In silico modeling of pathogenic point mutations in PSEN1 as studied in South-east Asia
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Abstract
In Asia, particularly in Korea and Japan, there is an increase in the aging population, and a subsequent increase in the number of Alzheimer’s disease (AD) patients. Early onset AD (EOAD) represents a minority of all cases. Three genes are associated with EOAD: APP, PSEN1, and PSEN2. PSEN1 is the most common causative gene of EOAD. Recently, more than 200 pathogenic mutations associated with EOAD were discovered in the coding region of PSEN1. To verify the damaging properties of mutations in pre-senilins, cell studies such as COS-1, HEK-293 were performed. The disadvantages of transfection analyses are that they are expensive and time-consuming. In addition, these studies cannot be performed for all mutations. In silico analyses (e.g., Sorting Intolerant from Tolerant [SIFT], PolyPhen2) can be useful in predicting which mutations are involved in disease progression. In addition, 3-D modeling can be also help to estimate the role of mutations in AD onset. This work focuses on AD-causative point mutations in PSEN1 as studied in South-East Asian countries. Predictions were performed for PSEN1 with point mutations to estimate their pathogenic nature and potential role in disease progression. In this study, PolyPhen 2 and SIFT software predictions, as well as 3-D modeling, were performed for all mutations. Most of the mutations were confirmed as pathogenic mutations by these algorithms; however, in silico modeling cannot replace clinical, functional, segregation, and association studies.
Keywords
Alzheimer’s disease Presenilin-1 Mutation ModellingPreview
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References
- 1.Catindig, J. A., Venketasubramanian, N., Ikram, M. K. & Chen, C. Epidemiology of dementia in Asia: insights on prevalence. trends and novel risk factors. J. Neurol. Sci. 321, 11–16 (2012).CrossRefPubMedGoogle Scholar
- 2.Bagyinszky, E., Youn, Y. C., An, S. S. & Kim, S. Y. The genetics of Alzheimer’s disease. Clin. Interv. Aging 9, 535–551 (2014).CrossRefPubMedPubMedCentralGoogle Scholar
- 3.Larner, A. J. & Doran, M. Clinical phenotypic heterogeneity of Alzheimer’s disease associated with mutations of the presenilin-1 gene. J. Neurol. 253, 139–158 (2006).CrossRefPubMedGoogle Scholar
- 4.Guerreiro, R. J. et al. Genetic screening of Alzheimer’s disease genes in Iberian and African samples yields novel mutations in presenilins and APP. Neurobiol. Aging 31, 725–731 (2010).CrossRefPubMedGoogle Scholar
- 5.Murayama, O. et al. Enhancement of amyloid beta 42 secretion by 28 different presenilin 1 mutations of familial Alzheimer’s disease. Neurosci. Lett. 265, 61–63 (1999).CrossRefPubMedGoogle Scholar
- 6.Kaneko, H. et al. Enhanced Accumulation of Phosphorylated a-Synuclein and Elevated β-Amyloid 42/40 Ratio Caused by Expression of the Presenilin-1 T440 Mutant Associated with Familial Lewy Body Disease and Variant Alzheimer’s Disease. J. Neurosci. 27, 13092–13097 (2007).CrossRefPubMedGoogle Scholar
- 7.Adzhubei, I. A. et al. A method and server for predicting damaging missense mutations. Nat. Methods 7, 248–249 (2010).CrossRefPubMedPubMedCentralGoogle Scholar
- 8.Ng, P. C. & Henikoff, S. SIFT: Predicting amino acid changes that affect protein function. Nucleic Acid. Res. 31, 3812–3814 (2003).CrossRefPubMedPubMedCentralGoogle Scholar
