Manipulation of the human tRNA pool reveals distinct tRNA sets that act in cellular proliferation or cell cycle arrest

Elife. 2020 Dec 24:9:e58461. doi: 10.7554/eLife.58461.

Abstract

Different subsets of the tRNA pool in human cells are expressed in different cellular conditions. The 'proliferation-tRNAs' are induced upon normal and cancerous cell division, while the 'differentiation-tRNAs' are active in non-dividing, differentiated cells. Here we examine the essentiality of the various tRNAs upon cellular growth and arrest. We established a CRISPR-based editing procedure with sgRNAs that each target a tRNA family. We measured tRNA essentiality for cellular growth and found that most proliferation-tRNAs are essential compared to differentiation- tRNAs in rapidly growing cell lines. Yet in more slowly dividing lines, the differentiation-tRNAs were more essential. In addition, we measured the essentiality of each tRNA family upon response to cell cycle arresting signals. Here we detected a more complex behavior with both proliferation-tRNAs and differentiation tRNAs showing various levels of essentiality. These results provide the so-far most comprehensive functional characterization of human tRNAs with intricate roles in various cellular states.

Keywords: CRISPR; cell biology; cell cycle arrest; cell proliferation; genetics; genomics; human; tRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CRISPR-Associated Protein 9
  • CRISPR-Cas Systems
  • Cell Cycle / genetics
  • Cell Cycle Checkpoints* / genetics
  • Cell Line
  • Cell Proliferation* / genetics
  • Cloning, Molecular
  • Gene Editing
  • Genomic Library
  • HeLa Cells
  • Humans
  • RNA, Transfer / genetics
  • RNA, Transfer / metabolism*

Substances

  • RNA, Transfer
  • CRISPR-Associated Protein 9

Associated data

  • GEO/GSE163611