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1.
Mar Pollut Bull ; 129(2): 573-591, 2018 Apr.
Article in English | MEDLINE | ID: mdl-29089114

ABSTRACT

Synoptic sediment quality triad (contaminants, benthic assemblages, toxicity testing) data were collected for sites in Sydney estuary, adjacent Cooks River and five less-modified southern estuaries. Matching data tested relationships between contaminants and benthic assemblages, correlations with specific contaminants, and the ability of sediment quality guidelines to predict the risk of adverse effects. Significant but weak relationships occurred in complex patterns between assemblages, contaminant concentrations and environmental variables. Maximum benthos abundance occurred where sediment contamination was high and was dominated by polychaetes. Spionidae (polychaete) and Galeommatidae (mollusc) abundances were strongly correlated with site environmental characteristics and with varying mixtures of metals and organic contaminants. The risk of adverse effects on benthic assemblage structure increased with increasing sediment toxicity except for areas of very high contamination and for non-bioavailable anthropogenic chemicals. The overall weight-of-evidence scores differentiated the highly modified sites from less-contaminated southern estuaries, where toxicity scores were higher than predicted.


Subject(s)
Environmental Monitoring/methods , Estuaries , Geologic Sediments/chemistry , Mollusca/drug effects , Polychaeta/drug effects , Water Pollutants, Chemical/toxicity , Animals , New South Wales , Rivers/chemistry , Water Pollutants, Chemical/analysis
3.
Tsitol Genet ; 50(6): 34-59, 2016.
Article in English, Russian | MEDLINE | ID: mdl-30484602

ABSTRACT

Thirty years after the Chernobyl explosion we still lack information regarding the genetic effects of radionuclide contamination on the plant population. For example, are plants adapting to the low dose of chronic ionising irradiation and showing improved resistance to radiation damage? Are they coping with changing/increased pathogenicity of fungi and viruses in the Chernobyl exclusion zone? Are plant populations rapidly accumulating mutational load and should we expect rapid microevolutionary changes in plants in the Chernobyl area? This review will try to summarise the current knowledge on these aspects of plant genetics and ecology and draw conclusions on the importance of further studies in the area around Chernobyl.


Subject(s)
Chromosome Aberrations/radiation effects , DNA Repair , DNA, Plant/radiation effects , Gamma Rays/adverse effects , Mutation/radiation effects , Plants/radiation effects , Chernobyl Nuclear Accident , DNA Damage , DNA, Plant/chemistry , Dose-Response Relationship, Radiation , Environmental Monitoring , Phytophthora/growth & development , Phytophthora/pathogenicity , Plant Diseases/genetics , Plant Diseases/microbiology , Plant Diseases/virology , Plants/genetics , Plants/microbiology , Plants/virology , Radioisotopes/analysis , Tobacco Mosaic Virus/growth & development , Tobacco Mosaic Virus/pathogenicity , Ukraine
4.
Anaesthesia ; 64(11): 1211-7, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19825057

ABSTRACT

The 2000-2002 Confidential Enquiry into Maternal and Child Health report highlighted several cases of maternal death where the staff who had been involved, were not offered support. The report recommended that 'Trusts must make provision for the prompt offer of support and/or counselling for all staff who have cared for a woman who has died.' We conducted a postal survey to firstly establish whether Trusts had implemented this, and also to ascertain the experience of consultant obstetric anaesthetists. Of 706 respondents (response rate 64%), 60% involved in a maternal death or other traumatic event received no offer of support, 65% were unaware of potential sources of support and only 5% received details of further help available. Furthermore, 69% were unaware of policies within their own Trusts for the provision of support services. We suggest that a formal structure should exist within all units that offers confidential support services and/or debriefing facilities to all staff involved in a maternal death or other traumatic event.


