Analyze Diet

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.
Amino acid sequence of horse colipase B.
Biochimica et biophysica acta    June 29, 1981   Volume 669, Issue 1 39-45 doi: 10.1016/0005-2795(81)90221-x
Bonicel J, Couchoud P, Foglizzo E, Desnuelle P, Chapus C.The complete sequence of the 96 residues composing horse colipase B has been determined by automated analysis of the intact protein, of two CNBr peptides and two tryptic peptides arising, respectively, from the citraconylated chain and from the unreduced protein. The single histidine of the protein is located at position 29 as in horse colipase A. His86, present in the C-terminal region of the pig cofactor and supposed to play a role in the folding molecule, is not conserved in horse B. Large pieces of the pig and horse B chains were found to be identical or very similar, especially the N-term...
Nucleic acid-protein interactions. Degradation of double-stranded RNA by glycosylated ribonucleases.
Biochimica et biophysica acta    June 26, 1981   Volume 654, Issue 1 77-85 doi: 10.1016/0005-2787(81)90138-6
Carsana A, Furia A, Gallo A, Beintema JJ, Libonati M.1. Extensively glycosylated ribonucleases, like the enzymes from pig and horse pancreas, show a much higher activity on double-stranded RNAs than similarly charged, carbohydrate-free RNAases under stranded assay conditions (relatively high salt concentrations). Glycosylated pig and horse pancreas RNAases also show a larger destabilizing effect on double-stranded poly[d(A-T)] X poly[d(A-T)], than that displayed by bovine RNAase A under these conditions. Both activities show a similar dependence on the ionic strength of the medium. 2. A partial enzymic removal of the heterosaccharide side chains...
Relationship of sialic acid residues to in vitro biological and immunological activities of equine gonadotropins.
Biology of reproduction    June 1, 1981   Volume 24, Issue 5 1082-1087 
Aggarwal BB, Papkoff H.No abstract available
Crystallization and properties of creatine kinase from equine skeletal muscle.
Journal of biochemistry    May 1, 1981   Volume 89, Issue 5 1619-1631 doi: 10.1093/oxfordjournals.jbchem.a133357
Takasawa T, Fukushi K, Shiokawa H.A crystalline creatine kinase was obtained from equine skeletal muscle. The enzyme was homogeneous, as judged by ultracentrifugation and disc electrophoresis on polyacrylamide gel. The crystalline enzyme had a specific activity of 110 units per mg of protein, that is, 14-fold purification over the crude extract of equine skeletal muscle. The molecular weight of the enzyme was determined to be 84,600 by the conventional low-speed sedimentation equilibrium method, and s020,w was 5.32S. Eight cysteine residues were found on amino acid analysis, two of which were essential for the enzymatic activi...
Isolation and characterization of two glycophorins from horse erythrocyte membranes.
Journal of biochemistry    May 1, 1981   Volume 89, Issue 5 1593-1598 doi: 10.1093/oxfordjournals.jbchem.a133354
Murayama JI, Takeshita K, Tomita M, Hamada A.Crude glycophorin fraction was prepared from horse erythrocyte membranes by extraction with lithium diiodosalicylate and partition in aqueous phenol. Two glycophorins, designated glycophorins HA and HB, were isolated by two different techniques: preparative gel electrophoresis in the presence of sodium dodecyl sulfate and ion-exchange chromatography in the presence of the nonionic detergent Ammonyx LO. Each glycophorin formed at least two bands on gel electrophoresis, which corresponded to a dimeric form and a monomeric form. Glycophorin HA, the major component, had a blocked amino-terminus an...
Hydrolysis by horse muscle acylphosphatase of (Ca2+ + Mg2+)-ATPase phosphorylated intermediate.
Archives of biochemistry and biophysics    April 15, 1981   Volume 208, Issue 1 37-41 doi: 10.1016/0003-9861(81)90120-x
Stefani M, Liguri G, Berti A, Nassi P, Ramponi G.No abstract available
The histidine residues in pig and horse colipases.
Biochemical and biophysical research communications    March 16, 1981   Volume 99, Issue 1 114-119 doi: 10.1016/0006-291x(81)91720-4
Granon S, Rahmani-Jourdheuil D, Desnuelle P, Chapus C.No abstract available
Stabilization of the C-terminal part of pig and horse colipase by carboxypeptidase and trypsin inhibitors.
European journal of biochemistry    March 16, 1981   Volume 115, Issue 1 99-105 doi: 10.1111/j.1432-1033.1981.tb06203.x
Chapus C, Desnuelle P, Foglizzo E.Pig and horse colipases have been purified by a common procedure using trypsin and carboxypeptidase inhibitors as stabilizers. Two forms of pig colipase were identified: a predominant A1 form with about 103-105 residues, and a minor slightly degraded A2 form in which the last two C-terminal residues, Asp and Ser, were lacking. This type of degradation is considerably slowed down by carboxypeptidase inhibitors. A total of four forms of the horse cofactor were characterized: two (A1 and B1) were probably isocolipases which differed by only a few substitutions. Both contained the same number of r...
