3,378 research outputs found
Therapeutic Opportunities in Infectious Diseases: Highlights from the Society of Medicines Research Symposium, held on March 14th 2013 at the National Heart & Lung Institute, London, UK
Structure of the PII signal transduction protein of Neisseria meningitidis at 1.85 Ȃ resolution
Copyright @ 2006 International Union of CrystallographyThe PII signal transduction proteins GlnB and GlnK are implicated in the regulation of nitrogen assimilation in Escherichia coli and other enteric bacteria. PII-like proteins are widely distributed in bacteria, archaea and plants. In contrast to other bacteria, Neisseria are limited to a single PII protein (NMB 1995), which shows a high level of sequence identity to GlnB and GlnK from Escherichia coli (73 and 62%, respectively). The structure of the PII protein from N. meningitidis (serotype B) has been solved by molecular replacement to a resolution of 1.85 Ȃ. Comparison of the structure with those of other PII proteins shows that the overall fold is tightly conserved across the whole population of related proteins, in particular the positions of the residues implicated in ATP binding. It is proposed that the Neisseria PII protein shares functions with GlnB/GlnK of enteric bacteria.This study is funded by the Medical Research Council UK and Europe (SPINE) consortium (European Commission Grant No. QLG2-CT-2002-00988)
Quality early education-quality food and nutrition practices?: Some initial results from a pilot research project into food and nutrition practices in early years settings in Kent, UK
TREX1 DNA exonuclease deficiency, accumulation of single stranded DNA and complex human genetic disorders
Aicardi-Goutieres syndrome (AGS) is an unusual condition that clinically mimics a congenital viral infection. Several genes have recently been implicated in the aetiology of this disorder. One of these genes encodes the DNA exonuclease TREX1. Recent work from Yang, Lindahl and Barnes has provided insight into the cellular consequence of TREX1-deficiency. They found that TREX1-deficiency resulted in the intracellular accumulation of single stranded DNA resulting in chronic activation of the DNA damage response network, even in cells from Trex1-mutated AGS patients. Here, I summarise their findings and discuss them in context with the other AGS causative genes which encode subunits of the RNase H2 complex. I describe mechanisms by which the inappropriate intracellular accumulation of nucleic acid species might deleteriously impact upon normal cell cycle progression. Finally, using the example of Systemic Lupus Erythematosus (SLE), I also summarise the evidence suggesting that the failure to process intermediates of nucleic acid metabolism can result in the activation of uncontrolled autoimmunity
Buried alive: Aquatic plants survive in ‘ghost ponds’ under agricultural fields
The widespread loss of wetlands due to agricultural intensification has been highlighted as a major threat to aquatic biodiversity. However, all is not lost as we reveal that the propagules of some aquatic species could survive burial under agricultural fields in the sediments of ‘ghost ponds’ - ponds in-filled during agricultural land consolidation. Our experiments showed at least eight aquatic macrophyte species to germinate from seeds and oospores, following 50–150 years of dormancy in the sediments of ghost ponds. This represents a significant proportion of the expected macrophyte diversity for local farmland ponds, which typically support between 6 and 14 macrophyte species. The rapid (< 6 months) re-colonisation of resurrected ghost ponds by a diverse aquatic vegetation similarly suggests a strong seed-bank influence. Ghost ponds represent abundant, dormant time capsules for aquatic species in agricultural landscapes around the globe, affording opportunities for enhancing landscape-scale aquatic biodiversity and connectivity. While reports of biodiversity loss through agricultural intensification dominate conservation narratives, our study offers a rare positive message, demonstrating that aquatic organisms survive prolonged burial under intensively managed agricultural fields. We urge conservationists and policy makers to consider utilizing and restoring these valuable resources in biodiversity conservation schemes and in agri-environmental approaches and policies
Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling
