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9C0I

Structure of the DRT2 reverse transcriptase in complex with its non-coding RNA

Summary for 9C0I
Entry DOI10.2210/pdb9c0i/pdb
EMDB information45085
DescriptorReverse transcriptase/maturase family protein, DNA primer, DRT2 ncRNA, ... (5 entities in total)
Functional Keywordsreverse transcriptase, rolling circle amplification, phage defense, transferase-dna-rna complex, transferase/dna/rna
Biological sourceKlebsiella pneumoniae
More
Total number of polymer chains3
Total formula weight142322.53
Authors
Wilkinson, M.E.,Zhang, F. (deposition date: 2024-05-25, release date: 2024-09-04, Last modification date: 2024-10-16)
Primary citationWilkinson, M.E.,Li, D.,Gao, A.,Macrae, R.K.,Zhang, F.
Phage-triggered reverse transcription assembles a toxic repetitive gene from a noncoding RNA.
Science, 386:eadq3977-eadq3977, 2024
Cited by
PubMed Abstract: 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 cryogenic electron microscopy provide a molecular basis for repeat synthesis. Gene synthesis from a noncoding RNA is a new mode of genetic regulation in prokaryotes.
PubMed: 39208082
DOI: 10.1126/science.adq3977
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.91 Å)
Structure validation

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PDB entries from 2024-11-13

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