Mutation in the platelet-derived growth factor receptor alpha inhibits adeno-associated virus type 5 transduction

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• 作者：Ingo H. Pilz^a ; ¹ ; ² ; ^{ingo.hinrich.pilz@uniklinik-freiburg.de} ; Giovanni Di Pasquale^a ; ² ; ^{gdipasqu@nidcr.nih.gov} ; Agnieszka Rzadzinska^b ; ^{agnieszka.rzadzinska@addenbrookes.nhs.uk} ; Stephen H. Leppla^c ; ^{sleppla@nih.gov} ; John A. Chiorini^a ; ^{jchiorini@dir.nidcr.nih.gov}
• 关键词：Forward genetics ; AAV5 ; Furin ; Toxin ; CHO cells ; Anthrax
• 刊名：Virology
• 出版年：2012
• 期刊代码：108_00426822
• 类别：imm
• 出版时间：20 June, 2012
• 卷：428
• 期：1
• 页码：58-63
• 文件大小：578 K

摘要

Due to its non-pathogenic lifecycle, little is known about the cellular determinants of infection by adeno-associated virus (AAV). To identify these critical cellular factors, we took advantage of the gene transfer abilities of AAV in combination with a forward genetic selection to identify proteins critical for transduction by this virus. AAV serotype 5 (AAV5) vectors encoding the furin gene were used to transduce furin-deficient cells followed by selection with furin-dependent toxins. A population of cells specifically resistant to AAV5 transduction was identified and sequence analysis suggested all had a single amino acid mutation in the leader sequence of the platelet-derived growth factor receptor alpha (PDGFR伪) gene. Characterization of this mutation suggested it inhibited PDGFR伪 trafficking resulting in limited expression on the plasma membrane. Mutagenesis and transfection experiments confirmed the effect of this mutation on PDGFR伪 trafficking, and the AAV5 resistant phenotype could be rescued by transfection with wild type PDGFR伪.