Orb2 enables rare-codon-enriched mRNA expression during Drosophila neuron differentiation

Nat Commun. 2024 Jun 20;15(1):5270. doi: 10.1038/s41467-024-48344-8.

Abstract

Regulation of codon optimality is an increasingly appreciated layer of cell- and tissue-specific protein expression control. Here, we use codon-modified reporters to show that differentiation of Drosophila neural stem cells into neurons enables protein expression from rare-codon-enriched genes. From a candidate screen, we identify the cytoplasmic polyadenylation element binding (CPEB) protein Orb2 as a positive regulator of rare-codon-dependent mRNA stability in neurons. Using RNA sequencing, we reveal that Orb2-upregulated mRNAs in the brain with abundant Orb2 binding sites have a rare-codon bias. From these Orb2-regulated mRNAs, we demonstrate that rare-codon enrichment is important for mRNA stability and social behavior function of the metabotropic glutamate receptor (mGluR). Our findings reveal a molecular mechanism by which neural stem cell differentiation shifts genetic code regulation to enable critical mRNA stability and protein expression.

MeSH terms

  • Animals
  • Brain / cytology
  • Brain / metabolism
  • Cell Differentiation* / genetics
  • Codon / genetics
  • Drosophila / genetics
  • Drosophila / metabolism
  • Drosophila Proteins* / genetics
  • Drosophila Proteins* / metabolism
  • Drosophila melanogaster / cytology
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / metabolism
  • Neural Stem Cells* / cytology
  • Neural Stem Cells* / metabolism
  • Neurons* / cytology
  • Neurons* / metabolism
  • RNA Stability*
  • RNA, Messenger* / genetics
  • RNA, Messenger* / metabolism
  • Receptors, Metabotropic Glutamate / genetics
  • Receptors, Metabotropic Glutamate / metabolism
  • Transcription Factors
  • mRNA Cleavage and Polyadenylation Factors / genetics
  • mRNA Cleavage and Polyadenylation Factors / metabolism

Substances

  • Drosophila Proteins
  • RNA, Messenger
  • Orb2 protein, Drosophila
  • Codon
  • Receptors, Metabotropic Glutamate
  • mRNA Cleavage and Polyadenylation Factors
  • Transcription Factors