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Transcriptome-wide piRNA profiling in human brains of Alzheimer's disease
Open accessAbstract
Discovered in the brains of multiple animal species, piRNAs may contribute to the pathogenesis of neuropsychiatric illnesses. The present study aimed to identify brain piRNAs across transcriptome that are associated with Alzheimer's disease (AD). Prefrontal cortical tissues of 6 AD cases and 6 controls were examined for piRNA expression levels using an Arraystar HG19 piRNA array (containing 23,677 piRNAs) and genotyped for 17 genome-wide significant and replicated risk SNPs. We examined whether piRNAs are expressed differently between AD cases and controls and explored the potential regulatory effects of risk SNPs on piRNA expression levels. We identified a total of 9453 piRNAs in human brains, with 103 nominally (p < 0.05) differentially (>1.5 fold) expressed in AD cases versus controls and most of the 103 piRNAs nominally correlated with genome-wide significant risk SNPs. We conclude that piRNAs are abundant in human brains and may represent risk biomarkers of AD.
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“Since flamenco is known to encode a major piRNA cluster3,26, and piRNAs have recently been reported to be differentially expressed in the human Alzheimer’s disease brain27,28, we next determined if piRNAs are involved in dysfunctional transposable element control in the tauopathy brain.”
From Pathogenic tau-induced piRNA depletion promotes neuronal death through transposable element dysregulation in neurodegenerative tauopathies (2018) · cites this paper as [28]
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Cites
Meta-Analysis of 74,046 Individuals Identifies 11 New Susceptibility Loci for Alzheimer’s Disease
(EADI), E. A. D. I., Lambert, J.-C., (GERAD), G. A. E. R. I. A. D., Alzheimer's Disease Genetic Consortium (ADGC), (CHARGE), C. F. H. A. A. R. I. G. E., Ibrahim-Verbaas, C. A., Harold, D., Naj, A. C., Sims, R., Bellenguez, C., et al. (2013) · Nature Genetics · doi:10.1038/ng.2802 · Cited by 4,336
Harold, D., Abraham, R., Hollingworth, P., Sims, R., Gerrish, A., Hamshere, M. L., Pahwa, J. S., Moskvina, V., Dowzell, K., Williams, A., et al. (2009) · Nature Genetics · doi:10.1038/ng.440 · Cited by 3,326
Discrete Small RNA-Generating Loci as Master Regulators of Transposon Activity in Drosophila
Brennecke, J., Aravin, A. A., Stark, A., Dus, M., Kellis, M., Sachidanandam, R., & Hannon, G. J. (2007) · Cell · doi:10.1016/j.cell.2007.01.043 · Cited by 2,524
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
the European Alzheimer's Disease Initiative Investigators, Lambert, J.-C., Heath, S., Even, G., Campion, D., Sleegers, K., Hiltunen, M., Combarros, O., Zelenika, D., Bullido, M. J., et al. (2009) · Nature Genetics · doi:10.1038/ng.439 · Cited by 2,234
Initiative, T. A. D. N., Hollingworth, P., CHARGE consortium, EADI1 consortium, Harold, D., Sims, R., Gerrish, A., Lambert, J.-C., Carrasquillo, M. M., Abraham, R., et al. (2011) · Nature Genetics · doi:10.1038/ng.803 · Cited by 1,997
Naj, A. C., Jun, G., Beecham, G. W., Wang, L.-S., Vardarajan, B. N., Buros, J., Gallins, P. J., Buxbaum, J. D., Jarvik, G. P., Crane, P. K., et al. (2011) · Nature Genetics · doi:10.1038/ng.801 · Cited by 1,901
