Other
17 Authors
- Gao G,
- Liu DR,
- Shen MW,
- Xie J,
- Levy JM,
- Burghes AHM,
- Arnold WD,
- Blatnik AJ,
- Kray KM,
- Newby GA,
- Wang D,
- Richter MF,
- Du A,
- Zhao KT,
- Raguram A,
- Matuszek Z,
- Arbab M
| First Author | Arbab M | Year | 2023 |
| Journal | Science | Volume | 380 |
| Issue | 6642 | Pages | eadg6518 |
| PubMed ID | 36996170 | Mgi Jnum | J:343015 |
| Mgi Id | MGI:7465231 | Doi | 10.1126/science.adg6518 |
| Citation | Arbab M, et al. (2023) Base editing rescue of spinal muscular atrophy in cells and in mice. Science 380(6642):eadg6518 |
| abstractText | Spinal muscular atrophy (SMA), the leading genetic cause of infant mortality, arises from survival motor neuron (SMN) protein insufficiency resulting from SMN1 loss. Approved therapies circumvent endogenous SMN regulation and require repeated dosing or may wane. We describe genome editing of SMN2, an insufficient copy of SMN1 harboring a C6>T mutation, to permanently restore SMN protein levels and rescue SMA phenotypes. We used nucleases or base editors to modify five SMN2 regulatory regions. Base editing converted SMN2 T6>C, restoring SMN protein levels to wild type. Adeno-associated virus serotype 9-mediated base editor delivery in Delta7SMA mice yielded 87% average T6>C conversion, improved motor function, and extended average life span, which was enhanced by one-time base editor and nusinersen coadministration (111 versus 17 days untreated). These findings demonstrate the potential of a one-time base editing treatment for SMA. |
