High-resolution linkage map in the proximity of the host resistance locus Cmv1

被引:42
作者
Depatie, C
Muise, E
Lepage, P
Gros, P
Vidal, SM
机构
[1] MCGILL UNIV,MONTREAL GEN HOSP,CTR STUDY HOST RESISTANCE,MONTREAL,PQ H3G 1A4,CANADA
[2] MCGILL UNIV,MONTREAL GEN HOSP,DEPT BIOCHEM,MONTREAL,PQ H3G 1A4,CANADA
[3] MCGILL UNIV,MONTREAL GEN HOSP,DEPT MED,MONTREAL,PQ H3G 1A4,CANADA
[4] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,BOSTON,MA 02115
[5] HARVARD UNIV,SCH MED,DEPT CELL BIOL,BOSTON,MA 02115
关键词
D O I
10.1006/geno.1996.4498
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The mouse chromosome 6 locus Cmv1 controls replication of mouse Cytomegalovirus (MCMV) in the spleen of the infected host. In our effort to clone Cmv1, we have constructed a high-resolution genetic linkage map in the proximity of the gene. For this, a total of 45 DNA markers corresponding to either cloned genes or microsatellites were mapped within a 7.9-cM interval overlapping the Cmv1 region. We have followed the cosegregation of these markers with respect to Cmv1 in a total of 2248 backcross mice from a preexisting interspecific backcross panel of 281 (Mus spretus x C57BL/6J)F1 x C57BL/6J and 2 novel panels of 989 (A/J x C57BL6)F1 x A/J and 978 (BALB/c x C57BL/6J)F1 x BALB/c segregating Cmv1. Combined pedigree analysis allowed us to determine the following gene order and intergene distances (in cM) on the distal region of mouse chromosome 6: D6Mit216-(1.9)-D6Mit336-(2.2)-D6Mit218-(1.0)-D6Mit52-(0.5)-D6Mit194-(0.2)-Nkrp1/D6Mit61/135/257/289/338-(0.4)-Cmv1/Ly49A/D6Mit370-(0.3)-Prp/Kap/D6Mit13/111/219-(0.3)-Tel/D6Mit374/290/220/196/195/110-(1.1)-D6Mit25. Therefore, the minimal genetic interval for Cmv1 of 0.7 cM is defined by 13 tightly linked markers including 2 markers, Ly49A and D6Mit370, that did not show recombination with Cmv1 in 1967 meioses analyzed; the proximal limit of the Cmv1 domain was defined by 8 crossovers between Nkrp1/D6Mit61/135/257/289/338 and Cmv1/Ly49A/D6Mit370, and the distal limit was defined by 5 crossovers between Cmv1/Ly49A/D6Mit370 and Prp/Kap/D6Mit13/111/219. This work demonstrates tight linkage between Cmv1 and genes from the natural killer complex (NKC), such as Nkrp1 and Ly49A, suggesting that Cmv1 may represent an NK cell recognition structure encoded in the NRC region. (C) 1997 Academic Press
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页码:154 / 163
页数:10
相关论文
共 54 条
[21]  
HO M, 1994, TRANSPL P, V26, P7
[22]   ANALYSIS INVITRO OF 2 BIOLOGICALLY DISTINCT STRAINS OF MURINE CYTOMEGALO-VIRUS [J].
HUDSON, JB ;
WALKER, DG ;
ALTAMIRANO, M .
ARCHIVES OF VIROLOGY, 1988, 102 (3-4) :289-295
[23]  
IWAMOTO T, 1993, ONCOGENE, V8, P1087
[24]   EVIDENCE THAT NK CELLS AND INTERFERON ARE REQUIRED FOR GENETIC-RESISTANCE TO LETHAL INFECTION WITH ECTROMELIA VIRUS [J].
JACOBY, RO ;
BHATT, PN ;
BROWNSTEIN, DG .
ARCHIVES OF VIROLOGY, 1989, 108 (1-2) :49-58
[25]   MHC CLASS-I ALLOANTIGEN SPECIFICITY OF LY-49+ IL-2-ACTIVATED NATURAL-KILLER-CELLS [J].
KARLHOFER, FM ;
RIBAUDO, RK ;
YOKOYAMA, WM .
NATURE, 1992, 358 (6381) :66-70
[26]  
KRAUTER K, 1995, NATURE, V377, P321
[27]   MOLECULAR-CLONING OF BETA-3 SUBUNIT, A 3RD FORM OF THE G-PROTEIN BETA-SUBUNIT POLYPEPTIDE [J].
LEVINE, MA ;
SMALLWOOD, PM ;
MOEN, PT ;
HELMAN, LJ ;
AHN, TG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (06) :2329-2333
[28]   SUSCEPTIBILITY TO URETHAN-INDUCED PULMONARY ADENOMAS BETWEEN A/J AND C57BL/6J MICE - USE OF AXB AND BXA RECOMBINANT INBRED LINES INDICATING A 3-LOCUS GENETIC MODEL [J].
MALKINSON, AM ;
NESBITT, MN ;
SKAMENE, E .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1985, 75 (05) :971-974
[29]   A MACINTOSH PROGRAM FOR STORAGE AND ANALYSIS OF EXPERIMENTAL GENETIC-MAPPING DATA [J].
MANLY, KF .
MAMMALIAN GENOME, 1993, 4 (06) :303-313
[30]   THE GENE CODING FOR THE KIDNEY ANDROGEN-REGULATED PROTEIN (KAP), MAPS BETWEEN THE GAPD AND KRAS-2 GENES ON MOUSE CHROMOSOME-6 [J].
MELANITOU, E ;
SIMONCHAZOTTES, D ;
GUENET, JL ;
ROUGEON, F .
MAMMALIAN GENOME, 1991, 1 (03) :191-192