Subject(s)
Attitude to Death , Counseling/supply & distribution , Maternal Mortality , Medical Staff, Hospital/psychology , Occupational Health Services/supply & distribution , Anesthesia, Obstetrical/mortality , Health Care Surveys , Humans , Occupational Diseases/epidemiology , Occupational Diseases/etiology , Occupational Diseases/prevention & control , Social Support , Stress, Psychological/epidemiology , Stress, Psychological/etiology , Stress, Psychological/prevention & control , Surveys and Questionnaires , United Kingdom/epidemiology
5.
Sci Total Environ ; 407(8): 2820-35, 2009 Apr 01.
Article in English | MEDLINE | ID: mdl-19211135

ABSTRACT

The current work aimed to compile existing information to better understand the source, fate and effects of metallic contaminants in one catchment-receiving basin system (Iron Cove) in Sydney Harbour (Australia). Copper, Pb and Zn concentrations of potential source materials, i.e. soils (mean 62, 410 and 340 microg g(-1), respectively) and road dust (mean 160, 490 and 520 microg g(-1), respectively) and in materials being transported to the estuary, i.e. in gully pots (mean 110, 200 and 260 microg g(-1) for Cu, Pb, and Zn, respectively), in bedload (mean 210, 880 and 1700 microg g(-1), respectively) and particulates in canals draining the catchment (mean 325, 290 and 1865 microg g(-1), respectively) were highly enriched. Estuarine sediments in the receiving basin are enriched 20 times over pre-anthropogenic concentrations and are toxic to benthic animals at the canal mouths. Stormwater remediation is required to reduce metal loads to the adjacent estuary.


Subject(s)
Geologic Sediments/chemistry , Water Pollutants, Chemical/analysis , Copper/analysis , Copper/chemistry , Dust/analysis , Environmental Monitoring , Fresh Water/chemistry , Lead/analysis , Lead/chemistry , New South Wales , Water Movements , Water Pollutants, Chemical/chemistry , Water Supply , Zinc/analysis , Zinc/chemistry
6.
Ann Bot ; 101(2): 267-76, 2008 Jan.
Article in English | MEDLINE | ID: mdl-17981881

ABSTRACT

BACKGROUND AND AIMS: The plants that have remained in the contaminated areas around Chernobyl since 1986 encapsulate the effects of radiation. Such plants are chronically exposed to radionuclides that they have accumulated internally as well as to alpha-, beta- and gamma-emitting radionuclides from external sources and from the soil. This radiation leads to genetic damage that can be countered by DNA repair systems. The objective of this study is to follow DNA repair and adaptation in haploid cells (birch pollen) and diploid cells (seed embryos of the evening primrose) from plants that have been growing in situ in different radionuclide fall-out sites in monitored regions surrounding the Chernobyl explosion of 1986. METHODS: Radionuclide levels in soil were detected using gamma-spectroscopy and radiochemistry. DNA repair assays included measurement of unscheduled DNA synthesis, electrophoretic determination of single-strand DNA breaks and image analysis of rDNA repeats after repair intervals. Nucleosome levels were established using an ELISA kit. KEY RESULTS: Birch pollen collected in 1987 failed to perform unscheduled DNA synthesis, but pollen at gamma/beta-emitter sites has now recovered this ability. At a site with high levels of combined alpha- and gamma/beta-emitters, pollen still exhibits hidden damage, as shown by reduced unscheduled DNA synthesis and failure to repair lesions in rDNA repeats properly. Evening primrose seed embryos generated on plants at the same gamma/beta-emitter sites now show an improved DNA repair capacity and ability to germinate under abiotic stresses (salinity and accelerated ageing). Again those from combined alpha- and gamma/beta-contaminated site do not show this improvement. CONCLUSIONS: Chronic irradiation at gamma/beta-emitter sites has provided opportunities for plant cells (both pollen and embryo cells) to adapt to ionizing irradiation and other environmental stresses. This may be explained by facilitation of DNA repair function.


Subject(s)
Adaptation, Physiological/radiation effects , Betula/radiation effects , Chernobyl Nuclear Accident , DNA Repair/radiation effects , Oenothera biennis/radiation effects , Pollen/radiation effects , Radioisotopes/pharmacology , Seeds/radiation effects , Adaptation, Physiological/drug effects , Betula/drug effects , Betula/genetics , Betula/physiology , DNA Breaks, Single-Stranded/drug effects , DNA Breaks, Single-Stranded/radiation effects , DNA Repair/drug effects , DNA Restriction Enzymes/metabolism , DNA, Plant/biosynthesis , Dose-Response Relationship, Radiation , Germination/drug effects , Germination/radiation effects , Nucleosomes/drug effects , Nucleosomes/radiation effects , Oenothera biennis/genetics , Oenothera biennis/physiology , Osmotic Pressure/drug effects , Osmotic Pressure/radiation effects , Pollen/drug effects , Pollen/genetics , Seedlings/drug effects , Seedlings/radiation effects , Seeds/drug effects , Seeds/genetics , Sodium Chloride/pharmacology , Time Factors
7.
Environ Monit Assess ; 120(1-3): 187-220, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16773229

