GeneSet Information

Tier II GS135227 • anticardiolipin antibody 1 (Acla1, Published QTL Chr 17)

DESCRIPTION:

QTL associated with anticardiolipin antibody 1. This interval was obtained by using a fixed interval width of 25 Mbp around the peak marker (33737692)

LABEL:

QTL-Acla1-Mouse-Chr 17

SCORE TYPE:

Binary

DATE ADDED:

2012-04-02

DATE UPDATED:

2020-05-06

SPECIES:

AUTHORS:

Ida A, Hirose S, Hamano Y, Kodera S, Jiang Y, Abe M, Zhang D, Nishimura H, Shirai T

TITLE:

Multigenic control of lupus-associated antiphospholipid syndrome in a model of (NZW x BXSB) F1 mice.

JOURNAL:

European journal of immunology Sep 1998, Vol 28, pp. 2694-703

ABSTRACT:

In a subset of systemic lupus erythematosus (SLE) patients, antiphospholipid syndrome, characterized by occurrence of anti-cardiolipin (CL) antibodies, thrombocytopenia, thrombosis and recurrent intrauterine fetal death occurs. Male (NZW x BXSB)F1 mice, carrying the BXSB Yaa gene, serve as a model for SLE-associated antiphospholipid syndrome. Using microsatellite markers in the NZW x (NZW x BXSB)F1 backcross male progeny, we mapped BXSB alleles contributing to the generation of anti-CL antibodies, platelet-binding antibodies, thrombocytopenia and myocardial infarction. Generation of each disease character was controlled by two major independently segregating dominant alleles, i.e. those on chromosomes (Chr.) 4 and 17 for anti-CL antibodies, Chr. 8 and 17 for both anti-platelet antibodies and thrombocytopenia and, to our surprise, Chr. 7 and 14 for myocardial infarction, and that a combination of the two alleles appeared to produce full expression of each character, as a complementary gene action. The alleles on Chr. 17 linked to the above three characters were all mapped in close proximity to the H-2 complex. Therefore, no single factor such as anti-CL antibodies can explain the pathogenesis of SLE-associated antiphospholipid syndrome. Rather, a combination of susceptibility alleles such as described here, along with additional modifying loci, i.e. BXSB Yaa and some from NZW, characterizes unique SLE features in male (NZW x BXSB) F1 mice. There are potentially important candidate genes which may be linked to the syndrome. PUBMED: 9754557
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Annotation Information



Alleles (D000483)
Myocardial Infarction (D009203)
Lupus Erythematosus, Systemic (D008180)
Antiphospholipid Syndrome (D016736)
Chromosomes (D002875)
Patients (D010361)
Microsatellite Repeats (D018895)
Lifting (D017770)
Fetal Death (D005313)
Antibodies, Anticardiolipin (D017153)
Infarction (D007238)
Antibodies (D000906)
Thrombocytopenia (D013921)
Thrombosis (D013927)
Character (D002605)
decreased platelet cell number (MP:0003179)
thrombosis (MP:0005048)
immunoglobulin complex, circulating (GO:0042571)
pathogenesis (GO:0009405)

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