Analyze Diet

Topic:DNA

DNA in horses refers to the genetic material that carries the hereditary information necessary for the growth, development, functioning, and reproduction of equine species. It consists of sequences of nucleotides that encode the genetic instructions used in the development and functioning of horses. DNA analysis in horses can provide insights into genetic diversity, lineage, and breed characteristics. It is also utilized in identifying genetic disorders, understanding hereditary traits, and assisting in selective breeding programs. This page compiles peer-reviewed research studies and scholarly articles that explore the structure, function, and applications of DNA analysis in equine genetics and breeding.
DNases in milk and blood sera from different species.
Acta veterinaria Scandinavica    January 1, 1979   Volume 20, Issue 3 404-416 doi: 10.1186/BF03546602
Gudding R.DNases were demonstrated in samples of colostrum and blood serum from man and various domestic animals. The measurable DNase activity recorded was highest in samples from cat and dog and lowest in samples from goat, horse, pig and sheep. In contrast to DNases produced by certain bacteria, these enzymes were thermo-labile and the activity was maximal in the area pH 5.0–5.5. A modification of an agar medium originally described for the demonstration of bacterial DNases was found to be suitable for assays of DNases from colostrum, milk and serum. DNaser ble påvist i prøver fra kolostrum og bl...
Hybridization of bovine papilloma virus type 1 and type 2 DNA to DNA from virus-induced hamster tumors and naturally occurring equine tumors.
Intervirology    January 1, 1979   Volume 11, Issue 4 227-233 doi: 10.1159/000149038
Lancaster WD, Theilen GH, Olson C.DNAs from bovine papilloma virus(BPV)-induced hamster tumors and from equine connective tissue tumors of unknown etiology were examined for BPV DNA sequences by molecular hybridization. DNA from two distinct classes of BPV (type 1 and type 2) was labeled in vitro and used as probes. Analysis of DNA-DNA reassociation kinetics indicated that both virus types were capable of tumor induction in the hamster. DNA isolated from 6 of 7 equine tumors accelerated the reassociation of the BPV DNA probes. BPV type 1 or type 2 DNA hybridized extensively to DNA from 3 tumors, while 3 other tumors contained ...
Analysis of mechanisms regulating the expression of parental alleles at the GPD locus in mule erythrocytes.
Biochemical genetics    June 1, 1978   Volume 16, Issue 5-6 379-386 doi: 10.1007/BF00484205
Serov OL, Zakijan SM, Kulichkov VA.Erythrocyte glucose-6-phosphate dehydrogenase (G6PD) was examined by 13% starch gel electrophoresis in 74 mules (42 females and 32 males), 35 donkeys, and ten horses. The quantitative expression of the parental alleles at the Gpd locus varies greatly in female mules from the hemizygous expression of the maternal allele to that of the paternal. The data obtained indicate that the X chromosomes are randomly inactivated in females mules. No selective advantage of a cell population with a maternally (or paternally) derived X active was found in female mule erythrocytes. It is suggested that the ph...
Detection of proviral DNA in horse cells infected with equine infectious anemia virus.
Journal of virology    June 1, 1978   Volume 26, Issue 3 577-583 doi: 10.1128/JVI.26.3.577-583.1978
Rice NR, Simek S, Ryder OA, Coggins L.Equine infectious anemia virus (EIAV) recently has been shown to possess a high-molecular-weight RNA genome and a virion reverse transcriptase. We completed the demonstration that EIAV is a retrovirus by showing the presence of proviral DNA in equine cells infected in vitro, but not in normal horse DNA. These studies were performed by using a highly representative cDNA probe synthesized by the virion polymerase. It was found that this cDNA reassociated extensively, and with high thermal stability, with either viral RNA or DNA extracted from infected cells, but showed no detectable reassociatio...
Replication of equine herpesvirus type 1 and type 3: resistance to hydroxyurea and thymidine.
