Publication: Thirteen novel mutations of the replicated region of PKD1 in an Asian population
Issued Date
2000-01-01
Resource Type
ISSN
00852538
Other identifier(s)
2-s2.0-0033802011
Rights
Mahidol University
Rights Holder(s)
SCOPUS
Bibliographic Citation
Kidney International. Vol.58, No.4 (2000), 1400-1412
Suggested Citation
Bunyong Phakdeekitcharoen, Terry J. Watnick, Curie Ahn, Dae Yeon Whang, Brian Burkhart, Gregory G. Germino Thirteen novel mutations of the replicated region of PKD1 in an Asian population. Kidney International. Vol.58, No.4 (2000), 1400-1412. doi:10.1046/j.1523-1755.2000.00302.x Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/26347
Research Projects
Organizational Units
Authors
Journal Issue
Thesis
Title
Thirteen novel mutations of the replicated region of PKD1 in an Asian population
Abstract
Background. Mutations of PKD1 are thought to account for approximately 85% of all mutations in autosomal dominant polycystic kidney disease (ADPKD). The search for PKD1 mutations has been hindered by both its large size and complicated genomic structure. To date, few mutations that affect the replicated segment of PKD1 have been described, and virtually all have been reported in Caucasian patients. Methods. In the present study, we have used a long-range polymerase chain reaction (PCR)-based strategy previously developed by our laboratory to analyze exons in the replicated region of PKD1 in a population of 41 unrelated Thai and 6 unrelated Korean families with ADPKD. We have amplified approximately 3.5 and approximately 5 kb PKD1 gene-specific fragments (5'MR and 5'LR) containing exons 13 to 15 and 15 to 21 and performed single-stand conformation analysis (SSCA) on nested PCR products. Results. Nine novel pathogenic mutations were detected, including six nonsense and three frameshift mutations. One of the deletions was shown to be a de novo mutation. Four potentially pathogenic variants, including one 3 bp insertion and three missense mutations, were also discovered. Two of the nonconservative amino acid substitutions were predicted to disrupt the three-dimensional structure of the PKD repeats. In addition, six polymorphisms, including two missense and four silent nucleotide substitutions, were identified. Approximately 25% of both the pathogenic and normal variants were found to be present in at least one of the homologous loci. Conclusion. To our knowledge, this is the first report of mutation analysis of the replicated region of PKD1 in a non-Caucasian population. The methods used in this study are widely applicable and can be used to characterize PKD1 in a number of ethnic groups using DNA samples prepared using standard techniques. Our data suggest that gene conversion may play a significant role in producing variability of the PKD1 sequence in this population. The identification of additional mutations will help guide the study of polycystin-1 and better help us to understand the pathophysiology of this common disease.