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41.
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Coevolution of the glucose dehydrogenase gene and the ejaculatory duct in the genus Drosophila 总被引:2,自引:0,他引:2
The glucose dehydrogenase gene (Gld) in Drosophila melanogaster exhibits a
unique spatial and temporal pattern of expression. GLD expression switches
from a non-sex-limited state at the pupal stage to a male-limited state at
the adult stage. At the adult stage, the enzyme is restricted to the
ejaculatory duct. Within the genus Drosophila, the ejaculatory duct has
undergone a simple morphological divergence. In order to determine whether
correlated changes in GLD expression had occurred, GLD activity during the
pupal and adult stages was determined for several Drosophila species. It
was found that virtually all of the species exhibit pupal GLD activity,
whereas only those species with an expanded ejaculatory duct express
male-limited GLD. The results of interspecific genital imaginal disc
transplantation experiments indicate that the expanded morphology and GLD
expression do not require any species- or sex-specific diffusible factors.
An apparent regulatory polymorphism exists within the D. takahashii species
with respect to male-limited GLD expression.
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DR. Myron A. Mehlman DR. Emil A. Pfitzer DR. Robert A. Scala The Committee to Promote Principles of Reduction Refinement Replacement of Animal Testing in Industrial Toxicology Laboratories 《Cell biology and toxicology》1989,5(3):349-358
The Committee to Promote Principles of Reduction, Refinement and Replacement of Animal Testing in Industrial Toxicology Laboratories was established in 1987 to work toward industrywide improvements in laboratory animal testing methods. The committee's goals are to gather information about effective nonanimal testing techniques and other methods of conserving and improving the care of laboratory animals, to work toward the systematic validation of nonanimal alternatives, and to disseminate useful information about progressive programs and policies throughout the industrial toxicology community. This is the first in a continuing series of reports the committee plans to produce as part of an ongoing program to promote communication among industrial toxicologists about successful methods of reducing, refining and replacing animal testing. Here are some of the report's major findings: (1) Animal care and use committees charged with the oversight of laboratory animal use are a universal practice at the companies surveyed. (2) Significant reductions in the number of animals used for acute toxicity testing have taken place at all the companies during the last 5- to 10-year period. (3) Structure-activity relationships (predicting a test compound's properties based on the known properties of familiar chemicals with similar structures) are widely used to minimize, but not replace, the use of animals. (4) Tissue and organ culture systems are being used with increasing frequency for screening and mechanistic studies, but are not completely replacing animal evaluations as a final step. (5) There is a pressing need for the systematic and scientifically sound validation of nonanimal alternative techniques to reduce the use of animals in toxicology testing while satisfying requirements for the protection of public safety. 相似文献
46.
Purified chloroplast tRNAs were isolated fromPisum sativum leaves and radioactively labeled at their 3′ end using tRNA nucleotidyl transferase and α32P-labeled CTP. Pea ctDNA was fragmented using a number of restriction endonucleases and hybridized with thein vitro labeled chloroplast tRNAs by DNA transfer method. Genes for tRNAs have been found to be dispersed throughout the chloroplast
genome. A closer analysis of the several hybrid regions using recombinant DNA plasmids have shown that tRNA genes are localized
in the chloroplast genome in both single and multiple arrangements. Two dimensional gel electrophoresis of total ct tRNA have
identified 36 spots. All of them have been found to hybridize withPisum sativum ctDNA. Using recombinant clones, 30 of the tRNA spots have been mapped inPisum sativum ctDNA. 相似文献
47.
Mutations which improve the efficiency of recombination should affect
either the proteins which mediate recombination or their substrate, DNA
itself. The former mutations would be localized to a few sites. The latter
would be dispersed. Studies of hybridization between RNA molecules have
suggested that recombination may be initiated by a homology search
involving the "kissing" of the tips of stem loops. This predicts that, in
the absence of other constraints, mutations which assist the formation of
stem loops would be favored. From comparisons of the folding of normal and
shuffled DNA sequences, I present evidence for an evolutionary selection
pressure to distribute stem loops generally throughout genomes. I propose
that this early pressure came into conflict with later local pressures to
impose information concerning specific function. The conflict was
accommodated by permitting sections of DNA concerned with a specific
function to evolve in dispersed segments. Traces of the conflict seem to be
present in some modern intron-containing genes. Thus, introns may have
allowed the interspersing of selectively advantageous stem loops in coding
regions of DNA.
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48.
A requirement for trypsin-sensitive cell-surface components for cell-cell interactions of embryonic neural retina cells 总被引:5,自引:3,他引:2 下载免费PDF全文
A quantitative assay was used to measure the rate of collection of a population of embryonic neural retina cells to the surface of cell aggregates. The rate of collection of freshly trysinized cells was limited in the initial stages by the rate of replacement of trypsin-sensitive cell- surface components. When cells were preincubated, or "recovered," and then added to cell aggregates, collection occurred at a linear rate and was independent of protein and glycoprotein synthesis. The adhesion of recovered cells was temperature and energy dependent, and was reversibly inhibited by cytochalasin B. Colchicine had little effect on collection of recovered cells. Antiserum directed against recovered cell membranes was shown to bind to recovered cells by indirect immunofluorescence. The antiserum also was shown to inhibit collection of recovered cells to aggregates, suggesting that at least some of the antigens identified might be involved in the adhesion process. The inhibitory effect of the antiserum was dose dependent . Freshly trypsinized cells absorbed neither the immunofluorescence activity nor the adhesion-inhibiting activity. Recovered cells absorbed away both activities. In specificity studies, dorsal neural retina cells adhered to aggregates of ventral optic tectum in preference to aggregates of dorsal optic tectum. The adhesive specificity of the dorsal retina cells was less sensitive to trypsin than the adhesive specificity of ventral retina cells which adhered preferentially to dorsal tectal aggregates only after a period of recovery. 相似文献
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50.
The self-incompatibility phenotype in brassica is altered by the transformation of a mutant S locus receptor kinase 总被引:2,自引:0,他引:2 下载免费PDF全文
The self-incompatible (SI) Brassica napus line W1, which carries the 910 S allele, was transformed with an inactive copy of the 910 S locus receptor kinase (SRK) gene. Two transformed lines were analyzed based on their heritable ability to set self-seed. The first line was virtually completely self-compatible (SC), and reciprocal pollinations with the original W1 line demonstrated that only the stigma side of the SI phenotype was altered. An analysis of the expression of endogenous SRK-910 demonstrated that the mechanism of transgene action is via gene suppression. Furthermore, the expression of the S locus glycoprotein gene present in the 910 allele (SLG-910), SLG-A10, which is derived from a nonfunctional S allele, and an S locus-related gene were also suppressed. When the transgene was crossed into another SI line carrying the A14 S allele, it was also capable of suppressing the expression of the endogenous genes and of making this line SC. The second transgenic line studied was only partly SC. In this case as well, only the stigma phenotype was affected, although no gene suppression was detected for endogenous SRK-910 or SLG-910. In this line, the expression of the transgene most likely was causing the change in phenotype, and no effect was observed when this transgene was crossed into the other SI line. Therefore, this work reinforces the hypothesis that the SRK gene is required, but only for the stigma side of the SI phenotype, and that a single transgene can alter the SI phenotype of more than one S allele. 相似文献