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A Ds insertion alters the nuclear localization of the maize transcriptional activator R.

机译:Ds插入会改变玉米转录激活因子R的核定位。

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摘要

The R-sc gene of maize is a member of the R gene family of transcriptional activators that regulate anthocyanin biosynthesis. A derivative of R-sc, r-m9 conditions a reduced level of aleurone pigmentation due to the presence of a 2.1-kb Ds insertion near the 3' end of the coding region. Excision of Ds from r-m9 leaves a 7-bp insertion in the darker but still mutant v24 derivative. Both the 7-bp insertion in v24 and the 2.1-kb Ds in r-m9 are predicted to truncate their respective R proteins proximal to the carboxyl terminus, which was shown previously to contain one of three nuclear localization sequences. We find that the reduced expression of r-m9 and v24 are not due to mRNA or protein instability, but most likely reflect the inefficient localization of truncated R proteins to the nucleus. To our knowledge this is the first example of a transposable element insertion that alters gene expression by affecting nuclear localization. In addition, our data indicate that the carboxyl terminus of the R protein is far more important than previously suspected and illustrates the utility of natural mutations for defining functional domains in proteins.
机译:玉米的R-sc基因是调节花色苷生物合成的转录激活因子R基因家族的成员。 R-sc,r-m9的衍生物由于在编码区3'端附近存在2.1-kb Ds插入而降低了糊粉色素的水平。从r-m9切除Ds在较暗但仍突变的v24衍生物中保留了7 bp的插入。预测v24中的7 bp插入和r-m9中的2.1 kb Ds都将截断它们各自靠近羧基末端的R蛋白,先前已显示它包含三个核定位序列之一。我们发现,r-m9和v24的减少表达不是由于mRNA或蛋白质的不稳定性,而是最有可能反映出截短的R蛋白到核的低效定位。据我们所知,这是可转座元件插入的第一个例子,它通过影响核定位来改变基因表达。此外,我们的数据表明R蛋白的羧基末端比以前怀疑的重要得多,并说明了天然突变在定义蛋白质功能结构域中的作用。

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