Phage-triggered reverse transcription assembles a toxic repetitive gene from a noncoding RNA
Reverse transcription has frequently been co-opted for cellular functions and in prokaryotes is associated with protection against viral infection, but the underlying mechanisms of defense are generally unknown. Here, we show that in the DRT2 defense system, the reverse transcriptase binds a neighboring pseudoknotted noncoding RNA. Upon bacteriophage infection, a template region of this RNA is reverse transcribed into an array of tandem repeats that reconstitute a promoter and open reading frame, allowing expression of a toxic repetitive protein and an abortive infection response. Biochemical reconstitution of this activity and cryo-electron microscopy provide a molecular basis for repeat synthesis. Gene synthesis from a noncoding RNA is a previously unknown mode of genetic regulation in prokaryotes.
Authors
- Linyi Gao (ORCID: https://orcid.org/0000-0002-3579-0327)
- Max E. Wilkinson (ORCID: https://orcid.org/0000-0003-4738-9503)
- Rhiannon K. Macrae (ORCID: https://orcid.org/0000-0002-7850-9056)
- Feng Zhang (ORCID: https://orcid.org/0000-0003-0178-7995)
- David Li (ORCID: https://orcid.org/0000-0002-8921-5168)
Institutions
- Broad Institute (US)
- Howard Hughes Medical Institute (US)
- McGovern Institute for Brain Research (US)
- Massachusetts Institute of Technology (US)
- Stanford University (US)
Publication Details
- Journal
- Science
- Published
- 2024-08-29
- DOI
- https://doi.org/10.1126/science.adq3977
- Citations
- 37
- Primary Topic
- Bacteriophages and microbial interactions
- Type
- article
- Field-Weighted Citation Impact
- 16.98
Funders
- Harvard University
- Broad Institute