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转座因子水手座可在非果蝇类昆虫中切除。

The transposable element mariner can excise in non-drosophilid insects.

作者信息

Coates C J, Turney C L, Frommer M, O'Brochta D A, Warren W D, Atkinson P W

机构信息

Commonwealth Scientific and Industrial Research Organisation, Division of Entomology, Canberra, Australia.

出版信息

Mol Gen Genet. 1995 Nov 15;249(2):246-52. doi: 10.1007/BF00290372.

Abstract

Plasmid-based excision assays performed in embryos of two non-drosophilid species using the mariner transposable element from Drosophila mauritiana resulted in empty excision sites identical to those observed after the excision of mariner from D. mauritiana chromosomes. In the presence of the autonomous mariner element Mos1, excision products were recovered from D. melanogaster, D. mauritiana and the blowfly Lucilia cuprina. When a hsp82 heat shock promoter-Mos1 construct was used to supply mariner transposase, excision products were also recovered from the Queensland fruitfly Bactrocera tryoni. Analysis of DNA sequences at empty excision sites led us to hypothesise that the mariner excision/repair process involves the formation of a heteroduplex at the excision breakpoint. The success of these assays suggests that they will provide a valuable tool for assessing the ability of mariner and mariner-like elements to function in non-drosophilid insects and for investigating the basic mechanisms of mariner excision and repair.

摘要

在两种非果蝇物种的胚胎中使用来自毛里求斯果蝇的水手转座元件进行基于质粒的切除试验,结果产生的空切除位点与从毛里求斯果蝇染色体上切除水手元件后观察到的位点相同。在自主水手元件Mos1存在的情况下,从黑腹果蝇、毛里求斯果蝇和绿蝇 Lucilia cuprina中回收了切除产物。当使用hsp82热休克启动子-Mos1构建体来提供水手转座酶时,也从昆士兰果蝇Bactrocera tryoni中回收了切除产物。对空切除位点的DNA序列分析使我们推测,水手切除/修复过程涉及在切除断点处形成异源双链体。这些试验的成功表明,它们将为评估水手元件和类水手元件在非果蝇昆虫中发挥功能的能力以及研究水手切除和修复的基本机制提供有价值的工具。

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