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缺乏env基因的LTR逆转座子mdg3水平转移的证据。

Evidence for horizontal transfer of the LTR retrotransposon mdg3, which lacks an env gene.

作者信息

Syomin B V, Leonova T Ya, Ilyin Y V

机构信息

V. A. Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Vavilova St. 32, Moscow B-334, 119991 Russia,

出版信息

Mol Genet Genomics. 2002 May;267(3):418-23. doi: 10.1007/s00438-002-0678-1. Epub 2002 May 9.

Abstract

Horizontal (interspecific) transfer is regarded as a possible strategy for the propagation of transposable elements through evolutionary time. To date, however, conclusive evidence that transposable elements are capable of horizontal transfer from one species to another has been limited to class II or DNA-type elements. We tested the possibility of such transfer for several Drosophila melanogaster LTR retrotransposons of the gypsy group in an experiment in which D. melanogaster and D. virilis somatic cell lines were used as donor and recipient cells, respectively. This approach was chosen in light of the high levels of LTR retrotransposon amplification and expression observed in cultured D. melanogaster cells. In the course of the experiment, parallel analysis for mdg1, mdg3, 17.6, 297, 412 and B104/roo retrotransposons was performed to detect their presence in the genome of recipient cells. Only the mdg3 retrotransposon, which lacks an env gene, was found to be transmitted into recipient cells. This model, based on the use of cultured cells, is a promising system for further investigating the mechanisms of LTR retrotransposon transfer.

摘要

水平(种间)转移被认为是转座元件在进化过程中进行传播的一种可能策略。然而,迄今为止,转座元件能够从一个物种水平转移到另一个物种的确凿证据仅限于II类或DNA型元件。我们在一项实验中测试了几种黑腹果蝇(Drosophila melanogaster)吉普赛族LTR逆转录转座子发生这种转移的可能性,在该实验中,黑腹果蝇和粗壮果蝇(D. virilis)的体细胞系分别用作供体细胞和受体细胞。鉴于在培养的黑腹果蝇细胞中观察到高水平的LTR逆转录转座子扩增和表达,所以选择了这种方法。在实验过程中,对mdg1、mdg3、17.6、297、412和B104/roo逆转录转座子进行了平行分析,以检测它们在受体细胞基因组中的存在情况。结果发现,只有缺少env基因的mdg3逆转录转座子被转移到了受体细胞中。这个基于使用培养细胞的模型,是进一步研究LTR逆转录转座子转移机制的一个很有前景的系统。

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