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- W4387364797 abstract "Certain classes of genetic variation still escape detection in clinical sequencing analysis. One such class is retroelement insertion, which has been reported as a cause of Mendelian diseases and may offer unique therapeutic implications. Here, we conducted retroelement profiling on whole-genome sequencing data from a cohort of 237 individuals with ataxia telangiectasia (A-T). We found 15 individuals carrying retroelement insertions in ATM, all but one of which integrated in noncoding regions. Systematic functional characterization via RNA sequencing, RT-PCR, and/or minigene splicing assays showed that 12 out of 14 intronic insertions led or contributed to ATM loss of function by exon skipping or activating cryptic splice sites. We also present proof-of-concept antisense oligonucleotides that suppress cryptic exonization caused by a deep intronic retroelement insertion. These results provide an initial systematic estimate of the contribution of retroelements to the genetic architecture of recessive Mendelian disorders as ∼2.1%–5.5%. Our study highlights the importance of retroelement insertions as causal variants and therapeutic targets in genetic diseases." @default.
- W4387364797 created "2023-10-06" @default.
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- W4387364797 date "2023-10-01" @default.
- W4387364797 modified "2023-10-08" @default.
- W4387364797 title "Contribution and therapeutic implications of retroelement insertions in ataxia telangiectasia" @default.
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- W4387364797 doi "https://doi.org/10.1016/j.ajhg.2023.09.008" @default.
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