Novel complex Re-Arrangement of ARG1 commonly shared by unrelated patients with Hyperargininemia
2014
Mohseni, Jafar | Boon Hock, Chia | Abdul Razak, Che | Othman, Syah Nor Iman | Hayati, Fatemeh | PeiTee, Winnie Ong | Haniffa, Muzhirah | Zilfalil, Bin Alwi | Mohd. Rawi, Rowani | Ngu, Lock-Hock | Sasongko, Teguh Haryo
Hyperargininemia is a very rare progressive neurometabolic disorder caused by deficiency of hepatic cytosolic arginase I, resulting from mutations in the ARG1 gene. Until now, some mutations were reported worldwide and none of them were of Southeast Asian origins. Furthermore, most reported mutations were point mutations and a few others deletions or insertions.This study aims at identifying the disease-causing mutation in the ARG1 gene of Malaysian patients with hyperargininemia.We employed a series of PCR amplifications and direct sequencing in order to identify the mutation. We subsequently used quantitative real-time PCR to determine the copy number of the exons flanking the mutation. We blasted our sequencing data with that of the reference sequence in the NCBI in order to obtain positional insights of the mutation.We found a novel complex re-arrangement involving insertion, inversion and gross deletion of ARG1 (designated g.insIVS1+1899GTTTTATCAT;g.invIVS1+1933_+1953;g.delIVS1+1954_IVS2+914;c.del116_188;p.Pro20SerfsX4) commonly shared by 5 patients with hyperargininemia, each originating from different family. None of the affected families share known relationship with each other, although four of the five patients were known to have first-cousin consanguineous parents.This is the first report of complex re-arrangement in the ARG1. Further analyses showing that the patients have shared the same geographic origin within the northeastern part of Malaysia prompted us to suggest a simple molecular screening of hyperargininemia within related ethnicities using a long-range PCR.
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