Mapping of the BALB/c Ly49 cluster defines a minimal natural killer cell receptor gene repertoire

Marie France Proteau, Etienne Rousselle, Andrew P. Makrigiannis

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41 Citas (Scopus)

Resumen

The BALB/c inbred mouse strain is one of the most commonly used for immunological studies and is an animal model for natural killer (NK) cell function during pathogen infection and tumorigenesis. To understand better NK cell function in this strain, the complete BALB/c Ly49 haplotype was deduced. The BALB/c haplotype spans approximately 300 kb with a gene order and content of Ly49q, e, x, i, g, l, c, and a. Functional BALB/c alleles of Ly49q and e were isolated and found to be conserved. The BALB/c cluster represents a minimal haplotype as it contains many fewer functional genes than the 129 or B6 mouse strains. The small number of BALB/c Ly49 genes is due mainly to an absent group of genes (relative to B6 and 129) between Ly49x and i, although other smaller deletions are present. These gene deletions provide a genetic basis for the lack of certain Ly49-associated NK cell functions in this mouse strain. Finally, the mapping of a third Ly49 haplotype reveals that the basic murine Ly49 repertoire is composed of three framework gene pairs (Ly49q and e, Ly49i and g, and Ly49c and a) that are interspersed with variable numbers of strain-specific Ly49.

Idioma originalEnglish
Páginas (desde-hasta)669-677
Número de páginas9
PublicaciónGenomics
Volumen84
N.º4
DOI
EstadoPublished - oct. 2004
Publicado de forma externa

Nota bibliográfica

Funding Information:
We gratefully acknowledge Dominic Messervier (IRCM, Montreal, QC, Canada) for technical assistance, Brian Wilhelm (Sanger Centre, UK) for advice on bootstrapping, and Stephen Anderson (SAIC–National Cancer Institute, Frederick, MD, USA) for critically reading the manuscript. This work was supported by an operating grant from the Canadian Institutes for Health Research. A.P.M. is a Scholar of the Canadian Institutes for Health Research (New Investigator Award).

ASJC Scopus Subject Areas

  • Genetics

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