Differentiation of sub-types of equine herpesvirus I by restriction endonuclease analysis.
Australian veterinary journal    March 1, 1981   Volume 57, Issue 3 148-149 doi: 10.1111/j.1751-0813.1981.tb00495.x
Sabine M, Robertson GR, Whalley JM.No abstract available
The cleavage of the Met-Lys bond in a bradykinin derivative by glandular kallikreins.
Hoppe-Seyler's Zeitschrift fur physiologische Chemie    March 1, 1981   Volume 362, Issue 3 337-345 doi: 10.1515/bchm2.1981.362.1.337
Araujo-Viel MS, Juliano L, Prado ES.The synthetic tridecapeptide Gly-Leu-Met-Lys-Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg was used as a model substrate for horse urinary and porcine pancreatic kallikreins. The Met-Lys bond is hydrolyzed selectively by both enzymes. Oxidation of the methionine residue to sulfoxide made the peptide resistant to both kallikreins. Substitution of either the methionine or lysine residues by norleucine led to peptides in which the Nle-Lys or the Met-Nle bonds, respectively, were susceptible to the urinary kallikrein. The esterolytic and Met-Lys bond-splitting activities of both enzymes were inhibited simil...
Physico-chemical properties of pregnant mare serum gonadotropin.
Biochimica et biophysica acta    February 27, 1981   Volume 667, Issue 2 267-276 doi: 10.1016/0005-2795(81)90192-6
Combarnous Y, Salesse R, Garnier J.Pregnant mare serum gonadotropin exhibits a dissociation at acid pH as shown by the drop of s20,w values from 3.52 S at pH 8.1 to 2.52 S at pH 2.0. The dissociation is accompanied by an absorbance change with a maximum at 287 nm and a parallel loss of both follicle-stimulating hormone (FSH) and luteinizing hormone (LH) activities as followed by radioreceptor assays. The apparent pKa of the acid transition is 3.45 with an extremely slow and temperature-dependent rate at pH 2.0 (1.8 . 10(-4) s-1 at 37 degrees C). By gel filtration the molecular weight of the active hormone is estimated to be 45 ...
Isolation and characterization of a new beta-melanotropin from horse pituitary glands.
Biochemical and biophysical research communications    February 12, 1981   Volume 98, Issue 3 621-627 doi: 10.1016/0006-291x(81)91159-1
Ng TB, Oosthuizen MM, Chung D, Li CH.No abstract available
Activation of pigeon erythrocyte adenylate cyclase by cholera toxin. Partial purification of an essential macromolecular factor from horse erythrocyte cytosol.
Biochimica et biophysica acta    February 5, 1981   Volume 672, Issue 3 248-261 doi: 10.1016/0304-4165(81)90291-9
Le Vine H, Cuatrecasas P.A cytosolic, macromolecular factor required for the cholera toxin-dependent activation of pigeon erythrocyte adenylate cyclase and cholera toxin-dependent ADP-ribosylation of a membrane-bound 43,000 dalton polypeptide has been purified 1100-fold from horse erythrocyte cytosol using organic solvent precipitation and heat treatment. This factor, 13,000 daltons, does not absorb to anionic or cationic exchange resins, is sensitive to trypsin or 10% trichloroacetic acid and is not extractable by diethyl ether. Activation of adenylate cyclase by cholera toxin requires the simultaneous presence of AT...
Rapid-scanning spectral evidence for catalytically nonequivalent but interconvertible forms of equine liver alcohol dehydrogenase.
Biochimie    February 1, 1981   Volume 63, Issue 2 97-102 doi: 10.1016/s0300-9084(81)80171-x
Koerber SC, Dunn MF.These rapid-scanning stopped-flow kinetic studies of the equine liver alcohol dehydrogenase-catalyzed reduction of p-nitrobenzaldehyde by NADH and (4R)-4-deuterio NADH (NADD) under single turnover conditions establish : (1) The reaction is biphasic using NADD as coenzyme, k1 approximately 200 sec-1, k2 = 0.5 sec-1 and the amplitude ratio (A1)/(A1 + A2) approximately equal to 0.5. (2) Each phase of the reaction involves the oxidation of enzyme-bound reduced coenzyme. (3) The recycling of sites in the presence of 20 mM pyrazole is negligible. (4) The rates of E(NAD-pyrazole) complex formation at...
Equine cytomegalovirus: cultural characteristics and properties of viral DNA.
