Abstract
While the life expectancy of the population has increased, Alzheimer’s disease (AD) has emerged as one of the greatest health problems of old age. AD is characterized by neuronal loss and cognitive decline. In the AD brain, there is a decrease in levels of acetylcholinesterase (AChE) and an increase in the levels of the related enzyme butyrylcholinesterase (BChE), that accumulate in plaques and tangles. Apolipoprotein E (ApoE) is a major cholesterol carrier and plays an important role in maintaining lipid homeostasis. APOE-ε4 constitutes the most important known genetic risk factor for late-onset AD. It has been proposed that the BCHE-K allele (Ala539Thr) acts in synergy with the APOE-ε4 allele to promote risk for AD. However, there is insufficient evidence to support a correlation. Most studies focused only on the coding regions of the genes. In this study, we analyzed sequence regions beyond the BCHE coding sequence. We found synergy between APOE-ε4 and SNPs localized in 5′UTR (rs1126680) and in intron 2 (rs55781031) of the BCHE-K allele (rs1803274) in 18% of patients with late-onset AD (n = 55). The results show that the coexistence of the APOE-ε4 allele and 3 SNPs in the BCHE gene is associated with a highly elevated risk of late-onset AD. SNP (rs1126680) in 5′UTR of the BCHE gene is located 32 nucleotides upstream of the 28 amino acid signal peptide. Mass spectrometry analysis of the BChE protein produced by SNP (rs1126680) showed that the mutation caused an in frame N-terminal extension of 41 amino acids of the BChE signal peptide. The resultant variant with a 69 amino acid signal peptide, designated N-BChE, may play a role in development of AD.
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Introduction
Alzheimer’s disease (AD), a neurodegenerative disease associated with cognitive decline is the most common form of dementia in elderly individuals. Approximately 13% of people over the age of 65 and 45% over the age of 85 are estimated to have AD. An estimated 50 million people worldwide lived with dementia in 2017. This number will almost double every 20 years, reaching 131.5 million in 20501. There are several types of human dementia of which AD is the most common2. Differentiation between AD and dementia with Lewy bodies, vascular dementia (VaD) and frontotemporal dementia (FTD) can be challenging at present and ambiguous. Diagnosis of AD requires a clinical syndrome of dementia, confirmed by postmortem brain autopsy by detecting cerebral pathology including β-amyloid (Aβ) plaques and tau neurofibrillary tangles (NFTs)3,4. However, the presence of Aβ in cognitively normal older individuals indicates that other markers are desirable to facilitate more accurate diagnosis of AD5,6,7,8,9,10.
Alzheimer’s disease (AD) is divided into 2 subtypes: early-onset AD occurring at age 30 to 65 years, with approximately 1% to 6% of all cases and late-onset AD, which is the most common form of AD at age later than 65. The cause for most Alzheimer’s cases is still unknown except for a few percent of cases where mutations in genes APP, PSEN1, and PSEN2 are associated with early-onset AD. Multiple genetic and environmental risk factors are involved in late-onset AD pathogenesis11,12. Many studies have shown that an imbalance between the production and clearance of amyloid-β (Aβ) forming amyloid plaques, is probably a major contributor to neurodegeneration and disease development. The toxicity of Aβ seems to depend on the presence of microtubule-associated hyperphosphorylated forms of the protein tau, which aggregate and deposit in AD brains as neurofibrillary tangles13. On the other hand, other factors can also be involved in AD development.
The results from genome-wide association studies (GWAS) have shown that the presence of the ε4 allele of APOE is the strongest genetic risk factor for AD14,15,16. Apolipoprotein E (ApoE) is a protein involved in lipid transport between cells and tissues and it seems to play a role in Aβ aggregation and clearance. The human APOE gene exists in three allelic forms (APOE-ε2, APOE-ε3, and APOE-ε4) which differ only by two amino acids in positions 112 and 158, encoding either cysteine or arginine: ApoE2 (Cys112, Cys158), ApoE3 (Cys112, Arg158), and ApoE4 (Arg112, Arg158). Individuals carrying the APOE-ε4 allele are at increased risk of AD compared with those carrying the more common ε3 or/and ε2 alleles. It has been hypothesized that ApoE2 and ApoE3 may enhance the clearance of Aβ more efficiently, compared to ApoE4, and/or ApoE4 promotes Aβ fibrillization more effectively than ApoE2 and ApoE317,18,19,20. Previous studies showed genes expression changes associated with lipid metabolism as well as inflammation and a role of ApoE4 in these processes among AD patients21,22. Other mechanisms, such as tau phosphorylation, neuroinflammation and a role of BCHE protein in the formation of plaques have been also considered as risk factors for AD. Accumulation of amyloid plaques, is thought to initiate a pathogenic cascade that leads to synaptic dysfunction and neurodegeneration10.
