| Literature DB >> 32197836 |
Charles Romeo1, Shih-Heng Chen1, Eugenia Goulding1, Lucas Van Gorder1, Maura Schwartz1, Mitzie Walker1, Gregory Scott2, Erica Scappini3, Manas Ray2, Negin P Martin4.
Abstract
Gene delivery to fertilized eggs is often the first step in creation of transgenic animals, CRISPR knock-out, or early developmental studies. The zona pellucida, a hardened glycoprotein matrix surrounding the mammalian fertilized eggs, often complicates gene delivery by forming a barrier against transfection reagents and viruses. High efficiency techniques to perforate or penetrate the zona allow for access and gene delivery to fertilized eggs. However, these techniques often rely on highly skilled technologists, are costly, and require specialized equipment for micromanipulation, laser perforation, or electroporation. Here, we report that adenoassociated viruses (AAVs) with serotypes 1 or DJ can efficiently diffuse across the zona to deliver genes without any manipulations to fertilized eggs. We observe lowered rates of embryo development after treatment of embryos with all AAV serotypes. However, we were able to reduce adverse effects on embryo development by exposing embryos to AAVs at later stages of in vitro development. AAVs have low immune response and do not incorporate into their host chromosomes to cause insertional mutations. Hence, AAVs can serve as a highly effective tool for transient delivery of genes to fertilized mammalian eggs. Published by Elsevier Inc.Entities:
Keywords: AAV; Embryos; Gene delivery; Mouse fertilized eggs; Transduction; Zona pellucida
Mesh:
Year: 2020 PMID: 32197836 PMCID: PMC7188573 DOI: 10.1016/j.bbrc.2020.03.026
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575