- 9.Hu, J. & Ng, P. C. SIFT Indel: predictions for the functional effects of amino acid insertions/deletions in proteins. PLo. One 8, e77940 (2013).CrossRefGoogle Scholar
- 10.Källberg, M. et al. Template-based protein structure modeling using the RaptorX web server. Natur. Protocols 7, 1511–1522 (2012).CrossRefGoogle Scholar
- 11.Ataka, S. et al. A novel presenilin-1 mutation (Leu85Pro) in early-onset Alzheimer disease with spastic paraparesis. Arch. Neurol. 61, 1773–1776 (2004).CrossRefPubMedGoogle Scholar
- 12.Kamino, K. et al. Three different mutations of presenilin 1 gene in early-onset Alzheimer’s disease families. Neurosci. Lett. 208, 195–198 (1996).CrossRefPubMedGoogle Scholar
- 13.Jia, J., Xu, E., Shao, Y., Jia, J., Sun, Y. & Li, D. One novel presenilin-1 gene mutation in a Chinese pedigree of familial Alzheimer’s disease. J. Alzheime. Dis. 7, 119–124 (2005).Google Scholar
- 14.Fang, B., Jia, L. & Jia, J. Chinese Presenilin-1 V97L mutation enhanced Abeta42 levels in SH-SY5Y neuroblastoma cells. Neurosci. Lett. 406, 33–37 (2006).CrossRefPubMedGoogle Scholar
- 15.Jiao, B. et al. Mutational analysis in early-onset familial Alzheimer’s disease in Mainland China. Neurobiol. Aging 35, 1957.e1–6 (2014).CrossRefPubMedGoogle Scholar
- 16.La Bella, V. et al. A novel mutation (Thr116Ile) in the presenilin 1 gene in a patient with early-onset Alzheimer’s disease. Eur J Neurol 11, 521–524 (2004).CrossRefPubMedGoogle Scholar
- 17.Raux, G. et al. Molecular diagnosis of autosomal dominant early onset Alzheimer’s disease: an update. J. Med. Genetics 42, 793–795 (2005).CrossRefGoogle Scholar
- 18.Romero, I. et al. A presenilin-1 Thr116Asn substitution in a family with early-onset Alzheimer’s disease. Neuroreport 10, 2255–2260 (1999).CrossRefPubMedGoogle Scholar
- 19.Yasuda, M. et al. A pedigree with a novel presenilin 1 mutation at a residue that is not conserved in presenilin 2. Arch. Neurology 56, 65–69 (1999).CrossRefGoogle Scholar
- 20.Fang, B. Y. & Jia, J. P. The effect of two newly Chinese presenilin-1 mutations on the sensitivity to trophic factor withdrawal in human neuroblastoma cells. Zhonghua Yi Xue Z. Zhi 87, 336–340 (2007).Google Scholar
- 21.Kim, H. J., Kim, H. Y., Ki, C. S. & Kim, S. H. Presenilin 1 gene mutation (M139I) in a patient with an early-onset Alzheimer’s disease: clinical characteristics and genetic identification. Neurol. Sci. 31, 781–783 (2010).CrossRefPubMedGoogle Scholar
- 22.Cruts, M. et al. Molecular genetic analysis of familial early-onset Alzheimer’s disease linked to chromosome 14q24.3. Hum. Mol. Genet. 4, 2363–2372 (1995).CrossRefPubMedGoogle Scholar
- 23.Arai, N. et al. Familial cases presenting very early onset autosomal dominant Alzheimer’s disease with I143T in presenilin-1 gene: implication for genotype-phenotype correlation. Neurogenetics 9, 65–67, 2008.CrossRefPubMedGoogle Scholar
- 24.Hattori, S. et al. A novel presenilin 1 mutation (Y154N) in a patient with early onset Alzheimer’s disease with spastic paraparesis. Neurosci. Lett. 368, 319–322 (2004).CrossRefPubMedGoogle Scholar
- 25.Hong, K. S. et al. Clinical and genetic analysis of a pedigree of a thirty-six-year-old familial Alzheimer’s disease patient. Biol. Psychiatry 42, 1172–1176 (1997).CrossRefPubMedGoogle Scholar
- 26.Kim, J. et al. A novel PSEN1 H163P mutation in a patient with early-onset Alzheimer’s disease: clinical, neuroimaging, and neuropathological findings. Neurosci. Lett. 530, 109–114 (2012).CrossRefPubMedGoogle Scholar
