Schatzle J, Bush J, Dharmawardhane S, Firtel R A, Gomer R H, Cardelli J
Department of Microbiology and Immunology, Louisiana State University Medical Center, Shreveport 71130.
J Biol Chem. 1993 Sep 15;268(26):19632-9.
The lysosomal alpha-mannosidase gene in Dictyostelium discoideum is representative of a small group of genes that are expressed under two different conditions: 1) immediately upon removal of the bacterial food source from exponentially growing cells at < 5 x 10(5) cells/ml (which also initiates the developmental cycle), and 2) when the concentration of a secreted glycoprotein termed the prestarvation response factor (PSF) reaches a critical threshold in cultures growing at densities > 5 x 10(5) cells/ml. In this report we show that transcription of the alpha-mannosidase gene induced by starvation did not require protein synthesis in axenic wild-type strains, whereas protein synthesis was required for the transcriptional induction observed in response to PSF. Northern blot analysis was also done using mRNA from G alpha 1 and G alpha 2 gene disruption mutants. These genes encode subunits of heterotrimeric G proteins found at the cell surface in growing cells and cells early in development. The pattern of alpha-mannosidase gene expression was normal in these mutants as well as in mutants unable to produce the secreted glycoprotein conditioned medium factor or the cAMP receptor-1 protein. These genes have been shown to regulate the expression of many genes during early development. Promoter analysis studies identified a 145-base pair sequence element containing a TTG box which was required for alpha-mannosidase transcriptional induction under both starvation conditions and in response to PSF. The TTG box identified is an important regulatory element in the promoter of another prestarvation response gene, the discoidin I gamma gene. A ts mutant was found to misregulate the expression of both discoidin I and alpha-mannosidase expression at restrictive temperatures. Taken together these results suggest that the prestarvation response genes may be coordinately regulated possibly through the TTG box.
盘基网柄菌中的溶酶体α-甘露糖苷酶基因是一小类基因的代表,这类基因在两种不同条件下表达:1)当指数生长的细胞(细胞密度<5×10⁵个细胞/毫升)中细菌食物源被移除时(这也启动了发育周期)立即表达;2)当一种称为饥饿前反应因子(PSF)的分泌糖蛋白的浓度在细胞密度>5×10⁵个细胞/毫升的培养物中达到临界阈值时表达。在本报告中,我们表明,在无菌野生型菌株中,饥饿诱导的α-甘露糖苷酶基因转录不需要蛋白质合成,而对PSF响应所观察到的转录诱导则需要蛋白质合成。还使用来自Gα1和Gα2基因破坏突变体的mRNA进行了Northern印迹分析。这些基因编码在生长细胞和发育早期细胞的细胞表面发现的异源三聚体G蛋白的亚基。在这些突变体以及无法产生分泌糖蛋白条件培养基因子或cAMP受体-1蛋白的突变体中,α-甘露糖苷酶基因的表达模式是正常的。这些基因已被证明在早期发育过程中调节许多基因的表达。启动子分析研究确定了一个包含TTG框的145个碱基对的序列元件,该元件在饥饿条件下和对PSF的响应中是α-甘露糖苷酶转录诱导所必需的。所确定的TTG框是另一个饥饿前反应基因盘状蛋白Iγ基因启动子中的重要调节元件。发现一个温度敏感突变体在限制温度下错误调节盘状蛋白I和α-甘露糖苷酶的表达。综合这些结果表明,饥饿前反应基因可能通过TTG框进行协调调节。