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缺失反向末端重复序列的 B-B' 和 C-C' 区会降低 rAAV 的生产效率,但会增加转基因的表达。

Deletion of the B-B' and C-C' regions of inverted terminal repeats reduces rAAV productivity but increases transgene expression.

机构信息

College of Life Sciences, Jilin University, Changchun, Jilin, China.

Beijing Ruicy Gene Therapy Institute for Rare Diseases, Beijing, China.

出版信息

Sci Rep. 2017 Jul 14;7(1):5432. doi: 10.1038/s41598-017-04054-4.

Abstract

Inverted terminal repeats (ITRs) of the adeno-associated virus (AAV) are essential for rescue, replication, packaging, and integration of the viral genome. While ITR mutations have been identified in previous reports, we designed a new truncated ITR lacking the B-B' and C-C' regions named as ITRΔBC and investigated its effects on viral genome replication, packaging, and expression of recombinant AAV (rAAV). The packaging ability was compared between ITRΔBC rAAV and wild-type (wt) ITR rAAV. Our results showed the productivity of ITRΔBC rAAV was reduced 4-fold, which is consistent with the 8-fold decrease in the replication of viral genomic DNA of ITRΔBC rAAV compared with wt ITR rAAV. Surprisingly, transgene expression was significantly higher for ITRΔBC rAAV. A preliminary exploration of the underlying mechanisms was carried out by inhibiting and degrading the ataxia telangiectasia mutated (ATM) protein and the Mre11 complex (MRN), respectively, since the rAAV expression was inhibited by the ATM and/or MRN through cis interaction or binding with wt ITRs. We demonstrated that the inhibitory effects were weakened on ITRΔBC rAAV expression. This study suggests deletion in ITR can affect the transgene expression of AAV, which provides a new way to improve the AAV expression through ITRs modification.

摘要

腺相关病毒(AAV)的反向末端重复序列(ITR)对于病毒基因组的拯救、复制、包装和整合是必不可少的。虽然在以前的报告中已经鉴定出 ITR 突变,但我们设计了一种新的截短的 ITR,缺失了 B-B'和 C-C'区域,命名为 ITRΔBC,并研究了它对病毒基因组复制、包装和重组 AAV(rAAV)表达的影响。我们比较了 ITRΔBC rAAV 和野生型(wt)ITR rAAV 的包装能力。结果表明,ITRΔBC rAAV 的产率降低了 4 倍,与 ITRΔBC rAAV 中病毒基因组 DNA 的复制减少 8 倍一致。令人惊讶的是,ITRΔBC rAAV 的转基因表达显著升高。通过抑制和降解共济失调毛细血管扩张突变(ATM)蛋白和 Mre11 复合物(MRN),分别对潜在机制进行了初步探索,因为 rAAV 表达通过顺式相互作用或与 wt ITRs 结合被 ATM 和/或 MRN 抑制。我们证明,对 ITRΔBC rAAV 表达的抑制作用减弱。这项研究表明,ITR 的缺失会影响 AAV 的转基因表达,这为通过 ITR 修饰来提高 AAV 表达提供了一种新的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6da/5511163/0efec225c15f/41598_2017_4054_Fig1_HTML.jpg

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