Intervirology    January 1, 1978   Volume 9, Issue 5 276-285 doi: 10.1159/000148945
Allen GP, Cohen JC, Randall CC, O'Callaghan DJ.The replication of equine herpesvirus type 1 (EHV-1) and type 3 (EHV-3) was unimpeded in three different cell types-equine epithelial cells, equine fibroblasts, and mouse fibroblasts-which had been blocked in their capacity to synthesize host DNA by 2.5 mM hydroxyurea (HU) or 2 mM thymidine (TdR). The rate of DNA synthesis in uninfected or equine herpesvirus-infected cells in the presence of HU or TdR was measured by pulse-labeling cell samples with a labeled DNA precursor at different times after infection. DNA synthesis in uninfected cultures was completely inhibited by both compounds. Howev...
Probing DNA quaternary ordering with circular dichroism spectroscopy: studies of equine sperm chromosomal fibers.
Biopolymers    March 1, 1977   Volume 16, Issue 3 573-582 doi: 10.1002/bip.1977.360160308
Sipski ML, Wagner TE.No abstract available
Bovine papilloma virus: presence of virus-specific DNA sequences in naturally occurring equine tumors.
Proceedings of the National Academy of Sciences of the United States of America    February 1, 1977   Volume 74, Issue 2 524-528 doi: 10.1073/pnas.74.2.524
Lancaster WD, Olson C, Meinke W.Four of five spontaneous benign equine connective tissue tumors of unknown etiology and a bovine papilloma virus (BPV)-induced equine tumor contained BPV-specific DNA sequences as determined by DNA-DNA hybridization of DNA from tumors with BPV DNA labeled in vitro. Analysis of the kinetics of reassociation indicated that 20-75% of the BPV genome was present in the various tumors. The number of partial BPV genome equivalents ranged from 60 to 500 copies per diploid quantity of cellular DNA. Thermal denaturation profiles of duplexes formed between labeled BPV DNA and DNA from tumor cells indicat...
[Mechanisms for the expression of parental alleles of the Gpd locus in mule erythrocytes].
Genetika    January 1, 1977   Volume 13, Issue 10 1761-1766 
Serov OL, Zakiian SM, Kulichkov VA.No abstract available
Purification and characterization of equine herpesvirus-induced DNA.
Virology    January 1, 1977   Volume 76, Issue 1 395-408 doi: 10.1016/0042-6822(77)90311-7
Allen GP, O'Callaghan DJ, Randall CC.Infection of cells with equine herpesvirus type 1 (EHV-1) or type 3 (EHV-3) resulted in the induction of a DNA polymerase activity distinguishable from host cell DNA polymerases by its high salt requirement for maximal activity. By column chromatography on DEAE-cellulose, DNA-cellulose, phosphocellulose, and hydroxyapatite, the EHV-1-induced polymerase was purified 500-fold with 1–2% recovery of total activity from the nuclei of infected hamster livers. The final enzyme preparation was homogeneous as judged by electrophoresis in sodium dodecyl sulfate-polyacrylamide gels. Calculations based ...
Comparison of serum DNA, native DNA-binding and deoxyribonuclease levels in ten animal species and man.
Life sciences    November 15, 1976   Volume 19, Issue 10 1609-1614 doi: 10.1016/0024-3205(76)90108-9
Cox RA, Gokcen M.No abstract available
Phenotype of mammalian spermatozoa in relation to genetic content.
Indian journal of experimental biology    September 1, 1976   Volume 14, Issue 5 610-611 
Bhattacharya BC, Gunther AH, Enos HL, Evans BM, Ghosh CR.No abstract available
The future use of cytogenetics in the manipulation of domestic animal populations.
New Zealand veterinary journal    December 1, 1975   Volume 23, Issue 12 295-298 doi: 10.1080/00480169.1975.34263
Bruere AN.No abstract available
Isolation and characterization of an adenovirus and isolation of its adenovirus-associated virus in cell culture from foals with respiratory tract disease.
American journal of veterinary research    March 1, 1975   Volume 36, Issue 3 247-250 
Dutta SK.An adenovirus was isolated from a foal with respiratory tract disease. The virus produced cytopathic effects (CPE) in equine embryo kidney (EEK) cell culture, contained deoxyribonucleic acid (DNA), was resistant to chloroform and pH 3, and was moderately resistant to heat. The virus caused hemagglutination of human (type O) erythrocytes. Viral density was 1.34 g/cm,3 and diameter was 75 nm. An adenovirus-associated virus (AAV) isolated from the infected cell culture was 22 nm in diameter. These viruses are classified as equine adenovirus and equine AAV.