ABSTRACT

Correlation analyses between measures of toxicity and concentrations of chemical contaminants were conducted for 103 surficial sediments from Sydney Harbour, Australia, and vicinity. Toxicity tests consisted of amphipod survival and reburial tests of whole sediments (Corophium colo), sea urchin fertilisation and larval development tests of pore waters (Heliocidaris tuberculata) and microbial bioluminescence (Microtox) tests of solvent extracts and pore waters. Toxicity in most tests correlated with concentrations of metallic contaminants, in particular, zinc, lead and copper. Organic contaminants did not correlate as significantly with toxicity. However, Heliocidaris tuberculata showed relationships with organochlorine compounds in samples with low to moderate metals contamination. Toxicity in the Microtox solvent extract test appeared to be primarily influenced by the presence of sulfur. This study has no precedent in Australia and the results support the validity of using local indigenous species in toxicity tests of field-collected sediments. This toxicity/chemistry dataset may be used in evaluations of sediment quality guidelines recently introduced to Australia.


Subject(s)
Environmental Monitoring , Geologic Sediments/chemistry , Water Pollutants, Chemical/analysis , Water Pollutants, Chemical/toxicity , Amphipoda/drug effects , Amphipoda/growth & development , Animals , Australia , Metals, Heavy/analysis , Metals, Heavy/toxicity , Sea Urchins/drug effects , Sea Urchins/growth & development , Toxicity Tests
8.
Arch Environ Contam Toxicol ; 50(3): 306-15, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16435089

ABSTRACT

Interim sediment quality guidelines (ISQGs) adapted recently to Australia from North American effects-based guidelines were evaluated with matching chemical and toxicological data collected for sediments (n = 103) from Sydney Harbour and south coast estuaries of New South Wales. The incidence of toxicity for the test battery was low (7%) among samples with all chemical concentrations below ISQG-Low values, indicating these guidelines are accurate and protective of non-toxic conditions. The incidence of toxicity increased greatly (to 73%) when one or more ISQG-Low values were exceeded, suggesting that ISQG-Low guidelines are appropriate for compliance. Frequent toxic effects (in >75% of samples) were associated with chemical concentrations exceeding ISQG-High guidelines. As expected, the high guideline values were more predictive of adverse effects than the low guidelines. Predictive abilities of ISQGs were not markedly affected by normalization of organic compounds to organic carbon or the use of dilute acid extractions for metals, suggesting that the guidelines are applicable to a wide range of conditions.


Subject(s)
Amphipoda/drug effects , Geologic Sediments , Guidelines as Topic , Sea Urchins/drug effects , Amphipoda/physiology , Animals , Australia , Conservation of Natural Resources , Environmental Monitoring , Evaluation Studies as Topic , Fertilization/drug effects , Geologic Sediments/analysis , Larva/drug effects , Larva/growth & development , Luminescence , Sea Urchins/physiology , Toxicity Tests , Water Pollutants, Chemical/analysis , Water Pollutants, Chemical/toxicity
9.
Environ Monit Assess ; 96(1-3): 53-83, 2004.
Article in English | MEDLINE | ID: mdl-15327149

