Freitag M, Dighde N, Sachs M S
Department of Chemistry, Biochemistry, and Molecular Biology, Oregon Graduate Institute of Science & Technology, Portland 97291-1000, USA.
Genetics. 1996 Jan;142(1):117-27. doi: 10.1093/genetics/142.1.117.
The Neurospora crassa arg-2 gene encodes the small subunit of arginine-specific carbamoyl phosphate synthetase. The levels of arg-2 mRNA and mRNA translation are negatively regulated by arginine. An upstream open reading frame (uORF) in the transcript's 5' region has been implicated in arginine-specific control. An arg-2-hph fusion gene encoding hygromycin phosphotransferase conferred arginine-regulated resistance to hygromycin when introduced into N. crassa. We used an arg-2-hph strain to select for UV-induced mutants that grew in the presence of hygromycin and arginine, and we isolated 46 mutants that had either of two phenotypes. One phenotype indicated altered expression of both arg-2-hph and arg-2 genes; the other, altered expression of arg-2-hph but not arg-2. One of the latter mutations, which was genetically closely linked to arg-2-hph, was recovered from the 5' region of the arg-2-hph gene using PCR. Sequence analyses and transformation experiments revealed a mutation at uORF codon 12 (Asp to Asn) that abrogated negative regulation. Examination of the distribution of ribosomes on arg-2-hph transcripts showed that loss of regulation had a translational component, indicating the uORF sequence was important for Arg-specific translational control. Comparisons with other uORF5 suggest common elements in translational control mechanisms.
粗糙脉孢菌的arg - 2基因编码精氨酸特异性氨甲酰磷酸合成酶的小亚基。arg - 2 mRNA的水平和mRNA翻译受到精氨酸的负调控。转录本5'区域的一个上游开放阅读框(uORF)与精氨酸特异性调控有关。当将编码潮霉素磷酸转移酶的arg - 2 - hph融合基因导入粗糙脉孢菌时,它赋予了对潮霉素的精氨酸调节抗性。我们使用arg - 2 - hph菌株来筛选在潮霉素和精氨酸存在下生长的紫外线诱导突变体,并分离出了46个具有两种表型之一的突变体。一种表型表明arg - 2 - hph和arg - 2基因的表达均发生改变;另一种表型是arg - 2 - hph的表达改变而arg - 2的表达未改变。后一种突变中的一个与arg - 2 - hph在遗传上紧密连锁,使用PCR从arg - 2 - hph基因的5'区域中分离得到。序列分析和转化实验揭示了uORF密码子12处的一个突变(天冬氨酸突变为天冬酰胺),该突变消除了负调控。对arg - 2 - hph转录本上核糖体分布的检查表明,调控的丧失具有翻译成分,这表明uORF序列对于精氨酸特异性翻译控制很重要。与其他uORF5的比较表明了翻译控制机制中的共同元件。