Butyrylcholinesterase (Uniprot P06276), also known as plasma cholinesterase or pseudocholinesterase, is a serine hydrolase present in most tissues with the highest levels in plasma and liver23,24. BChE has a widespread distribution in the human body and it serves as an inherent protector from damages caused by toxic compounds before they reach acetylcholinesterase (AChE) in synapses. In the brain BChE is found in glia and white matter, and it has been shown to be involved, along with AChE, in cholinergic neurotransmission25,26. In the human brain, BChE is mainly expressed in glial cells, particularly astrocytes in contrast to AChE which is found in neurons. Nevertheless, BChE is also found in specific populations of neurons, particularly localized in the amygdala and hippocampus27 and thalamus25,28. BChE was found in amyloid plaques and neurofibrillary tangles (NFTs), which suggests that the protein may be involved in pathogenesis of AD29,30,31. Other researchers demonstrated that BChE may participate in the transformation of beta-amyloid (Aβ) from an initially benign to an eventually malignant form32. The accumulation of BChE in cortical grey matter in association with AD pathology, an area that normally has scant BChE activity, suggests an opportunity to detect this pathology during life by imaging BChE33,34. Other findings showed that the most frequent genetic variant of the BCHE gene – the K-variant (c.1699G> A, p.Ala539Thr, rs1803274), was considerably less effective in attenuating the accumulation of Aβ fibrils than BChE wild type35,36. The association between the BChE-K variant and AD risk in patients carrying the ApoE4 allele has been debated and studied many times, but no definitive correlation has been established, as some support the idea37,38,39, while other researchers remain doubtful40,41,42. Despite the fact that many of these studies are based on meta-analysis, GWAS and cohort study, the results are inconsistent and a role for BChE in AD pathology remains unclear43,44.
Nearly all previous reports regarding BChE involvement in the development of AD focused only on the K-variant alteration located in the tetramerization domain of BChE.
Our study shows that mutations in the 5′UTR and intron 2 of the BCHE gene increase the probability of an association of the BChE-K variant and APOE-ε4 allele with late-onset AD.
Results
Previous studies reported an association between the K variant (BCHE-K) and late-onset AD risk in carriers of APOE-ε4. We attempted to replicate this finding in 55 confirmed AD and 18 age matched controls, while expanding the analysis to include noncoding regions of the BCHE gene. Genotype and allele frequencies of the BCHE and APOE-ε4 variants analyzed are summarized in Table 1. We found a subpopulation of 10 subjects with compound alterations in BCHE (rs1126680, rs55781031, rs1803274) and APOE-ε4 alleles among 55 people with late-onset AD. The rs1803274 and APOE-ε4 alleles were found in 8 out of 45 AD patients and in 6 out of 18 controls. The mutations were mainly heterozygous so that only one allele carried a mutation and the other allele was wild-type.
Alterations in noncoding regions of a gene can play various roles in protein synthesis. 5′ UTR modifications can change the protein translation start site and modifications in introns can be involved in splicing regulation and gene expression pattern. To determine whether rs1126680 and rs55781031 (c.−32G> A and c.1518-121 T > C) affected the protein sequence of serum BChE, we isolated BChE from homozygous individuals from our serum collection45 by affinity chromatography on Hupresin and size exclusion chromatography. Isolated proteins were analyzed by mass spectrometry of trypsin-digested proteins. Peptides were found that corresponded to a new translational start site of BChE (Fig. 1A,B, Supplementary Fig. S2) located −69 amino acids from Glu1 of the mature, secreted BChE protein. Furthermore, the extended 69-residue signal peptide was not clipped off the secreted BChE protein. To predict the rs1126680 effect on local RNA secondary structure of the first 200 nucleotides of the BChE transcript MFOLD algorithm and RNAsnp Web Server were used46,47,48. We did not observe significant changes in the predicted secondary structures outside of the region containing the alteration (Fig. 1C).
