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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.
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 ...
Horse erythrocyte gangliosides: preparation of the major hematoside NeuNG1-Lac-Cer.
Lipids    September 1, 1980   Volume 15, Issue 9 682-685 doi: 10.1007/BF02534019
Maget-Dana R, Michalski JC.A simple method for the isolation of hematoside NeuNG1-Lac-Cer from horse erythrocytes is described. An aliquot of the crude ganglioside fraction was labeled by tritiated sodium borohydride after mild periodate oxidation. The compounds obtained were used as radioactive tracers in column chromatography. Gangliosides were applied onto a silicic acid column and eluted stepwise by solvents of steadily increasing polarity. The major ganglioside, NeuNG1-Lac-Cer, was eluted in a high yield by the solvent mixture chloroform/methanol/water (60:35:8, v/v/v).
The complete amino acid sequence of horse muscle acylphosphatase.
The Journal of biological chemistry    July 25, 1980   Volume 255, Issue 14 6868-6874 
Cappugi G, Manao G, Camici G, Ramponi G.The amino acid sequence of horse muscle acylphosphatase is given in the present paper. The carboxymethylated enzyme consists of a single polypeptide chain of 98 amino acid residues with an acetyl group blocking the NH2 terminus and a tyrosine at the COOH terminus. The calculated molecular weight of the native protein, a mixed disulfide with glutathione, is 11,365. The carboxymethylated protein was cleaved by cyanogen bromide. The three expected fragments were purified; moreover, an additional fragment, derived from a partial failure of cleavage at methionine-24, was purified and characterized....
Assembly of intra- and interspecies hybrid apoferritins.
The Journal of biological chemistry    July 10, 1980   Volume 255, Issue 13 6234-6237 
Otsuka S, Listowsky I, Niitsu Y, Urushizaki I.An intraspecies hybrid apoferritin was assembled by mixing subunits of horse heart ferritin, which consists mainly of H-type subunits, and horse spleen ferritin, in which L-type subunits predominate. Interspecies hybrid apoferritins were reconstituted from subunits of human liver-horse spleen ferritins and from rat liver-horse spleen ferritins. All the hybrid ferritins migrated as single zones with electrophoretic mobilities intermediate between those of the parent ferritins. Isoelectric focusing data and immunological patterns were consistent with the view that the reassembled apoferritins we...
[Hemoglobins, XXXIII. Note on the Sequence of the hemoglobins of the horse (author’s transl)].
Hoppe-Seyler's Zeitschrift fur physiologische Chemie    July 1, 1980   Volume 361, Issue 7 1107-1116 
Matsuda G, Maita T, Braunitzer G, Schrank B.The sequence analysis of the slow migrating component of the hemoglobins of horse was repeated with the automatic methode in the sequenator and the sequence of the beta-chains completed. In the alpha-chains the positions of alpha63 and alpha65 (Gly, Ala) and alpha82 and alpha85 (amides) were changed and the remaining 40 sequences of the beta-chains are reported. According to these data and biological contributions of other authors, the biological aspects of the primary structure and the polymorphism of the hemoglobins of the horse are discussed.
Selectivity of oxidase and reductase activity of horse heart cytochrome c.
Biochemical and biophysical research communications    June 30, 1980   Volume 94, Issue 4 1106-1112 doi: 10.1016/0006-291x(80)90533-1
Myer YP, Thallum KK, Pande J, Verma BC.No abstract available
Identification by gas-liquid chromatography-mass spectrometry of 4-O-acetyl-9-O-lactyl-N-acetyl-neuraminic acid, a new sialic acid from horse submandibular gland.
Biochimica et biophysica acta    June 19, 1980   Volume 630, Issue 2 306-310 doi: 10.1016/0304-4165(80)90435-3
Reuter G, Pfeil R, Kamerling JP, Vliegenthart JF, Schauer R.The novel sialic acid 4-O-acetyl-9-O-lactyl-N-acetylneuraminic acid has been identified as a constituent of horse submandibular gland glycoproteins in addition to the already known equine sialic acids, N-acetylneuraminic acid, 4-O-acetyl-N-acetylneuraminic acid, 9-O-acetyl-N-acetylneuraminic acid, 4,9-di-O-acetyl-N-acetylneuraminic acid, N-glycolylneuraminic acid, 4-O-acetyl-N-glycolylneuraminic acid and 9-O-acetyl-N-glycolylneuraminic acid. The structure has been established by combined gas-liquid chromatography-mass spectrometry.
Biochemical characterization of equine herpesvirus type 3-induced deoxythymidine kinase purified from lytically infected horse embryo dermal fibroblasts.
Journal of virology    May 1, 1980   Volume 34, Issue 2 474-483 doi: 10.1128/JVI.34.2.474-483.1980
McGowan JJ, Allen GP, Barnett JM, Gentry GA.Infection of horse KyED cells with equine herpesvirus type 3 (EHV-3) resulted in a sevenfold increase in cytosol deoxythymidine kinase (dTK) activity. The EHV-3 dTK was purified from KyED cytosol dTK by affinity chromatography on deoxythymidine-Sepharose and characterized with respect to its electrophoretic mobility, molecular weight, substrate specificity, phosphate donor specificity, and immunological specificity. The purified EHV-3 dTK migrated in polyacrylamide gels with an Rf of 0.30 and sedimented in glycerol gradients with an S value of 5.13, corresponding to a molecular weight of 83,00...
