p.Val19Glyfs*21 and p.Leu228* variants in the survival of motor neuron 1 trigger nonsense-mediated mRNA decay causing the SMN1 PTC+ transcripts degradation

- p.Val19Glyfs*21 and p.Leu228* can trigger NMD, causing rapid degradation of SMN1 transcripts.
- Treatment with translation inhibitors (puromycin and Cycloheximide (CHX)) can sharply increased the levels of FL-SMN1 transcripts with PTCs in the cultured primary fibroblast and lymphoblastoid cell lines.
- The knockdown efficiency of UPF1 in the cultured primary fibroblast cell lines was much higher(>85%) than in the lymphoblastoid cell lines by using shRNA −mediated silencing of UPF1.
- Different responses to drug treatments (both puromycin and CHX) were observed in different cell lines and individuals.

Spinal Muscular Atrophy (SMA) results from loss-of-function mutations in the survival of motor neuron 1 (SMN1) gene. Our previous research showed that 40% of variants were nonsense or frameshift variants and SMN1 mRNA levels in the patients carrying these variants were significantly decreased. Here we selected one rare variant (p.Val19Glyfs*21) and one common variant (p.Leu228*) to explore the degradation mechanism of mutant transcripts. The levels of full-length (FL)-SMN1 transcripts and SMN protein in the cell lines from the patients with these variants were both significantly reduced (p < 0.01). Treatment with two translation inhibitors (puromycin and Cycloheximide (CHX)) markedly increased the levels of FL-SMN1 transcripts with premature translation termination codons (PTCs) (p < 0.01) and showed time-dependent (10 h > 5.5 h) but not dose-dependent effects. Moreover, the knockdown of UPF1, a key factor in nonsense-mediated mRNA decay (NMD) by lentivirus, led to a 3.1-fold increase (p < 0.01) in FL-SMN1 transcript levels in patient fibroblasts. Our research provides evidence that these two PTC-generating variants (p.Val19Glyfs*21 and p.Leu228*) can trigger NMD, causing rapid degradation of SMN1 transcripts thereby resulting in SMN protein deficiency. These two variants are highly pathogenic and are associated with more severe SMA phenotypes. Varying NMD efficiency after treatment with puromycin and CHX in different cell types was also observed.