| Autor: |
Backlund, Michael P., Repo, Pauliina, Kangas, Harri, Donner, Kati, Sankila, Eeva-Marja, Krootila, Julia, Paavo, Maarjaliis, Wartiovaara, Kirmo, Kivelä, Tero T., Turunen, Joni A. |
| Zdroj: |
Human Mutation; 2/9/2024, Vol. 2024, p1-10, 10p |
| Abstrakt: |
Retinitis pigmentosa (RP) is a group of inherited degenerative retinal disorders affecting more than 1.5 million people worldwide. For 30-50% of individuals with RP, the genetic cause remains unresolved by current clinical diagnostic gene panels. It is likely explained by variants in novel RP-associated genes or noncoding regulatory regions, or by complex genetic alterations such as large structural variants. Recent developments in long-read sequencing techniques have opened an opportunity for efficient analysis of complex genetic variants. We analysed a Finnish family with dominantly inherited RP affecting six individuals in three generations. Two affected individuals underwent a comprehensive clinical examination in combination with a clinical diagnostic gene panel, followed by whole exome sequencing in our laboratory. They exhibited typical signs of RP, yet initial sequence analysis found no causative variants. Reanalysis of the sequencing data detected a LINE-1 (L1) retrotransposon insertion of unknown size in exon 4 of the RP1 axonemal microtubule-associated (RP1) gene. The large chimeric L1 insertion that segregated with the disease was further characterised using targeted adaptive nanopore sequencing of RP1, allowing us to identify a 5.6 kb L1 transposable element insertion in RP1 as the cause of RP in this family with dominantly inherited RP. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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