B-COMPLEX RECOMBINANTS AND SARCOMA REGRESSION - ROLE OF B-L/B-F REGION GENES

被引:6
作者
AUCLAIR, BW
COLLINS, WM
ZSIGRAY, RM
BRILES, WE
机构
[1] UNIV NEW HAMPSHIRE,DEPT ANIM & NUTR SCI,DURHAM,NH 03824
[2] UNIV NEW HAMPSHIRE,DEPT MICROBIOL,DURHAM,NH 03824
[3] NO ILLINOIS UNIV,DEPT BIOL SCI,DE KALB,IL 60115
关键词
ROUS SARCOMA VIRUS; B COMPLEX; TUMOR REGRESSION; CHICKENS; GENE;
D O I
10.3382/ps.0740434
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
The anti-sarcoma response of three B complex recombinant haplotypes B-R1(F24-G23), B-R2(F2-G23), and B-R3(F2-G23) was investigated. In a preliminary experiment, one male heterozygous for the B-R1 recombinant haplotype and another heterozygous for the B-R2 recombinant haplotype were each mated to females, some of which carried the respective recombinant. The anti-sarcoma response of progeny carrying the B-R1 recombinant differed significantly from that of progeny carrying the B-R2 recombinant. Subsequently, each of the three recombinant haplotypes was placed on each of four B haplotype complex backgrounds, and compared to B-G and B-L/B-F region controls on the same background haplotype. For each recombinant, significant differences in tumor growth were found between the recombinant and B-L/B-F control chickens on either one, two, or three of the four genetic backgrounds tested. For each recombinant, no differences were found between chickens carrying the recombinant and B-G region controls, which is further evidence that the gene(s) controlling Rous sarcoma growth lies in or near the B-L/B-F chromosomal region. Moreover, although the B-R2 and B-R3 recombinants appear to be identical serologically, they differed significantly in tumor growth suggesting that the two haplotypes are genetically different.
引用
收藏
页码:434 / 440
页数:7
相关论文
共 24 条
[1]  
AEED PA, 1993, ANIM GENET, V24, P177, DOI 10.1111/j.1365-2052.1993.tb00283.x
[2]  
[Anonymous], STATISTICAL PACKAGE
[3]  
BRILES W E, 1980, Animal Blood Groups and Biochemical Genetics, V11, P38
[4]  
Briles W E, 1977, Adv Exp Med Biol, V88, P221
[5]   IDENTIFICATION OF HAPLOTYPES OF THE CHICKEN MAJOR HISTOCOMPATIBILITY COMPLEX (B) [J].
BRILES, WE ;
BRILES, RW .
IMMUNOGENETICS, 1982, 15 (05) :449-459
[6]  
BRILES WE, 1979, GENETICS, V91, P514
[7]   COMPLEMENTATION OF MAJOR HISTOCOMPATIBILITY HAPLOTYPES IN REGRESSION OF ROUS-SARCOMA VIRUS-INDUCED TUMORS IN NON-INBRED CHICKENS [J].
BROWN, DW ;
COLLINS, WM ;
WARD, PH ;
BRILES, WE .
POULTRY SCIENCE, 1982, 61 (03) :409-413
[8]  
COLLINS W, 1980, Animal Blood Groups and Biochemical Genetics, V11, P38
[9]   B-LOCUS (MHC) EFFECT UPON REGRESSION OF RSV-INDUCED TUMORS IN NONINBRED CHICKENS [J].
COLLINS, WM ;
BRILES, WE ;
CORBETT, AC ;
CLARK, KK ;
ZSIGRAY, RM ;
DUNLOP, WR .
IMMUNOGENETICS, 1979, 9 (01) :97-100
[10]   B LOCUS (MHC) IN CHICKEN - ASSOCIATION WITH FATE OF RSV-INDUCED TUMORS [J].
COLLINS, WM ;
BRILES, WE ;
ZSIGRAY, RM ;
DUNLOP, WR ;
CORBETT, AC ;
CLARK, KK ;
MARKS, JL ;
MCGRAIL, TP .
IMMUNOGENETICS, 1977, 5 (04) :333-343