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Chromosomal location of the genes encoding complement components C5 and factor H in the mouse.

TLDR
This genetic analysis raises the possibility that C5 and factor H are both encoded by complex loci composed of distinct structural and regulatory genes.
Abstract
Complementary DNA probes corresponding to the factor H and C5 polypeptides have been used to determine the chromosomal localizations of these two complement components. Both probes revealed complex and polymorphic arrays of DNA fragments in Southern blot analysis of mouse genomic DNA. Following the distribution of these bands in panels of somatic cell hybrids carrying various combinations of mouse chromosomes on a constant rat or Chinese hamster background allowed the localization of the C5-associated fragments to proximal chromosome 2 and the localization of the factor H-associated fragments to chromosome 1 or chromosome 3. Following the inheritance of DNA restriction fragment-length polymorphisms revealed by the probes in recombinant inbred mouse strains allowed the factor H-associated fragments to be mapped to Sas-1 on chromosome 1, and the C5-associated fragments to be mapped to Hc. Analysis of three-point crosses, in turn, placed the latter locus 19 cM distal to Sd on chromosome 2. We have designated the two loci Cfh and C5, respectively. This genetic analysis raises the possibility that C5 and factor H are both encoded by complex loci composed of distinct structural and regulatory genes.

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Deficiency of the murine fifth complement component (C5). A 2-base pair gene deletion in a 5'-exon.

TL;DR: There is an identical 2 base pair deletion in an exon of the C5 gene in several different C5-deficient mouse strains and this mutation should result in C5 protein deficiency.
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Structure, organization , and regulation of the complement genes

TL;DR: Cl cloning studies have provided information which emphasizes the manner in which the members of the complement system may be divided into families of structurally and functionally related proteins many of which are coded for on the same chromosome and are closely linked.
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Genetic analysis of autoimmune gld mice. I. Identification of a restriction fragment length polymorphism closely linked to the gld mutation within a conserved linkage group

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Comparative map for mice and humans.

TL;DR: This report summarizes the status of this comparative map and provided a listing of homologous genes and anonymous loci that have been mapped in mice and humans together with references documenting homology and the chromosomal and linkage assignments.
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Multiple roles for Bordetella lipopolysaccharide molecules during respiratory tract infection.

TL;DR: Biosynthesis of a full-length LPS molecule by these three bordetellae is essential for the expression of full virulence for mice, and the different distal structures modifying the LPS molecules on these three closely related subspecies serve different purposes in respiratory tract infection, highlighting the diversity of functions attributable to LPS of gram-negative bacteria.
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