RNA polymerase II CTD interactome with 3′ processing and termination factors in fission yeast and its impact on phosphate homeostasis Academic Article uri icon


MeSH Major

  • Manganese
  • Phosphoric Diester Hydrolases
  • RNA Nucleotidyltransferases
  • Saccharomyces cerevisiae
  • Saccharomyces cerevisiae Proteins


  • © 2018 BioMed Central Ltd..All right reserved. The carboxy-terminal domain (CTD) code encrypted within the Y1S2P3T4S5P6S7 heptad repeats of RNA polymerase II (Pol2) is deeply rooted in eukaryal biology. Key steps to deciphering the code are identifying the events in gene expression that are governed by individual "letters" and then defining a vocabulary of multiletter "words" and their meaning. Thr4 and Ser7 exert opposite effects on the fission yeast pho1 gene, expression of which is repressed under phosphate-replete conditions by transcription of an upstream flanking long noncoding RNA (lncRNA). Here we attribute the derepression of pho1 by a CTD-S7A mutation to precocious termination of lncRNA synthesis, an effect that is erased by mutations of cleavage-polyadenylation factor (CPF) subunits Ctf1, Ssu72, Ppn1, Swd22, and Dis2 and termination factor Rhn1. By contrast, a CTD-T4A mutation hyperrepresses pho1, as do CPF subunit and Rhn1 mutations, implying that T4A reduces lncRNA termination. Moreover, CTD-T4A is synthetically lethal with ppn1Δ and swd22Δ, signifying that Thr4 and the Ppn1·Swd22 module play important, functionally redundant roles in promoting Pol2 termination. We find that Ppn1 and Swd22 become essential for viability when the CTD array is curtailed and that S7A overcomes the need for Ppn1·Swd22 in the short CTD context. Mutational synergies highlight redundant essential functions of (i) Ppn1·Swd22 and Rhn1, (ii) Ppn1·Swd22 and Ctf1, and (iii) Ssu72 and Dis2 phosphatases. CTD alleles Y1F, S2A, and T4A have overlapping synthetic lethalities with ppn1Δ and swd22Δ, suggesting that Tyr1-Ser2-Thr4 form a three-letter CTD word that abets termination, with Rhn1 being a likely "reader" of this word.

publication date

  • November 6, 2018



  • Academic Article



  • eng

PubMed Central ID

  • PMC6233144

Digital Object Identifier (DOI)

  • 10.1073/pnas.1810711115

PubMed ID

  • 30355770

Additional Document Info

start page

  • E10652

end page

  • E10661


  • 115


  • 45