scholarly journals A Further Study of the Role of Copper in Regard to the Antimutagenic Action of Sodium Copper Chlorophyllin (SCC) in Somatic Cells of Drosophila melanogaster

2013 ◽  
Vol 8 ◽  
pp. BMI.S11081 ◽  
Author(s):  
Emilio Pimentel ◽  
Martha P. Cruces ◽  
Stanley Zimmering
Keyword(s):  
Drosophila Melanogaster ◽  
Gamma Rays ◽  
Copper Content ◽  
Gamma Ray ◽  
Somatic Cells ◽  
Food Supplement ◽  
Genetic Damage ◽  
Sodium Copper Chlorophyllin ◽  
Antimutagenic Action

Previous findings suggest that copper plays a crucial role in the antimutagenic effect of sodium copper chlorophyllin (SCC). The objective of the current research was to compare the antimutagenic effects of two SCC compounds with different amounts of copper (3.7% and 5.4%, respectively) on the genetic damage induced by gamma rays in somatic cells of Drosophila. Data indicate that an increase in copper content of 31.5% in SCC-5.4 resulted in a greater inhibition of gamma ray genetic damage of 49% whereas only a 2% inhibition with SCC-3.7 occurred. Of greater interest is the association of SCC with a variety of uses in humans, such as a chemo preventive agent and food supplement. A greater attention to the concentration of copper in the SCC product in use should be required.

scholarly journals Improving the performance of 241Am-Be for PGNAA applications using a proper shielding for neutron source and the NaI detector

2010 ◽  
Vol 25 (3) ◽  
pp. 205-211 ◽  
Author(s):  
Hamed Panjeh ◽  
Hashem Hakimabad ◽  
Lalle Motavalli
Keyword(s):  
Gamma Rays ◽  
Energy Region ◽  
Gamma Ray ◽  
Region Of Interest ◽  
High Rate ◽  
Prompt Gamma ◽  
Peak Resolution ◽  
Set Up ◽  
Gamma Ray Detector

The gamma ray spectrum resolution from a 241Am-Be source-based prompt gamma ray activation analysis set-up has been observed to increase in the energy region of interest with enclosing the NaI detector in a proper neutron and gamma ray shield. We have investigated the tact that the peak resolution of prompt gamma rays in the region of interest from the set-up depends on the source activity to the great extent, size and kind of the detector and the geometry of the detector shield. In order to see the role of a detector shield, five kinds of the detector shield were used and finally the proper kind was introduced. Since the detector shield has an important contribution in the reduction of the undesirable and high rate gamma rays coming to the gamma ray detector, a good design of a proper shield enables the elimination of the unwanted events, such as a pulse pile-up. By improving the shielding design, discrete and distinguishable photoelectric peaks in the energy region of interest have been observed in the spectrum of prompt gamma rays.

scholarly journals Genetic damage induced by CrO3 can be reduced by low doses of Protoporphyrin-IX in somatic cells of Drosophila melanogaster

2014 ◽  
Vol 1 ◽  
pp. 894-899 ◽  
Author(s):  
Luz M. Vidal E. ◽  
Emilio Pimentel P. ◽  
M. Patricia Cruces M. ◽  
Juan C. Sánchez M.
Keyword(s):  
Drosophila Melanogaster ◽  
Somatic Cells ◽  
Protoporphyrin Ix ◽  
Low Doses ◽  
Genetic Damage

Gonad formation and development requires the abd-A domain of the bithorax complex in Drosophila melanogaster

Development ◽  
1992 ◽  
Vol 115 (2) ◽  
pp. 395-402 ◽  
Author(s):  
S. Cumberledge ◽  
J. Szabad ◽  
S. Sakonju
Keyword(s):  
Drosophila Melanogaster ◽  
Germ Line ◽  
Somatic Cells ◽  
Gonadal Development ◽  
Somatic Tissue ◽  
Bithorax Complex ◽  
Wild Type ◽  
Pole Cells ◽  
Transplantation Experiments

The abdominal-A (abd-A) gene, a member of the bithorax complex, is required for the correct identity of parasegments (PS) 7 through 13. Mutations in iab-4, one of the cis-regulatory regions of abd-A, transform epidermal structures of PS 9 and also cause loss of gonads in adult flies. Here, we describe a developmental and molecular analysis of the role of iab-4 functions in gonadal development. In flies homozygous for a strong iab-4 allele, gonadogenesis is not initiated in the embryo because the mesodermal cells fail to encapsulate the pole cells. Flies homozygous for weaker iab-4 mutations sometimes form ovaries. The ovary-oviduct junctions are abnormal, however, and egg transfer from the ovary to the uterus is blocked in the adult. To localize the sites that require iab-4 function, we have analyzed animals chimeric for the mutant and wild-type cells. These chimeras were generated by three kinds of transplantation experiments: pole cells, embryonic somatic nuclei or larval ovaries. Our results suggest that iab-4 is required in the somatic cells of the gonadal primordia, but not the germ line. In addition, the formation of functional ovary-oviduct junctions and egg transfer also requires iab-4 functions in the somatic cells of the ovary and in at least one additional somatic tissue.

