首页> 外文期刊>Nucleic Acids Research >Two groups of phenylalanine biosynthetic operon leader peptides genes: a high level of apparently incidental frameshifting in decoding Escherichia coli pheL
【24h】

Two groups of phenylalanine biosynthetic operon leader peptides genes: a high level of apparently incidental frameshifting in decoding Escherichia coli pheL

机译:两组苯丙氨酸生物合成操纵子前导肽基因:解码大肠杆菌pheL时明显发生偶然的移码

获取原文
获取原文并翻译 | 示例
           

摘要

The bacterial pheL gene encodes the leader peptide for the phenylalanine biosynthetic operon. Translation of pheL mRNA controls transcription attenuation and, consequently, expression of the downstream pheA gene. Fifty-three unique pheL genes have been identified in sequenced genomes of the gamma subdivision. There are two groups of pheL genes, both of which are short and contain a run(s) of phenylalanine codons at an internal position. One group is somewhat diverse and features different termination and 5'-flanking codons. The other group, mostly restricted to Enterobacteria and including Escherichia coli pheL, has a conserved nucleotide sequence that ends with UUC_CCC_UGA. When these three codons in E. coli pheL mRNA are in the ribosomal E-, P- and A-sites, there is an unusually high level, 15%, of +1 ribosomal frameshifting due to features of the nascent peptide sequence that include the penultimate phenylalanine. This level increases to 60% with a natural, heterologous, nascent peptide stimulator. Nevertheless, studies with different tRNA(Pro) mutants in Salmonella enterica suggest that frameshifting at the end of pheL does not influence expression of the downstream pheA. This finding of incidental, rather than utilized, frameshifting is cautionary for other studies of programmed frameshifting.
机译:细菌pheL基因编码苯丙氨酸生物合成操纵子的前导肽。 pheL mRNA的翻译控制转录的衰减,进而控制下游pheA基因的表达。在γ细分的测序基因组中已鉴定出53个独特的pheL基因。有两组pheL基因,它们都很短,并且在内部位置包含一系列苯丙氨酸密码子。一组稍有不同,具有不同的终止和5'侧翼密码子。另一类主要限于肠杆菌,包括大肠杆菌pheL,其保守核苷酸序列以UUC_CCC_UGA结尾。当大肠杆菌pheL mRNA中的这三个密码子位于核糖体E,P和A位点时,由于新生肽序列的特征,其中包括15%的+1核糖体移码率异常高。倒数第二个苯丙氨酸。使用天然的,异源的,新生的肽刺激剂,该水平增加到60%。但是,在沙门氏菌中使用不同tRNA(Pro)突变体的研究表明,在pheL末端移码不会影响下游pheA的表达。对于程序化移码的其他研究,偶然发现而不是利用移码的这一发现是谨慎的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号