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BF2  -  Major histocompatibility complex class I...

Gallus gallus

Synonyms: B-F, B-F-S01, B-F-S02, B-F-S03, B-F-S09, ...
 
 
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Disease relevance of BF2

  • In this study, an avian leukosis virus (ALV) vector system, RCASBP, expressing MHC chicken class I (B-F) cDNA was used to develop target cells expressing the chicken class I glycoproteins complexed with ALV antigens on the cell surface [1].
  • A btuB::Tn10 insertion which disrupts the gene encoding the vitamin B12 receptor from E. coli K-12 was P1 transduced into a virulent E. coli K1 strain [2].
  • Marek's disease virus down-regulates surface expression of MHC (B Complex) Class I (BF) glycoproteins during active but not latent infection of chicken cells [3].
  • The peptide binding motifs for this major B-F12 molecule in chickens of Rous sarcoma regressor line CB (B12/B12) have been determined [4].
  • Clinically significant vitamin B12 deficiency secondary to malabsorption of protein-bound vitamin B12 [5].
 

Psychiatry related information on BF2

  • The results of this series of experiments with chicks trained on a single trial, passive avoidance task, demonstrate that methotrexate-induced folate deficiency, and excess levels of folate and B12 lead to amnesia in these subjects [6].
 

High impact information on BF2

  • Evidence is presented that the immune response to B-G antigens is responsible for the development of autoimmunity and other pathological events that follow and that tolerance to class I MHC antigens (B-F antigens) shared by lymphocytes erythrocytes is maintained at the same time that B-G tolerance is broken [7].
  • This transcript, that is by far the most divergent known member of the class I gene family, hybridized to six B-F genes present in the cosmids [8].
  • Second, we find, for the B4, B12, and B15 haplotypes, that one cDNA is at least 10-fold more abundant than the other [9].
  • Compared with the MHC of typical mammals, the chicken MHC is smaller and simpler, with only two class I genes found in the B12 haplotype [9].
  • The kinetics of the reaction of cyanide with free aquocobalamin (H2OCbl) and with aquocobalamin bound to a vitamin B12-binding protein (haptocorrin) from chicken serum (HC-H2OCbl) have been investigated as a function of temperature and pH [10].
 

Chemical compound and disease context of BF2

 

Biological context of BF2

 

Anatomical context of BF2

  • B-FIV amino acid residues predicted to interact with the CDR1alpha region of the T-cell receptor (Tcr) demonstrate less variability than in mouse and human class I alleles [16].
  • Functional analysis employing site-directed mutagenesis identified BF amino acid residues forming serologic epitopes as well as residues important in antigen presentation to ALV-induced cytotoxic T lymphocytes [15].
  • The chicken major histocompatibility complex (MHC) is commonly defined by serologic reactions of erythrocytes with antibodies specific to the highly polymorphic MHC class I (BF) and MHC class IV (BG) antigens [17].
  • These studies demonstrate that following transepithelial flux of vitamin B12 through the ileal mucosa, the vitamin becomes coupled to TCII [18].
  • Two of these classes are homologous to classes I and II of mammals (B-F and B-L, respectively), while the third (B-G) is a differentiation antigen of the erythroid cell-line; the mammalian homologue of this class is still undefined [19].
 

Associations of BF2 with chemical compounds

  • Monoclonal antibodies to the FLAG epitope served to monitor cell-surface expression for functional analysis of the BFIV21 class I glycoprotein [15].
  • Parenteral injection of 1000 microgram of nonlabeled vitamin B12 did not interfere with the absorption of the radio-B12 from the meat [20].
  • We demonstrate here that B-G molecules purified with monoclonal antibodies exert this adjuvant effect on the production of alloantibodies to chicken class I (B-F) molecules, when the two are in the same liposome [21].
  • MDV-induced T-cell tumors suffer a nearly complete loss of cell surface BF upon virus reactivation with 5-bromo-2'-deoxyuridine (BUdR) [3].
  • A study was made of the effect of low-dose gamma irradiation on the content of thiamine (B1), riboflavin (B2), niacin, pyridoxine (B6) and cobalamin (B12) in pork chops, and thiamine, riboflavin and niacin in chicken breasts [22].
 