ABSTRACT

The toxicological responses of three species to 103 surficial saltwater sediment samples from Sydney Harbour, and coastal lakes and estuaries on the south-east coast of New South Wales, Australia, were tested in a battery of four to six laboratory toxicity tests. This is the first large-scale toxicological study of sediments in Australia, the objective of which is to assess the protective and predictive abilities of North American biological effects-based sediment quality guidelines, recently adopted in Australia. Amphipods were exposed to whole sediments in survival and reburial tests, sea urchin fertilisation and larval development tests were conducted on porewaters, and bacterial bio-luminescence (Microtox) tests were conducted on organic solvent extracts and porewaters. Local indigenous species were used for the amphipod and sea urchin tests (Corophium sp. and Heliocidaris tuberculata, respectively). A wide range of responses, from <25 to 100% of negative controls were observed in all tests. Mean control-adjusted responses ranged from 46 to 96% for all tests. The percentages of highly toxic samples ranged from 11 to 83% in the various tests. The order of test sensitivity was: amphipod survival < Microtox test of porewaters < amphipod reburial < sea urchin larval development < sea urchin fertilisation < Microtox test of solvent extracts. Concordance between toxicity tests in classifying samples as highly toxic or not, ranged from 47 to 79%, indicating some similarities between test results, but not complete equivalence. Combined toxicity test results showed that the incidence of highly toxic responses occurring in the majority of tests (75-100% of tests) was low (5% of samples), but a large percentage of samples had highly toxic results in at least one test (76% of samples). Toxicity was more pervasive in the Sydney region than in coastal lakes and estuaries south of Sydney. The current study demonstrated the utility of indigenous invertebrate species and the Microtox bacterium in a sediment toxicity test battery for Australian saltwater sediments.


Subject(s)
Geologic Sediments/analysis , Sea Urchins/drug effects , Animals , Environmental Monitoring/methods , Luminescent Measurements , New South Wales , Toxicity Tests , Vibrio/drug effects , Water Pollutants, Chemical/toxicity
10.
Biochem Soc Trans ; 31(Pt 3): 694-8, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12773185

ABSTRACT

Halobacterium is one of the few known Archaea that tolerates high levels of sunlight in its natural environment. Photoreactivation is probably its most important strategy for surviving UV irradiation and we have shown that both of the major UV photoproducts, cyclobutane pyrimidine dimers (CPDs) and (6-4) photoproducts, can be very efficiently repaired by photoreactivation in this organism. There are two putative photolyase gene homologues in the published genome sequence of Halobacterium sp. NRC-1. We have made a mutant deleted in one of these, phr2, and confirmed that this gene codes for a CPD photolyase. (6-4) photoproducts are still photoreactivated in the mutant so we are currently establishing whether the other homologue, phr1, codes for a (6-4) photolyase. We have also demonstrated an excision repair capacity that operates in the absence of visible light but the nature of this pathway is not yet known. There is probably a bacteria-type excision-repair mechanism, since homologues of uvrA, uvrB, uvrC and uvrD have been identified in the Halobacterium genome. However, there are also homologues of eukaryotic nucleotide-excision-repair genes ( Saccharomyces cerevisiae RAD3, RAD25 and RAD2 ) so there may be multiple repair mechanisms for UV damage in Halobacterium.


Subject(s)
DNA Damage/radiation effects , DNA Repair/radiation effects , DNA, Archaeal/radiation effects , Halobacterium salinarum/genetics , Animals , DNA Repair/genetics , DNA, Archaeal/genetics , Deoxyribodipyrimidine Photo-Lyase/radiation effects , Halobacterium salinarum/classification , Halobacterium salinarum/radiation effects , Phylogeny
11.
Mol Microbiol ; 48(2): 465-80, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12675805

ABSTRACT

Endonuclease III (Nth) enzyme from Escherichia coli is involved in base excision repair of oxidised pyrimidine residues in DNA. The Schizosaccharomyces pombe Nth1 protein is a sequence and functional homologue of E. coli Nth, possessing both DNA glycosylase and apurinic/apyrimidinic (AP) lyase activity. Here, we report the construction and characterization of the S. pombe nth1 mutant. The nth1 mutant exhibited no enhanced sensitivity to oxidising agents, UV or gamma-irradiation, but was hypersensitive to the alkylating agent methyl methanesulphonate (MMS). Analysis of base excision from DNA exposed to [3H]methyl-N-nitrosourea showed that the purified Nth1 enzyme did not remove alkylated bases such as 3-methyladenine and 7-methylguanine whereas methyl-formamidopyrimidine was excised efficiently. The repair of AP sites in S. pombe has previously been shown to be independent of Apn1-like AP endonuclease activity, and the main reason for the MMS sensitivity of nth1 cells appears to be their lack of AP lyase activity. The nth1 mutant also exhibited elevated frequencies of spontaneous mitotic intrachromosomal recombination, which is a phenotype shared by the MMS-hypersensitive DNA repair mutants rad2, rhp55 and NER repair mutants rad16, rhp14, rad13 and swi10. Epistasis analyses of nth1 and these DNA repair mutants suggest that several DNA damage repair/tolerance pathways participate in the processing of alkylation and spontaneous DNA damage in S. pombe.


