Tail-tape-fused virion and non-virion RNA polymerases of a thermophilic virus with an extremely long tail

Author:

Chaban Anastasiia,Minakhin Leonid,Goldobina Ekaterina,Bae Brain,Hao Yue,Borukhov Sergei,Putzeys Leena,Boon Maarten,Lavigne RobORCID,Makarova Kira S.,Koonin Eugene V.,Nair Satish K.,Tagami Shunsuke,Severinov Konstantin,Sokolova Maria L.ORCID

Abstract

AbstractThermus thermophilusbacteriophage P23-45 encodes a giant 5,002-residue tail tape measure protein (TMP)1that defines the length of its extraordinarily long 800 nm tail2,3. We found that the N-terminal portion of P23-45 TMP is an unusual RNA polymerase (RNAP) homologous to cellular and viral ‘two-barrel’ RNAPs. The TMP-fused virion RNAP transcribes pre-early phage genes, including a gene that encodes another, non-virion RNAP, that transcribes early and some middle phage genes. We determined the crystal structures of both P23-45 RNAPs. The non-virion RNAP has a crab claw-like architecture similar to previously reported two-barrel RNAPs. The virion RNAP adopts a unique flat structure without a clamp, which likely reflects the requirement for its extrusion through the narrow channel in the phage tail for delivery into the cell. Structure and sequence comparisons of the P23-45 RNAPs with other phage and cellular RNAPs suggest that, despite the extensive functional differences, the two P23-45 RNAPs originate from an ancient gene duplication in an ancestral phage. Our findings demonstrate remarkable adaptability of two-barrel RNAPs that can be attained within a single virus species.

Publisher

Cold Spring Harbor Laboratory

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