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人类基质附着区域对于在黑腹果蝇中建立转基因隔离是必要的,但对于维持转基因隔离则不是必需的。

Human matrix attachment regions are necessary for the establishment but not the maintenance of transgene insulation in Drosophila melanogaster.

作者信息

Namciu Stephanie J, Fournier R E K

机构信息

Division of Basic Sciences, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave. N., Seattle, WA 98109, USA.

出版信息

Mol Cell Biol. 2004 Dec;24(23):10236-45. doi: 10.1128/MCB.24.23.10236-10245.2004.

Abstract

Human matrix attachment regions (MARs) can insulate transgene expression from chromosomal position effects in Drosophila melanogaster. To gain insight into the mechanism(s) by which chromosomal insulation occurs, we studied the expression phenotypes of Drosophila transformants expressing mini-white transgenes in which MAR sequences from the human apoB gene were arranged in a variety of ways. In agreement with previous reports, we found that a single copy of the insulating element was not sufficient for position-independent transgene expression; rather, two copies were required. However, the arrangement of the two elements within the transgene was unimportant, since chromosomal insulation was equally apparent when both copies of the insulator were upstream of the mini-white reporter as when the transcription unit was flanked by insulator elements. Moreover, experiments in which apoB 3' MAR sequences were removed from integrated transgenes in vivo by site-specific recombination demonstrated that MAR sequences were required for the establishment but not for the maintenance of chromosomal insulation. These observations are not compatible with the chromosomal loop model in its simplest form. Alternate mechanisms for MAR function in this system are proposed.

摘要

人类基质附着区域(MARs)能够使转基因表达免受果蝇染色体位置效应的影响。为深入了解染色体绝缘发生的机制,我们研究了在果蝇转化体中表达微型白色转基因的表达表型,其中来自人类载脂蛋白B基因的MAR序列以多种方式排列。与之前的报道一致,我们发现单个绝缘元件不足以实现转基因的位置独立表达;相反,需要两个拷贝。然而,转基因内两个元件的排列并不重要,因为当两个绝缘拷贝都在微型白色报告基因上游时,与转录单元两侧都有绝缘元件时一样,染色体绝缘同样明显。此外,通过位点特异性重组在体内从整合的转基因中去除载脂蛋白B 3' MAR序列的实验表明,MAR序列对于建立染色体绝缘是必需的,但对于维持染色体绝缘则不是必需的。这些观察结果与最简单形式的染色体环模型不相符。本文提出了该系统中MAR功能的替代机制。

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