A germline-specific class of small RNAs binds mammalian Piwi proteins
Girard, A., Sachidanandam, R., Hannon, G. J., & Carmell, M. A. (2006) · Nature · doi:10.1038/nature04917 · Cited by 1,762
A novel class of small RNAs bind to MILI protein in mouse testes
Aravin, A., Gaidatzis, D., Pfeffer, S., Lagos-Quintana, M., Landgraf, P., Iovino, N., Morris, P., Brownstein, M. J., Kuramochi-Miyagawa, S., Nakano, T., et al. (2006) · Nature · doi:10.1038/nature04916 · Cited by 1,516
Small non-coding RNAs in animal development
Stefani, G., & Slack, F. J. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2347 · Cited by 1,390
Genome-wide Analysis of Genetic Loci Associated With Alzheimer Disease
Seshadri, S. (2010) · JAMA · doi:10.1001/jama.2010.574 · Cited by 1,219
A Slicer-Mediated Mechanism for Repeat-Associated siRNA 5' End Formation in Drosophila
Gunawardane, L. S., Saito, K., Nishida, K. M., Miyoshi, K., Kawamura, Y., Nagami, T., Siomi, H., & Siomi, M. C. (2007) · Science · doi:10.1126/science.1140494 · Cited by 1,173
Characterization of the piRNA Complex from Rat Testes
Lau, N. C., Seto, A. G., Kim, J., Kuramochi‐Miyagawa, S., Nakano, T., Bartel, D. P., & Kingston, R. E. (2006) · Science · doi:10.1126/science.1130164 · Cited by 987
Somatic mosaicism in neuronal precursor cells mediated by L1 retrotransposition
Muotri, A. R., Chu, V. T., Marchetto, M. C. N., Deng, W., Moran, J. V., & Gage, F. H. (2005) · Nature · doi:10.1038/nature03663 · Cited by 942
A novel class of small RNAs in mouse spermatogenic cellsPreprint
Grivna, S. T., Beyret, E., Wang, Z., & Lin, H. (2006) · Genes & Development · doi:10.1101/gad.1434406 · Cited by 874
L1 retrotransposition in human neural progenitor cells
Coufal, N. G., Garcia-Perez, J. L., Peng, G. E., Yeo, G. W., Mu, Y., Lovci, M. T., Morell, M., O’Shea, K. S., Moran, J. V., & Gage, F. H. (2009) · Nature · doi:10.1038/nature08248 · Cited by 814
Characterization of the piRNA Complex from Rat Testes
Iseni, F., Barge, A., Baudin, F., Blondel, D., Ruigrok, R. W. H., Schoehn, G., & Mavrakis, M. (2006) · Cited by 714
A Role for Neuronal piRNAs in the Epigenetic Control of Memory-Related Synaptic Plasticity
Rajasethupathy, P., Antonov, I., Sheridan, R., Frey, S., Sander, C., Tuschl, T., & Kandel, E. R. (2012) · Cell · doi:10.1016/j.cell.2012.02.057 · Cited by 582
Coon, K. D., Myers, A. J., Craig, D. W., Webster, J. A., Pearson, J. V., Lince, D. H., Zismann, V. L., Beach, T. G., Leung, D., Bryden, L., et al. (2007) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.v68n0419 · Cited by 569
One Loop to Rule Them All: The Ping-Pong Cycle and piRNA-Guided Silencing
Czech, B., & Hannon, G. J. (2016) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2015.12.008 · Cited by 513
Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease
Li, H., Wetten, S., Li, L., St. Jean, P. L., Upmanyu, R., Surh, L., Hosford, D., Barnes, M. R., Briley, J. D., Borrie, M., et al. (2008) · Archives of Neurology · doi:10.1001/archneurol.2007.3 · Cited by 499
PIWI proteins and PIWI-interacting RNAs in the soma
Ross, R. J., Weiner, M. M., & Lin, H. (2014) · Nature · doi:10.1038/nature12987 · Cited by 436
