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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.
Comparison of the interaction of equine LH and human chorionic gonadotrophin to equine testicular receptors.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 113-121 
Evans JW, Roser JF, Mikuckis GM.Human chorionic gonadotrophin (hCG) can be used to study horse luteinizing hormone (LH) receptors in stallion testicular tissue. hCG was more stable than horse LH during radioiodination when compared by their abilities to bind to testicular receptor sites. During incubation, neither hormone lost binding activity at 4 degrees C. Horse LH lost binding activity during incubation at 25 degrees C and both hormones lost binding activity at 37 degrees C. Both hormones bound to the same receptor sites which are specific for the hormones. The receptor sites were not degraded when incubated at 4 degrees...
Effect of PGF-2 alpha on LH receptors in the equine corpus luteum.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 235-245 
Roser JF, Evans JW, Mikuckis GM, Adams TE, Hughes JP.As quantified by Scatchard analysis, a 27 000 g crude luteal membrane fraction contained a single population of unoccupied LH receptors characterized by high affinity, ka = 0.647 +/- 0.158 X 10(11) M-1 and low binding capacity, Rt = 4.91 +/- 0.78 X 10(-11) M/mg membrane fraction. Acceptable hormonal specificity, reversibility, saturability, high affinity and tissue specificity indicated that the binding protein was a physiological receptor. To ensure that the methods used for Scatchard analysis were valid, hCG was characterized for specific activity and maximum bindability, non-specific bindin...
Cibacron Blue-induced modification of neutral proteinase from horse blood leukocytes.
Acta biologica et medica Germanica    January 1, 1982   Volume 41, Issue 1 47-52 
Potempa J.The proteolytic activity of the elastase-like proteinase from granules of horse blood leukocytes is retained on a column of Cibacron Blue-Sepharose and can be eluted with 0.5 M KSCN. During this procedure its mol. wt. is reduced from 49000 to 30000 and isoelectric point is shifted towards higher pH. The inactive protein not adsorbed on Cibacron Blue-Sepharose is strongly acidic and shows a mol. wt. of 20000. Upon mixing this protein with the modified enzyme the native proteinase is reconstituted as shown by polyacrylamide gel electrophoresis at pH 8.3 and isoelectric focusing in a sucrose grad...
Limited trypsinolysis of porcine and equine colipases. Spectroscopic and kinetic studies.
Biochimica et biophysica acta    December 29, 1981   Volume 671, Issue 2 155-163 doi: 10.1016/0005-2795(81)90129-x
Rathelot J, Canioni P, Bosc-Bierne I, Sarda L, Kamoun A, Kaptein R, Cozzone PJ.Porcine and equine colipases have been submitted to mild tryptic digestion. Proteolysis occurs at the Arg5-Gly6 bond with the loss of the N-terminal pentapeptide. Studies of native and trypsin-treated colipases by circular dichroism and laser chemically induced dynamic nuclear polarization indicate that proteolysis induces conformational changes in the region of the tyrosine cluster. Experiments in the presence of phospholipid provide further evidence showing that these residues are in or close to the region of the protein interacting with aggregated lipids. Kinetic studies of the reaction of ...
Serologic and molecular comparisons of several equine herpesvirus type 1 strains.
American journal of veterinary research    December 1, 1981   Volume 42, Issue 12 2099-2104 
Turtinen LW, Allen GP, Darlington RW, Bryans JT.The molecular and serologic relatedness of 2 recent respiratory tract isolates of equine herpesvirus type 1, designated T1 and T2, were compared with the Army 183, Kentucky-A hamster-adapted (KyA-ha), and L-M cell-adapted (KyA-LM) strains. Electrophoresis in polyacrylamide gels revealed differences in virion structural proteins among 4 purified strains. Seven envelope glycoproteins (molecular weight of 93,000, 65,000, 62,000, 60,000, 36,000, 20,000, and 18,000) corresponding to virion proteins 13, 16, 17, 18, 23, 25, and 26a, respectively, found in both the Army 183 and KyA-ha strains had slig...
Analysis of the genome of equine herpesvirus type 1: arrangement of cleavage sites for restriction endonucleases EcoRI, BglII and BamHI.
The Journal of general virology    December 1, 1981   Volume 57, Issue Pt 2 307-323 doi: 10.1099/0022-1317-57-2-307
Whalley JM, Robertson GR, Davison AJ.The genome of an Australian isolate of equine herpesvirus type 1 (equine abortion virus) has been analysed using the restriction endonucleases EcoRI, BglII and BamHI, and a physical map constructed. Terminal fragments were identified by exonuclease treatments, and linkage of fragments was deduced by a combination of single- and double-digest experiments and cross-blot hybridizations. The genome has a mol. wt. of 100 x 10(6) and is comprised of a short unique region bounded by repetitive sequences, which is present in both orientations in approximately equal amounts in the DNA population, and a...
