4.8 Article

Coding-Sequence Determinants of Gene Expression in Escherichia coli

期刊

SCIENCE
卷 324, 期 5924, 页码 255-258

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1170160

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资金

  1. Burroughs Wellcome Fund
  2. James S. McDonnell Foundation
  3. Penn Genome Frontiers Institute
  4. Defense Advanced Research Projects Agency [HR0011-05-1-0057]
  5. Foundation for Polish Science
  6. European Molecular Biology Organization
  7. Wellcome Trust/BBSRC [BB/DO19621/1]
  8. Biotechnology and Biological Sciences Research Council [BB/D019621/1] Funding Source: researchfish
  9. BBSRC [BB/D019621/1] Funding Source: UKRI

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Synonymous mutations do not alter the encoded protein, but they can influence gene expression. To investigate how, we engineered a synthetic library of 154 genes that varied randomly at synonymous sites, but all encoded the same green fluorescent protein (GFP). When expressed in Escherichia coli, GFP protein levels varied 250-fold across the library. GFP messenger RNA (mRNA) levels, mRNA degradation patterns, and bacterial growth rates also varied, but codon bias did not correlate with gene expression. Rather, the stability of mRNA folding near the ribosomal binding site explained more than half the variation in protein levels. In our analysis, mRNA folding and associated rates of translation initiation play a predominant role in shaping expression levels of individual genes, whereas codon bias influences global translation efficiency and cellular fitness.

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