Sequence analysis using the Kozak sequence prediction algorithm showed that the new translation start site at residue −69 (nucleotide −123 in Table 2) scored higher for the Kozak consensus sequence than the start site at residue −28 in wild-type BChE (nucleotide + 1 in Table 2). A perfect Kozak sequence would have a score of 1. Scores of 0.17 and 0.14 for the 2 ATG start sites in Table 2 indicate that BChE expression levels are modulated through inefficient start site sequences. The slightly higher score of 0.17 suggests the homozygous mutant would have higher plasma BChE activity. Contrary to expectation, plasma samples with 3 BCHE SNPs had a lower BChE activity. The N-terminus extended BChE protein variant, designated N-BChE, is 41 aa longer than wt and carries a substitution at nucleotide −32 position TGC > TAC (c.−32G > A) p.C-11Y (rs1126680) (Fig. 1).
Discussion
Genetically, the ε4 allele of the apolipoprotein E (APOE) gene is the strongest risk factor for late-onset AD49. Several competing hypotheses explain the cause of the disease. An early hypothesis, that AD is defined by the presence of Aβ plaques and neurofibrillary tangles became inadequate when it was found that the brains of up to 40% of cognitively normal older adults also had Aβ plaques and tangles. Additional markers of AD are required to facilitate a more accurate diagnosis of the disease. This study shows that the coexistence of the APOE-ε4 allele and 3 SNPs in the BCHE gene, localized in 5′UTR (rs1126680) and in intron 2 (rs55781031) of the BCHE-K allele (rs1803274), is associated with a highly elevated risk of late-onset AD.
Little is known about regulation of BCHE gene expression. Our previous studies and results presented by others have shown that c.−32G> A (rs1126680) (also known as −116A) substitution in exon 1 was associated with lower BChE activity45,50. It was shown that 5′ UTR c.−32G> A, (rs1126680) variant is preferentially found in cis with K variant (c.1699G> A, p.A567T) and intron 2 alteration (c.1518-121 T > C, rs55781031). It was also discussed that c.−32G> A is responsible for lowering of BChE activity by affecting transcription and/or translation. It was considered that 5′ UTR c.−32G> A, (rs1126680) variant can directly modulate protein translation through alterations in mRNA secondary structure. Protein translation is often regulated by mRNA secondary structure. Complementary sequences within the 5′ UTR can form stable stem-loop structures that may disturb initiation of translation51,52. A theoretical model of the mRNA secondary structure of the BCHE 5′ UTR region presented in Fig. 1C was predicted using mFold46. It is possible that the position of substitutions in the loop of the stem could affect binding of the regulatory proteins and disturb translation efficiency. Such a process was previously described for 5′ UTR of the ferritin receptor mRNA, which contains a stem loop that recruits binding proteins and controls translation efficiency53. Here, we observed two effects of c.−32G> A, (rs1126680): change in initiation codon of BChE protein resulting in N-extension of the 41 amino acids of the protein and alteration in the extended amino acid sequence p.C-11Y. Furthermore, we showed that the N-extension of the BChE protein was associated with some cases of late-onset AD. It is noteworthy, that N-terminally extended membrane variants of AChE were observed in brain neurons and hematopoietic cells as an effect of alternative splicing54. Extended N-AChE proteins may have transmembrane domains at their N terminus and play a role in apoptosis55. Our research shows N-terminally extended BChE variant produced as an effect of alternative translation start.
Our results show no association between AD risk in patients carrying the ApoE4 allele and the BChE K-variant when no other BCHE gene mutations are evaluated. This conclusion is based on the finding that 6 out of 18 control cases (33%) and 18/55 AD patients (33%) were positive for the BChE K-variant. However, a strong association (100%) was found between late-onset AD in patients carrying the ApoE4 allele and the BChE K-variant when 2 additional mutations in noncoding regions of the BCHE gene were present.