piRNAs: from biogenesis to function
Weick, E., & Miska, E. A. (2014) · Development · doi:10.1242/dev.094037 · Cited by 416
Shen, L., Kim, S., Risacher, S. L., Nho, K. T., Swaminathan, S., West, J. D., Foroud, T., Pankratz, N., Moore, J. H., Sloan, C., et al. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.01.042 · Cited by 383
piRNABank: a web resource on classified and clustered Piwi-interacting RNAs
Lakshmi, S. S., & Agrawal, S. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm696 · Cited by 377
A novel Alzheimer disease locus located near the gene encoding tau protein
Jun, G., Ibrahim-Verbaas, C. A., Vronskaya, M., Lambert, J.-C., Chung, J., Naj, A. C., Kunkle, B. W., Wang, L.-S., Bis, J. C., Bellenguez, C., et al. (2016) · Molecular Psychiatry · doi:10.1038/mp.2015.23 · Cited by 297
Identification of piRNAs in the central nervous system
Lee, E. J., Banerjee, S., Zhou, H., Jammalamadaka, A., Arcila, M., Manjunath, B. S., & Kosik, K. S. (2011) · RNA · doi:10.1261/rna.2565011 · Cited by 289
A Comprehensive Genetic Association Study of Alzheimer Disease in African Americans
Logue, M. W. (2011) · Archives of Neurology · doi:10.1001/archneurol.2011.646 · Cited by 250
Transposition-Driven Genomic Heterogeneity in the Drosophila Brain
Perrat, P. N., Dasgupta, S., Wang, J., Theurkauf, W. E., Weng, Z., Rosbash, M., & Waddell, S. (2013) · Science · doi:10.1126/science.1231965 · Cited by 245
Genome-wide association study of Alzheimer's disease
Kamboh, M. I., Demirci, F. Y., Wang, X., Minster, R. L., Carrasquillo, M. M., Pankratz, V. S., Younkin, S. G., Saykin, A. J., Initiative, A. D. N., Jun, G., et al. (2012) · Translational Psychiatry · doi:10.1038/tp.2012.45 · Cited by 242
Widespread expression of piRNA-like molecules in somatic tissues
Zheng, Y., Hu, H., Jiang, X., Maierhofer, V., Neb, E., He, L., Hu, Y., Hu, H., Li, N., Chen, W., et al. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr298 · Cited by 220
Genome-wide association study of CSF biomarkers Aβ 1-42 , t-tau, and p-tau 181p in the ADNI cohort
Kim, S., Swaminathan, S., Shen, L., Risacher, S. L., Nho, K., Foroud, T., Shaw, L. M., Trojanowski, J. Q., Potkin, S. G., Huentelman, M. J., et al. (2011) · Neurology · doi:10.1212/wnl.0b013e318204a397 · Cited by 206
Ramanan, V. K., Risacher, S. L., Nho, K. T., Kim, S., Swaminathan, S., Shen, L., Foroud, T., Hakonarson, H. H., Huentelman, M. J., Aisen, P. S. S., et al. (2013) · Molecular Psychiatry · doi:10.1038/mp.2013.19 · Cited by 200
Miyashita, A., Koike, A., Jun, G., Wang, L.-S., Takahashi, S., Matsubara, E., Kawarabayashi, T., Shoji, M., Tomita, N., Arai, H., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058618 · Cited by 196
A genome-wide association study for late-onset Alzheimer's disease using DNA pooling
Abraham, R., Moskvina, V., Sims, R., Hollingworth, P., Morgan, A., Georgieva, L., Dowzell, K., Cichon, S., Hillmer, A. M., O'Donovan, M. C., et al. (2008) · BMC Medical Genomics · doi:10.1186/1755-8794-1-44 · Cited by 195
Mice that lack astrotactin have slowed neuronal migration
Adams, N. C., Tomoda, T., Cooper, M. A., Dietz, G. P. H., & Hatten, M. E. (2002) · Development · doi:10.1242/dev.129.4.965 · Cited by 182