Large brain size is one of the defining characteristics of modern humans. Seckel syndrome (MIM 210600), a disorder of markedly reduced brain and body size, is associated with defective ATR-dependent DNA damage signaling. Only a single hypomorphic mutation of ATR has been identified in this genetically heterogeneous condition. We now report that mutations in the gene encoding pericentrin (PCNT)--resulting in the loss of pericentrin from the centrosome, where it has key functions anchoring both structural and regulatory proteins--also cause Seckel syndrome. Furthermore, we find that cells of individuals with Seckel syndrome due to mutations in PCNT (PCNT-Seckel) have defects in ATR-dependent checkpoint signaling, providing the first evidence linking a structural centrosomal protein with DNA damage signaling. These findings also suggest that other known microcephaly genes implicated in either DNA repair responses or centrosomal function may act in common developmental pathways determining human brain and body size
Myanmar and Asia united, Australia left behind long ago
It is well known that western Myanmar is underlain by a continental fragment, the West Burma Block, but there are arguments about its origin and the time of its arrival in SE Asia. This study presents the first petrological, XRD diffraction, heavy mineral and detrital zircon U-Pb age data from turbidite sandstones in the Chin Hills that were deposited on West Burma crust in the Triassic. These sandstones contain detritus derived from areas surrounding West Burma and thus help resolve arguments about its location in the Palaeozoic and Mesozoic. West Burma, Sibumasu and Western Australia have similar populations of Archean zircons derived from Western Australian cratons. Until the Devonian all formed part of the Gondwana supercontinent. The abundance of Archean zircons decreases from Western Australia to West Burma and then to Sibumasu. This is consistent with their relative positions in the Gondwana margin, with Sibumasu furthest outboard from Western Australia. Differences in zircon populations indicate that Indochina was not close to West Burma or Sibumasu in Gondwana. West Burma contains abundant Permian and Triassic zircons. These are unknown in Western Australia and different from those of the Carnarvon Basin; they were probably derived from SE Asian tin belt granitoids. Cr spinel is present in most West Burma sandstones; it is common in SE Asia but rare in Western Australia. These new data show that West Burma was part of SE Asia before the Mesozoic and support suggestions that the Argo block that rifted in the Jurassic is not West Burma
Crystal structure of nitrogen regulatory protein IIA from
BACKGROUND: The NMB0736 gene of Neisseria meningitidis serogroup B strain MC58 encodes the putative nitrogen regulatory protein, IIANtr (abbreviated to NM-IIANtr). The homologous protein present in Escherichia coli is implicated in the control of nitrogen assimilation. As part of a structural proteomics approach to the study of pathogenic Neisseria spp., we have selected this protein for structure determination by X-ray crystallography. RESULTS: The NM-IIANtr was over-expressed in E. coli and was shown to be partially mono-phosphorylated, as assessed by mass spectrometry of the purified protein. Crystals of un-phosphorylated protein were obtained and diffraction data collected to 2.5 A resolution. The structure of NM-IIANtr was solved by molecular replacement using the coordinates of the E. coli nitrogen regulatory protein IIAntr [PDB: 1A6J] as the starting model. The overall fold of the Neisseria enzyme shows a high degree of similarity to the IIANtr from E. coli, and the position of the phosphoryl acceptor histidine residue (H67) is conserved. The orientation of an adjacent arginine residue (R69) suggests that it may also be involved in coordinating the phosphate group. Comparison of the structure with that of E. coli IIAmtl complexed with HPr [PDB: 1J6T] indicates that NM-IIANtr binds in a similar way to the HPr-like enzyme in Neisseria. CONCLUSION: The structure of NM-IIANtr confirms its assignment as a homologue of the IIANtr proteins found in a range of other Gram-negative bacteria. We conclude that the NM- IIANtr protein functions as part of a phosphorylation cascade which, in contrast to E. coli, shares the upstream phosphotransfer protein with the sugar uptake phosphoenolpyruvate:sugar phosphotransferase system (PTS), but in common with E. coli has a distinct downstream effector mechanism
Epidemiological associations between brachycephaly and upper respiratory tract disorders in dogs attending veterinary practices in England
