Mobile Element Insertion in the APOB Exon 3 Coding Sequence: A New Challenge in Hypobetalipoproteinemia Diagnosis

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Surles, Laurie | Janin, Alexandre | Molitor, Corentin | Chatron, Nicolas | Moret, Myriam | Nony, Séverine | Dumont, Sabrina | Marmontel, Oriane | Simonet, Thomas | Sassolas, Agnès | Moulin, Philippe | Di Filippo, Mathilde

Edité par CCSD ; Wiley -

International audience. ABSTRACT Mobile elements (ME) can transpose by copy‐and‐paste mechanisms. A heterozygous insertion in APOB exon 3 coding sequence was suspected in a patient with hypobetalipoproteinemia (HBL), by gel electrophoresis of the PCR products. An insertion of a 85 bp fragment flanked by a polyA stretch and a target replication site duplication was identified as a ME insertion (MEI) from the AluYa5 subfamily, NM_000384.3(APOB):c.135_136ins(160). Then, the DNA was reanalyzed using our NGS custom panel. Routine analysis did not reveal any causative variant, but manual inspection of the alignments and MELT enabled us to detect this MEI from NGS data. A functional study revealed that this MEI introduces a stop codon p.(Phe46Alafs*2) and additionally leads to p.(Lys41Serfs*2) due to an exon skipping. This is the first report of a MEI into APOB , as a cause of HBL. Furthermore, our study highlights the value of including MEI‐callers in routine pipelines to improve primary dyslipidemia diagnosis.

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