Yeast 18 S rRNA Is directly involved in the ribosomal response to stringent AUG selection during translation initiation

Naoki Nemoto, Chingakham Ranjit Singh, Tsuyoshi Udagawa, Suzhi Wang, Elizabeth Thorson, Zachery Winter, Takahiro Ohira, Miki Ii, Leoš Valášek, Susan J. Brown, Katsura Asano

研究成果: Article査読

18 被引用数 (Scopus)

抄録

In eukaryotes, the 40 S ribosomal subunit serves as the platform of initiation factor assembly, to place itself precisely on the AUG start codon. Structural arrangement of the 18 S rRNA determines the overall shape of the 40 S subunit. Here, we present genetic evaluation of yeast 18 S rRNA function using 10 point mutations altering the polysome profile. All the mutants reduce the abundance of the mutant 40 S, making it limiting for translation initiation. Two of the isolated mutations, G875A, altering the core of the platform domain that binds eIF1 and eIF2, and A1193U, changing the h31 loop located below the P-site tRNAiMet, show phenotypes indicating defective regulation of AUG selection. Evidence is provided that these mutations reduce the interaction with the components of the preinitiation complex, thereby inhibiting its function at different steps. These results indicate that the 18 S rRNA mutations impair the integrity of scanning-competent preinitiation complex, thereby altering the 40 S subunit response to stringent AUG selection. Interestingly, nine of the mutations alter the body/platform domains of 18 S rRNA, potentially affecting the bridges to the 60 S subunit, but they do not change the level of 18 S rRNA intermediates. Based on these results, we also discuss the mechanism of the selective degradation of the mutant 40 S subunits.

本文言語English
ページ(範囲)32200-32212
ページ数13
ジャーナルJournal of Biological Chemistry
285
42
DOI
出版ステータスPublished - 2010 10月 15
外部発表はい

ASJC Scopus subject areas

  • 生化学
  • 分子生物学
  • 細胞生物学

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