Isolation of equine muscle carbonic anhydrase in crystalline form.
Biochemical and biophysical research communications    November 30, 1981   Volume 103, Issue 2 573-580 doi: 10.1016/0006-291x(81)90490-3
Nishita T, Deutsch HF.No abstract available
Isolation and properties of beta-endorphin-(1-27), N alpha-acetyl-beta-endorphin, corticotropin, gamma-lipotropin and neurophysin from equine pituitary glands.
International journal of peptide and protein research    November 1, 1981   Volume 18, Issue 5 443-450 doi: 10.1111/j.1399-3011.1981.tb03005.x
Ng TB, Chung D, Li CH.No abstract available
Molecular cloning of equine herpesvirus type 1 DNA: analysis of standard and defective viral genomes and viral sequences in oncogenically transformed cells.
Proceedings of the National Academy of Sciences of the United States of America    November 1, 1981   Volume 78, Issue 11 6684-6688 doi: 10.1073/pnas.78.11.6684
Robinson RA, Tucker PW, Dauenhauer SA, O'Callaghan DJ.Genomic DNA sequences of equine herpesvirus type 1 (EHV-1) have been cloned as BamHI and EcoRI restriction fragments into the plasmid pBR322 and propagated in Escherichia coli. With the exception of two EcoRI restriction fragments that reside in the S region of the viral genome, all of the cloned fragments demonstrated the same electrophoretic mobilities, restriction cleavage sites, and blot-hybridization patterns as did the parent fragments produced by BamHI or EcoRI digestion of virion DNA. The EcoRI J fragment and the BamHI E fragment of the L-region terminus were cloned after the addition ...
Circular dichroism study of horse colipase interaction with bile salt.
Biochimica et biophysica acta    October 28, 1981   Volume 670, Issue 3 305-311 doi: 10.1016/0005-2795(81)90101-x
Canioni P, Julien R, Romanetti R, Cozzone P, Sarda L.No abstract available
Primary structure of 3-phosphoglycerate kinase from horse muscle. I. Purification of cyanogen bromide peptides and amino acid sequence of peptide CB5 (104 residues).
The Journal of biological chemistry    October 25, 1981   Volume 256, Issue 20 10284-10292 
Hardy GW, Darbre A, Merrett M.3-Phosphoglycerate kinase was isolated from horse muscle and subjected to the action of cyanogen bromide. The resulting peptides were separated using gel filtration combined with either ion exchange chromatography on phosphocellulose in 6 M urea or high voltage paper electrophoresis. The sequence of the largest peptide, CB5, has been determined by a combination of automated and manual Edman degradation carried out on the intact peptide and derivatives obtained by proteolytic digestion. The isolation of two peptides derived from CB5 by cleavage of the bond between Asp109 and Pro110 facilitated ...
Analysis of the potentiometric titration of reduced horse heart cytochrome c.
Biopolymers    October 1, 1981   Volume 20, Issue 10 2243-2252 doi: 10.1002/bip.1981.360201016
Marini MA, Martin CJ, Forlani L.No abstract available
Antigenic and structural conservation of herpesvirus DNA-binding proteins.
The Journal of general virology    October 1, 1981   Volume 56, Issue Pt 2 409-419 doi: 10.1099/0022-1317-56-2-409
Littler E, Yeo J, Killington RA, Purifoy DJ, Powell KL.Previously, we have shown a common antigen of several herpesviruses (pseudorabies virus, equine abortion virus and bovine mammillitis virus) to be antigenically related to the major DNA-binding proteins of herpes simplex virus types 1 and 2. In this study we have purified the cross-reacting polypeptide from cells infected with pseudorabies virus, equine abortion virus and bovine mammillitis virus and shown the cross-reacting protein to be a major DNA-binding protein for each virus. Tryptic peptide analysis of the cross-reacting DNA-binding proteins of all five viruses has shown structural simi...
Equine follicle-stimulating hormone. Purification, acid dissociation, and binding to equine testicular tissue.
The Journal of biological chemistry    September 25, 1981   Volume 256, Issue 18 9567-9572 
Combarnous Y, Hengé MH.A simple method of purification of equine follicle-stimulating hormone is described by which two forms of the hormone are obtained. The acid dissociation of the most active preparation was studied and a pKa of 5.8 was determined at 37 degrees C. This value is 2 pH units higher than that observed for pregnant mare serum gonadotropin suggesting that the binding areas between subunits are not identical in the two hormones. We also describe an homologous radioreceptor assay of equine follicle-stimulating hormone which is highly specific for this hormone in contrast to the heterologous systems desc...