Linkage between the K blood group locus and the 6-PGD locus in horses.
Animal blood groups and biochemical genetics    January 1, 1974   Volume 5, Issue 3 137-141 doi: 10.1111/j.1365-2052.1974.tb01323.x
Sandberg K.No abstract available
Equine herpesviruses: antigenic relationships and deoxyribonucleic acid densities.
Infection and immunity    October 1, 1973   Volume 8, Issue 4 621-627 doi: 10.1128/iai.8.4.621-627.1973
Plummer G, Goodheart CR, Studdert MJ.Equine herpesviruses with a deoxyribonucleic acid density of 1.716 to 1.717 g/cm(3) were compared with one another by the plaque-reduction test and by the rate of development of cytopathic effect as indicated by plaque size in rabbit kidney cultures. Of the 19 isolates studied, the 9 which had already been tentatively labeled equine abortion viruses were serologically similar to one another; each of them grew more quickly than did any of the other 10 isolates although the mean plaque sizes formed a series of gradations with no clear hiatus which would permit the unequivocal delineation of the ...
A DNA-binding protein in the serum of certain mammalian species.
Proceedings of the National Academy of Sciences of the United States of America    November 1, 1972   Volume 69, Issue 11 3327-3330 doi: 10.1073/pnas.69.11.3327
Thoburn R, Hurvitz AI, Kunkel HG.Various mammalian species contain an anionic serum protein that reacts specifically with native DNA. It is considerably less reactive with single-strand DNA and does not react with monodeoxyribonucleotides, homopolyribonucleotides, or duplexes of homopolyribonucleotides. Synthetic dA.dT was an effective inhibitor of the reaction with native DNA, while Micrococcus luteus DNA and dG.dC were not inhibitory. This protein was encountered in the course of studies on DNA antibodies. Although it reacted with red cells coated with DNA and gave agar precipitation bands, it was clearly distinct from DNA ...
Further proof of genetic inactivation of the X chromosome in the female mule.
Nature    June 16, 1972   Volume 237, Issue 5355 393-396 doi: 10.1038/237393a0
Rattazzi MG, Cohen MM.No abstract available
G6PD expression and X chromosome late replication in fibroblast clones from a female mule.
Nature    June 16, 1972   Volume 237, Issue 5355 396-397 doi: 10.1038/237396a0
Ray M, Gee PA, Richardson BJ, Hamerton JL.No abstract available
[Individual and species specificity differences in the DNA content of spermatozoas].
Zentralblatt fur Veterinarmedizin. Reihe A    April 1, 1972   Volume 19, Issue 4 327-336 
Stolla R.No abstract available
Evidence for a relationship between equine abortion (herpes) virus deoxyribonucleic acid synthesis and the S phase of the KB cell mitotic cycle.
Journal of virology    June 1, 1971   Volume 7, Issue 6 736-748 doi: 10.1128/JVI.7.6.736-748.1971
Lawrence WC.Autoradiographic analyses of deoxyribonucleic acid (DNA) synthesis in randomly growing KB cell cultures infected with equine abortion virus (EAV) suggested that viral DNA synthesis was initiated only at times that coincided with the entry of noninfected control cells into the S phase of the cell cycle. Synchronized cultures of KB cells were infected at different stages of the cell cycle, and rates of synthesis of cellular and viral DNA were measured. When cells were infected at different times within the S phase, viral DNA synthesis was initiated 2 to 3 hr after infection. However, when cells ...
Comparison of four horse herpesviruses.
Journal of virology    November 1, 1969   Volume 4, Issue 5 738-741 doi: 10.1128/JVI.4.5.738-741.1969
Plummer G, Bowling CP, Goodheart CR.Four equine herpesviruses (equine abortion virus, equine herpesvirus types 2 and 3, and equine cytomegalovirus) were compared. The equine abortion virus did not cross-neutralize with any of the other viruses, but the other three did show varying degrees of cross-neutralization among themselves. Equine abortion virus grew more quickly in tissue cultures than did the others, and attained higher titers of infectivity in the culture fluid; it also formed plaques in a wider range of tissue culture species, although the other three were not specific for one tissue culture system only, in that they w...
