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• W4280553610 abstract "ABSTRACT Myotonic dystrophy type 2 (DM2) is caused by CCTG repeat expansions in the CNBP gene, comprising 75 to >11,000 units and featuring extensive mosaicism, making it challenging to sequence fully-expanded alleles. To overcome these limitations, we used PCR-free Cas9-mediated nanopore sequencing to characterize CNBP repeat expansions at the single-nucleotide level in nine DM2 patients. The length of normal and expanded alleles can be assessed precisely using this strategy, agreeing with traditional methods, and revealing the degree of mosaicism. We also sequenced an entire ∼50-kbp expansion, which has not been achieved previously for DM2 or any other repeat-expansion disorders. Our approach precisely counted the repeats and identified the repeat pattern for both short interrupted and uninterrupted alleles. Interestingly, in the expanded alleles, only two DM2 samples featured the expected pure CCTG repeat pattern, while the other seven presented also TCTG blocks at the 3′ end, which have not been reported before in DM2 patients, but confirmed hereby with orthogonal methods. The demonstrated approach simultaneously determines repeat length, structure/motif and the extent of somatic mosaicism, promising to improve the molecular diagnosis of DM2 and achieve more accurate genotype– phenotype correlations for the better stratification of DM2 patients in clinical trials." @default.
• W4280553610 created "2022-05-22" @default.
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• W4280553610 date "2022-05-12" @default.
• W4280553610 modified "2023-10-13" @default.
• W4280553610 title "Characterization of full-length <i>CNBP</i> expanded alleles in myotonic dystrophy type 2 patients by Cas9-mediated enrichment and nanopore sequencing" @default.
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• W4280553610 doi "https://doi.org/10.1101/2022.05.12.491603" @default.
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