Article ID Journal Published Year Pages File Type
2820991 Genomics 2012 7 Pages PDF
Abstract

In this study, through linkage analysis of a four-generation Chinese family with multiple members afflicted with DGI (type II), we identified a novel missense mutation in DSPP. The mutation was located in exon 2 at the second nucleotide position of the last codon and resulted in a substitution of a proline with a leucine residue (c.50C>T, p.P17L, g.50C>T). To assess the potential effects of this novel mutation, we utilized various bioinformatics analysis programs. The results indicate that the mutation likely affects protein cleavage/trafficking. We also analyzed previously reported mutations of DSPP. In summary, our finding supports that the genomic sequence that corresponds to the P17 residue of DSPP is a mutational hotspot and P17 may be critical for the function of DSPP.

► We identified a novel missense DSPP mutation in a Chinese family with DGI-II. ► Basing on bioinformatics analysis, the mutation is likely to affect protein cleavage. ► Using bioinformatics programs, we analyzed previously reported DSPP mutations. ► Our study enhances the understanding of a molecular basis for the DGI-II.

Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Genetics
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