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黑腹果蝇中I因子转座的多步控制证据。

Evidence for a multistep control in transposition of I factor in Drosophila melanogaster.

作者信息

de La Roche Saint André C, Bregliano J C

机构信息

Institut de Biologie du Développement de Marseille, France.

出版信息

Genetics. 1998 Apr;148(4):1875-84. doi: 10.1093/genetics/148.4.1875.

Abstract

Drosophila melanogaster strains belong to one of two interactive categories, inducer (I) or reactive (R), with respect to the I-R system of hybrid dysgenesis. The dysgenic interaction results from the presence of several transposition-competent copies of a LINE-like element, the I factor, only in the genome of I strains. When a cross is performed between I males and R females, I factor transposes at high frequency in the germ line of F1 daughters, known as SF females. This transposition burst results in the sterility of SF females. I factor transposes by reverse transcription of a full-length transcript. Specific RT-PCR experiments were done to compare the amount of I factor transcript in samples corresponding to various transposition frequencies. The sensitivity of the method allowed the ready detection of the I factor RNA in every tissue and genetic background examined. Comparison of amplification signals suggests that I factor activity in ovaries is regulated at different levels. First, the amount of I factor RNA subjected to negative and positive regulation. Whereas the negative control, which limits transposition in nonpermissive contexts, may be exerted by an I factor encoded repressor function, the positive control is linked to reactivity level, a cellular state maternally inherited from R mothers. Additionally, negative regulation is also exerted downstream of I factor RNA. This differs notably from previous conclusions in which transcription was envisaged as the main level of regulation of the I factor transposition.

摘要

就杂种不育的I-R系统而言,黑腹果蝇品系属于两个相互作用的类别之一,即诱导型(I)或反应型(R)。这种不育相互作用是由于仅在I品系的基因组中存在几个具有转座能力的类LINE元件I因子拷贝。当I雄蝇与R雌蝇杂交时,I因子在F1代雌蝇(称为SF雌蝇)的生殖系中高频转座。这种转座爆发导致SF雌蝇不育。I因子通过全长转录本的逆转录进行转座。进行了特定的RT-PCR实验,以比较对应于各种转座频率的样品中I因子转录本的量。该方法的灵敏度使得能够在检查的每个组织和遗传背景中轻松检测到I因子RNA。扩增信号的比较表明,卵巢中I因子的活性在不同水平上受到调节。首先,I因子RNA的量受到正负调节。限制在非允许环境中转座的负调控可能由I因子编码的阻遏功能施加,而正调控与反应性水平相关,反应性水平是从R母本遗传的一种细胞状态。此外,负调控也在I因子RNA的下游发挥作用。这与之前认为转录是I因子转座主要调控水平的结论明显不同。

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