Linkage Study Revealed Complex Haplotypes in a Multifamily Due to Different Mutations in Capn3 Gene in an Iranian Ethnic Group Publisher Pubmed



Mojbafan M^{1, 2} ; Tonekaboni SH³ ; Abiri M^{1, 2} ; Kianfar S⁴ ; Sarhadi A⁴ ; Nilipour Y⁵ ; Tavakkolybazzaz J² ; Zeinali S^{1, 4} Show Affiliations
Source: Journal of Molecular Neuroscience Published:2016

Abstract

Calpainopathy is an autosomal recessive form of limb girdle muscular dystrophies which is caused by mutation in CAPN3 gene. In the present study, co-segregation of this disorder was analyzed with four short tandem repeat markers linked to the CAPN3 gene. Three apparently unrelated Iranian families with same ethnicity were investigated. Haplotype analysis and sequencing of the CAPN3 gene were performed. DNA sample from one of the patients was simultaneously sent for next-generation sequencing. DNA sequencing identified two mutations. It was seen as a homozygous c.2105C>T in exon 19 in one family, a homozygous novel mutation c.380G>A in exon 3 in another family, and a compound heterozygote form of these two mutations in the third family. Next-generation sequencing also confirmed our results. It was expected that, due to the rare nature of limb girdle muscular dystrophies, affected individuals from the same ethnic group share similar mutations. Haplotype analysis showed two different homozygote patterns in two families, yet a compound heterozygote pattern in the third family as seen in the mutation analysis. This study shows that haplotype analysis would help in determining presence of different founders. © 2016, Springer Science+Business Media New York.