Different types of dementia may be caused by different molecular mechanisms. Many factors can be involved in development of late-onset AD. In this study, we found synergy between APOE-ε4 and SNPs localized in the BCHE gene (rs1126680, rs55781031, rs1803274) in 18% of patients with late-onset AD (n = 55). Despite the small number of patients, we propose that the presence of the APOE-ε4 allele and 3 SNPs in the BCHE provides 100% confidence in predicting late-onset AD. These multiple gene alterations were present only in patients with late-onset AD. The limitation of our study is that only 18% of late-onset AD patients carried all these mutations. A larger cohort study that considers additional genetic and environmental factors may account for the 82% of late-onset AD cases that did not contain this set of mutations.
Materials and Methods
AD patients (n = 55) enrolled in the study were selected by specialists in geriatric psychiatry as described earlier56. Briefly, the diagnosis of AD was based on medical interviews, clinical symptoms, appropriate imaging examinations and clinical tests including the Hachinski Ischemic Scale, the Geriatric Depression Scale, the Mini Mental State Examination (MMSE) and the Clock Drawing Test. In order to exclude other possible causes of impairments in cognitive function, complete blood count, a lipidogram and other tests clinically appropriate for somatic diseases were performed during the diagnostic process. The patient group consisted of 26 males and 29 females with a mean age of 83 years (range 65–102 years). The control group (n = 18) had no signs or symptoms of dementia or a severe somatic disorder. Controls consisted of 9 males and 9 females with a mean age of 76 years (range 68–87 years). All participants were of European origin and homogeneous ethnic (Polish) background. Serum collection and genotyping of the control group (n = 1200) was described earlier45.
DNA Extraction, PCR Amplification and Sanger Sequencing
Genomic DNA was extracted from 1 mL of peripheral blood leukocytes using Blood Mini kit in accordance with the manufacturer’s protocol (A&A Biotechnology, Poland). Sequences of 4 amplicons of the BCHE gene were determined using the method previously described45. Briefly, 4 regions of the BCHE gene were amplified by PCR using the following primers M1F, 5′-F- AGACTACCTGCAATTGTAAAGCA, and M1R, 5′-TCTCATCCCACAGAATGAGC; M2-2F, 5′- GCCACAGTCTCTGACCAAGTG and M2-2R-5′- TTCTGTTCCTAGCTTCATAAAGAG; M3-F, 5′- CACTAAGCCCAGTTCACATACG, M3-R, 5′- CATCACCGTGCCTTGGAG; M4-1F, 5′- TGTACTGTGTAGTTAGAGAAAATGGC; M4-1R, 5′- TACTAAGTTAAAGATGTGAGGAATC.
APOE- ε2/ε3/ε4 alleles (rs429358, rs7412) polymorphism were determined using the following primers APO4F 5′-ACGCGGGCACGGCTGTCCAAGGAG and APO4R 5′-CTCGCGGGCCCCGGCCTGGTACAC. A 25-μL PCR mixture contained 60 ng of extracted DNA, 10 pmoles of each forward and reverse primer, dNTPs, buffer, and Marathon Taq DNA polymerase (A&A Biotechnology, Poland). Amplification was performed with an initial denaturation at 95 °C for 5 minutes, followed by 35 cycles of denaturation at 95 °C for 30 s, annealing at 55 °C for 30 s, and extension at 72 °C for 30 s with a final extension at 72 °C for 10 minutes. PCR products were purified using Clean Up kit (A&A Biotechnology, Poland). Bidirectional DNA sequencing of PCR amplification products was performed using BigDye Terminator v.3.1 cycle sequencing kit and 3130 Genetic Analyzer according to the manufacturer’s protocol (ThermoFischer Scientific, USA). Sequences were analyzed by Sequencher v.4.10 DNA Software (Gene Codes Corporation, USA) and aligned with BCHE APOE reference genomic sequences.
