GeneSet Information

Tier II GS136083 • keratoconus 1 (Krcn1, Published QTL Chr 17)

DESCRIPTION:

QTL associated with keratoconus 1. This interval was obtained by using a fixed interval width of 25 Mbp around the peak marker (34880993)

LABEL:

QTL-Krcn1-Mouse-Chr 17

SCORE TYPE:

Binary

DATE ADDED:

2012-04-02

DATE UPDATED:

2024-04-25

SPECIES:

AUTHORS:

Tachibana M, Adachi W, Kinoshita S, Kobayashi Y, Honma Y, Hiai H, Matsushima Y

TITLE:

Androgen-dependent hereditary mouse keratoconus: linkage to an MHC region.

JOURNAL:

Investigative ophthalmology & visual science Jan 2002, Vol 43, pp. 51-7

ABSTRACT:

To better understand the pathogenesis of hereditary keratoconus, an inbred line of spontaneous mutant mice with keratoconus-affected corneas (SKC mice) was established and studied with a multidisciplinary approach.Using a mutant mouse with corneas having a keratoconical appearance as the progenitor, an inbred line of SKC mouse was established by repeated sibling mating. Morphology, cell growth, apoptosis and protein expression of SKC mouse corneas were examined. Castration of males and androgen treatment for females were conducted to determine any androgen dependency of the phenotype. Linkage analysis was conducted to reveal the responsible or predisposing gene of SKC mouse keratoconus.Corneas of the SKC mouse resemble those of human eyes with keratoconus. Both are conical and show similar corneal changes, including apoptosis of keratocytes and increased expression of c-fos protein. The SKC mouse phenotype was transmitted in an autosomal recessive manner, although it was observed almost exclusively in males. Intriguingly, female mice showed the phenotype when injected with testosterone, whereas male incidence of the phenotype diminished drastically when mice were castrated. Linkage analysis localized a predisposition locus to an MHC region on mouse chromosome 17, which includes a locus for the gene for sex-limited protein (Slp).SKC mouse keratoconus is a potential model for a subset of human keratoconus, which is a disease entity with heterogeneous pathogeneses. Alternatively, SKC mouse keratoconus could be a model for other human or mouse-specific keratopathies. PUBMED: 11773012
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Annotation Information

No sequence read archive data associated with this GeneSet.


Major Histocompatibility Complex (D008285)
Incidence (D015994)
Chromosomes (D002875)
Chromosomes, Human, Pair 17 (D002886)
Therapeutics (D013812)
Siblings (D035781)
Testosterone (D013739)
Castration (D002369)
Keratoconus (D007640)
Apoptosis (D017209)
Dependency (Psychology) (D003858)
pathogenesis (GO:0009405)
cell growth (GO:0016049)
chromosome (GO:0005694)

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