Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3
-
Published:2019-10-29
Issue:1
Volume:10
Page:
-
ISSN:2041-1723
-
Container-title:Nature Communications
-
language:en
-
Short-container-title:Nat Commun
Author:
Florian Rahel T., , Kraft FlorianORCID, Leitão ElsaORCID, Kaya Sabine, Klebe Stephan, Magnin Eloi, van Rootselaar Anne-FleurORCID, Buratti JulienORCID, Kühnel Theresa, Schröder Christopher, Giesselmann Sebastian, Tschernoster Nikolai, Altmueller Janine, Lamiral AnaideORCID, Keren Boris, Nava Caroline, Bouteiller Delphine, Forlani Sylvie, Jornea Ludmila, Kubica Regina, Ye TaoORCID, Plassard DamienORCID, Jost Bernard, Meyer Vincent, Deleuze Jean-François, Delpu Yannick, Avarello Mario D. M., Vijfhuizen Lisanne S., Rudolf GabrielleORCID, Hirsch Edouard, Kroes Thessa, Reif Philipp S., Rosenow Felix, Ganos Christos, Vidailhet Marie, Thivard Lionel, Mathieu Alexandre, Bourgeron Thomas, Kurth IngoORCID, Rafehi Haloom, Steenpass Laura, Horsthemke BernhardORCID, LeGuern Eric, Klein Karl MartinORCID, Labauge PierreORCID, Bennett Mark F.ORCID, Bahlo MelanieORCID, Gecz JozefORCID, Corbett Mark A.ORCID, Tijssen Marina A. J.ORCID, van den Maagdenberg Arn M. J. M., Depienne ChristelORCID
Abstract
Abstract
Familial Adult Myoclonic Epilepsy (FAME) is a genetically heterogeneous disorder characterized by cortical tremor and seizures. Intronic TTTTA/TTTCA repeat expansions in SAMD12 (FAME1) are the main cause of FAME in Asia. Using genome sequencing and repeat-primed PCR, we identify another site of this repeat expansion, in MARCH6 (FAME3) in four European families. Analysis of single DNA molecules with nanopore sequencing and molecular combing show that expansions range from 3.3 to 14 kb on average. However, we observe considerable variability in expansion length and structure, supporting the existence of multiple expansion configurations in blood cells and fibroblasts of the same individual. Moreover, the largest expansions are associated with micro-rearrangements occurring near the expansion in 20% of cells. This study provides further evidence that FAME is caused by intronic TTTTA/TTTCA expansions in distinct genes and reveals that expansions exhibit an unexpectedly high somatic instability that can ultimately result in genomic rearrangements.
Funder
Fondations Maladies rares University Hospital Essen
Publisher
Springer Science and Business Media LLC
Subject
General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry
Reference46 articles.
1. van den Ende, T., Sharifi, S., van der Salm, S. M. A. & van Rootselaar, A. F. Familial cortical myoclonic tremor and epilepsy, an enigmatic disorder: from phenotypes to pathophysiology and genetics. A systematic review. Tremor Other Hyperkinet Mov. 8, 503 (2018). 2. Striano, P. & Zara, F. Autosomal dominant cortical tremor, myoclonus and epilepsy. Epileptic Disord. 18, 139–144 (2016). 3. van Rootselaar, A. F. et al. Familial cortical myoclonic tremor with epilepsy: a single syndromic classification for a group of pedigrees bearing common features. Mov. Disord. 20, 665–673 (2005). 4. Mikami, M. et al. Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23.3-q24.1. Am. J. Hum. Genet. 65, 745–751 (1999). 5. Guerrini, R. et al. Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures: a newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2. Brain 124, 2459–2475 (2001).
Cited by
117 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|