Virology    February 1, 1981   Volume 109, Issue 1 106-119 doi: 10.1016/0042-6822(81)90475-x
Wharton JH, Henry BE, O'Callaghan DJ.No abstract available
Fibrinolytic activity without fibrinogenolysis during long-distance racing in horses.
Journal of applied physiology: respiratory, environmental and exercise physiology    February 1, 1981   Volume 50, Issue 2 245-249 doi: 10.1152/jappl.1981.50.2.245
Ferguson EW, Bernier LL, Shaughness GP, Boucher JH.Fourteen horses were studied during a 157-km endurance ride. Two humans who ran the 157 km were also evaluated at the finish. Fibrin monomer samples were examined by two-dimensional gel electrophoresis and sodium dodecyl sulfate polyacrylamide gel electrophoresis. Two major species of horse Beta-chain with higher molecular weights and different isoelectric mobilities than human beta-chain were observed. Horse alpha-chains had higher molecular weights than human alpha-chains but similar alpha-chain heterogeneities. Mean euglobulin lysis time (ELT) in the horses was accelerated to similar levels...
Effects of limited denaturation by heat on the dynamic conformation of equine immunoglobulin M antibody and on interaction with antigen and complement.
Biochemistry    January 6, 1981   Volume 20, Issue 1 192-198 doi: 10.1021/bi00504a032
Siegel RC, Cathou RE.No abstract available
Alcohol dehydrogenase from Leuconostoc mesenteroides: molecular properties in comparison with the yeast and horse liver enzyme.
The International journal of biochemistry    January 1, 1981   Volume 13, Issue 12 1215-1224 doi: 10.1016/0020-711x(81)90067-7
Schneider-Bernlöhr H, Fiedler H, Gerber M, Weber C, Zeppezauer M.No abstract available
Predicted secondary structure of horse muscle acylphosphatase. Comparison with circular dichroism measurements.
Physiological chemistry and physics    January 1, 1981   Volume 13, Issue 3 267-273 
Camici G, Manao G, Cappugi G, Ramponi G.We have predicted the secondary structure of horse muscle acylphosphatase by the statistical method of Chou and Fasman. In addition, we have studied the circular dichroism spectra of the enzyme, obtaining values for comparison to the predicted results. Discrepancies were found for the alpha-helix content estimated by the two methods.
Characterization of the binding of Triton X-100 to equine and rabbit serum albumin.
Physiological chemistry and physics    January 1, 1981   Volume 13, Issue 5 455-459 
Sukow WW, Bailey J.The binding isotherms for Triton X-100 binding to equine and rabbit serum albumin were determined by equilibrium dialysis at 16 degrees C in pH 7.0, I = 0.05 phosphate buffer. Presented in a Scatchard plot, the binding isotherms are a straight line, indicating thermodynamically independent and identical binding sites. In this model equine serum albumin is characterized as having 11 such sites with an equilibrium constant of 6.0 x 10(3) M-1. Similarly, rabbit serum albumin is characterized as having 9 such sites with an equilibrium constant of 8.0 x 10(3) M-1.
Fractionation and partial characterization of alpha-1-protease isoinhibitors of horse.
Biochimica et biophysica acta    December 4, 1980   Volume 616, Issue 2 351-361 doi: 10.1016/0005-2744(80)90152-7
Pellegrini A, von Fellenberg R.The principal alpha-1-protease inhibitor of horse was fractionated by classical methods and analysed with a modified fibrinogen-agarose gel electrophoretic method of high sensitivity and resolving power. Starting with an electrophoretically homogeneous inhibitor in unfractionated serum, two isoinhibitor bands became apparent after fractionation with (NH4)2SO4 and DEAE-cellulose DE-52 ion-exchange chromatography. The isoinhibitors differed in electrophoretic migration and in the elution pattern from Sephadex G-100 gel filtration, but possessed identical antigenic determinants and enzyme specifi...
Equine infectious anemia virus, a putative lentivirus, contains polypeptides analogous to prototype-C oncornaviruses.
Virology    December 1, 1980   Volume 107, Issue 2 520-525 doi: 10.1016/0042-6822(80)90319-0
Parekh B, Issel CJ, Montelaro RC.No abstract available
Restriction in IgM expression–I. The VH regions of equine anti-lactose antibodies.
Molecular immunology    December 1, 1980   Volume 17, Issue 12 1553-1561 doi: 10.1016/0161-5890(80)90181-9
Rodwell JD, Karush F.No abstract available
[Effect of 2 methods of demineralization on the on the preservation of glycoproteins and proteoglycans in the intertubular and peritubular dentin in the horse].
