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Topic:Molecular biology

Molecular biology in horses involves the study of molecular processes and genetic mechanisms that underpin equine physiology and health. This field encompasses the analysis of DNA, RNA, proteins, and other biomolecules to understand gene expression, genetic variation, and cellular functions in horses. Techniques such as genomic sequencing, gene expression profiling, and molecular diagnostics are employed to explore topics like hereditary diseases, performance traits, and immune responses in equines. This page assembles peer-reviewed research studies and scholarly articles that investigate the molecular biology of horses, focusing on genetic research, molecular techniques, and their applications in equine science.
Molecular epizootiologic studies of equine herpesvirus-1 infections by restriction endonuclease fingerprinting of viral DNA.
American journal of veterinary research    February 1, 1983   Volume 44, Issue 2 263-271 
Allen GP, Yeargan MR, Turtinen LW, Bryans JT, McCollum WH.No abstract available
Difference in sizes of human compared to murine alpha-subunits of the glycoprotein hormones arises by four-codon gene deletion or insertion.
Endocrinology    February 1, 1983   Volume 112, Issue 2 482-485 doi: 10.1210/endo-112-2-482
Chin WW, Maizel JV, Habener JF.The sizes of the human and subhuman alpha-subunits of the glycoprotein hormones differ by four amino acids (hCG alpha, 92 amino acids; murine, equine, bovine, and ovine alpha, 96 amino acids). The shortening of the human alpha-subunit has been attributed to posttranslational proteolysis. We have recently determined the nucleotide sequences of the mRNAs encoding the precursors of the alpha-subunit of mouse TSH and rat gonadotropins using recombinant DNA techniques. In this report, we have compared these nucleotide sequences and their deduced amino acid sequences with those of the pre- alpha-sub...
Further study of the chemical structure of the equine erythrocyte hematoside containing O-acetyl ester.
The Journal of biological chemistry    January 25, 1983   Volume 258, Issue 2 876-881 
Gasa S, Makita A, Kinoshita Y.The chemical structure of an equine hematoside, which contained an ester group and comprised 72% of the total erythrocyte gangliosides, was determined by means of nondestructive and destructive procedures. A 400-MHz nuclear magnetic resonance spectrum of the ganglioside in perdeuterodimethyl sulfoxide demonstrated three protons due to a methyl group of an acetyl moiety, as well as amide and anomeric protons which were compatible with those of the ordinary hematoside. The spin decoupling difference spectroscopy of the ganglioside revealed the presence of the following structures. [formula: see ...
Effects of common radioiodination procedures on the binding of glycoproteins to immobilized lectins.
Biochemical and biophysical research communications    January 14, 1983   Volume 110, Issue 1 103-107 doi: 10.1016/0006-291x(83)91266-4
Montelaro RC, West M, Ivey M.Representative glycoproteins including fetuin, protein A, ovalbumin, alpha 1 acid glycoprotein, and the major glycoprotein of equine infectious anemia virus were labelled with 125I by the chloramine-T or Bolton-Hunter procedure and their binding to immobilized Con A or lentil lectin compared to untreated samples of each glycoprotein. Glycoprotein modification was no greater than one substituted residue per protein molecule. Yet the radioiodinated glycoproteins typically displayed only 0-50% of the lectin binding observed with untreated samples. These results indicate that lectin glycoprotein b...
Intestinal alkaline phosphatase-like properties of horse kidney alkaline phosphatase.
Enzyme    January 1, 1983   Volume 30, Issue 4 269-272 doi: 10.1159/000469588
Hoffmann WE, Dorner JL, Morris H.Two isoenzymes of alkaline phosphatase from horse kidney were identified by cellulose acetate electrophoresis. Horse kidney alkaline phosphatase was similar to horse intestinal alkaline phosphatase, in regard to both antigenicity and response to levamisole inhibition, but different from horse liver alkaline phosphatase. This study suggests that horse kidney alkaline phosphatase is an expression of the intestinal gene locus and not the hepatic gene locus.
Identification of the second alpha-2-antiprotease of equine serum as antithrombin III.