Hu, X., Pickering, E. H., Liu, Y. C., Hall, S., Fournier, H., Katz, E., DeChairo, B. M., John, S., Eerdewegh, P. V., Soares, H. D., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016616 · Cited by 167
Naj, A. C., Beecham, G. W., Martin, E. R., Gallins, P. J., Powell, E. H., Konidari, I., Whitehead, P. L., Cai, G., Haroutunian, V. H., Scott, W. K., et al. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001130 · Cited by 148
Beyond transposons: the epigenetic and somatic functions of the Piwi-piRNA mechanism
Peng, J. C., & Lin, H. (2013) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2013.01.010 · Cited by 146
Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease
Heinzen, E. L., Need, A. C., Hayden, K. M., Chiba‐Falek, O., Roses, A. D., Strittmatter, W. J., Burke, J. R., Hulette, C. M., Welsh-Bohmer, K. A., & Goldstein, D. B. (2010) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-1212 · Cited by 131
Roy, J., Sarkar, A., Parida, S., Ghosh, Z., & Mallick, B. (2017) · Molecular BioSystems · doi:10.1039/c6mb00699j · Cited by 130
Examination of the current top candidate genes for AD in a genome-wide association study
Feulner, T. M., Laws, S. M., Friedrich, P., Wagenpfeil, S., Wurst, S. H. R., Riehle, C., Kuhn, K. A., Krawczak, M., Schreiber, S., Nikolaus, S., et al. (2010) · Molecular Psychiatry · doi:10.1038/mp.2008.141 · Cited by 128
Hébert, S. S., Wang, W.-X., Zhu, Q., & Nelson, P. T. (2013) · Journal of Alzheimer's Disease · doi:10.3233/jad-122350 · Cited by 125
Untangling the web: The diverse functions of the PIWI/piRNA pathway
Mani, S. R., & Juliano, C. E. (2013) · Molecular Reproduction and Development · doi:10.1002/mrd.22195 · Cited by 118
Meda, S. A., Narayanan, B., Liu, J., Perrone-Bizzozero, N. I., Stevens, M. C., Calhoun, V. D., Glahn, D. C., Shen, L., Risacher, S. L., Saykin, A. J., et al. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.12.076 · Cited by 115
Non-coding RNA interact to regulate neuronal development and function
Iyengar, B. R., Choudhary, A., Sarangdhar, M. A., Venkatesh, K. V., Gadgil, C. J., & Pillai, B. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00047 · Cited by 115
Altered Expression of PIWI RNA in the Rat Brain After Transient Focal Ischemia
Dharap, A. A., Nakka, V. P., & Vemuganti, R. (2011) · Stroke · doi:10.1161/strokeaha.110.598391 · Cited by 109
Antúnez, C., Boada, M., González‐Pérez, A., Gayán, J., Ramírez‐Lorca, R., Marín, J., Hernández, I., Moreno‐Rey, C., Morón, F. J., López‐Arrieta, J., et al. (2011) · Genome Medicine · doi:10.1186/gm249 · Cited by 100
Genome-wide association analysis of age-at-onset in Alzheimer's disease
Kamboh, M. I., Barmada, M. M., Demirci, F. Y., Minster, R. L., Carrasquillo, M. M., Pankratz, V. S., Younkin, S. G., Saykin, A. J., Initiative, T. A. D. N., Sweet, R. A., et al. (2012) · Molecular Psychiatry · doi:10.1038/mp.2011.135 · Cited by 100
ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology
Nelson, P. T., Estus, S., Abner, E. L., Parikh, I. J., Malik, M., Neltner, J. H., Ighodaro, E. T., Wang, W., Wilfred, B. R., Wang, L., et al. (2014) · Acta Neuropathologica · doi:10.1007/s00401-014-1282-2 · Cited by 92
Sorl1 as an Alzheimer’s Disease Predisposition Gene?