Purification of BChE from serum by affinity chromatography on Hupresin® and mass spectrometry
Human BChE was purified from 0.1 mL of serum on 50 ul of Hupresin AC Sepharose (Chemforase, Mont-Saint-Aignan, France). Hupresin AC was equilibrated with 100 mM NaCl, 20 mM TrisCl pH 7.4 and serum proteins were loaded on the 50 µl resin in 1.5 ml filter tubes and washed using 100 mM NaCl, 20 mM TrisCl pH 7.4 buffer. BChE complexes were eluted with 50 µl of 0.5 M trimethylammonium chloride (TMA Cl) in 100 mM NaCl, 20 mM TrisCl pH 7.4 buffer. Eluted proteins were dialyzed and concentrated to 20 µl in Amicon Ultra 10 K Centrifugal Filters. Subsequently, eluted proteins were applied to a gel filtration chromatography column, TSK gel 3000 SWXL (300 × 7.8 mm, Tosoh) equilibrated with 10 mM phosphate buffer pH 7.4; 8 g/L NaCl at a flow rate of 1 ml/min at RT. The column was connected to a Merck Hitachi LaChrom HPLC system equipped with an L-7420 UV-Vis detector. Eluted fractions with BChE activity were collected and concentrated to 20 µl in Amicon Ultra 10 K Centrifugal Filters. BChE activity of each fraction was determined spectrophotometrically by modified Ellman’s method using BTC (S-butyrylthiocholine iodide) as a substrate. The assay was performed in 96-well microtiter plates in a final reaction volume of 200 μl of 100 mM PB buffer (pH 7.4) with a final concentration of 0.5 mM DTNB (5,5′-dithiobis(2-nitrobenzoic acid)) and 5 mM BTC. The absorbance was monitored at 412 nm by repeated measurements at 1 min intervals for 10 minutes by a thermostated microplate reader spectrophotometer (Tecan Infinite M200Pro) at 25 °C. 50 μL of 100 mM ammonium bicarbonate buffer was added to the each protein sample, reduced with 5 mM TCEP for 30 min at 60 °C, blocked with 10 mM MMTS for 15 min at RT and digested overnight, shaking with 10 ng/ml trypsin (CAT NO V5280, Promega) at 37 °C. Finally, to stop digestion trifluoroacetic acid was added at a final concentration of 0.1%. The digest was centrifuged at 4 °C, 14 000 g for 30 min, to pellet solids. The particle-free supernatant was analyzed by LC-MS/MS in the Laboratory of Mass Spectrometry (IBB PAS, Warsaw) using a nanoAcquity UPLC system (Waters) coupled to an Orbitrap Elite mass spectrometer (Thermo Fisher Scientific). The mass spectrometer was operated in the data-dependent MS2 mode, and data were acquired in the m/z range of 300–2000. Peptides were separated by a 180 min linear gradient of 95% solution A (0.1% formic acid in water) to 35% solution B (acetonitrile and 0.1% formic acid). The measurement of each sample was preceded by three washing runs to avoid cross-contamination. The final MS washing run was searched for the presence of cross-contamination between samples. Data were searched with the Max-Quant (Version 1.5.7.4) platform search parameters: match between runs (match time window 0.7 min, alignment time 20 min), enzyme: trypsin/p; specific; max missed 2, minimal peptide length 7aa, variable modification: methionine oxidation, N-term acetylation, fixed: cysteine alkylation, main search peptide tolerance 4.5 ppm, protein FDR 0.01. Data were searched against home made protein database including isoforms of BChE.
Ethical approval and consent to participate
All patients and healthy individuals gave written informed consent for molecular genetic testing. The study was approved by the Independent Bioethics Commission for Research at the Medical University of Gdansk. The experiments were done in accordance with the Helsinki Declaration of 1975.
References
Alzheimer’s Disease International (ADI), London, World Alzheimer Report Available at: https://www.alz.co.uk/research/world-report-2018 (2018).
Scheltens, P. et al. Alzheimer’s disease. Lancet 388, 505–517 (2016).
Beach, T. G., Monsell, S. E., Phillips, L. E. & Kukull, W. Accuracy of the Clinical Diagnosis of Alzheimer Disease at National Institute on Aging Alzheimer Disease Centers, 2005–2010. J. Neuropathol. Exp. Neurol. 71, 266–273 (2012).
