/chemistry , Hemoglobins/metabolism , Humans , Hydrogen Peroxide/pharmacology , Hydrogen-Ion Concentration , Iron/chemistry , Iron/metabolism , Male , Myoglobin/chemistry , Myoglobin/metabolism , Oxidation-Reduction/drug effects , Rats , Rats, Sprague-Dawley , Renal Insufficiency/etiology , Renal Insufficiency/pathology , Rhabdomyolysis/metabolism , Spectrophotometry
4.
BMJ Case Rep ; 14(6)2021 Jun 15.
Article in English | MEDLINE | ID: mdl-34130974

ABSTRACT

We present a case of non-surgically managed bilateral osteonecrosis of the external auditory canal with a history of long-term medical therapy for osteoporosis. A 79-year-old woman with severe osteoporosis and destructive osteoarthritis received >10 years of once weekly bisphosphonate therapy before switching to denosumab. Four months later, the patient presented with bilateral loss of hearing and right-sided otalgia. Necrotising otitis externa, cholesteatoma and malignancy were considered but with histology, microbiological and CT assessment, bilateral osteonecrosis of the external auditory canal was diagnosed. Surgical debridement with canalplasty was avoided due to our patient's comorbidities. Treatment continued for 5 months with regular aural toilet, Terra-Cortril ointment and bismuth-iodine-paraffin paste packing. At 1-year follow-up, bilateral external auditory canals were completely re-epithelialised with no pain or affected hearing. We report the first case of bilateral osteonecrosis of the external auditory canal associated with denosumab and bisphosphonates with successful conservative management.


Subject(s)
Bisphosphonate-Associated Osteonecrosis of the Jaw , Cholesteatoma , Aged , Bisphosphonate-Associated Osteonecrosis of the Jaw/diagnostic imaging , Bisphosphonate-Associated Osteonecrosis of the Jaw/surgery , Denosumab/adverse effects , Diphosphonates , Ear Canal/diagnostic imaging , Female , Humans
5.
J Exp Bot ; 61(10): 2549-60, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20406786

ABSTRACT

Expression of FLOWERING LOCUS T (FT) and its homologues has been shown to accelerate the onset of flowering in a number of plant species, including poplar (Populus spp.). The application of FT should be of particular use in forest trees, as it could greatly accelerate and enable new kinds of breeding and research. Recent evidence showing the extent to which FT is effective in promoting flowering in trees is discussed, and its effectiveness in poplar is reported. Results using one FT gene from Arabidopsis and two from poplar, all driven by a heat-inducible promoter, transformed into two poplar genotypes are also described. Substantial variation in flowering response was observed depending on the FT gene and genetic background. Heat-induced plants shorter than 30 cm failed to flower as well as taller plants. Plants exposed to daily heat treatments lasting 3 weeks tended to produce fewer abnormal flowers than those in heat treatments of shorter durations; increasing the inductive temperature from 37 degrees C to 40 degrees C produced similar benefits. Using optimal induction conditions, approximately 90% of transgenic plants could be induced to flower. When induced FT rootstocks were grafted with scions that lacked FT, flowering was only observed in rootstocks. The results suggest that a considerable amount of species- or genotype-specific adaptation will be required to develop FT into a reliable means for shortening the generation cycle for breeding in poplar.


Subject(s)
Botany/methods , Breeding , Flowers/genetics , Genes, Plant/genetics , Plant Proteins/genetics , Populus/genetics , Trees/genetics , Arabidopsis/genetics , Arabidopsis Proteins/genetics , Clone Cells , Flowers/anatomy & histology , Flowers/growth & development , Fruit/anatomy & histology , Genotype , Hot Temperature , Plant Proteins/metabolism , Pollen/growth & development , Populus/anatomy & histology , Research
6.
J Orthop Trauma ; 33(12): 601-607, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31356446

ABSTRACT

OBJECTIVE: To investigate the risk of postoperative surgical site infections after plate fixation of the anterior pelvic ring subsequent to preperitoneal pelvic packing (PPP). DESIGN: Retrospective observational cohort study. SETTING: Level I academic trauma center. PATIENTS: Adult trauma patients with unstable pelvic ring injuries requiring surgical fixation of the anterior pelvic ring. INTERVENTION: Pelvic plate fixation was performed as a staged procedure after external fixation and PPP/depacking (PPP group; n = 25) or as a single-stage primary internal fixation (control group; n = 87). MAIN OUTCOME MEASURE: Incidence of postoperative surgical site infections of the pelvic space. RESULTS: Anterior pelvic plate fixation was performed in 112 patients during a 5-year study period. The PPP group had higher injury severity scores and transfused packed red blood cells than the control group (injury severity score: 46 ± 12.2 vs. 29 ± 1.5; packed red blood cells: 13 ± 10 vs. 5 ± 2; P < 0.05). The mean time until pelvic depacking was 1.7 ± 0.6 days (range: 1-3 days) and 3.4 ± 3.7 days (range: 0-15 days) from depacking until pelvic fracture fixation. Two patients in the PPP group and 8 patients in the control group developed a postoperative infection requiring a surgical revision (8.0% vs. 9.2%; n.s.). Both PPP patients with a pelvic space infection had undergone anterior plate fixation for associated acetabular fractures. CONCLUSIONS: These data support the safety of the PPP protocol for bleeding pelvic ring injuries due to the lack of increased infection rates after fracture fixation. Caution should be applied when considering PPP in patients with associated acetabular fractures. LEVEL OF EVIDENCE: Therapeutic Level III. See Instructions for Authors for a complete description of levels of evidence.


