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8GH6

Bombyx mori R2 retrotransposon initiating target-primed reverse transcription

This is a non-PDB format compatible entry.
Summary for 8GH6
Entry DOI10.2210/pdb8gh6/pdb
EMDB information40033
DescriptorReverse transcriptase-like protein, 28S DNA bottom strand, 3' side, 28S DNA bottom strand, 5' side (priming strand), ... (8 entities in total)
Functional Keywordsretrotransposon, line, reverse transcriptase, endonuclease, rna binding protein, rna binding protein-rna-dna complex, rna binding protein/rna/dna
Biological sourceBombyx mori (domestic silkworm)
More
Total number of polymer chains5
Total formula weight255812.02
Authors
Wilkinson, M.E.,Zhang, F. (deposition date: 2023-03-09, release date: 2023-04-05, Last modification date: 2023-08-16)
Primary citationWilkinson, M.E.,Frangieh, C.J.,Macrae, R.K.,Zhang, F.
Structure of the R2 non-LTR retrotransposon initiating target-primed reverse transcription.
Science, 380:301-308, 2023
Cited by
PubMed Abstract: Non-long terminal repeat (non-LTR) retrotransposons, or long interspersed nuclear elements (LINEs), are an abundant class of eukaryotic transposons that insert into genomes by target-primed reverse transcription (TPRT). During TPRT, a target DNA sequence is nicked and primes reverse transcription of the retrotransposon RNA. Here, we report the cryo-electron microscopy structure of the R2 non-LTR retrotransposon initiating TPRT at its ribosomal DNA target. The target DNA sequence is unwound at the insertion site and recognized by an upstream motif. An extension of the reverse transcriptase (RT) domain recognizes the retrotransposon RNA and guides the 3' end into the RT active site to template reverse transcription. We used Cas9 to retarget R2 in vitro to non-native sequences, suggesting future use as a reprogrammable RNA-based gene-insertion tool.
PubMed: 37023171
DOI: 10.1126/science.adg7883
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.08 Å)
Structure validation

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