Alexander S, Leone S, Ostermeyer E
Division of Biological Sciences, University of Missouri, Columbia 65211.
Mol Cell Biol. 1991 Jun;11(6):3171-9. doi: 10.1128/mcb.11.6.3171-3179.1991.
Genetic analysis in Dictyostelium discoideum has identified regulatory genes which control the developmental expression of the discoidin lectin multigene family. Among these, the drsA mutation is a dominant second-site suppressor of another mutation, disB, which has the discoidinless phenotype. We now demonstrate a novel mechanism by which the drsA allele exerts its suppressive effect on the disB mutation. Interestingly, drsA does not merely bypass the disB mutation and restore the wild-type pattern of lectin expression. Rather, drsA mutant cells have high levels of discoidin lectin synthesis during growth but do not express lectins during aggregation. In contrast, wild-type cells only express lectin protein during the aggregation period of development. Phenocopies of the drsA mutation show a pattern of discoidin expression similar to that seen in the bona fide mutant. These data suggest that there may be a mechanism of negative feedback, resulting from the high levels of discoidin lectin made during growth, which inhibits further discoidin lectin expression during development. Northern (RNA) analysis of developing drsA mutant cells shows that these cells contain high levels of discoidin mRNA, although no discoidin lectin protein is being translated from these messages. Therefore, expression of the discoidin gene family can be controlled at the level of translation as well as transcription.
对盘基网柄菌的遗传分析已鉴定出控制盘状菌素凝集素多基因家族发育表达的调控基因。其中,drsA突变是另一个具有无盘状菌素表型的突变disB的显性第二位点抑制子。我们现在证明了一种新机制,通过该机制drsA等位基因对disB突变发挥其抑制作用。有趣的是,drsA不仅仅是绕过disB突变并恢复凝集素表达的野生型模式。相反,drsA突变细胞在生长期间具有高水平的盘状菌素凝集素合成,但在聚集期间不表达凝集素。相比之下,野生型细胞仅在发育的聚集期表达凝集素蛋白。drsA突变的拟表型显示出与真正突变体中相似的盘状菌素表达模式。这些数据表明,可能存在一种负反馈机制,由生长期间产生的高水平盘状菌素凝集素导致,该机制在发育过程中抑制进一步的盘状菌素凝集素表达。对发育中的drsA突变细胞的Northern(RNA)分析表明,这些细胞含有高水平的盘状菌素mRNA,尽管没有从这些信息中翻译出盘状菌素凝集素蛋白。因此,盘状菌素基因家族的表达可以在翻译水平以及转录水平上受到控制。