Subject(s)
Fracture Fixation, Internal/adverse effects , Fractures, Bone/surgery , Hemostatic Techniques/adverse effects , Pelvic Bones/injuries , Surgical Wound Infection/epidemiology , Adult , Aged , Bone Plates , Female , Fracture Healing , Humans , Incidence , Male , Middle Aged , Retrospective Studies , Treatment Outcome , Young Adult
8.
J Telemed Telecare ; 12 Suppl 2: S72-6, 2006.
Article in English | MEDLINE | ID: mdl-16989678

ABSTRACT

While a networked, nationwide health information system is financially and logistically impractical, the development of independent, regional systems is realistic and feasible. A Telemedicine Research Network (TRN) could connect a number of geographically disparate health systems. This would require the reconciliation of policies and practices in five principal areas: partner agreement on project scope; privacy, security and confidentiality; technical standards; telecommunications and computer infrastructure; change management and training. Initial establishment of a first-stage TRN would require very little technical development and would, instead, rely on trust among the partners. The development of standards-based TRNs will greatly increase the quality and quantity of telemedicine research.


Subject(s)
Data Collection/standards , Telemedicine/standards , Confidentiality/standards , Data Collection/methods , Medical Records Systems, Computerized/standards , Research , Telemedicine/methods , Telemedicine/organization & administration
9.
Biochem J ; 374(Pt 2): 521-7, 2003 Sep 01.
Article in English | MEDLINE | ID: mdl-12797864

ABSTRACT

Reactive nitrogen species, such as peroxynitrite, can nitrate tyrosine in proteins to form nitrotyrosine. Nitrotyrosine is metabolized to 3-nitro-4-hydroxyphenylacetic acid (NHPA), which is excreted in the urine. This has led to the notion that measurement of urinary NHPA may provide a time-integrated index of nitrotyrosine formation in vivo. However, it is not known whether NHPA is derived exclusively from metabolism of nitrotyrosine, or whether it can be formed by nitration of circulating para -hydroxyphenylacetic acid (PHPA), a metabolite of tyrosine. In the present study, we have developed a gas chromatography MS assay for NHPA and PHPA to determine whether or not NHPA can be formed directly by nitration of PHPA. Following the injection of nitrotyrosine, 0.5+/-0.16% of injected dose was recovered unchanged as nitrotyrosine, and 4.3+/-0.2% as NHPA in the urine. To determine whether or not NHPA could be formed by the nitration of PHPA, deuterium-labelled PHPA ([(2)H(6)]PHPA) was injected, and the formation of deuterated NHPA ([(2)H(5)]NHPA) was measured. Of the infused [(2)H(6)]PHPA, 78+/-2% was recovered in the urine unchanged, and approx. 0.23% was recovered as [(2)H(5)]NHPA. Since the plasma concentration of PHPA is markedly higher than free nitrotyrosine (approx. 400-fold), the nitration of high-circulating endogenous PHPA to form NHPA becomes very significant and accounts for the majority of NHPA excreted in urine. This is the first study to demonstrate that NHPA can be formed by nitration of PHPA in vivo, and that this is the major route for its formation.


Subject(s)
Nitrates/metabolism , Nitrophenols/metabolism , Phenylacetates/metabolism , Tyrosine/analogs & derivatives , Tyrosine/metabolism , Animals , Deuterium/administration & dosage , Deuterium/metabolism , Gas Chromatography-Mass Spectrometry , Humans , Injections, Intravenous , Lipopolysaccharides/administration & dosage , Lipopolysaccharides/pharmacology , Male , Models, Chemical , Nitrophenols/blood , Nitrophenols/urine , Nitrosation , Phenylacetates/blood , Phenylacetates/urine , Rats , Rats, Sprague-Dawley , Reference Standards , Tyrosine/administration & dosage , Tyrosine/pharmacology
10.
Am J Disaster Med ; 6(3): 155-62, 2011.
Article in English | MEDLINE | ID: mdl-21870664