On the possible gamma-ray source in Cygnus

1967 ◽  
Vol 31 ◽  
pp. 469-471
Author(s):  
J. G. Duthie ◽  
M. P. Savedoff ◽  
R. Cobb
Keyword(s):  
Gamma Rays ◽  
Gamma Ray ◽  
Right Ascension

A source of gamma rays has been found at right ascension 20h15m, declination +35°, with an uncertainty of 6° in each coordinate. Its flux is (1·5 ± 0·8) x 10-4photons cm-2sec-1at 100 MeV. Possible identifications are reviewed, but no conclusion is reached. The mechanism producing the radiation is also uncertain.

Solar Flare Energetic Neutral Emission Measurements in the Project Coronas-I

1994 ◽  
Vol 144 ◽  
pp. 635-639
Author(s):  
J. Baláž ◽  
A. V. Dmitriev ◽  
M. A. Kovalevskaya ◽  
K. Kudela ◽  
S. N. Kuznetsov ◽  
...  
Keyword(s):  
Solar Flare ◽  
Energy Range ◽  
Gamma Rays ◽  
Pulse Shape ◽  
Gamma Ray ◽  
Pulse Shape Discrimination ◽  
Shape Discrimination ◽  
Solar Neutron ◽  
Low Altitude

AbstractThe experiment SONG (SOlar Neutron and Gamma rays) for the low altitude satellite CORONAS-I is described. The instrument is capable to provide gamma-ray line and continuum detection in the energy range 0.1 – 100 MeV as well as detection of neutrons with energies above 30 MeV. As a by-product, the electrons in the range 11 – 108 MeV will be measured too. The pulse shape discrimination technique (PSD) is used.

scholarly journals MULTIPLE ALLELE APPROACH TO THE STUDY OF GENES IN DROSOPHILA MELANOGASTER THAT ARE INVOLVED IN IMAGINAL DISC DEVELOPMENT

Genetics ◽  
1978 ◽  
Vol 89 (2) ◽  
pp. 355-370 ◽  
Author(s):  
Allen Shearn ◽  
Grafton Hersperger ◽  
Evelyn Hersperger ◽  
Ellen Steward Pentz ◽  
Paul Denker
Keyword(s):  
Drosophila Melanogaster ◽  
Phenotypic Variation ◽  
Mutant Allele ◽  
Imaginal Disc ◽  
Reference Allele ◽  
Multiple Allele ◽  
Significant Difference ◽  
Chromosome Mutations ◽  
Cold Sensitive

ABSTRACT The phenotypes of five different lethal mutants of Drosophila melanogaster that have small imaginal discs were analyzed in detail. From these results, we inferred whether or not the observed imaginal disc phenotype resulted exclusively from a primary imaginal disc defect in each mutant. To examine the validity of these inferences, we employed a multiple-allele method. Lethal alleles of the five third-chromosome mutations were identified by screening EMS-treated chromosomes for those which fail to complement with a chromosome containing all five reference mutations. Twenty-four mutants were isolated from 13,197 treated chromosomes. Each of the 24 was then tested for complementation with each of the five reference mutants. There was no significant difference in the mutation frequencies at these five loci. The stage of lethality and the imaginal disc morphology of each mutant allele were compared to those of its reference allele in order to examine the range of defects to be found among lethal alleles of each locus. In addition, hybrids of the alleles were examined for intracistronic complementation. For two of the five loci, we detected no significant phenotypic variation among lethal alleles. We infer that each of the mutant alleles at these two loci cause expression of the null activity phenotype. However, for the three other loci, we did detect significant phenotypic variation among lethal alleles. In fact, one of the mutant alleles at each of these three loci causes no detectable imaginal disc defect. This demonstrates that attempting to assess the developmental role of a gene by studying a single mutant allele may lead to erroneous conclusions. As a byproduct of the mutagenesis procedure, we have isolated two dominant, cold-sensitive mutants.

scholarly journals A novel transvection phenomenon affecting the white gene of Drosophila melanogaster.

Genetics ◽  
1990 ◽  
Vol 126 (1) ◽  
pp. 167-176
Author(s):  
D Gubb ◽  
M Ashburner ◽  
J Roote ◽  
T Davis
Keyword(s):  
Drosophila Melanogaster ◽  
Homologous Chromosome ◽  
Tandem Duplication ◽  
Gamma Ray ◽  
Insertion Site ◽  
Hairpin Loop ◽  
Homologous Chromosomes ◽  
Inverted Order ◽  
In Trans ◽  
In Cis

Abstract The zeste mutation of Drosophila melanogaster suppresses the expression of white genes in the eye. This suppression is normally dependent on there being two copies of w+ located close to each other in the genome--they may either be in cis (as in a tandem duplication of w+) or in trans, i.e. on homologous chromosomes. Duplicated w+ genes carried by a giant transposing element, TE146(Z), are suppressed by z whether they are in direct (tandem) or inverted order. The tandem form of the TE is very sensitive to a rearrangement on the homologous chromosome--many rearrangements with breakpoints "opposite" the TE's insertion site prevent the interaction between the white genes on a z background. These aberrations act as dominant suppressors of zeste that are specific to the tandemly duplicated form of TE146(Z). The inverted form of the TE146(Z) presumably pairs as a hairpin loop; this is more stable than the tandem form by the criterion that its zeste phenotype is unaffected by any of the aberrations. This effect of rearrangements has been used as the basis for a screen, gamma-ray induced aberrations with at least one breakpoint opposite the TE site were recovered by their suppression of the zeste phenotype.

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