Mobilization of iron from ferritin by isolated mitochondria. Effects of species compatibility between ferritin and mitochondria and iron content of ferritin.
Biochimica et biophysica acta    September 18, 1981   Volume 677, Issue 1 50-56 doi: 10.1016/0304-4165(81)90144-6
Ulvik RJ, Romslo I, Roland F, Crichton RR.Mitochondria mobilize iron from ferritin by a mechanism that depends on external FMN. With rat liver mitochondria, the rate of mobilization of iron is higher from rat liver ferritin than from horse spleen ferritin. With horse liver mitochondria, the rate of iron mobilization is higher from horse spleen ferritin than from rat liver ferritin. The results are explained by a higher affinity between mitochondria and ferritins of the same species. The mobilization of iron increases with the iron content of the ferritin and then levels off. A maximum is reached with ferritins containing about 1 200 i...
Nucleolus organizer regions in the chromosomes of the domestic horse.
The Journal of heredity    September 1, 1981   Volume 72, Issue 5 357-358 doi: 10.1093/oxfordjournals.jhered.a109525
Kopp E, Mayr B, Czaker R, Schleger W.No abstract available
beta-Endorphin: isolation, amino acid sequence and synthesis of the hormone from horse pituitary glands.
International journal of peptide and protein research    September 1, 1981   Volume 18, Issue 3 242-248 doi: 10.1111/j.1399-3011.1981.tb02978.x
Li CH, Ng TB, Yamashiro D, Chung D, Hammonds RG, Tseng LF.Beta-endorphin has been isolated from equine pituitaries. Its amino acid sequence is identical to that of ovine, bovine and camel beta-endorphins except for substitution of the threonine residue at position 6 by serine. The equine beta-endorphin has also been synthesized by the solid-phase method. In comparison with the human hormone, equine beta-endorphin was shown to possess 3 times the receptor-binding activity in rat membrane preparations and 1.6 times the analgesic potency in the mouse tail-flick assay.
The interaction of equine platelet tropomyosin with skeletal muscle actin.
The Journal of biological chemistry    July 25, 1981   Volume 256, Issue 14 7257-7261 
Côté GP, Smillie LB.Whereas skeletal muscle tropomyosin binds strongly to muscle F-actin in a buffer containing 30 mM KCl and 1-2 mM free Mg2+, equine platelet tropomyosin only binds stoichiometrically (1 tropomyosin molecule per 6 actin monomers) at higher Mg2+ concentrations (7-8 mM free Mg2+). At low free Mg2+ concentrations (1.5 mM) the binding of the platelet protein is only marginally increased by raising the KCl concentration to an optimal value (0.10-0.20 M). This weaker binding can be attributed to the relatively poor head-to-tail polymerization of platelet tropomyosin and its fewer actin-binding sites. ...
Amino acid sequence of horse spleen apoferritin.
FEBS letters    July 6, 1981   Volume 129, Issue 2 322-327 doi: 10.1016/0014-5793(81)80193-7
Heusterspreute M, Crichton RR.No abstract available
Biological functions and receptor binding activities of equine chorionic gonadotrophins.
Journal of reproduction and fertility    July 1, 1981   Volume 62, Issue 2 527-536 doi: 10.1530/jrf.0.0620527
Stewart F, Allen WR.The role of equine chorionic gonadotrophin (CG, formerly termed Pregnant Mare serum Gonadotrophin, PMSG) in maintaining equine pregnancy was investigated by examining the effects of this hormone on the maternal ovaries during early gestation and relating these findings to the receptor binding activities of CG in vitro. Measurement of plasma progestagen profiles in mares and donkeys carrying horse, donkey, mule ( female horse X male donkey) and hinny (female donkey X male horse) conceptuses confirmed that CG induced several secondary ovulations and thus maintained maternal progestagen concentra...
Electron transfer between horse heart and Candida krusei cytochromes c in the free and bound states.
Biochimica et biophysica acta    July 1, 1981   Volume 636, Issue 2 129-135 doi: 10.1016/0005-2728(81)90085-2
Yoshimura T, Sogabe T, Aki K.Electron transfer between horse heart and Candida krusei cytochromes c in the free and phosvitin-bound states was examined by difference spectrum and stopped-flow methods. The difference spectra in the wavelength range of 540-560 nm demonstrated that electrons are exchangeable between the cytochromes c of the two species. The equilibrium constants of the electron transfer reaction for the free and phosvitin-bound forms, estimated from these difference spectra, were close to unity at 20 degrees C in 20 mM Tris-HCl buffer (pH 7.4). The electron transfer rate for free cytochrome c was (2-3).10(4)...
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