Nature Communications (Jan 2024)

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

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

DOI
https://doi.org/10.1038/s41467-023-44630-z
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 12

Abstract

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Abstract Thermus thermophilus bacteriophage P23-45 encodes a giant 5,002-residue tail tape measure protein (TMP) that defines the length of its extraordinarily long tail. Here, we show that the N-terminal portion of P23-45 TMP is an unusual RNA polymerase (RNAP) homologous to cellular 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 report the crystal structures of both P23-45 RNAPs. The non-virion RNAP has a crab-claw-like architecture. By contrast, the virion RNAP adopts a unique flat structure without a clamp. Structure and sequence comparisons of the P23-45 RNAPs with other 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 striking adaptability of RNAPs that can be attained within a single virus species.