Other interactions of BF2

  • The humoral response of 1 pair of recombinants isolated from a Red Jungle Fowl (BW3 and BW4) being identical on BF and BG, but different on BL, indicated that part of the primary vaccine response was an MHC II restricted T-cell dependent response [23].
  • The MHC of a broiler chicken line: serology, B-G genotypes, and B-F/B-LB sequences [24].
 

Analytical, diagnostic and therapeutic context of BF2

  • Third, we use 2D gel electrophoresis of class I molecules from pulse-labeled cells to show that there is only one heavy chain spot for the B4 and B15 haplotypes, and one major spot for the B12 haplotype [9].
  • The B serotypes were compared by B-G restriction fragment length polymorphism (RFLP) analysis, allele-specific PCR typing test for B-LBII family genes and nucleotide sequence analysis of expressed B-F and B-LBII family genes [25].
  • Subsequently, the monomers were further separated, and the purified MBP-BF2, -beta2m, and MBP were analyzed by circular dichroism (CD) spectrum [26].
  • A vitamin B12-binding protein (haptocorrin) from chicken serum has been purified to homogeneity by photodissociative affinity chromatography and characterized by gel electrophoresis and UV-visible spectrophotometry of its aquocobalamin, hydroxocobalamin, and cyanocobalamin complexes [27].
  • The urinary radioactivities, which were as low as those after oral administration of radioactive hydroxocobalamin and vitamin B12 coenzyme, suggested that the radio-B12 was present in meat in coenzyme form or was converted into the stable hydroxoform during the process of cooking and digestion [20].