- 27.Higuchi, S. et al. A novel PS1 Mutation (W165G) in a Japanese family with early-onset Alzheimer’s disease. Alzheimer’. Reports 3, 227–231 (2000).Google Scholar
- 28.Guo, J. et al. A novel presenilin 1 mutation (Ser169del) in a Chinese family with early-onset Alzheimer’s disease. Neurosci. Lett. 468, 34–37 (2010).CrossRefPubMedGoogle Scholar
- 29.Kasuga, K. et al. Depression and psychiatric symptoms preceding onset of dementia in a family with early-onset Alzheimer disease with a novel PSEN1 mutation. J. Neurology 256, 1351–1353 (2009).CrossRefGoogle Scholar
- 30.Yasuda, M. et al. A novel missense mutation in the presenilin-1 gene in a familial Alzheimer’s disease pedigree with abundant amyloid angiopathy. Neurosci. Lett. 232, 29–32 (1997).CrossRefPubMedGoogle Scholar
- 31.Janssen, J. C. et al. Early onset familial Alzheimer’s disease: Mutation frequency in 31 families. Neurology 60, 235–239 (2003).CrossRefPubMedGoogle Scholar
- 32.Park, H. K. et al. Identification of PSEN1 and APP gene mutations in Korean patients with early-onset Alzheimer’s disease. J. Korean Med. Sci. 23, 213–217 (2008).CrossRefPubMedPubMedCentralGoogle Scholar
- 33.Sugiyama, N. et al. A novel missense mutation (G209R) in exon 8 of the presenilin 1 gene in a Japanese family with presenile familial Alzheimer’s disease. Hum. Mutat. 14, 90 (1999).CrossRefPubMedGoogle Scholar
- 34.Takao, M. et al. A novel mutation (G217D) in the Presenilin 1 gene (PSEN1) in a Japanese family: presenile dementia and parkinsonism are associated with cotton wool plaques in the cortex and striatum. Acta. Neuropathol. 104, 155–170 (2002).CrossRefPubMedGoogle Scholar
- 35.Zekanowski, C. et al. Two novel presenilin 1 gene mutations connected with frontotemporal dementia-like clinical phenotype: genetic and bioinformatic assessment. Exp. Neurol. 200, 82–88 (2006).CrossRefPubMedGoogle Scholar
- 36.Jiang, H. Y. et al. Identification of PSEN1 mutations p.M233L and p.R352C in Han Chinese families with early-onset familial Alzheimer’s disease. Neurobiol. Aging 36, 1602.e3–6 (2015).CrossRefPubMedGoogle Scholar
- 37.Sodeyama, N. et al. Very early onset Alzheimer’s disease with spastic paraparesis associated with a novel presenilin 1 mutation (Phe237Ile). J. Neurology. Neurosurgery Psychiatry 71, 556–557 (2001).CrossRefGoogle Scholar
- 38.Jiao, B. et al. Mutational analysis in early-onset familial Alzheimer’s disease in Mainland China. Neurobiol. Aging 35, 1957.e1–6 (2014).CrossRefPubMedGoogle Scholar
- 39.Furuya, H. et al. A novel mutation (L250V) in the presenilin 1 gene in a Japanese familial Alzheimer’s disease with myoclonus and generalized convulsion. J. Neurol. Sci. 209, 75–77 (2003).CrossRefPubMedGoogle Scholar
- 40.Ikeda, M. et al. The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients. Ann. Neurol. 40, 912–917 (1996).CrossRefPubMedGoogle Scholar
- 41.Matsubara-Tsutsui, M. et al. Molecular evidence of presenilin 1 mutation in familial early onset dementia. Am. J. Med. Genet. 114, 292–298 (2002).CrossRefPubMedGoogle Scholar
- 42.Kamimura K. et al. Familial Alzheimer’s disease genes in Japanese. J. Neurol. Sci. 160, 76–81 (1998).CrossRefPubMedGoogle Scholar
- 43.Gomez-Isla, T. et al. A novel presenilin-1 mutation: increased beta-amyloid and neurofibrillary changes. Ann. Neurol. 41, 809–813 (1997).CrossRefPubMedGoogle Scholar
- 44.Larner, A. J., Ray, P. S. & Doran, M. The R269H mutation in presenilin-1 presenting as late-onset autosomal dominant Alzheimer’s disease. J. Neurol. Sci. 252, 173–176 (2007).CrossRefPubMedGoogle Scholar
