Scofield S R, Harrison K, Nurrish S J, Jones J D
Sainsbury Laboratory, John Innes Centre, Norwich, United Kingdom.
Plant Cell. 1992 May;4(5):573-82. doi: 10.1105/tpc.4.5.573.
To explore the effects of altering the level of Activator (Ac) transposase (TPase) expression, a series of plasmids was constructed in which heterologous promoters were fused to the TPase gene. Promoters for the cauliflower mosaic virus (CaMV) 35S transcript and the octopine synthase (ocs) and nopaline synthase (nos) genes were tested. These fusions, and constructs expressing TPase from the wild-type Ac promoter, were introduced into tobacco, and their activity was monitored by crossing to a line carrying Dissociation (Ds) in a streptomycin phosphotransferase gene (Ds::SPT). The SPT marker provides a record of somatic excisions of Ds that occur during embryo development. The patterns of somatic variegation that resulted from transactivation by each fusion were distinct and strikingly different from the pattern triggered by the wild-type Ac constructs. Unlike wild-type Ac, which caused transposition throughout embryo development, each fusion gave rise to sectors of discrete size. Sectors triggered by the CaMV 35S fusion were largest, ocs sectors were intermediate, and nos were smallest. These patterns appear to indicate differential timing of the activation of these promoters during embryogeny. Measurement of transcript abundance for each transformant indicated that the CaMV 35S-transformed plants accumulated approximately 1000-fold more TPase mRNA than plants containing wild-type Ac, whereas ocs- and nos-transformed lines accumulated about 100-fold and 20-fold higher levels, respectively. Measurements of germinal excision frequencies driven by the chimeric TPase fusions, however, indicated that increasing transcription does not necessarily result in an increase in germinal excision. These measurements showed that the ocs and nos fusions have very low rates of germinal excision. Only the CaMV 35S fusion transformants were found to have higher rates than the Ac constructs, although significant pod-to-pod variation was observed. Gel blot analysis of DNA from progeny carrying germinal excision events resulting from the CaMV 35S fusion showed that excision is associated with reinsertion and that siblings sometimes carry the same transposition events. These findings suggest that in tobacco there is no direct proportionality between TPase expression and Ac-Ds transposition activity. This possibility has important implications for understanding the regulation of Ac transposition and for designing efficient gene tagging systems.
为了探究改变激活子(Ac)转座酶(TPase)表达水平的影响,构建了一系列质粒,其中异源启动子与TPase基因融合。对花椰菜花叶病毒(CaMV)35S转录本、章鱼碱合酶(ocs)和胭脂碱合酶(nos)基因的启动子进行了测试。将这些融合体以及从野生型Ac启动子表达TPase的构建体导入烟草中,并通过与携带链霉素磷酸转移酶基因解离(Ds)的品系(Ds::SPT)杂交来监测它们的活性。SPT标记记录了胚胎发育过程中发生的Ds体细胞切除情况。每种融合体通过反式激活导致的体细胞斑驳模式各不相同,且与野生型Ac构建体引发的模式显著不同。与在整个胚胎发育过程中引起转座的野生型Ac不同,每种融合体都产生了大小离散的扇形区域。由CaMV 35S融合体引发的扇形区域最大,ocs扇形区域居中,nos扇形区域最小。这些模式似乎表明这些启动子在胚胎发生过程中激活的时间不同。对每个转化体转录本丰度的测量表明,CaMV 35S转化的植物积累的TPase mRNA比含有野生型Ac的植物多约1000倍,而ocs和nos转化系分别积累的水平高约100倍和20倍。然而,对嵌合TPase融合体驱动的生殖细胞切除频率的测量表明,转录增加不一定会导致生殖细胞切除增加。这些测量表明ocs和nos融合体的生殖细胞切除率非常低。仅发现CaMV 35S融合体转化体的切除率高于Ac构建体,尽管观察到显著的荚间变异。对携带由CaMV 35S融合体导致的生殖细胞切除事件的后代DNA进行凝胶印迹分析表明,切除与重新插入有关,并且同胞有时携带相同的转座事件。这些发现表明,在烟草中TPase表达与Ac-Ds转座活性之间不存在直接的比例关系。这种可能性对于理解Ac转座的调控以及设计高效的基因标签系统具有重要意义。