Pears C J, Williams J G
Imperial Cancer Research Fund, Clare Hall Laboratories, Herts, UK.
Nucleic Acids Res. 1988 Sep 12;16(17):8467-86. doi: 10.1093/nar/16.17.8467.
The cysteine proteinase 1 (CP1) and cysteine proteinase 2 (CP2) genes of Dictyostelium discoideum encode co-ordinately expressed mRNA sequences which are inducible by extracellular cAMP. There are short, G-rich sequence elements upstream of both genes and we have previously shown that deletion of these elements from the CP2 gene abolishes cAMP-inducibility. We show here that the G-rich element from the CP1 gene is functionally homologous to that in the CP2 gene by reconstituting cAMP-inducibility in a deletion mutant of the CP2 gene using CP1-derived sequences. Both the CP1 and CP2 genes contain multiple G-rich elements. We show that efficient induction requires at least two copies of the CP1 element and that their relative orientation is unimportant. Two copies of an inverted relative orientation are, however, inactive when moved upstream of their normal position and are incapable of conferring cAMP-inducibility on a heterologous gene. These observations suggest that these sequences are either essential promoter elements, not themselves interacting with the inducer, or that their interaction with a separate class of control sequences is necessary for inducible expression.
盘基网柄菌的半胱氨酸蛋白酶1(CP1)和半胱氨酸蛋白酶2(CP2)基因编码由细胞外cAMP诱导协同表达的mRNA序列。两个基因上游都有短的富含G的序列元件,我们之前已经表明从CP2基因中删除这些元件会消除cAMP诱导性。我们在此表明,通过使用CP1衍生序列在CP2基因的缺失突变体中重建cAMP诱导性,CP1基因的富含G的元件在功能上与CP2基因中的元件同源。CP1和CP2基因都包含多个富含G的元件。我们表明,有效的诱导至少需要两个CP1元件拷贝,并且它们的相对方向并不重要。然而,两个反向相对方向的拷贝在移至其正常位置上游时无活性,并且不能赋予异源基因cAMP诱导性。这些观察结果表明,这些序列要么是必不可少的启动子元件,本身不与诱导剂相互作用,要么它们与另一类控制序列的相互作用对于诱导表达是必要的。