The DOI matches its Crossref record; 155 of the 157 references it cites were found in a registry or an index.
Repeat instability: mechanisms of dynamic mutations
Abstract
Disease-causing repeat instability is an important and unique form of mutation that is linked to more than 40 neurological, neurodegenerative and neuromuscular disorders. DNA repeat expansion mutations are dynamic and ongoing within tissues and across generations. The patterns of inherited and tissue-specific instability are determined by both gene-specific cis-elements and trans-acting DNA metabolic proteins. Repeat instability probably involves the formation of unusual DNA structures during DNA replication, repair and recombination. Experimental advances towards explaining the mechanisms of repeat instability have broadened our understanding of this mutational process. They have revealed surprising ways in which metabolic pathways can drive or protect from repeat instability.
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“By a process that is poorly understood, a small number of specific normal-length STRs undergo somatic or germline expansion and transition to intermediate, pre-mutation, and mutation (affected) repeat unit tract lengths (Mirkin, 2007; Pearson et al., 2005).”
From Disease-Associated Short Tandem Repeats Co-localize with Chromatin Domain Boundaries (2018) · cites this paper as Pearson et al., 2005
In the citing paper
“Notably, a large number of daSTRs known to undergo paternal instability (McMurray, 2010; Pearson et al., 2005) co-localized to boundaries in mouse sperm and not in mouse oocytes (Du et al., 2017), suggesting that daSTRs could be at boundaries when germ line expansion takes place (Figure S3).”
From Disease-Associated Short Tandem Repeats Co-localize with Chromatin Domain Boundaries (2018) · cites this paper as Pearson et al., 2005
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Oxidative DNA Damage Modulates Trinucleotide Repeat Instability Via DNA Base Excision Repair
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“TNR expansion is associated with more than 40 neurodegenerative diseases such as Huntington’s disease, myotonic dystrophy, fragile X syndrome, and Friedreich’s ataxia (74,253,258).”
BackgroundInfluentialGenetics of Familial and Idiopathic Pulmonary Arterial Hypertension
Austin, E. D., Loyd, J. E., & PhillipsIII, J. A. (2010) · Springer eBooks · doi:10.1007/978-0-387-87429-6_69
“Trinucleotide repeat expansion was discovered for fragile X syndrome in the early 1990s, and this mechanism is known to be the basis for more than 40 different neurologic diseases, most of which exhibit genetic anticipation [ 20 ].”
BackgroundSales, L. M. (2007) · TDX (Tesis Doctorals en Xarxa)
A two-pronged model of polyglutamine disease
Skipper, M. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2366
Casci, T. (2009) · Nature Reviews Genetics · doi:10.1038/nrg2655
Fragile X for the obstetrician and gynecologist
Seungdamrong, A., & McGovern, P. G. (2008) · Expert Review of Obstetrics & Gynecology · doi:10.1586/17474108.3.6.761
Burne, T. H. J., Eyles, D. W., & McGrath, J. J. (2008) · Behavioral and Brain Sciences · doi:10.1017/s0140525x08004251
Pathirana, E., Takemon, Y., Takayanagi, A., Abbas, E. M., Tanida, K., Shimizu, N., & Kato, M. (2012) · Journal of Advanced Science · doi:10.2978/jsas.24.1
Chen, R., HOU, M. T., CHANG, N. W., Chen, Y. T., & Tsai, J. J. P. (2011) · International Journal of Artificial Intelligence Tools · doi:10.1142/s0218213011000073
Limited variability of CTG/CAG repeats in Lycopersicon nuclear DNA
Dimitrova, D., Georgiev, O., Valkova, C., Atanassova, B. Y., & Karagyozov, L. K. (2008) · Biologia Plantarum · doi:10.1007/s10535-008-0031-6
Freschi, V., Bogliolo, A., & Liso, A. (2012) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2012.09.001
Danielak-Czech, B., Kozubska-Sobocińska, A., Babicz, M., Kruczek, K., & Rejduch, B. (2013) · Annales Universitatis Mariae Curie-Skłodowska. Sectio EE: Zootechnica
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Drosophila as a Model for Neurodegenerative Disease: Roles of RNA Pathways in Pathogenesis
Bonini, N. M. (2009) · Research and perspectives in neurosciences · doi:10.1007/978-3-642-04298-0_9
“The polyglutamine diseases are a subclass of a much larger set of human diseases known as the trinucleotide repeat diseases, all due to small repeat expansions, typically of triplet repeats within genes (Pearson et al. 2005).”
BackgroundThe Role of XPG in Processing (CAG) n /(CTG) n
Hou, C., Zhang, T. Z., Tian, L., Huang, J., Gu, L., & Li, G. (2011)
Functional analysis of Drosophila melanogaster linker histone dH1
Vujatovic, O. (2012) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
Mrkonjic, M. (2009) · TSpace (University of Toronto)
Análise de repetições em dados biológicos
Lousado, J. P., & Oliveira, J. L. (2010) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
Morales, H. F., & Vásquez, M. (2012)
Petit, A. (2015) · TDX (Tesis Doctorals en Xarxa)
Metadata
- Authors
- Pearson, C. E., Edamura, K. N., & Cleary, J. D.
- Affiliations
- University of Toronto (CA)
- Hospital for Sick Children (CA)
- Corresponding author
- Pearson, Christopher E.
- Venue
- Nature Reviews Genetics
- Published
- 2005-10
- Volume
- 6
- Issue
- 10
- Pages
- 729-742
- ISSN
- 1471-0056 (ISSN-L)
- 1471-0064
- OpenAlex
- W2087505473
- Cited by
- 924
- References
- 157
- Citations by year
- 2026: 13 · 2025: 23 · 2024: 45 · 2023: 29 · 2022: 25 · 2021: 54 · 2020: 27 · 2019: 38 · 2018: 53 · 2017: 45 · 2016: 58 · 2015: 41 · 2014: 55 · 2013: 46 · 2012: 56
- FWCI
- 3.89
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Genetics (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Genetic Neurodegenerative Diseases
- Health Sciences › Medicine › Pathology and Forensic Medicine › Genetic factors in colorectal cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Keywords
- repeat instability, dynamic mutation, trinucleotide repeat disorders, neurodegenerative diseases, neuromuscular disorders, cis-regulatory elements, trans-acting proteins, DNA replication, DNA repair, DNA recombination, DNA secondary structure
- MeSH terms
- DNA Repair, DNA Replication, Humans, Models, Genetic, Mutation, Recombination, Genetic, Trinucleotide Repeat Expansion, Heredodegenerative Disorders, Nervous System, DNA Repeat Expansion, Genomic Instability
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