Yoo So Yeon, Bomblies Kirsten, Yoo Seung Kwan, Yang Jung Won, Choi Mi Suk, Lee Jong Seob, Weigel Detlef, Ahn Ji Hoon
Plant Signaling Network Research Center, School of Life Sciences and Biotechnology, Korea University, Seoul, 136-701, Korea.
Planta. 2005 Jun;221(4):523-30. doi: 10.1007/s00425-004-1466-4. Epub 2005 Jan 29.
Positive selection of transgenic plants is essential during plant transformation. Thus, strong promoters are often used in selectable marker genes to ensure successful selection. Many plant transformation vectors, including pPZP family vectors, use the 35S promoter as a regulatory sequence for their selectable marker genes. We found that the 35S promoter used in a selectable marker gene affected the expression pattern of a transgene, possibly leading to a misinterpretation of the result obtained from transgenic plants. It is likely that the 35S enhancer sequence in the 35S promoter is responsible for the interference, as in the activation tagging screen. This affected expression mostly disappeared in transgenic plants generated using vectors without the 35S sequences within their T-DNA region. Therefore, we suggest that caution should be used in selecting a plant transformation vector and in the interpretation of the results obtained from transgenic approaches using vectors carrying the 35S promoter sequences within their T-DNA regions.
在植物转化过程中,转基因植物的阳性选择至关重要。因此,强启动子常用于选择标记基因以确保成功筛选。许多植物转化载体,包括pPZP家族载体,使用35S启动子作为其选择标记基因的调控序列。我们发现,选择标记基因中使用的35S启动子会影响转基因的表达模式,可能导致对转基因植物所获结果的错误解读。如在激活标签筛选中一样,35S启动子中的35S增强子序列可能是造成这种干扰的原因。在使用T-DNA区域内没有35S序列的载体产生的转基因植物中,这种受影响的表达大多消失了。因此,我们建议在选择植物转化载体以及解读使用T-DNA区域内携带35S启动子序列的载体进行转基因方法所获结果时应谨慎。