The nucleic acid content of skeletal muscle and liver in mammals of different body size.
Comparative biochemistry and physiology    February 1, 1969   Volume 28, Issue 2 897-905 doi: 10.1016/0010-406x(69)92123-9
Munro HN, Gray JA.No abstract available
Kinetics of cellular and viral DNA synthesis in equine abortion (herpes) virus infection of L-M cells.
Virology    September 1, 1968   Volume 36, Issue 1 104-114 doi: 10.1016/0042-6822(68)90120-7
O'Callaghan DJ, Cheevers WP, Gentry GA, Randall CC.No abstract available
Kinetics of viral deoxyribonucleic acid, protein, and infectious particle production and alterations in host macromolecular syntheses in equine abortion (herpes) virus-infected cells.
Journal of virology    August 1, 1968   Volume 2, Issue 8 793-804 doi: 10.1128/JVI.2.8.793-804.1968
O'Callaghan DJ, Hyde JM, Gentry GA, Randall CC.Infection of exponential-phase suspension cultures of mouse fibroblast cells (L-M) with equine abortion virus (EAV) resulted in inhibition of cell growth and marked alterations in host metabolic processes. The synthesis of deoxyribonucleic acid (DNA) and ribonucleic acid was inhibited within 4 hr after infection and was suppressed by more than 90% by the time of maximal virus replication (14 to 18 hr). The overall rate of protein synthesis, however, was similar in uninfected and virus-producing cells as determined by measurements of net protein and isotope incorporation. The time course of vir...
[Biochemical polymorphism and the detection of paternity in horses].
Schweizer Archiv fur Tierheilkunde    July 1, 1967   Volume 109, Issue 7 378-385 
Baer A.No abstract available
Estimation of Blood Leukocyte Numbers by Means of a DNA Viscosity Test.
Journal of the American Veterinary Medical Association    December 15, 1964   Volume 145 1177-1183 
SCHALM OW, MURRAY R.No abstract available
On the Nucleic Acid Content in Spermatozoa of Certain Farm Animals. BRATANOV K, YOSIFOV K, MATLIEVA M, TSEKOVA E.No abstract available
Degradation of Deoxyribonucleic Acid and Alteration of Nucleic Acid Metabolism in Suspension Cultures of L-M Cells Infected with Equine Abortion Virus.
Journal of bacteriology    July 1, 1963   Volume 86, Issue 1 138-146 doi: 10.1128/jb.86.1.138-146.1963
RANDALL CC, WALKER BM.Randall, Charles C. (University of Mississippi School of Medicine, Jackson) and Barbara M. Walker. Degradation of deoxyribonucleic acid and alteration of nucleic acid metabolism in suspension cultures of L-M cells infected with equine abortion virus. J. Bacteriol. 86:138-146. 1963.-Metabolic alterations in log-phase suspension cultures infected with equine abortion virus (EAV) were determined in L-M cells simultaneously labeled or prelabeled with H(3)- or C(14)-thymidine. Although infection produced an early stimulation of the uptake of labeled thymidine (TdR) into the acid-soluble fraction of...
Composition of RNA and DNA of citric acid-isolated liver nuclei from hamsters infected with equine abortion virus (EAV).
Virology    August 1, 1960   Volume 11 773-775 doi: 10.1016/0042-6822(60)90121-5
GENTRY GA, RANDALL CC, DARLINGTON RW.No abstract available
Some aspects of the desoxyribonuclease activities of animal tissues.
The Journal of general physiology    November 1, 1952   Volume 36, Issue 2 227-241 doi: 10.1085/jgp.36.2.227
ALLFREY V, MIRSKY AE.It has been found that many animal tissues contain "acid" desoxyribonucleases with pH optima near 5.2. A chemical method for the determination of this activity is described. The pancreatic desoxyribonuclease crystallized by Kunitz and shown to have a neutral pH optimum occurs in the pancreas together with the "acid" enzyme, but only the "neutral" enzyme occurs in the pancreatic juice. The ratio of "neutral" to "acid" DNAase activities in the pancreas is greater than 200, but in all other tissues examined there is no appreciable concentration of the neutral enzyme. It is concluded that neutral ...