The International journal of biochemistry    January 1, 1983   Volume 15, Issue 7 917-922 doi: 10.1016/0020-711x(83)90167-2
Pellegrini A, Zweifel HR, von Fellenberg R.The alpha-2-protease inhibitor, of 65,000 daltons molecular weight, described by several authors in horse plasma and also present as a contaminant in alpha-1-isoinhibitor isolates previously described by us (Pellegrini & von Fellenberg (1980) Biochim. biophys. Acta 616, 351-361) has now been isolated to purity and identified as antithrombin III. The inhibitor is composed of a single polypeptide chain as judged by SDS polyacrylamide gel electrophoresis. The inhibitor was effective only against trypsin and thrombin. Serological cross-reaction existed between the inhibitor and the antiserum t...
Studies on prolactin 48: isolation and properties of the hormone from horse pituitary glands.
Archives of biochemistry and biophysics    January 1, 1983   Volume 220, Issue 1 208-213 doi: 10.1016/0003-9861(83)90402-2
Li CH, Chung D.Isolation of prolactin from equine pituitary glands has been described. It has a potency of 42 IU/mg in the pigeon crop-sac test and consists of 199 amino acids. The hormone has only four half-cystine residues in contrast to other mammalian prolactins which have six residues. From NH2-terminal sequence analysis and amino acid composition of cyanogen bromide fragments, the NH2-terminal disulfide loop is missing in the equine prolactin molecule. Circular dichroism spectra indicate that the alpha-helical content of equine prolactin appears to be lower (50%) than that found in the ovine hormone (6...
Characterisation of the alpha 1-protease inhibitor system in Thoroughbred horse plasma by horizontal two-dimensional (ISO-DALT) electrophoresis. 1. Protein staining.
Animal blood groups and biochemical genetics    January 1, 1983   Volume 14, Issue 2 83-105 doi: 10.1111/j.1365-2052.1983.tb01065.x
Pollitt CC, Bell K.The isoelectric points and the molecular weights of the major components of the eight Thoroughbred protease inhibitor (Pi) types have been determined by polyacrylamide gel isoelectric focusing and polyacrylamide gel pore gradient (ISO-DALT) electrophoresis respectively. The major Pi proteins focus in the range pH 3.74-4.43 and have molecular weights ranging from 55 000-72 000 daltons. Using the ISO-DALT method of electrophoresis, protein maps for the eight Thoroughbred Pi types have been presented for the first time. None of the homozygous Pi types are identical except for the types S1 and S2 ...
Genetic linkage between the loci for phosphohexose isomerase (PHI) and a serum protein (Xk) in horses.
Animal blood groups and biochemical genetics    January 1, 1983   Volume 14, Issue 1 45-50 doi: 10.1111/j.1365-2052.1983.tb01059.x
Andersson L, Juneja RK, Sandberg K.Genetic linkage between the equine loci for phosphohexose isomerase (PHI) and serum Xk protein was demonstrated by means of segregation data from three sire families. The recombination frequency was estimated from pooled data to be 0.23 +/- 0.02; a significant heterogeneity between sires for estimates of the recombination frequency was observed. No indication of linkage was detected between Xk and 14 other blood marker loci. Linkage between the Xk locus and the locus for soluble malic enzyme (ME1) has recently been reported in horses. An equine linkage group designated LG IV comprising the thr...
Subcellular localization and properties of the NAD(P)H oxidase from equine polymorphonuclear leukocytes.
Enzyme    January 1, 1983   Volume 29, Issue 3 198-207 doi: 10.1159/000469633
Heyneman RA.The subcellular distribution of the superoxide-forming enzyme in horse polymorphonuclear leukocytes was investigated. After activation of the cells with sodium oleate, a relatively stable and NAD(P)H-dependent oxygen consumption and superoxide production was found in association with the plasma membranes. The pH dependence displayed an optimum near neutrality. The apparent Km values were 38 x 10(-6) mol/l for NADPH and 1,560 x 10(-6) mol/l for NADH, suggesting that NADPH is the physiological donor. The rates of oxygen uptake, O2- production, and NADP consumption were consistent with the stoich...
Isolation and characterization of horse alpha 2-macroglobulin protease inhibitor.
The International journal of biochemistry    January 1, 1983   Volume 15, Issue 8 1003-1011 doi: 10.1016/0020-711x(83)90036-8
Pellegrini A, Zweifel HR, von Fellenberg R.Several publications have described in the past properties of partly purified horse alpha 2-macroglobulin (alpha 2M) which are strikingly different from the human alpha 2M. Horse alpha 2M was therefore isolated to purity by classical procedures, i.e. affinity chromatography, ion exchange chromatography and gel filtration, and its properties are compared with those of its human counterpart. The molecular weight of the native protein and its subunits, the isoelectrofocusing pattern and the change in electrophoretic mobility caused by interaction with protease were similar to those of human alpha...
