Using an interspecific cross, gene linkage relationships among members of the murine complement receptor-related genes, C4bp, Cfh, Mcry, and Mcr2, were analyzed by segregation of RFLP in 200 mice. The human homologues of these genes are tightly linked, composing the RCA locus, which maps to human chromosome (Chr.)1q32, within a large linkage group conserved between human Chr.1q21-32 and mouse Chr.1. RFLP associated with C4bp and Cfh map within this conserved linkage group; Cfh is located 9 cM telomeric to C4bp, which is consistent with linkage data for their human homologues. Mcry and Mcr2, while tightly linked, are located outside the conserved group, 40 cM telomeric to C4bp. These data suggest that a translocation or inversion occurred within the RCA family during the evolution of the mouse, defining a breakpoint of this large conserved linkage group.
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1 April 1989
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April 01 1989
Genetic organization of complement receptor-related genes in the mouse.
S F Kingsmore,
S F Kingsmore
Department of Medicine, Duke University, Durham, North Carolina 27710.
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D P Vik,
D P Vik
Department of Medicine, Duke University, Durham, North Carolina 27710.
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C B Kurtz,
C B Kurtz
Department of Medicine, Duke University, Durham, North Carolina 27710.
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P Leroy,
P Leroy
Department of Medicine, Duke University, Durham, North Carolina 27710.
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B F Tack,
B F Tack
Department of Medicine, Duke University, Durham, North Carolina 27710.
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J H Weis,
J H Weis
Department of Medicine, Duke University, Durham, North Carolina 27710.
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M F Seldin
M F Seldin
Department of Medicine, Duke University, Durham, North Carolina 27710.
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S F Kingsmore
,
D P Vik
,
C B Kurtz
,
P Leroy
,
B F Tack
,
J H Weis
,
M F Seldin
Department of Medicine, Duke University, Durham, North Carolina 27710.
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1989) 169 (4): 1479–1484.
Citation
S F Kingsmore, D P Vik, C B Kurtz, P Leroy, B F Tack, J H Weis, M F Seldin; Genetic organization of complement receptor-related genes in the mouse.. J Exp Med 1 April 1989; 169 (4): 1479–1484. doi: https://doi.org/10.1084/jem.169.4.1479
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