Subject(s)
Deoxyribonuclease (Pyrimidine Dimer)/metabolism , Escherichia coli Proteins/metabolism , Fungal Proteins/metabolism , Mutation , Schizosaccharomyces/genetics , Cell Survival , DNA Damage , DNA Glycosylases/metabolism , DNA Repair , DNA, Fungal/drug effects , DNA, Fungal/radiation effects , Deoxyribonuclease (Pyrimidine Dimer)/genetics , Escherichia coli Proteins/genetics , Fungal Proteins/genetics , Methyl Methanesulfonate/pharmacology , Microbial Sensitivity Tests , Mutagens/pharmacology , Pyrimidines/metabolism , Recombination, Genetic , Schizosaccharomyces/drug effects , Schizosaccharomyces/metabolism , Schizosaccharomyces/radiation effects , Ultraviolet Rays
12.
Mol Microbiol ; 45(2): 533-42, 2002 Jul.
Article in English | MEDLINE | ID: mdl-12123462

ABSTRACT

In common with other apicomplexan parasites, Plasmodium falciparum, a causative organism of human malaria, harbours a residual plastid derived from an ancient secondary endosymbiotic acquisition of an alga. The function of the 35 kb plastid genome is unknown, but its evolutionary origin and genetic content make it a likely target for chemotherapy. Pulsed field gel electrophoresis and ionizing radiation have shown that essentially all the plastid DNA comprises covalently closed circular monomers, together with a tiny minority of linear 35 kb molecules. Using two-dimensional gels and electron microscopy, two replication mechanisms have been revealed. One, sensitive to the topoisomerase inhibitor ciprofloxacin, appears to initiate at twin D-loops located in a large inverted repeat carrying duplicated rRNA and tRNA genes, whereas the second, less drug sensitive, probably involves rolling circles that initiate outside the inverted repeat.


Subject(s)
DNA Replication , DNA, Circular/biosynthesis , DNA, Protozoan/biosynthesis , Plasmodium falciparum/genetics , Plastids/genetics , Animals , Anti-Infective Agents/pharmacology , Ciprofloxacin/pharmacology , DNA Replication/drug effects , DNA, Circular/genetics , DNA, Circular/ultrastructure , DNA, Protozoan/genetics , DNA, Protozoan/ultrastructure , Electrophoresis, Gel, Pulsed-Field , Electrophoresis, Gel, Two-Dimensional , Microscopy, Electron , Models, Genetic , Plasmodium falciparum/drug effects , Plasmodium falciparum/ultrastructure , Plastids/drug effects , Plastids/ultrastructure , Protozoan Proteins/antagonists & inhibitors , Topoisomerase II Inhibitors
13.
Biochim Biophys Acta ; 1544(1-2): 196-206, 2001 Jan 12.
Article in English | MEDLINE | ID: mdl-11341929

ABSTRACT

A heat-soluble protein present in substantial quantities in Typha latifolia pollen was purified to homogeneity. The protein was subjected to cyanogen bromide cleavage, and the peptides produced were separated by HPLC chromatography and sequenced. The two sequences determined were found to be related to the putative D76 LEA protein from Brassica napus seeds and one of them to the D-7 LEA protein from upland cotton. This suggests the pollen protein to be a member of the LEA group III family of proteins. The secondary structure of the protein in solution and in the dry state was investigated using Fourier transform IR spectroscopy. Whereas the protein in solution was highly unordered, being largely in a random coil conformation, the conformation was largely alpha-helical after fast drying. Slow drying reversibly led to both alpha-helical and intermolecular extended beta-sheet structures. When dried in the presence of sucrose, the protein adopted alpha-helical conformation, irrespective of drying rate. The effect of the protein on the stability of sucrose glasses was also investigated. The dehydrated mixture of sucrose and the LEA protein had higher glass transition temperatures and average strength of hydrogen bonding than dehydrated sucrose alone. We suggest that LEA proteins may play a role together with sugars in the formation of a tight hydrogen bonding network in the dehydrating cytoplasm, thus conferring long-term stability.