Hyman, B. T. & Trojanowski, J. Q. Editorial on Consensus Recommendations for the Postmortem Diagnosis of Alzheimer Disease from the National Institute on Aging and the Reagan Institute Working Group on Diagnostic Criteria for the Neuropathological Assessment of Alzheimer Disease. J. Neuropathol. Exp. Neurol. 56, 1095–1097 (1997).
Johnson, K. A. et al. Appropriate Use Criteria for Amyloid PET: A Report of the Amyloid Imaging Task Force, the Society of Nuclear Medicine and Molecular Imaging, and the Alzheimer’s Association. J. Nucl. Med. 54, 476–490 (2013).
Clark, C. M. et al. Cerebral PET with florbetapir compared with neuropathology at autopsy for detection of neuritic amyloid-β plaques: a prospective cohort study. Lancet Neurol. 11, 669–678 (2012).
Sabri, O. et al. Florbetaben PET imaging to detect amyloid beta plaques in Alzheimer’s disease: Phase 3 study. Alzheimer’s Dement. 11, 964–974 (2015).
Curtis, C. et al. Phase 3 Trial of Flutemetamol Labeled With Radioactive Fluorine 18 Imaging and Neuritic Plaque Density. JAMA Neurol. 72, 287 (2015).
Wang, L. et al. Evaluation of Tau Imaging in Staging Alzheimer Disease and Revealing Interactions Between β-Amyloid and Tauopathy. JAMA Neurol. 73, 1070 (2016).
Hardy, J. The Amyloid Hypothesis of Alzheimer’s Disease: Progress and Problems on the Road to Therapeutics. Science 297, 353–356 (2002).
Liu, C. C., Kanekiyo, T., Xu, H. & Bu, G. Apolipoprotein E and Alzheimer disease: risk, mechanisms and therapy. Nat. Rev. Neurol. 9, 106–118 (2013).
Bekris, L. M., Yu, C.-E., Bird, T. D. & Tsuang, D. W. Review Article: Genetics of Alzheimer Disease. J. Geriatr. Psychiatry Neurol. 23, 213–227 (2010).
Ballatore, C., Lee, V. M. Y. & Trojanowski, J. Q. Tau-mediated neurodegeneration in Alzheimer’s disease and related disorders. Nat. Rev. Neurosci. 8, 663–72 (2007).
Jun, G. Meta-analysis Confirms CR1, CLU, and PICALM as Alzheimer Disease Risk Loci and Reveals Interactions With APOE Genotypes. Arch. Neurol. 67, 1473 (2010).
Lambert, J. C. et al. Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer’s disease. Nat. Genet. 41, 1094–1099 (2009).
Seshadri, S. Genome-wide Analysis of Genetic Loci Associated With Alzheimer Disease. JAMA 303, 1832 (2010).
Corder, E. et al. Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer’s disease in late onset families. Science 261, 921–923 (1993).
Bu, G. Apolipoprotein E and its receptors in Alzheimer’s disease: pathways, pathogenesis and therapy. Nat. Rev. Neurosci. 10, 333–344 (2009).
Mahley, R. W. & Rall, S. C. APOLIPOPROTEIN E: Far More Than a Lipid Transport Protein. Annu. Rev. Genomics Hum. Genet. 1, 507–537 (2000).
Farrer, L. A. Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium. JAMA J. Am. Med. Assoc. 278, 1349–1356 (1997).
Haroutunian, V., Katsel, P. & Schmeidler, J. Transcriptional vulnerability of brain regions in Alzheimer’s disease and dementia. Neurobiol. Aging 30, 561–573 (2009).
Barbash, S. et al. Alzheimer’s brains show inter-related changes in RNA and lipid metabolism. Neurobiol. Dis. 106, 1–13 (2017).
Johnson, G. & Moore, S. W. Why has butyrylcholinesterase been retained? Structural and functional diversification in a duplicated gene. Neurochemistry International 61, 783–797 (2012).
Lockridge, O. Review of human butyrylcholinesterase structure, function, genetic variants, history of use in the clinic, and potential therapeutic uses. Pharmacol. Ther. 148, 34–46 (2015).
Darvesh, S., Hopkins, D. A. & Geula, C. Neurobiology of butyrylcholinesterase. Nat. Rev. Neurosci. 4, 131–138 (2003).