Kinetic and structural relationships of transition monomeric and oligomeric carboxyl- and choline-esterases.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes    January 1, 1983   Volume 18, Issue 1 29-63 doi: 10.1080/03601238309372357
Main AR.The kinetic and structural relationships of eight electrophoretically pure mammalian serum and liver serine carboxylesterases (CE) and cholinesterases (ChE) have been studied. Eight CE's and ChE's, which were fully resolved but only partially purified, provided additional information. Five of the electrophoretically pure esterases were monomeric, and of these, four belonged to a new and widely distributed class. These four monomeric esterases hydrolyzed choline esters, but at widely differing rates. Thus two were termed monomeric butyrylcholinesterases, mBuChE I and II, and two were monomeric ...
Structural and functional properties of the non-muscle tropomyosins.
Molecular and cellular biochemistry    January 1, 1983   Volume 57, Issue 2 127-146 doi: 10.1007/BF00849190
Côté GP.The non-muscle tropomyosins (TMs), isolated from such tissues as platelets, brain and thyroid, are structurally very similar to the muscle TMs, being composed of two highly alpha-helical subunits wound around each other to form a rod-like molecule. The non-muscle TMs are shorter than the muscle TMs; sequence analysis demonstrates that each subunit of equine platelet TM consists of 247 amino acids, 37 fewer than for skeletal muscle TM. The major differences in sequence between platelet and skeletal muscle TM are found near the amino and carboxyl terminal ends of the proteins. Probably as the re...
Pyrimidine metabolism in peripheral and phytohemagglutinin-stimulated mammalian lymphocytes.
The International journal of biochemistry    January 1, 1983   Volume 15, Issue 1 51-55 doi: 10.1016/0020-711x(83)90010-1
Peters GJ, Oosterhof A, Veerkamp JH.1. Activity of uridine kinase was very low in ovine lymphocytes and in those of some pigs. Lymphocytes of other pigs showed a significantly higher activity of this enzyme. Activity of uridine kinase in lymphocytes of man, horse and cattle was intermediate. 2. Activity of uridine phosphorylase was higher than that of uridine kinase with lymphocytes of all species. 3. Activity of uridine kinase in equine lymphocytes increases at PHA-stimulation and also in porcine lymphocytes with a low activity at the start of the culture. Activity of uridine kinase decreased in porcine lymphocytes with a high ...
Streptokinase-dependent delayed activation of horse plasminogen.
Biochimica et biophysica acta    December 6, 1982   Volume 709, Issue 1 19-27 doi: 10.1016/0167-4838(82)90416-2
Marcum JA, Highsmith RF, Kline DL.Complete activation of purified horse plasminogen to plasmin was obtained with a 1:10 molar ratio of streptokinase to plasminogen after 5 min of incubation at 37 degrees C. At a 1:1 molar ratio, maximal activity did not appear until 15-30 min, while at a ratio of 6:1 complete activation was delayed for 120-180 min. Gel filtration studies of isotopically labeled streptokinase and horse plasminogen suggest that the delay was due to impaired formation of a streptokinase-plasminogen complex. The predominant streptokinase moiety within the streptokinase-plasmin complex which forms from the streptok...
Characterization of the major antigens of Haemophilus equigenitalis (contagious equine metritis organism).
The Journal of hygiene    December 1, 1982   Volume 89, Issue 3 529-538 doi: 10.1017/s0022172400071102
Corbel MJ, Brewer RA.Immunoelectrophoresis of ultrasonically disrupted Haemophilus equigenitalis (contagious equine metritis organism) cells against rabbit and equine antisera disclosed at least 11 precipitating antigens. Two of these, a polysaccharide and a lipopolysaccharide-protein complex, were of high molecular weight and located on the cell surface. The remaining antigens were intracellular and were small- to medium-sized proteins. The surface antigens were the most significant in relation to the serological response in infected horses. They also reacted with sera from apparently healthy cattle, but the reas...
The use of capillary column gas chromatography and negative ion chemical ionization mass spectrometry to confirm the administration of synthetic corticosteroids to horses.