Subject(s)
Glass , Plant Proteins/isolation & purification , Pollen/chemistry , Amino Acid Sequence , Brassica/chemistry , Carbohydrate Conformation , Electrophoresis, Polyacrylamide Gel , Gossypium/chemistry , Plant Proteins/chemistry , Protein Structure, Secondary , Spectroscopy, Fourier Transform Infrared , Sucrose/chemistry
14.
J Mol Biol ; 306(2): 159-68, 2001 Feb 16.
Article in English | MEDLINE | ID: mdl-11237591

ABSTRACT

The Phylum Apicomplexa comprises thousands of obligate intracellular parasites, some of which cause serious disease in man and other animals. Though not photosynthetic, some of them, including the malaria parasites (Plasmodium spp.) and the causative organism of Toxoplasmosis, Toxoplasma gondii, possess a remnant plastid partially determined by a highly derived residual genome encoded in 35 kb DNA. The genetic maps of the plastid genomes of these two organisms are extremely similar in nucleotide sequence, gene function and gene order. However, a study using pulsed field gel electrophoresis and electron microscopy has shown that in contrast to the malarial version, only a minority of the plastid DNA of Toxoplasma occurs as circular 35 kb molecules. The majority consists of a precise oligomeric series of linear tandem arrays of the genome, each oligomer terminating at the same site in the genetic map, i.e. in the centre of a large inverted repeat (IR) which encodes duplicated tRNA and rRNA genes. This overall topology strongly suggests that replication occurs by a rolling circle mechanism initiating at the centre of the IR, which is also the site at which the linear tails of the rolling circles are processed to yield the oligomers. A model is proposed which accounts for the quantitative structure of the molecular population. It is relevant that a somewhat similar structure has been reported for at least three land plant chloroplast genomes.


Subject(s)
DNA Replication , DNA, Protozoan/biosynthesis , DNA, Protozoan/chemistry , Nucleic Acid Conformation , Plastids/genetics , Toxoplasma/genetics , Animals , DNA Restriction Enzymes/metabolism , DNA, Circular/biosynthesis , DNA, Circular/chemistry , DNA, Circular/genetics , DNA, Circular/ultrastructure , DNA, Protozoan/genetics , DNA, Protozoan/ultrastructure , Electrophoresis, Gel, Pulsed-Field , Gamma Rays , Microscopy, Electron , Models, Genetic
15.
Curr Genet ; 38(3): 113-25, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11057444

ABSTRACT

An artificially created non-tandem hetero-allelic duplication was constructed to assay mitotic intrachromosomal recombination in Schizosaccharomyces pombe. Two classes of recombinants could be distinguished: deletion-types, in which one copy of the duplicated sequence and the intervening sequence were lost, and conversion-types which retained the duplication. For spontaneous recombination, compared to wild-type cells, a rad22 mutant (corresponding to a Saccharomyces cerevisiae rad52 mutant) had wild-type levels of deletion-types, but was hypo-recombinant for conversion-types; rad16 (S. cerevisiae rad1), rad22 rad16 (S. cerevisiae rad52 rad1) and swi10 (S. cerevisiae rad10) mutants were hyper-recombinant for both types; rad22 swi10 (S. cerevisiae rad52 rad10) mutants were hypo-recombinant for both types; rhp51 (S. cerevisiae rad51) and rhp54 (S. cerevisiae rad54) mutants were hyper-recombinant for deletion-types, but almost completely lacked conversion-types. For wild-type cells, UV-irradiation induced both types of recombinant, but mainly conversion-types. All of the mutants lacked UV-induced recombination.


