PLA2G6 mutations in PARK14-linked young-onset parkinsonism and sporadic Parkinson's disease

Chin Song Lu, Szu Chia Lai, Ruey Meei Wu, Yi Hsin Weng, Chia Ling Huang, Rou Shayn Chen, Hsiu Chen Chang, Yah Huei Wu-Chou, Tu Hsueh Yeh

研究成果: 雜誌貢獻文章

45 引文 斯高帕斯(Scopus)

摘要

Mutations of PLA2G6 gene have been lately proposed to be the causative gene for PARK14 in patients with autosomal recessive young-onset parkinsonism (YOPD). The role of PLA2G6 mutations as a risk factor for Parkinson's disease is not clear. To study the PLA2G6 mutations in PARK14-linked patients and its association with the onset of sporadic Parkinson's disease (sPD), sequencing and gene dosage analyses were carried out in 25 patients (onset age ≦30 years) then the identified variants were assessed in 956 sporadic PD (sPD) patients and 802 age-matched healthy controls. Four genetic variants were identified; one patient had homozygous c.991G>T (p.Asp331Tyr) mutation, two had compound heterozygous c.991G>T/c.1077G>A (p.Met358IlefsX) mutation, one had single c.1976A>G (p.Asn659Ser) mutation, and one patient had an exon 1 hetero-deletion. The c.1077G>A mutation resulted in a 4-bp deletion in leukocyte mRNA by activating a cryptic splice site in exon 7. Only p.Asp331Tyr was identified in four sPD patients and four controls. The onset age for PLA2G6 mutation carriers was younger than that for sPD (29.86±8.59 vs. 56.84±11.33 years, P=0.0002). The analysis of previously reported PARK14 patients revealed that those who carried a truncated mutation tended to have a complicated phenotype and atrophies of cortex and cerebellum. In conclusion, PLA2G6 mutation was the second common genetic cause after PRKN mutation in our YOPD patients and might be a risk factor for early-onset PD in Han Chinese. Additionally, mutation data should be interpreted carefully because even a synonymous mutation could cause abnormal mRNA splicing.
原文英語
頁(從 - 到)183-191
頁數9
期刊American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
159 B
發行號2
DOIs
出版狀態已發佈 - 三月 2012
對外發佈Yes

ASJC Scopus subject areas

  • Genetics(clinical)
  • Psychiatry and Mental health
  • Cellular and Molecular Neuroscience

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