Alu Retrotransposition Event in SPAST Gene as a Novel Cause of Hereditary Spastic Paraplegia

• Published in: Movement disorders Vol. 38; no. 9; pp. 1750 - 1755
• Main Authors: Chen, Yi‐Jun, Wang, Meng‐Wen, Qiu, Yu‐Sen, Yuan, Ru‐Ying, Wang, Ning, Lin, Xiang, Chen, Wan‐Jin
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.09.2023
• Subjects: Autosomal dominant inheritance; Hereditary spastic paraplegia; Leukocytes; Movement disorders; Paralysis; Peripheral blood; Phenotypes; Polymerase chain reaction; Retrotransposition; Reverse transcription; Ribonucleic acid; RNA; RNA sequencing; SPAST; mobile element insertion; hereditary spastic paraplegia
• ISSN: 0885-3185; 1531-8257; 1531-8257
• DOI: 10.1002/mds.29522

To diagnose the molecular cause of hereditary spastic paraplegia (HSP) observed in a four-generation family with autosomal dominant inheritance. Multiplex ligation-dependent probe amplification (MLPA), whole-exome sequencing (WES), and RNA sequencing (RNA-seq) of peripheral blood leukocytes were performed. Reverse transcription polymerase chain reaction (RT-PCR) and Sanger sequencing were used to characterize target regions of SPAST. A 121-bp AluYb9 insertion with a 30-bp poly-A tail flanked by 15-bp direct repeats on both sides was identified in the edge of intron 16 in SPAST that segregated with the disease phenotype. We identified an intronic AluYb9 insertion inducing splicing alteration in SPAST causing pure HSP phenotype that was not detected by routine WES analysis. Our findings suggest RNA-seq is a recommended implementation for undiagnosed cases by first-line diagnostic approaches. © 2023 International Parkinson and Movement Disorder Society.