Subject(s)
Chromosomes, Fungal/genetics , DNA Repair , Gene Conversion/genetics , Recombination, Genetic/radiation effects , Schizosaccharomyces/genetics , Cell Survival , DNA, Fungal/radiation effects , Gene Deletion , Hot Temperature , Mitosis , Mutation , Time Factors
16.
Mutat Res ; 451(1-2): 197-210, 2000 Jun 30.
Article in English | MEDLINE | ID: mdl-10915873

ABSTRACT

This review is concerned with repair and tolerance of UV damage in the fission yeast, Schizosaccharomyces pombe and with the differences between Sch. pombe and budding yeast, Saccharomyces cerevisiae in their response to UV irradiation. Sch. pombe is not as sensitive to ultra-violet radiation as Sac. cerevisiae nor are any of its mutants as sensitive as the most sensitive Sac. cerevisiae mutants. This can be explained in part by the fact that Sch. pombe, unlike budding yeast or mammalian cells, has an extra pathway (UVER) for excision of UV photoproducts in addition to nucleotide excision repair (NER). However, even in mutants lacking this additional pathway, there are significant differences between the two yeasts. Sch. pombe mutants that lack the alternative pathway are still more UV-resistant than wild-type Sac. cerevisiae; recombination mutants are significantly UV sensitive (unlike their Sac. cerevisiae equivalents); mutants lacking the second pathway are sensitized to UV by caffeine; and checkpoint mutants are relatively more sensitive than the budding yeast equivalents. In addition, Sch. pombe has no photolyase. Thus, the response to UV in the two yeasts has a number of significant differences, which are not accounted for entirely by the existence of two alternative excision repair pathways. The long G2 in Sch. pombe, its well-developed recombination pathways and efficient cell cycle checkpoints are all significant components in survival of UV damage.


Subject(s)
DNA Damage/radiation effects , DNA Repair/physiology , DNA-Binding Proteins , Endodeoxyribonucleases , Saccharomyces cerevisiae Proteins , Schizosaccharomyces/genetics , Ultraviolet Rays , Caffeine/pharmacology , DNA Repair/drug effects , DNA Repair/radiation effects , Fungal Proteins/genetics , Fungal Proteins/metabolism , Photochemistry , Schizosaccharomyces/metabolism , Schizosaccharomyces/radiation effects , Transcription, Genetic
18.
Mol Gen Genet ; 260(4): 319-34, 1998 Nov.
Article in English | MEDLINE | ID: mdl-9870697

ABSTRACT

Caffeine potentiates the lethal effects of ultraviolet and ionising radiation on wild-type Schizosaccharomyces pombe cells. In previous studies this was attributed to the inhibition by caffeine of a novel DNA repair pathway in S. pombe that was absent in the budding yeast Saccharomyces cerevisiae. Studies with radiation-sensitive S. pombe mutants suggested that this caffeine-sensitive pathway could repair ultraviolet radiation damage in the absence of nucleotide excision repair. The alternative pathway was thought to be recombinational and to operate in the G2 phase of the cell cycle. However, in this study we show that cells held in G1 of the cell cycle can remove ultraviolet-induced lesions in the absence of nucleotide excision repair. We also show that recombination-defective mutants, and those now known to define the alternative repair pathway, still exhibit the caffeine effect. Our observations suggest that the basis of the caffeine effect is not due to direct inhibition of recombinational repair. The mutants originally thought to be involved in a caffeine-sensitive recombinational repair process are now known to be defective in arresting the cell cycle in S and/or G2 following DNA damage or incomplete replication. The gene products may also have an additional role in a DNA repair or damage tolerance pathway. The effect of caffeine could, therefore, be due to interference with DNA damage checkpoints, or inhibition of the DNA damage repair/tolerance pathway. Using a combination of flow cytometric analysis, mitotic index analysis and fluorescence microscopy we show that caffeine interferes with intra-S phase and G2 DNA damage checkpoints, overcoming cell cycle delays associated with damaged DNA. In contrast, caffeine has no effect on the DNA replication S phase checkpoint in response to inhibition of DNA synthesis by hydroxyurea.


