Literature DB >> 32197836

AAV diffuses across zona pellucida for effortless gene delivery to fertilized eggs.

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


  31 in total

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Journal:  Mol Cell       Date:  2018-12-20       Impact factor: 17.970

3.  Enhanced selective gene delivery to neural stem cells in vivo by an adeno-associated viral variant.

Authors:  Melissa A Kotterman; Tandis Vazin; David V Schaffer
Journal:  Development       Date:  2015-05-15       Impact factor: 6.868

4.  En masse lentiviral gene delivery to mouse fertilized eggs via laser perforation of zona pellucida.

Authors:  Negin P Martin; Page Myers; Eugenia Goulding; Shih-Heng Chen; Mitzie Walker; Thomas M Porter; Lucas Van Gorder; Amanda Mathew; Artiom Gruzdev; Charles Romeo
Journal:  Transgenic Res       Date:  2018-02-13       Impact factor: 2.788

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Authors:  Matthew J Mahon
Journal:  Adv Biosci Biotechnol       Date:  2011-06

Review 6.  Recombinant Viral Vectors as Neuroscience Tools.

Authors:  Shih-Heng Chen; Juhee Haam; Mitzie Walker; Erica Scappini; John Naughton; Negin P Martin
Journal:  Curr Protoc Neurosci       Date:  2019-03-22

7.  Rapid, simple, and versatile manufacturing of recombinant adeno-associated viral vectors at scale.

Authors:  Martin Lock; Mauricio Alvira; Luk H Vandenberghe; Arabinda Samanta; Jaan Toelen; Zeger Debyser; James M Wilson
Journal:  Hum Gene Ther       Date:  2010-10       Impact factor: 5.695

8.  CRISPR-READI: Efficient Generation of Knockin Mice by CRISPR RNP Electroporation and AAV Donor Infection.

Authors:  Sean Chen; Sabrina Sun; Dewi Moonen; Clancy Lee; Angus Yiu-Fai Lee; David V Schaffer; Lin He
Journal:  Cell Rep       Date:  2019-06-25       Impact factor: 9.423

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Journal:  Nature       Date:  2013-07-18       Impact factor: 49.962

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Review 4.  A most formidable arsenal: genetic technologies for building a better mouse.

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