Datta N, Cashmore A R
Department of Biology, University of Pennsylvania, Philadelphia 19104.
Plant Cell. 1989 Nov;1(11):1069-77. doi: 10.1105/tpc.1.11.1069.
There have been numerous recent reports documenting phosphorylation of DNA-binding proteins [Montminy and Bilezikjian (1987); Sorger, Lewis, and Pelham (1987); Hoeffler, Kovelman, and Roeder (1988); Jones et al. (1988); Prywes et al. (1988); Sorger and Pelham (1988); Yamamoto et al. (1988)], and the transcriptional regulatory activity of at least one of these proteins appears to be modulated by this modification [Montminy and Bilezikjian (1987); Yamamoto et al. (1988)]. We report here on a plant nuclear protein, the DNA-binding activity of which is strongly affected by phosphorylation. This protein, AT-1, binds to specific AT-rich elements (the AT-1 box) within promoters of certain nuclear genes encoding the small subunit of ribulose-1,5-bisphosphate carboxylase and the polypeptide components of the light-harvesting chlorophyll a/b protein complex. A consensus sequence of AATATTTTTATT was derived for the AT-1 box. We demonstrate that the DNA-binding ability of AT-1, from nuclear extracts of pea, can be reversibly modulated by phosphorylation. AT-1 is active in the nonphosphorylated form and loses all DNA-binding ability as a result of phosphorylation. The kinase that phosphorylates AT-1 uses both Mg-ATP and Mg-GTP as a substrate and is inhibited by heparin and spermine, indicative of an NII-type casein kinase.
最近有许多报道记录了DNA结合蛋白的磷酸化[蒙特米尼和比莱齐基安(1987年);索尔格、刘易斯和佩勒姆(1987年);赫夫勒、科韦尔曼和罗德(1988年);琼斯等人(1988年);普赖韦斯等人(1988年);索尔格和佩勒姆(1988年);山本等人(1988年)],并且这些蛋白中至少有一种的转录调节活性似乎受到这种修饰的调节[蒙特米尼和比莱齐基安(1987年);山本等人(1988年)]。我们在此报道一种植物核蛋白,其DNA结合活性受到磷酸化的强烈影响。这种蛋白,即AT-1,与某些编码1,5-二磷酸核酮糖羧化酶小亚基的核基因启动子以及光捕获叶绿素a/b蛋白复合体的多肽成分中的特定富含AT的元件(AT-1盒)结合。推导出了AT-1盒的一致序列AATATTTTTATT。我们证明,来自豌豆核提取物的AT-1的DNA结合能力可通过磷酸化被可逆调节。AT-1以非磷酸化形式具有活性,磷酸化后会丧失所有DNA结合能力。使AT-1磷酸化的激酶将Mg-ATP和Mg-GTP都用作底物,并受到肝素和精胺的抑制,这表明它是一种NII型酪蛋白激酶。