Copy number variation and mosaicism
- PMID: 19287164
- DOI: 10.1159/000184717
Copy number variation and mosaicism
Abstract
Mosaicism is the presence of cells within an organism that have a different genetic composition despite deriving from a single zygote. The consequence of this depends on the number and type of cells that are affected as well as the specific DNA involved. There are several diseases where mosaicism is known to occur, but the currently observed frequency is presumably an underestimation due to the difficulty of detecting changes in only a percentage of cells. Recent advances in technology have provided a greater insight into the frequency and mechanisms of mosaicism in all forms. This review will cover the different techniques that can be used for detecting copy number variation (CNV) in mosaic form, and describe some of the insights that different diseases have given on the true frequencies and mechanisms responsible for somatic rearrangements. It will conclude with a discussion of the implications of the recent description of CNV in identical twins, and what remains to be elucidated in the world of mosaic CNV.
Copyright 2009 S. Karger AG, Basel.
Similar articles
-
Expression divergence and copy number variation in the human genome.Cytogenet Genome Res. 2008;123(1-4):278-82. doi: 10.1159/000184718. Epub 2009 Mar 11. Cytogenet Genome Res. 2008. PMID: 19287165
-
Copy number variants, diseases and gene expression.Hum Mol Genet. 2009 Apr 15;18(R1):R1-8. doi: 10.1093/hmg/ddp011. Hum Mol Genet. 2009. PMID: 19297395 Review.
-
Somatic mosaicism for copy number variation in differentiated human tissues.Hum Mutat. 2008 Sep;29(9):1118-24. doi: 10.1002/humu.20815. Hum Mutat. 2008. PMID: 18570184
-
Copy number variation of beta-defensins and relevance to disease.Cytogenet Genome Res. 2008;123(1-4):148-55. doi: 10.1159/000184702. Epub 2009 Mar 11. Cytogenet Genome Res. 2008. PMID: 19287149 Review.
-
Copy number alterations and copy number variation in cancer: close encounters of the bad kind.Cytogenet Genome Res. 2008;123(1-4):176-82. doi: 10.1159/000184706. Epub 2009 Mar 11. Cytogenet Genome Res. 2008. PMID: 19287153 Review.
Cited by
-
Quantitative assessment of low-level parental mosaicism of SNVs and CNVs in Waardenburg syndrome.Hum Genet. 2023 Mar;142(3):419-430. doi: 10.1007/s00439-022-02517-x. Epub 2022 Dec 28. Hum Genet. 2023. PMID: 36576601
-
Detection of Mosaic Variants in Mothers of MPS II Patients by Next Generation Sequencing.Front Mol Biosci. 2021 Nov 5;8:789350. doi: 10.3389/fmolb.2021.789350. eCollection 2021. Front Mol Biosci. 2021. PMID: 34805285 Free PMC article.
-
Incident disease associations with mosaic chromosomal alterations on autosomes, X and Y chromosomes: insights from a phenome-wide association study in the UK Biobank.Cell Biosci. 2021 Jul 23;11(1):143. doi: 10.1186/s13578-021-00651-z. Cell Biosci. 2021. PMID: 34301302 Free PMC article.
-
MONTAGE: a new tool for high-throughput detection of mosaic copy number variation.BMC Genomics. 2021 Feb 24;22(1):133. doi: 10.1186/s12864-021-07395-7. BMC Genomics. 2021. PMID: 33627065 Free PMC article.
-
Parental somatic mosaicism for CNV deletions - A need for more sensitive and precise detection methods in clinical diagnostics settings.Genomics. 2020 Sep;112(5):2937-2941. doi: 10.1016/j.ygeno.2020.05.003. Epub 2020 May 6. Genomics. 2020. PMID: 32387503 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