Biomedical mass spectrometry    November 1, 1982   Volume 9, Issue 11 459-465 doi: 10.1002/bms.1200091102
Houghton E, Teale P, Dumasia MC, Wellby JK.The negative ion chemical ionization mass spectra of the MO-TMS derivatives of the corticosteroids prednisolone, betamethasone and dexamethasone have been obtained using capillary column gas chromatography mass spectrometry. The spectra showed abundant diagnostic ions at m/z greater than 300 allowing for clear discrimination between the three steroid derivatives. A capillary column gas chromatographic mass spectrometric method using negative ion chemical ionization mass spectrometry has been developed to confirm the presence of the parent steroids in horse urine following the administration of...
Estrogens in seminal plasma of human and animal species: identification and quantitative estimation by gas chromatography-mass spectrometry associated with stable isotope dilution.
Journal of steroid biochemistry    November 1, 1982   Volume 17, Issue 5 567-572 doi: 10.1016/0022-4731(82)90017-6
Reiffsteck A, Dehennin L, Scholler R.Estrone, 2-methoxyestrone and estradiol-17 beta have been definitely identified in seminal plasma of man, bull, boar and stallion by high resolution gas chromatography associated with selective monitoring of characteristic ions of suitable derivatives. Quantitative estimations were performed by isotope dilution with deuterated analogues and by monitoring molecular ions of trimethylsilyl ethers of labelled and unlabelled compounds. Concentrations of unconjugated and total estrogens are reported together with the statistical evaluation of accuracy and precision.
[Some physicochemical properties of native and polymerized glutaraldehyde-treated horse heart cytochrome c].
Ukrainskii biokhimicheskii zhurnal (1978)    September 1, 1982   Volume 54, Issue 5 497-501 
Skok MV, Denisiuk PV, Komissarenko SV.Glutaraldehyde treatment does not change the absorption of cytochrome c either in the visible or in UV spectra. It brings about the formation of dimers, trimers and high-polymeric forms of cytochrome c and shifts the pI of all cytochrome c isoelectric fractions to more acid pH. Polymerization also results in changes of kinetic parameters of cytochrome c benzidine reaction increasing its affinity to 3,3-diaminobenzidine with a simultaneous decrease in the effectiveness of H2O2 binding. These biochemical changes can be related to immunochemical differences of native and glutaraldehyde-treated cy...
Purification and identification of horse serum IgA.
Nihon juigaku zasshi. The Japanese journal of veterinary science    August 1, 1982   Volume 44, Issue 4 661-668 doi: 10.1292/jvms1939.44.661
Kurimoto T, Ikeda A, Tanaka K.ウマ分泌型IgA (初乳, 涙) の分離精製については, すでに報告されているが, ウマ血清IgAの分離精製に関する明確な手法を示した報告は見あたらない. われわれは, ウマ血清を脱塩, 硫安塩析し, ついでDEAEセルロース, 免疫吸着体のカラム操作により, 抗原性および分子サイズにおいて, IgG, IgG(T), IgM とは明らかに区別される免疫グロブリンを分離精製した. この免疫グロブリンは抗イヌIgAとの交差反応性により, IgAと同定された. さらに作製した抗分泌型...
Identification of a transforming retrovirus from cultured equine dermal fibrosarcoma.
Virology    July 30, 1982   Volume 120, Issue 2 490-494 doi: 10.1016/0042-6822(82)90050-2
Fatemi-Nainie S, Anderson LW, Cheevers WP.No abstract available
Specific fragmentation of natural inhibitor of mitochondrial ATPase by thrombin.
Biochemical and biophysical research communications    July 30, 1982   Volume 107, Issue 2 435-441 doi: 10.1016/0006-291x(82)91510-8
Dianoux AC, Freyssinet JM.No abstract available
Iron binding by horse spleen apoferritin. A vanadyl(IV) EPR spin probe study.
The Journal of biological chemistry    July 10, 1982   Volume 257, Issue 13 7672-7677 
Chasteen ND, Theil EC.No abstract available
Equine luteinizing hormone possesses follicle-stimulating hormone activity in hypophysectomized female rats.