Journal de biologie buccale    December 1, 1980   Volume 8, Issue 4 315-330 
Goldberg M, Molon Noblot M, Septier D.The effect of 2 methods of demineralization on the preservation of proteoglycans and glycoproteins was studied in the intertubular and peritubular dentine of the horse. The specimens embedded in Epon were demineralized with a 2% acid formic solution (Bonucci and Gheradi, 1975). Other fragments were treated with an organic solution of EDTA alkylammonium salt (Scott and Kyffin, 1979). These methods preserved in a satisfactory way these labile organic components. In the intertubular dentine, glycoproteins and proteoglycans were also identified, either associated with collagen fibres as a glue and...
Helix packing and subunit conformation in horse spleen apoferritin.
Nature    November 20, 1980   Volume 288, Issue 5788 298-300 doi: 10.1038/288298a0
Clegg GA, Stansfield RF, Bourne PE, Harrison PM.An electron density map of horse spleen apoferritin at 0.28-nm (2.8 A) resolution and its preliminary interpretation have been described previously. Rigorous examination of this and newer maps at the same nominal resolution but calculated from more extensive data sets, including model building in a Richards' comparator, now allows us to report on structural features in more detail. We list inter-helical angles within and between neighbouring subunits, and describe a new short region of inter-subunit anti-parallel pleated sheet. A short section of electron density not properly accounted for in ...
Conformation of Immunoglobulin M. III. Structural requirements of antigen for complement fixation by equine IgM.
Journal of immunology (Baltimore, Md. : 1950)    November 1, 1980   Volume 125, Issue 5 1910-1915 
Siegel RC, Cathou RE.Complexes of IgM equine anti-dansyl antibodies and different dansyl substituted carriers were tested for their ability to fix complement (C). Only dansyl92-Ficoll and dansyl12-poly-L-lysine were found to be effective. Dansyl13-bovine serum albumin, dansyl127-keyhole limpet hemocyanin, and reduced and alkylated dansyl10-ribonuclease were all ineffective. Lack of C fixation by the dansyl-ribonuclease was not due to lack of antibody-antigen complex formation, since binding at the concentrations employed for C fixation was established. However, in contrast, polymerized dansyl-ribonuclease (polydis...
The complete amino acid sequence of human Cu/Zn superoxide dismutase.
FEBS letters    October 20, 1980   Volume 120, Issue 1 53-56 doi: 10.1016/0014-5793(80)81044-1
Barra D, Martini F, Bannister JV, Schininà ME, Rotilio G, Bannister WH, Bossa F.No abstract available
Sequence of the low activity equine erythrocyte carbonic anhydrase and delineation of the amino acid substitutions in various polymorphic forms.
The Journal of biological chemistry    October 10, 1980   Volume 255, Issue 19 9196-9204 
Jabusch JR, Bray RP, Deutsch HF.the sequence of the low activity form of equine erythrocyte carbonic anhydrase has been determined. The most common electrophoretic form, designated D, has been found to have five substitutions. Amino acid exchanges in the electrophoretic variants known as A1, A2, B, and T have been found at six other positions. The data do not permit calculation of the number of polymorphic forms of this enzyme. The equine D isozyme and the analogous human enzyme are quite homologous, 211 of their 260 residues, or 81%, being identical.
Characterization of gangliosides from equine kidney and spleen.
Journal of biochemistry    October 1, 1980   Volume 88, Issue 4 1119-1128 doi: 10.1093/oxfordjournals.jbchem.a133065
Gasa S, Makita A.Gangliosides were isolated from equine kidney and spleen, and their carbohydrate and lipid moieties were characterized. Among the long-chain bases, considerable proportions of trihydroxy bases (42.3 to 61.2% of the total bases), in which phytosphingosine was predominant were found in all the ganglioside classes. The other major base was sphingosine. Among the constituent fatty acids, long-chain acids (with a carbon number of more than 20), comprised approximately half the total acids, with some alpha-hydroxy and mono-unsaturated acids. By means of sequential hydrolysis with glycosidases couple...
Equine connective tissue tumors contain unintegrated bovine papilloma virus DNA.
Journal of virology    September 1, 1980   Volume 35, Issue 3 962-964 doi: 10.1128/JVI.35.3.962-964.1980
Amtmann E, Müller H, Sauer G.Bovine papilloma virus (BPV) appears to be the etiological agent of common equine connective tissue tumors. We investigated the physical state of the viral DNA within such tumors and found no indication for integration into the host genome. The BPV genomes were present as free circular episomes. Two equine sarcoids were shown to contain multiple copies of free circular BPV type 1 (BPV-1) DNA. When the tumors were digested with several single-cut restriction enzymes, there were only form III BPV-1 DNA sequences could be revealed. One of the sarcoids contained, apart from wild-type BPV-1 DNA, a ...