Webster, J., Myers, A., Pearson, J. V., Craig, D. W., Hu‐Lince, D., Coon, K. D., Zismann, V., Beach, T. G., Leung, D. G., Bryden, L., et al. (2007) · Neurodegenerative Diseases · doi:10.1159/000110789 · Cited by 74
Transposon Silencing by piRNAs
Halić, M., & Moazed, D. (2009) · Cell · doi:10.1016/j.cell.2009.08.030 · Cited by 68
Multiple loci influencing hippocampal degeneration identified by genome scan
Melville, S. A., Buros, J. L., Parrado, A., Vardarajan, B. N., Logue, M. W., Shen, L., Risacher, S. L., Kim, S., Jun, G., DeCarli, C. S., et al. (2012) · Annals of Neurology · doi:10.1002/ana.23644 · Cited by 67
Pérez‐Palma, E., Bustos, B. I., Villamán, C., Alarcón, M. A., Ávila, M. E., Ugarte, G. D., Reyes, A. E., Opazo, C., Ferrari, G. V. D., Initiative, T. A. D. N., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0095413 · Cited by 64
piRNAs and Their Functions in the Brain
Zuo, L., Wang, Z., Tan, Y., Chen, X., & Luο, X. (2016) · International Journal of Human Genetics · doi:10.1080/09723757.2016.11886278 · Cited by 61
Self-citationMaternally deposited germline piRNAs silence the tirant retrotransposon in somatic cells
Akkouche, A., Grentzinger, T., Fablet, M., Armenise, C., Burlet, N., Braman, V., Chambeyron, S., & Vieira, C. P. (2013) · EMBO Reports · doi:10.1038/embor.2013.38 · Cited by 57
Variation at APOE and STH loci and Alzheimer's disease
Zuo, L., van Dyck, C. H., Luο, X., Kranzler, H. R., Yang, B., & Gelernter, J. E. (2006) · Behavioral and Brain Functions · doi:10.1186/1744-9081-2-13 · Cited by 51
Self-citationRamirez, A., van der Flier, W. M., Herold, C., Ramonet, D., Heilmann, S., Lewczuk, P., Popp, J., Lacour, A., Drichel, D., Louwersheimer, E., et al. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu372 · Cited by 49
Long noncoding RNAs in psychiatric disorders
Zuo, L., Tan, Y., Wang, Z., Wang, K.-S., Zhang, X., Chen, X., Li, C. R., Wang, T., & Luο, X. (2016) · Psychiatric Genetics · doi:10.1097/ypg.0000000000000129 · Cited by 49
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Metadata
- Authors
- Qiu, W., Guo, X., Lin, X., Yang, Q., Zhang, W., Zhang, Y., Zuo, L., Zhu, Y., Li, C.-S. R., Ma, C., & Luo, X.
- Affiliations
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
- Shanghai Mental Health Center (CN)
- Fujian Medical University (CN)
- Tianjin Anding Hospital (CN)
- Yale University (US)
- Corresponding author
- Ma, Chao
- ORCID
- Venue
- Neurobiology of Aging
- Publisher
- Elsevier BV
- Published
- 2017-09
- Volume
- 57
- Pages
- 170-177
- ISSN
- 0197-4580 (ISSN-L)
- PMC
- PMC5542056
- OpenAlex
- W2620580060
- Cited by
- 105
- References
- 58
- Citations by year
- 2026: 5 · 2025: 17 · 2024: 11 · 2023: 14 · 2022: 14 · 2021: 14 · 2020: 10 · 2019: 12 · 2018: 7 · 2017: 1
- FWCI
- 6.07
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Neurobiology of Aging (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- China Human Brain Bank Consortium
- National Natural Science Foundation of China (81373150, 81271239, 81202371, 81201057, 81171091, 91632113)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer-related molecular mechanisms research
- Keywords
- piRNA, Alzheimer's disease, prefrontal cortex, risk biomarkers, gene expression profiling
- MeSH terms
- Alzheimer Disease, Brain, Humans, Risk, Biomarkers, Gene Expression, Polymorphism, Single Nucleotide, RNA, Small Interfering, Microarray Analysis, Genome-Wide Association Study, Transcriptome
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