Luo Z, Freitag M, Sachs M S
Department of Chemistry, Biochemistry, and Molecular Biology, Oregon Graduate Institute of Science and Technology, Portland, Oregon 97291-1000, USA.
Mol Cell Biol. 1995 Oct;15(10):5235-45. doi: 10.1128/MCB.15.10.5235.
We examined the regulation of Neurospora crassa arg-2 and cpc-1 in response to amino acid availability.arg-2 encodes the small subunit of arginine-specific carbamoyl phosphate synthetase; it is subject to unique negative regulation by Arg and is positively regulated in response to limitation for many different amino acids through a mechanism known as cross-pathway control. cpc-1 specifies a transcriptional activator important for crosspathway control. Expression of these genes was compared with that of the cytochrome oxidase subunit V gene, cox-5. Analyses of mRNA levels, polypeptide pulse-labeling results, and the distribution of mRNA in polysomes indicated that Arg-specific negative regulation of arg-2 affected the levels of both arg-2 mRNA and arg-2 mRNA translation. Negative translational effects on arg-2 and positive translational effects on cpc-1 were apparent soon after cells were provided with exogenous Arg. In cells limited for His, increased expression of arg-2 and cpc-1, and decreased expression of cox-5, also had translational and transcriptional components. The arg-2 and cpc-1 transcripts contain upstream open reading frames (uORFs), as do their Saccharomyces cerevisiae homologs CPA1 and GCN4. We examined the regulation of arg-2-lacZ reporter genes containing or lacking the uORF start codon; the capacity for arg-2 uORF translation appeared critical for controlling gene expression.
我们研究了粗糙脉孢菌中arg-2和cpc-1基因在氨基酸可利用性变化时的调控情况。arg-2编码精氨酸特异性氨甲酰磷酸合成酶的小亚基;它受到精氨酸独特的负调控,并且在多种不同氨基酸受限的情况下,通过一种称为交叉途径控制的机制受到正调控。cpc-1编码一种对交叉途径控制很重要的转录激活因子。将这些基因的表达与细胞色素氧化酶亚基V基因cox-5的表达进行了比较。对mRNA水平、多肽脉冲标记结果以及mRNA在多核糖体中的分布分析表明,arg-2的精氨酸特异性负调控影响了arg-2 mRNA的水平及其翻译。在向细胞提供外源精氨酸后不久,对arg-2的负翻译效应和对cpc-1的正翻译效应就很明显。在组氨酸受限的细胞中,arg-2和cpc-1表达增加,而cox-5表达减少,这也具有翻译和转录成分。arg-2和cpc-1转录本含有上游开放阅读框(uORF),它们在酿酒酵母中的同源物CPA1和GCN4也是如此。我们研究了含有或缺少uORF起始密码子的arg-2-lacZ报告基因的调控;arg-2的uORF翻译能力似乎对控制基因表达至关重要。