Mesulam, M. M. et al. Acetylcholinesterase knockouts establish central cholinergic pathways and can use butyrylcholinesterase to hydrolyze acetylcholine. Neuroscience 110, 627–639 (2002).
Darvesh, S., Grantham, D. L. & Hopkins, D. A. Distribution of butyrylcholinesterase in the human amygdala and hippocampal formation. J. Comp. Neurol. 393, 374–390 (1998).
Darvesh, S. & Hopkins, D. A. Differential distribution of butyrylcholinesterase and acetylcholinesterase in the human thalamus. J. Comp. Neurol. 463, 25–43 (2003).
Mesulam, M. M. & Geula, C. Butyrylcholinesterase reactivity differentiates the amyloid plaques of aging from those of dementia. Ann. Neurol. 36, 722–727 (1994).
Geula, C. & Mesulam, M. M. Cholinesterases and the Pathology of Alzheimer Disease. Alzheimer Dis. Assoc. Disord. 9, 23–28 (1995).
Gómez-Ramos, P., Bouras, C. & Morán, M. A. Ultrastructural localization of butyrylcholinesterase on neurofibrillary degeneration sites in the brains of aged and Alzheimer’s disease patients. Brain Res. 640, 17–24 (1994).
Guillozet, A. L., Mesulam, M. M., Smiley, J. F. & Mash, D. C. Butyrylcholinesterase in the life cycle of amyloid plaques. Ann. Neurol. 42, 909–918 (1997).
Darvesh, S. Butyrylcholinesterase as a Diagnostic and Therapeutic Target for Alzheimer’s Disease. Curr. Alzheimer Res. 13, 1173–1177 (2016).
Macdonald, I. R. et al. Quantification of Butyrylcholinesterase Activity as a Sensitive and Specific Biomarker of Alzheimer’s Disease. J. Alzheimer’s Dis. 58, 491–505 (2017).
Diamant, S. et al. Butyrylcholinesterase attenuates amyloid fibril formation in vitro. Proc. Natl. Acad. Sci. USA 103, 8628–8633 (2006).
Podoly, E. et al. The Butyrylcholinesterase K Variant Confers Structurally Derived Risks for Alzheimer Pathology. J. Biol. Chem. 284, 17170–17179 (2009).
Lehmann, D. J., Johnston, C. & Smith, A. D. Synergy Between the Genes for Butyrylcholinesterase K Variant and Apolipoprotein E4 in Late-Onset Confirmed Alzheimer’s Disease. Hum. Mol. Genet. 6, 1933–1936 (1997).
Lehmann, D. J., Nagy, Z., Litchfield, S., Cortina Borja, M. & Smith, A. D. Association of butyrylcholinesterase K variant with cholinesterase-positive neuritic plaques in the temporal cortex in late-onset Alzheimer’s disease. Hum. Genet. 106, 447–452 (2000).
McIlroy, S. P. Butyrylcholinesterase K variant is genetically associated with late onset Alzheimer’s disease in Northern Ireland. J. Med. Genet. 37, 182–185 (2000).
Crawford, F. et al. The butyrylcholinesterase gene is neither independently nor synergistically associated with late-onset AD in clinic- and community-based populations. Neurosci. Lett. 249, 115–118 (1998).
Singleton, A. B. et al. No association between the K variant of the butyrylcholinesterase gene and pathologically confirmed Alzheimer’s disease. Hum. Mol. Genet. 7, 937–939 (1998).
Ki, C. S. et al. No association between the genes for butyrylcholinesterase K variant and apolipoprotein E4 in late-onset Alzheimer’s disease. Am. J. Med. Genet. - Neuropsychiatr. Genet. 88, 113–115 (1999).
Lehmann, D. J., Williams, J., Mcbroom, J. & Smith, A. D. Using meta-analysis to explain the diversity of results in genetic studies of late-onset Alzheimer’s disease and to identify high-risk subgroups. Neuroscience 108, 541–554 (2001).
Wang, Z. et al. Butyrylcholinesterase K Variant and Alzheimer’s Disease Risk: A Meta-Analysis. Med. Sci. Monit. 21, 1408–1413 (2015).
