Volume 46, Issue 4 pp. 1067-1074
Original Article

Arthritis in MRL/lpr mice is under the control of multiple gene loci with an allelic combination derived from the original inbred strains

Junji Kamogawa

Junji Kamogawa

Ehime University School of Medicine, Shigenobu, Ehime, Japan

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Miho Terada

Miho Terada

Ehime University School of Medicine, Shigenobu, Ehime, Japan

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Shinichi Mizuki

Shinichi Mizuki

Ehime University School of Medicine, Shigenobu, Ehime, Japan

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Miyuki Nishihara

Miyuki Nishihara

Ehime University School of Medicine, Shigenobu, Ehime, Japan

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Haruyasu Yamamoto

Haruyasu Yamamoto

Ehime University School of Medicine, Shigenobu, Ehime, Japan

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Shiro Mori

Shiro Mori

Tohoku University School of Dentistry, Sendai, Japan

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Yoriko Abe

Yoriko Abe

KAN Research Institute, Kyoto, Japan

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Koji Morimoto

Koji Morimoto

KAN Research Institute, Kyoto, Japan

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Syuichi Nakatsuru

Syuichi Nakatsuru

KAN Research Institute, Kyoto, Japan

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Yusuke Nakamura

Yusuke Nakamura

Human Genome Center, University of Tokyo, Tokyo, Japan

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Masato Nose

Corresponding Author

Masato Nose

Ehime University School of Medicine, Shigenobu, Ehime, Japan

Department of Pathology, Ehime University School of Medicine, Shigenobu-cho, Onsen-gun, Ehime 791-0295, JapanSearch for more papers by this author
First published: 05 April 2002
Citations: 40

Abstract

Objective

To clarify the mode of inheritance and the genome origins of arthritis in a lupus-prone strain of mice, MRL/MpJ, bearing a Fas deletion mutant gene, lpr (MRL/lpr).

Methods

Using non–lupus-prone strains of mice, C3H/HeJ-lpr/lpr (C3H/lpr), (MRL/lpr × C3H/lpr)F1 intercross and MRL/lpr × (MRL/lpr × C3H/lpr)F1 backcross mice were prepared. Arthritis in individual mice was analyzed by histopathologic grading, and the genomic DNA of the backcross mice was examined by simple sequence-length polymorphism analysis to determine the polymorphic microsatellite markers highly associated with arthritis.

Results

Arthritis-susceptibility loci with significant linkage were mapped between D15Mit111 and D15Mit18 (map position 17.8–18.7 cM) on chromosome 15 and between D19Mit112 and D19Mit72 (map position 43.0–55.0) on chromosome 19 (logarithm of odds scores 3.5 and 4.3, respectively). Three other loci, one mapped to each of chromosomes 1, 2, and 7, showed suggestive linkage. Loci homozygous for MRL alleles on chromosomes 1 and 19 enhanced arthritis in both sexes, whereas other loci on chromosomes 2 and 15 selectively affected males. A locus homozygous for MRL alleles on chromosome 7 inhibited arthritis in both sexes. Three of these loci were found to originate from an LG/J strain and 1 from an AKR/J strain. Some combinations of these loci showed an additive effect in a hierarchical manner on the development of arthritis.

Conclusion

Arthritis in MRL/lpr mice is a complex pathologic manifestation resulting from the cumulative effect of multiple gene loci with an allelic combination derived from the original inbred strains.

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