Biology of reproduction    June 1, 1982   Volume 26, Issue 5 935-942 doi: 10.1095/biolreprod26.5.935
Moudgal NR, Papkoff H.The ability of equine luteinizing hormone (eLH) to promote follicular growth and maturation in hypophysectomized rats has been assessed. A single injection of equine LH has been shown to promote the growth of a large number of antral and preovulatory follicles. In addition, equine LH markedly increased serum estrogen levels and uterine weight. Furthermore, equine LH, like equine chorionic gonadotropin (eCG; PMSG) was able to significantly enhance the incorporation of [3H]thymidine into ovarian DNA, an activity shown to be specific to hormones having follicle-stimulating hormone (FSH) activity....
Resonance-enhanced Raman identification of a ternary chemical intermediate during the equine liver alcohol dehydrogenase reduction of p-(dimethylamino)benzaldehyde.
Biochemistry    April 27, 1982   Volume 21, Issue 9 2193-2202 doi: 10.1021/bi00538a031
Jagodzinski PW, Funk GF, Peticolas WL.The nature of the binding of aromatic aldehyde and aromatic alcohol substrates to the catalytic zinc of equine liver alcohol dehydrogenase has been studied by using resonance-enhanced Raman spectroscopy. When an excess of both enzyme and coenzyme to substrate is used, a stable ternary chemical intermediate is formed between liver alcohol dehydrogenase and the reduced coenzyme, nicotinamide adenine dinucleotide, and the aldehyde, p-(dimethylamino)benzaldehyde, in the pH range 8.5-0.6. Resonance-enhanced Raman spectra clearly show that this same intermediate is formed between the excess enzyme, ...
Persistent infection by equine infectious anemia virus: asymmetry of nucleotide sequence reiteration in the integrated provirus of persistently infected cells.
Virology    April 15, 1982   Volume 118, Issue 1 246-253 doi: 10.1016/0042-6822(82)90340-3
Cheevers WP, Watson SG, Klevjer-Anderson P.No abstract available
Cytotaxin-induced cAMP peak in granulocytes: its relationship to crawling movements, chemokinesis and chemotaxis.
Biochemical pharmacology    April 15, 1982   Volume 31, Issue 8 1573-1577 doi: 10.1016/0006-2952(82)90382-3
Naef A, Damerau B, Keller HU.The relationship between the short transient intracellular increase in cAMP levels on the one hand and chemotaxis or crawling movements on the other hand was investigated using human and equine granulocytes. C5ades arg, f-met-leu-phe, human serum albumin and immunoglobulin were used as stimulating agents. There was no strict correlation between the induction of crawling movements or of chemokinesis in general and the generation of the cAMP peak. But there was so far a strict parallelism between the occurrence of the chemotactic response and the cAMP peak. However, the magnitude of the peak was...
The conformational transition of horse heart porphyrin c.
The Journal of biological chemistry    April 10, 1982   Volume 257, Issue 7 3864-3868 
Brems DN, Liu YC, Stellwagen E.The heme iron of horse heart cytochrome c was selectively removed using anhydrous HF. The product, porphyrin c, exhibits the viscosity, far ultraviolet circular dichroic, and fluorescence properties characteristic for native cytochrome c. However, porphyrin c is more susceptible to denaturation by guanidine hydrochloride and by heat than is the parent cytochrome. All of the conformational parameters of porphyrin c exhibit a common reversible transition centered at 0.95 m guanidine hydrochloride at 23 degrees C and pH 7.0. Guanidine denatured porphyrin c refolds in two kinetic phases having tim...
Pancreatic colipase: crystallographic and biochemical aspects.
European journal of biochemistry    April 1, 1982   Volume 123, Issue 2 347-354 doi: 10.1111/j.1432-1033.1982.tb19774.x
Pierrot M, Astier JP, Astier M, Charles M, Drenth J.A detailed study of the crystallization of hog and horse colipases has been undertaken. Several crystallographic varieties have been obtained and a 0.3-nm resolution structure determination is actually in progress. The sequence of the A form of horse colipase (one methionine) is given. From spectrophotometric experiments and sequence comparisons, the involvement of the aromatic residue in position 52 in the micelle binding site has been demonstrated.
Synthesis and properties of equine beta-melanotropin and its naturally occurring des-Asp analog.
International journal of peptide and protein research    April 1, 1982   Volume 19, Issue 4 327-333 doi: 10.1111/j.1399-3011.1982.tb02611.x
Izdebski J, Yamashiro D, Ng TB, Li CH.No abstract available