Genome-wide CRISPR screenings identified SMCHD1 as a host-restricting factor for AAV transduction.
Chenlu WangYu LiuJingfei XiongKun XieTianshu WangYu HuHuancheng FuBaiquan ZhangXiaochao HuangHui BaoHaoyang CaiBiao DongZhonghan LiPublished in: PLoS pathogens (2024)
AAV-mediated gene therapy typically requires a high dose of viral transduction, risking acute immune responses and patient safety, part of which is due to limited understanding of the host-viral interactions, especially post-transduction viral genome processing. Here, through a genome-wide CRISPR screen, we identified SMCHD1 (Structural Maintenance of Chromosomes Hinge Domain 1), an epigenetic modifier, as a critical broad-spectrum restricting host factor for post-entry AAV transgene expression. SMCHD1 knock-down by RNAi and CRISPRi or knock-out by CRISPR all resulted in significantly enhanced transgene expression across multiple viral serotypes, as well as for both single-strand and self-complementary AAV genome types. Mechanistically, upon viral transduction, SMCHD1 effectively repressed AAV transcription by the formation of an LRIF1-HP1-containing protein complex and directly binding with the AAV genome to maintain a heterochromatin-like state. SMCHD1-KO or LRIF1-KD could disrupt such a complex and thus result in AAV transcriptional activation. Together, our results highlight the host factor-induced chromatin remodeling as a critical inhibitory mechanism for AAV transduction and may shed light on further improvement in AAV-based gene therapy.
Keyphrases
- gene therapy
- genome wide
- dna methylation
- patient safety
- sars cov
- high dose
- gene expression
- copy number
- crispr cas
- genome editing
- poor prognosis
- transcription factor
- liver failure
- dna damage
- hepatitis b virus
- quality improvement
- high throughput
- drug induced
- amino acid
- extracorporeal membrane oxygenation
- single cell
- respiratory failure
- inflammatory response
- low dose