Background: Brachycephalic dog breeds are increasingly common. Canine brachycephaly has been associated with upper respiratory tract (URT) disorders but reliable prevalence data remain lacking. Using primary-care veterinary clinical data, this study aimed to report the prevalence and breed-type risk factors for URT disorders in dogs. Results: The sampling frame included 170,812 dogs attending 96 primary-care veterinary clinics participating within the VetCompass Programme. Two hundred dogs were randomly selected from each of three extreme brachycephalic breed types (Bulldog, French Bulldog and Pug) and three common small-to medium sized breed types (moderate brachycephalic: Yorkshire Terrier and non-brachycephalic: Border Terrier and West Highland White Terrier). Information on all URT disorders recorded was extracted from individual patient records. Disorder prevalence was compared between groups using the chi-squared test or Fisher’s test, as appropriate. Risk factor analysis used multivariable logistic regression modelling. During the study, 83 (6.9 %) study dogs died. Extreme brachycephalic dogs (median longevity: 8.6 years, IQR: 2.4-10.8) were significantly younger at death than the moderate and non-brachycephalic group of dogs (median 12.7 years, IQR 11.1-15.0) (P \u3c 0.001). A higher proportion of deaths in extreme brachycephalic breed types were associated with URT disorders (4/24 deaths, 16.7 %) compared with the moderate and non-brachycephalic group (0/59 deaths, 0.0 %) (P = 0.001). The prevalence of having at least one URT disorder in the extreme brachycephalic group was higher (22.0 %, 95 % confidence interval (CI): 18.0-26.0) than in the moderate and non-brachycephalic group (9.7 %, 95 % CI: 7.1-12.3, P \u3c 0.001). The prevalence of URT disorders varied significantly by breed type: Bulldogs 19.5 %, French Bulldogs 20.0 %, Pugs 26.5 %, Border Terriers 9.0 %, West Highland White Terriers 7.0 % and Yorkshire Terriers 13.0 % (P \u3c 0.001). After accounting for the effects of age, bodyweight, sex, neutering and insurance, extreme brachycephalic dogs had 3.5 times (95 % CI: 2.4-5.0, P \u3c 0.001) the odds of at least one URT disorder compared with the moderate and non-brachycephalic group. Conclusions: In summary, this study reports that URT disorders are commonly diagnosed in Bulldog, French Bulldog, Pug, Border Terrier, WHWT and Yorkshire Terrier dogs attending primary-care veterinary practices in England. The three extreme brachycephalic breed types (Bulldog, French Bulldog and Pug) were relatively short-lived and predisposed to URT disorders compared with three other small-to-medium size breed types that are commonly owned (moderate brachycephalic Yorkshire Terrier and non-brachycephalic: Border Terrier and WHWT). Conclusions: In summary, this study reports that URT disorders are commonly diagnosed in Bulldog, French Bulldog, Pug, Border Terrier, WHWT and Yorkshire Terrier dogs attending primary-care veterinary practices in England. The three extreme brachycephalic breed types (Bulldog, French Bulldog and Pug) were relatively short-lived and predisposed to URT disorders compared with three other small-to-medium size breed types that are commonly owned (moderate brachycephalic Yorkshire Terrier and non-brachycephalic: Border Terrier and WHWT)
Buried alive: Aquatic plants survive in ‘ghost ponds’ under agricultural fields
The widespread loss of wetlands due to agricultural intensification has been highlighted as a major threat to aquatic biodiversity. However, all is not lost as we reveal that the propagules of some aquatic species could survive burial under agricultural fields in the sediments of ‘ghost ponds’ - ponds in-filled during agricultural land consolidation. Our experiments showed at least eight aquatic macrophyte species to germinate from seeds and oospores, following 50–150 years of dormancy in the sediments of ghost ponds. This represents a significant proportion of the expected macrophyte diversity for local farmland ponds, which typically support between 6 and 14 macrophyte species. The rapid (< 6 months) re-colonisation of resurrected ghost ponds by a diverse aquatic vegetation similarly suggests a strong seed-bank influence. Ghost ponds represent abundant, dormant time capsules for aquatic species in agricultural landscapes around the globe, affording opportunities for enhancing landscape-scale aquatic biodiversity and connectivity. While reports of biodiversity loss through agricultural intensification dominate conservation narratives, our study offers a rare positive message, demonstrating that aquatic organisms survive prolonged burial under intensively managed agricultural fields. We urge conservationists and policy makers to consider utilizing and restoring these valuable resources in biodiversity conservation schemes and in agri-environmental approaches and policies
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