- 45.Tanahashi, H. et al. Sequence analysis of presenilin-1 gene mutation in Japanese Alzheimer’s disease patients. Neurosci. Lett. 218, 139–141 (1996).CrossRefPubMedGoogle Scholar
- 46.Lendon, C. L. et al. E280A PS-1 mutation causes Alzheimer’s disease but age of onset is not modified by ApoE alleles. Hum. Mutation 10, 186–195 (1997).CrossRefGoogle Scholar
- 47.Shioi, J. et al. FAD mutants unable to increase neurotoxic Abeta 42 suggest that mutation effects on neurodegeneration may be independent of effects on Abeta. J. Neurochem. 101, 674–681 (2007).CrossRefPubMedGoogle Scholar
- 48.Ch’ng, G. S., An, S. S., Bae, S. O., Bagyinszky, E. & Kim, S. Identification of two novel mutations, PSEN1 E280K and PRNP G127S, in a Malaysian family. Neuropsychiatr. Dis. Treat 11, 2315–23122 (2015).PubMedPubMedCentralGoogle Scholar
- 49.Hamaguchi, T. et al. A novel presenilin 1 mutation (L282F) in familial Alzheimer’s disease. J. Neurology 256, 1575–1577 (2009).CrossRefGoogle Scholar
- 50.Tabira, T. et al. Alzheimer’s disease with spastic paresis and cotton wool type plaques. J. Neurosci. Res. 70, 367–372, (2002).CrossRefPubMedGoogle Scholar
- 51.Aoki, M. et al. A presenilin-1 mutation in a Japanese family with Alzheimer’s disease and distinctive abnormalities on cranial MRI. Neurology 48,1118–1120 (1997).CrossRefPubMedGoogle Scholar
- 52.Ikeuchi, T. et al. Mutational analysis in early-onset familial dementia in the Japanese population. The role of PSEN1 and MAPT R406W mutations. Dement. Geriatr. Cogn. Disord. 26, 43–49 (2008).CrossRefPubMedGoogle Scholar
- 53.Sherrington, R. et al. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer’s disease. Nature 375, 754–760 (1995).CrossRefPubMedGoogle Scholar
- 54.Besançon, R. et al. Missense mutation in exon 11 (Codon 378) of the presenilin-1 gene in a French family with early-onset Alzheimer’s disease and transmission study by mismatch enhanced allele specific amplification. Hum. Mutat. 11, 481 (1998).CrossRefPubMedGoogle Scholar
- 55.Finckh, U. et al. Novel mutations and repeated findings of mutations in familial Alzheimer disease. Neurogenetics 6, 85–89 (2005).CrossRefPubMedGoogle Scholar
- 56.Traykov, D. L. et al. Novel PSEN1 mutation in a Bulgarian patient with very early-onset Alzheimer’s disease, spastic paraparesis, and extrapyramidal signs. Am. J. Alzheimers Dis. Other Dement. 24, 404–407 (2009).CrossRefGoogle Scholar
- 57.Campion, D. et al. Mutations of the presenilin I gene in families with early-onset Alzheimer’s disease. Hum. Mol. Genet. 4, 2373–2377 (1995).CrossRefPubMedGoogle Scholar
- 58.Yasuda, M. et al. Novel presenilin-1 mutation with widespread cortical amyloid deposition but limited cerebral amyloid angiopathy. J. Neurol. Neurosurg. Psychiatry 68, 220–223 (2000).CrossRefPubMedPubMedCentralGoogle Scholar
- 59.Matsushita, S. et al. Clinical and biomarker investigation of a patient with a novel presenilin-1 mutation (A431V) in the mild cognitive impairment stage of Alzheimer’s disease. Biol. Psychiatry 52, 907–910 (2002).CrossRefPubMedGoogle Scholar
- 60.Ishikawa, A. et al. A mutant PSEN1 causes dementia with Lewy bodies and variant Alzheimer’s disease. Ann. Neurology 57, 429–434 (2005).CrossRefGoogle Scholar
- 61.Tchernitchko, D., Goossens, M. & Wajcman, H. In silico prediction of the deleterious effect of a mutation: proceed with caution in clinical genetics. Clin. Chem. 50, 1974–1978 (2004).CrossRefPubMedGoogle Scholar