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T313M PINK1 Mutation in an Extended Highly Consanguineous Saudi Family With Early-Onset Parkinson Disease
Muhammad A. Chishti, DVM, PhD;
Saeed Bohlega, MD;
Maqbool Ahmed, PhD;
Arslan Loualich, BSc;
Pamela Carroll, BSc;
Christine Sato, BSc;
Peter St George-Hyslop, MD, FRCP;
David Westaway, PhD;
Ekaterina Rogaeva, PhD
Arch Neurol. 2006;63:1483-1485.
Background To date, 5 well-confirmed genes for Parkinson disease (PD) have been identified, including 3 autosomal recessive genes: PTEN-induced putative kinase 1 (PINK1), parkin, and DJ-1. Almost nothing is known about the genetics of PD in Saudi Arabia; however, consanguineous families, not infrequent in this population, could be important in the evaluation of known PD genes and the search for new PD factors in the future.
Objective To investigate known recessive PD genes in 5 consanguineous Saudi families with PD.
Design The entire open frame as well as the untranslated region and all 5' and 3' intron-exon boundaries of the PINK1, parkin, and DJ-1 genes were sequenced in 5 probands in Saudi families.
Results Four of 5 probands tested negative for PINK1, parkin, and DJ-1 mutations. However, in a large Saudi family with PD with at least 3 consanguineous marriages between first cousins, we detected a threonine to methionine substitution at codon 313 (T313M) PINK1 mutation that affected the kinase domain. Manifestations of the disease in this family included early onset (age, 28-38 years), tremulous movement, slow progression, diurnal fluctuations, bradykinesia, good response to levodopa therapy, and only mild dyskinesias. A neurologist blinded to genetic status clinically evaluated 15 family members, all older than 20 years, and diagnosed PD only in individuals who were later found to be homozygous for the T313M mutation. None of the 13 heterozygotes demonstrated any sign of PD.
Conclusion A homozygous T313M mutation is responsible for PD in this large Saudi family. However, the heterozygous T313M mutation does not act as a PD susceptibility factor, which is in contrast to several reports of mutations affecting only 1 PINK1 allele discovered in sporadic PD.
Author Affiliations: Departments of Comparative Medicine (Drs Chishti and Ahmed and Mr Loualich) and Neuroscience (Dr Bohlega), and Aragene Laboratory (Ms Carroll), King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia; Centre for Research in Neurodegenerative Diseases, Department of Medicine (Ms Sato and Drs St George-Hyslop, Westaway, and Rogaeva) and Toronto Western Hospital Research Institute (Dr St George-Hyslop), University of Toronto, Toronto, Ontario.
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