ABSTRACT

OBJECTIVE: To investigate the capabilities of Radio Frequency Identification (RFID) tracking of patients and medical equipment during a simulated disaster response scenario. DESIGN: RFID infrastructure was deployed at two small rural hospitals, in one large academic medical center and in two vehicles. Several item types from the mutual aid equipment list were selected for tracking during the demonstration. A central database server was installed at the UC Davis Medical Center (UCDMC) that collected RFID information from all constituent sites. The system was tested during a statewide disaster drill. During the drill, volunteers at UCDMC were selected to locate assets using the traditional method of locating resources and then using the RFID system. RESULTS: This study demonstrated the effectiveness of RFID infrastructure in real-time resource identification and tracking. Volunteers at UCDMC were able to locate assets substantially faster using RFID, demonstrating that real-time geolocation can be substantially more efficient and accurate than traditional manual methods. A mobile, Global Positioning System (GPS)-enabled RFID system was installed in a pediatric ambulance and connected to the central RFID database via secure cellular communication. This system is unique in that it provides for seamless region-wide tracking that adaptively uses and seamlessly integrates both outdoor cellular-based mobile tracking and indoor WiFi-based tracking. CONCLUSIONS: RFID tracking can provide a real-time picture of the medical situation across medical facilities and other critical locations, leading to a more coordinated deployment of resources. The RFID system deployed during this study demonstrated the potential to improve the ability to locate and track victims, healthcare professionals, and medical equipment during a region-wide disaster.


Subject(s)
Disaster Medicine/methods , Disaster Planning/methods , Patient Identification Systems/methods , Radio Frequency Identification Device/methods , Geographic Information Systems , Humans , Radio Waves
11.
Hepatology ; 45(6): 1517-26, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17523148

ABSTRACT

UNLABELLED: This study explores the hypothesis that the inflammatory response induced by administration of lipopolysaccharide (LPS) exacerbates brain edema in cirrhotic rats; and if so whether this is associated with altered brain metabolism of ammonia or anatomical disturbance of the blood-brain barrier. Adult Sprague-Dawley rats 4 weeks after bile duct ligation (BDL)/Sham-operation, or naïve rats fed a hyperammonemic diet (HD), were injected with LPS (0.5 mg/kg, intraperitoneally) or saline, and killed 3 hours later. LPS administration increased brain water in HD, BDL, and sham-operated groups significantly (P < 0.05), but this was associated with progression to pre-coma stages only in BDL rats. LPS induced cytotoxic brain swelling and maintained anatomical integrity of the blood-brain barrier. Plasma/brain ammonia levels were higher in HD and BDL rats than in sham-operated controls and did not change with LPS administration. Brain glutamine/myoinositol ratio was increased in the HD group but reduced in the BDL animals. There was a background pro-inflammatory cytokine response in the brains of cirrhotic rats, and plasma/brain tumor necrosis factor alpha (TNF-alpha) and IL-6 significantly increased in LPS-treated animals. Plasma nitrite/nitrate levels increased significantly in LPS groups compared with non-LPS controls; however, frontal cortex nitrotyrosine levels only increased in the BDL + LPS rats (P < 0.005 versus BDL controls). CONCLUSION: Injection of LPS into cirrhotic rats induces pre-coma and exacerbates cytotoxic edema because of the synergistic effect of hyperammonemia and the induced inflammatory response. Although the exact mechanism of how hyperammonemia and LPS facilitate cytotoxic edema and pre-coma in cirrhosis is not clear, our data support an important role for the nitrosation of brain proteins.


Subject(s)
Brain Edema/etiology , Cholestasis, Extrahepatic/complications , Coma/etiology , Endotoxemia/complications , Liver Cirrhosis, Experimental/complications , Ammonia/blood , Animals , Brain/blood supply , Brain/metabolism , Brain/pathology , Brain Edema/pathology , Capillaries/pathology , Capillaries/ultrastructure , Cholestasis, Extrahepatic/pathology , Coma/pathology , Consciousness , Cytokines/blood , Disease Models, Animal , Endotoxemia/chemically induced , Hyperammonemia/complications , Ligation , Lipopolysaccharides/pharmacology , Liver Cirrhosis, Experimental/pathology , Magnetic Resonance Spectroscopy , Male , Microscopy, Electron, Transmission , Nitrates/blood , Nitrites/blood , Rats , Rats, Sprague-Dawley , Tyrosine/analogs & derivatives , Tyrosine/metabolism
12.
Genome ; 46(5): 914-24, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14608408

ABSTRACT

A primary linkage map of the domestic turkey (Meleagris gallopavo) was developed by segregation analysis of genetic markers within a backcross family. This reference family includes 84 offspring from one F1 sire mated to two dams. Genomic DNA was digested using one of five restriction enzymes, and restriction fragment length polymorphisms were detected on Southern blots using probes prepared from 135 random clones isolated from a whole-embryo cDNA library. DNA sequence was subsequently determined for 114 of these cDNA clones. Sequence comparisons were done using BLAST searches of the GenBank database, and redundant sequences were eliminated. High similarity was found between 23% of the turkey sequences and mRNA sequences reported for the chicken. The current map, based on expressed genes, includes 138 loci, encompassing 113 loci arranged into 22 linkage groups and an additional 25 loci that remain unlinked. The average distance between linked markers is 6 cM and the longest linkage group (17 loci) measures 131 cM. The total map distance contained within linkage groups is 651 cM. The present map provides an important framework for future genome mapping in the turkey.


Subject(s)
Chromosome Mapping , Genome , Turkeys/genetics , Animals , Female , Gene Expression , Genetic Linkage , Genetic Markers , Lod Score , Male , Polymorphism, Restriction Fragment Length , Sequence Analysis, DNA
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