advertisement
Abstract #92849 Published in IGR 22-1
Genetic background modifies vulnerability to glaucoma-related phenotypes in mutant mice
Tolman NG; Balasubramanian R; MacAlinao DG; Kearney AL; Macnicoll KH; Montgomery CL; de Vries WN; Jackson IJ; Cross SH; Kizhatil K; Nair KS; John SWMDisease models & mechanisms 2021; 14:
Variants in the LIM homeobox transcription factor 1-beta () gene predispose individuals to elevated intraocular pressure (IOP), a key risk factor for glaucoma. However, the effect of mutations varies widely between individuals. To better understand the mechanisms underlying LMX1B-related phenotypes and individual differences, we backcrossed the (also known as ) allele onto the C57BL/6J (B6), 129/Sj (129), C3A/BLiA- /J (C3H) and DBA/2J- (D2-G) mouse strain backgrounds. Strain background had a significant effect on the onset and severity of ocular phenotypes in mutant mice. Mice of the B6 background were the most susceptible to developing abnormal IOP distribution, severe anterior segment developmental anomalies (including malformed eccentric pupils, iridocorneal strands and corneal abnormalities) and glaucomatous nerve damage. By contrast, mice of the 129 background were the most resistant to developing anterior segment abnormalities, had less severe IOP elevation than B6 mutants at young ages and showed no detectable nerve damage. To identify genetic modifiers of susceptibility to -induced glaucoma-associated phenotypes, we performed a mapping cross between mice of the B6 (susceptible) and 129 (resistant) backgrounds. We identified a modifier locus on Chromosome 18, with the 129 allele(s) substantially lessening severity of ocular phenotypes, as confirmed by congenic analysis. By demonstrating a clear effect of genetic background in modulating -induced phenotypes, providing a panel of strains with different phenotypic severities and identifying a modifier locus, this study lays a foundation for better understanding the roles of LMX1B in glaucoma with the goal of developing new treatments.
Full article
Classification:
3.4.2 Gene studies (Part of: 3 Laboratory methods > 3.4 Molecular genetics)
3.9 Pathophysiology (Part of: 3 Laboratory methods)