Subject(s)
Caffeine/pharmacology , Cell Cycle/drug effects , DNA Damage/drug effects , Radiation Tolerance/drug effects , Schizosaccharomyces/genetics , DNA Repair/drug effects , DNA Replication/drug effects , Flow Cytometry , G2 Phase/drug effects , Mitotic Index , Recombination, Genetic/drug effects , S Phase/drug effects , Schizosaccharomyces/drug effects , Schizosaccharomyces/radiation effects , Ultraviolet Rays
19.
Semin Arthritis Rheum ; 28(2): 97-106, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9806370

ABSTRACT

OBJECTIVE: To identify patterns of maternal antibodies associated with an increased risk of having a child with congenital heart block (CHB) and to provide a basis for counseling women with a previously affected child. METHODS: This retrospective clinical study of the obstetric histories of 46 Finnish women with a CHB child compared the strength and specificity of the immune response to SS-A/Ro and SS-B/La, as determined by immunoblot and ELISA, in 44 affected women with 85 women with systemic lupus erythematosus (SLE) and 32 women with primary Sjögren's syndrome (SS) with healthy children. RESULTS: High levels of anti-SS-A/Ro and anti-SS-B/La by practically all assays were associated with a significantly increased risk of having a CHB child. The best single test to identify high-risk mothers was anti-52 kd SS-A/Ro by immunoblot (OR 18.9), and it was the only assay to detect mothers at increased risk of CHB as compared with controls with primary SS. Low risk of CHB was indicated by undetectable or low levels of antibodies in the ELISA assays and no reactivity on immunoblot. Mothers with a previous child with CHB had a history of fetal loss (mostly spontaneous abortions) or a history of recurrent fetal losses (> or = 3) slightly more often than controls. Late-trimester obstetric complications in non-CHB pregnancies were insignificant. The relative risk for a female child compared with a male child to have CHB was 1.9 (1.2-2.9, P = .009), and the risk of the mother having another child with CHB was 12% (4 of 34). CONCLUSION: Although there is no unique antibody profile specific for CHB, mothers with a high or low risk of having a child with CHB can be identified. Female children appear to have an increased risk of CHB, but the risk of the mother having another child with CHB is low.


Subject(s)
Autoantigens/immunology , Counseling , Heart Block/congenital , Heart Block/immunology , RNA, Small Cytoplasmic , Ribonucleoproteins/immunology , Abortion, Spontaneous/immunology , Abortion, Spontaneous/prevention & control , Adult , Antibody Specificity , Autoantibodies/analysis , Child , Enzyme-Linked Immunosorbent Assay , Female , Fetal Death/immunology , Fetal Death/prevention & control , Finland , Heart Block/epidemiology , Humans , Incidence , Male , Pregnancy , Pregnancy Outcome , Prevalence , Recurrence , Retrospective Studies , Risk Factors , SS-B Antigen
20.
Bioessays ; 20(4): 291-7, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9619100

ABSTRACT

Ultraviolet light (UV) is thought to have had a major impact on the early evolution of life. UV is absorbed by nucleic acids and produces several types of DNA damage, which interfere with DNA replication and transcription. This damage can result in mutagenesis and cell killing. Several mechanisms for repairing UV-induced DNA damage have been identified. Besides the widely distributed nucleotide excision repair, two alternative repair mechanisms for specific lesions in UV-damaged DNA are known, involving photolyases and DNA glycosylases. Recently, a novel endonuclease for UV-induced DNA damage was identified that initiates an excision repair pathway completely different from previously established repair mechanisms. The finding of this "alternative excision repair" suggests the presence of a new category of DNA repair, initiated by single-strand breaks in DNA. Homologues of the UVDE enzyme have been found in eukaryotic microorganisms, as well as in bacteria, indicating that the enzyme originated early in evolution, and suggesting the existence of multirepair systems for UV-induced DNA damage during early evolution.


Subject(s)
DNA Damage , DNA Glycosylases , DNA Repair , DNA/radiation effects , Ultraviolet Rays/adverse effects , DNA Ligases/physiology , DNA, Fungal/genetics , DNA, Fungal/radiation effects , Deoxyribodipyrimidine Photo-Lyase/genetics , Fungal Proteins/physiology , Humans , Mutagenesis , N-Glycosyl Hydrolases/physiology , Neurospora crassa/genetics , Saccharomyces cerevisiae/genetics , Schizosaccharomyces/genetics , Substrate Specificity
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