The effect of trypsin digestion on the structure and iron-donating properties of transferrins from several species.
Biochimica et biophysica acta    April 25, 1980   Volume 622, Issue 2 297-307 doi: 10.1016/0005-2795(80)90040-9
Esparza I, Brock JH.The effect of trypsin digestion on iron-saturated and iron-free (apo) human, rabbit, bovine, pig and horse tranferrins has been studied. Iron-binding fragments were produced only from iron-saturated pig and bovine transferrins although some cleavage of the polypeptide chain occurred in all cases. The apo-transferrins were generally degraded to a greater extent than the corresponding iron-saturated proteins. The ability of the different transferrins to donate iron to rabbit reticulocytes varied in the order rabbit approximately pig greater than human approximately horse greater than bovine. Try...
Species distribution of gamma-glutamyl transpeptidase in the parotid gland.
Journal of dental research    April 1, 1980   Volume 59, Issue 4 728 doi: 10.1177/00220345800590041401
Hata K, Abiko Y, Takiguchi H.No abstract available
Involvement of lysines-72 and -79 in the alkaline isomerization of horse heart ferricytochrome c.
Biochemistry    March 18, 1980   Volume 19, Issue 6 1117-1120 doi: 10.1021/bi00547a012
Smith HT, Millett F.Spectrophotometric titrations of five singly modified horse heart ferricytochromes c, specifically (trifluoromethyl)phenylcarbamylated (CF3PhNHCO-) or trifluoroacetylated (CF3CO-) at lysines-13, -72, and -79, were carried out. The CF3PhNHCO-Lys-13, Lys-79, and CF3CO-Lys-79 derivatives all underwent alkaline isomerization with loss of the 695-nm band to low-spin species with an apparent pK of about 8.9, as did the unmodified cytochrome. However, modification of lysine-72 appeared to alter the reaction pathway since the CF3PhNHCO-Lys-72 derivative isomerized to a high-spin form with an apparent ...
Purification by affinity chromatography and characterization of a neutral alpha-glucosidase from horse kidney.
Biochimica et biophysica acta    March 14, 1980   Volume 612, Issue 1 85-96 doi: 10.1016/0005-2744(80)90281-8
Giudicelli J, Emiliozzi R, Vannier C, de Burlet G, Sudaka P.A horse kidney neutral alpha-D-glucosidase (alpha-D-glucoside glucohydrolase, EC 3.2.1.20) was purified about 580-fold with a yield of 33% by an affinity chromatography technique using the p-aminophenyl-beta-D-maltoside, a substrate derivative, as ligand. The purified enzyme, homogeneous in polyacrylamide gel electrophoresis, was a glycoprotein with a molecular weight of 280 000 as calculated by gel filtration and its isoelectric focusing points was found to be pH 4.1. The purified enzyme was able to hydrolyze various substrates having (alpha-1,2), (alpha-1,3), (alpha-1,4), and (alpha-1,6) glu...
Deoxythymidine kinase metabolism in equine herpesvirus type 3 infected horse embryo dermal fibroblasts.
Virology    March 1, 1980   Volume 101, Issue 2 516-519 doi: 10.1016/0042-6822(80)90465-1
McGowan JJ, Allen GP, Barnett JM, Gentry GA.No abstract available
Methylation of histidine-48 in pancreatic phospholipase A2. Role of histidine and calcium ion in the catalytic mechanism.
Biochemistry    February 19, 1980   Volume 19, Issue 4 743-750 doi: 10.1021/bi00545a021
Verheij HM, Volwerk JJ, Jansen EH, Puyk WC, Dijkstra BW, Drenth J, de Haas GH.It is known that His-48 is part of the active center in pancreatic phospholipase. To further elucidate the role of histidine-48 in the active center of pancreatic phospholipase A2, we have modified the enzyme with a number of bromo ketones and methyl benzenesulfonates. Rapid methylation occurred with methyl p-nitrobenzenesulfonate. Methylated phospholipase shows total loss of enzymatic activity whereas binding of substrate and the cofactor Ca2+ remains intact. Amino acid analysis of methylated equine phospholipase showed the loss of the single molecule of histidine and the formation of one mol...
A biologically active, three-fragment complex of horse heart cytochrome c.
The Journal of biological chemistry    February 10, 1980   Volume 255, Issue 3 845-853 
Juillerat M, Parr GR, Taniuchi H.No abstract available
Characterization of horse thyroid cyclic nucleotide phosphodiesterases.
European journal of biochemistry    February 1, 1980   Volume 104, Issue 1 297-304 doi: 10.1111/j.1432-1033.1980.tb04428.x
Erneux C, Couchie D, Dumont JE.No abstract available
Further studies on gangliosides of erythrocytes from horses and cattle.
Journal of biochemistry    February 1, 1980   Volume 87, Issue 2 639-643 
Hamanaka S, Handa S, Inoue J, Hasegawa A, Yamakawa T.The ganglioside patterns of erythrocytes from individual horses and cattle were examined. Variations in the ganglioside patterns were found in both horses and cattle. In the erythrocytes of most horses examined, NeuGc-Gal-Glc-ceramide (NeuGc-GM3) of 25 horses examined had only NeuGc-GM3 with no 4-O-Ac-NeuGc-GM3. The erythrocytes of various breeds of cattle had a characteristic ganglioside pattern, but they could be divided into 4 types on the basis of the composition of their gangliosides.