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腺病毒5型dl309突变体E3区域插入片段的潜在鲑鱼精子起源

Potential salmon sperm origin of the E3 region insert of the adenovirus 5 dl309 mutant.

作者信息

Gingras M C, Arevalo P, Aguilar-Cordova E

机构信息

Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.

出版信息

Cancer Gene Ther. 1996 May-Jun;3(3):151-4.

PMID:8725878
Abstract

The plasmid pJM17 is a commonly used adenoviral backbone derived from the dl309 mutant virus. It contains unknown sequences inserted in the E3 region during construction of the dl309 mutant. Complete description of the backbone sequence is required for interpretation of potential vector effects and for regulatory approval of a vector to be used in clinical trials. The anonymous E3 insert was sequenced and analyzed. The insert fragment is 646 base pairs (bp) long and is 100 bp shorter than the vector sequences it replaces. It interrupts the expression of the E3B 10.4K, 14.6K, and 14.7K genes, but not the E3A glycoprotein (gp) 19K gene. Sequence analysis and Southern blotting suggest that the insert might originate from salmon sperm DNA used as carrier during the construction of dl309. Transcription from the insert was not detected by Northern blot analysis of vector-transduced cells but was detected by reverse transcriptase polymerase chain reaction.

摘要

质粒pJM17是一种常用的腺病毒骨架,源自dl309突变病毒。在构建dl309突变体的过程中,其E3区域插入了未知序列。为了解潜在载体效应并获得用于临床试验的载体的监管批准,需要对骨架序列进行完整描述。对匿名的E3插入片段进行了测序和分析。插入片段长646个碱基对(bp),比它所取代的载体序列短100 bp。它中断了E3B 10.4K、14.6K和14.7K基因的表达,但没有中断E3A糖蛋白(gp)19K基因的表达。序列分析和Southern印迹表明,该插入片段可能源自dl309构建过程中用作载体的鲑鱼精子DNA。通过对载体转导细胞的Northern印迹分析未检测到插入片段的转录,但通过逆转录酶聚合酶链反应检测到了。

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