References

  1. In vitro analysis of a primary, major histocompatibility complex (MHC)-restricted, cytotoxic T-lymphocyte response to avian leukosis virus (ALV), using target cells expressing MHC class I cDNA inserted into a recombinant ALV vector. Thacker, E.L., Fulton, J.E., Hunt, H.D. J. Virol. (1995) [Pubmed]
  2. Elimination of the vitamin B12 uptake or synthesis pathway does not diminish the virulence of Escherichia coli K1 or Salmonella typhimurium in three model systems. Sampson, B.A., Gotschlich, E.C. Infect. Immun. (1992) [Pubmed]
  3. Marek's disease virus down-regulates surface expression of MHC (B Complex) Class I (BF) glycoproteins during active but not latent infection of chicken cells. Hunt, H.D., Lupiani, B., Miller, M.M., Gimeno, I., Lee, L.F., Parcells, M.S. Virology (2001) [Pubmed]
  4. v-src oncogene-specific carboxy-terminal peptide is immunoprotective against Rous sarcoma growth in chickens with MHC class I allele B-F12. Hofmann, A., Plachy, J., Hunt, L., Kaufman, J., Hala, K. Vaccine (2003) [Pubmed]
  5. Clinically significant vitamin B12 deficiency secondary to malabsorption of protein-bound vitamin B12. King, C.E., Leibach, J., Toskes, P.P. Dig. Dis. Sci. (1979) [Pubmed]
  6. Effect of folate deficiency and folate and B12 excess on memory functioning in young chicks. Crowe, S.F., Ross, C.K. Pharmacol. Biochem. Behav. (1997) [Pubmed]
  7. Tolerance and autoimmunity to erythroid differentiation (B-G) major histocompatibility complex alloantigens of the chicken. Havele, C., Wegmann, T.G., Longenecker, B.M. J. Exp. Med. (1982) [Pubmed]
  8. A molecular map of the chicken major histocompatibility complex: the class II beta genes are closely linked to the class I genes and the nucleolar organizer. Guillemot, F., Billault, A., Pourquié, O., Béhar, G., Chaussé, A.M., Zoorob, R., Kreibich, G., Auffray, C. EMBO J. (1988) [Pubmed]
  9. Peptide motifs of the single dominantly expressed class I molecule explain the striking MHC-determined response to Rous sarcoma virus in chickens. Wallny, H.J., Avila, D., Hunt, L.G., Powell, T.J., Riegert, P., Salomonsen, J., Skjødt, K., Vainio, O., Vilbois, F., Wiles, M.V., Kaufman, J. Proc. Natl. Acad. Sci. U.S.A. (2006) [Pubmed]
  10. Kinetics and activation parameters of the reaction of cyanide with free aquocobalamin and aquocobalamin bound to a haptocorrin from chicken serum. Marques, H.M., Brown, K.L., Jacobsen, D.W. J. Biol. Chem. (1988) [Pubmed]
  11. Critical vitamin supplementation of broiler diets high in alfalfa juice protein. Tsiagbe, V.K., Straub, R.J., Cook, M.E., Harper, A.E., Sunde, M.L. Poult. Sci. (1987) [Pubmed]
  12. Development of a specific radioimmunoassay for vitamin B12 and its application in the diagnosis of cobalt deficiency in sheep. Kennedy, D.G., O'Harte, F.P., Blanchflower, W.J., Rice, D.A. Vet. Res. Commun. (1990) [Pubmed]
  13. Diversity and locus specificity of chicken MHC B class I sequences. Livant, E.J., Brigati, J.R., Ewald, S.J. Anim. Genet. (2004) [Pubmed]
  14. Non-association between Rfp-Y major histocompatibility complex-like genes and susceptibility to Marek's disease virus-induced tumours in 6(3) x 7(2) F2 intercross chickens. Vallejo, R.L., Pharr, G.T., Liu, H.C., Cheng, H.H., Witter, R.L., Bacon, L.D. Anim. Genet. (1997) [Pubmed]
  15. Functional analysis of avian class I (BFIV) glycoproteins by epitope tagging and mutagenesis in vitro. Fulton, J.E., Thacker, E.L., Bacon, L.D., Hunt, H.D. Eur. J. Immunol. (1995) [Pubmed]
  16. Analysis of polymorphisms in the major expressed class I locus (B-FIV) of the chicken. Hunt, H.D., Fulton, J.E. Immunogenetics (1998) [Pubmed]
  17. Molecular genotype identification of the Gallus gallus major histocompatibility complex. Fulton, J.E., Juul-Madsen, H.R., Ashwell, C.M., McCarron, A.M., Arthur, J.A., O'Sullivan, N.P., Taylor, R.L. Immunogenetics (2006) [Pubmed]
  18. Formation of transcobalamin II--vitamin B12 complex by guinea-pig ileal mucosa in organ culture after in vivo incubation with intrinsic factor--vitamin B12. Rothenberg, S.P., Weiss, J.P., Cotter, R. Br. J. Haematol. (1978) [Pubmed]
  19. The MHC haplotypes of the chicken. Simonsen, M., Crone, M., Koch, C., Hála, K. Immunogenetics (1982) [Pubmed]
  20. Vitamin B12 assimilation from chicken meat. Doscherholmen, A., McMahon, J., Ripley, D. Am. J. Clin. Nutr. (1978) [Pubmed]
  21. The "adjuvant effect" of the polymorphic B-G antigens of the chicken major histocompatibility complex analyzed using purified molecules incorporated in liposomes. Salomonsen, J., Eriksson, H., Skjødt, K., Lundgreen, T., Simonsen, M., Kaufman, J. Eur. J. Immunol. (1991) [Pubmed]
  22. Effect of gamma irradiation on the B vitamins of pork chops and chicken breasts. Fox, J.B., Thayer, D.W., Jenkins, R.K., Phillips, J.G., Ackerman, S.A., Beecher, G.R., Holden, J.M., Morrow, F.D., Quirbach, D.M. Int. J. Radiat. Biol. (1989) [Pubmed]
  23. Immune response to a killed infectious bursal disease virus vaccine in inbred chicken lines with different major histocompatibility complex haplotypes. Juul-Madsen, H.R., Dalgaard, T.S., Røntved, C.M., Jensen, K.H., Bumstead, N. Poult. Sci. (2006) [Pubmed]
  24. The MHC of a broiler chicken line: serology, B-G genotypes, and B-F/B-LB sequences. Li, L., Johnson, L.W., Livant, E.J., Ewald, S.J. Immunogenetics (1999) [Pubmed]
  25. Three new MHC haplotypes in broiler breeder chickens. Livant, E.J., Zheng, D., Johnson, L.W., Shi, W., Ewald, S.J. Anim. Genet. (2001) [Pubmed]
  26. Structures and homology modeling of chicken major histocompatibility complex protein class I (BF2 and beta2m). Yan, R.Q., Li, X.S., Yang, T.Y., Xia, C. Mol. Immunol. (2006) [Pubmed]
  27. Heteronuclear NMR studies of cobalamins. 31P NMR observations of cobalamins bound to a haptocorrin from chicken serum. Brown, K.L., Marques, H.M., Jacobsen, D.W. J. Biol. Chem. (1988) [Pubmed]
 
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