SOX4-mediated repression of specific tRNAs inhibits proliferation of human glioblastoma cells

Proc Natl Acad Sci U S A. 2020 Mar 17;117(11):5782-5790. doi: 10.1073/pnas.1920200117. Epub 2020 Mar 2.

Abstract

Transfer RNAs (tRNAs) are products of RNA polymerase III (Pol III) and essential for mRNA translation and ultimately cell growth and proliferation. Whether and how individual tRNA genes are specifically regulated is not clear. Here, we report that SOX4, a well-known Pol II-dependent transcription factor that is critical for neurogenesis and reprogramming of somatic cells, also directly controls, unexpectedly, the expression of a subset of tRNA genes and therefore protein synthesis and proliferation of human glioblastoma cells. Genome-wide location analysis through chromatin immunoprecipitation-sequencing uncovers specific targeting of SOX4 to a subset of tRNA genes, including those for tRNAiMet Mechanistically, sequence-specific SOX4-binding impedes the recruitment of TATA box binding protein and Pol III to tRNA genes and thereby represses their expression. CRISPR/Cas9-mediated down-regulation of tRNAiMet greatly inhibits growth and proliferation of human glioblastoma cells. Conversely, ectopic tRNAiMet partially rescues SOX4-mediated repression of cell proliferation. Together, these results uncover a regulatory mode of individual tRNA genes to control cell behavior. Such regulation may coordinate codon usage and translation efficiency to meet the demands of diverse tissues and cell types, including cancer cells.

Keywords: SOX4; glioblastoma; mRNA translation; tRNA expression; tRNAiMet.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brain Neoplasms / metabolism*
  • Cell Line, Tumor
  • Cell Proliferation*
  • DNA Polymerase III / metabolism
  • Glioblastoma / metabolism*
  • HEK293 Cells
  • Humans
  • RNA, Transfer / genetics
  • RNA, Transfer / metabolism*
  • SOXC Transcription Factors / genetics
  • SOXC Transcription Factors / metabolism*
  • TATA-Box Binding Protein / genetics
  • TATA-Box Binding Protein / metabolism

Substances

  • SOX4 protein, human
  • SOXC Transcription Factors
  • TATA-Box Binding Protein
  • TBP protein, human
  • RNA, Transfer
  • DNA Polymerase III