Jasiecki, J. et al. Activity and polymorphisms of butyrylcholinesterase in a Polish population. Chem. Biol. Interact. 259, 70–77 (2016).
Zuker, M. Mfold web server for nucleic acid folding and hybridization prediction. Nucleic Acids Res. 31, 3406–3415 (2003).
Sabarinathan, R. et al. The RNAsnp web server: predicting SNP effects on local RNA secondary structure. Nucleic Acids Res. 41, W475–W479 (2013).
Sabarinathan, R. et al. RNAsnp: Efficient Detection of Local RNA Secondary Structure Changes Induced by SNPs. Hum. Mutat. 34, 546–556 (2013).
Kim, J., Basak, J. M. & Holtzman, D. M. The Role of Apolipoprotein E in Alzheimer’s Disease. Neuron 63, 287–303 (2009).
Furtado-Alle, L. et al. Association of variants of the -116 site of the butyrylcholinesterase BCHE gene to enzyme activity and body mass index. Chem. Biol. Interact. 175, 115–118 (2008).
Hinnebusch, A. G., Ivanov, I. P. & Sonenberg, N. Translational control by 5′-untranslated regions of eukaryotic mRNAs. Science 352, 1413–1416 (2016).
Leppek, K., Das, R. & Barna, M. Author Correction: Functional 5′ UTR mRNA structures in eukaryotic translation regulation and how to find them. Nat. Rev. Mol. Cell Biol. 19, 673–673 (2018).
Muckenthaler, M., Gray, N. K. & Hentze, M. W. IRP-1 Binding to Ferritin mRNA Prevents the Recruitment of the Small Ribosomal Subunit by the Cap-Binding Complex eIF4F. Mol. Cell 2, 383–388 (1998).
Meshorer, E. et al. Combinatorial Complexity of 5′ Alternative Acetylcholinesterase Transcripts and Protein Products. J. Biol. Chem. 279, 29740–29751 (2004).
Toiber, D. et al. N-Acetylcholinesterase-Induced Apoptosis in Alzheimer’s Disease. PLoS One 3, e3108 (2008).
Limon-Sztencel, A. et al. The algorithm for Alzheimer risk assessment based on APOE promoter polymorphisms. Alzheimers. Res. Ther. 8, 19 (2016).
De Rijk, P., Wuyts, J. & De Wachter, R. RnaViz 2: an improved representation of RNA secondary structure. Bioinformatics 19, 299–300 (2003).
Salamov, A. A., Nishikawa, T. & Swindells, M. B. Assessing protein coding region integrity in cDNA sequencing projects. Bioinformatics 14, 384–90 (1998).
Acknowledgements
The equipment used was sponsored in part by the Centre for Preclinical Research and Technology (CePT), a project co-sponsored by European Regional Development Fund and Innovative Economy, The National Cohesion Strategy of Poland. Dr. Dominik Cysewski was financed within the TEAM TECH programme of the Foundation for Polish Science co-financed by the European Union under the European Regional Development Fund. (TEAM TECH CORE FACILITY/2016-2/2). This work was supported by the Ministry of Science and Higher Education Republic of Poland from the quality-promoting subsidy under the Leading National Research Centre (KNOW) programme 2012–2017 Faculty of Pharmacy with Subfaculty of Laboratory Medicine [dec. MNiSW-DS-6002-4693-23/WA/12].
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Conceived the study: J.J., B.W. Designed and supervised the experiments: J.J., A.L.-S., M.Ż., M.C., D.C., J.L., B.W. Performed the experiments: J.J., A.L.-S., M.Ż., M.C., D.C., J.L., B.W. Analyzed and interpreted data: J.J., A.L.-S., M.Ż., M.C., D.C., J.L., B.W. Wrote the paper: J.J., B.W. All authors read and approved the final manuscript.
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Jasiecki, J., Limon-Sztencel, A., Żuk, M. et al. Synergy between the alteration in the N-terminal region of butyrylcholinesterase K variant and apolipoprotein E4 in late-onset Alzheimer’s disease. Sci Rep 9, 5223 (2019). https://doi.org/10.1038/s41598-019-41578-3
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DOI: https://doi.org/10.1038/s41598-019-41578-3
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