The Role of S. cerevisiae Sub1/PC4 in Transcription Elongation Depends on the C-Terminal Region and Is Independent of the ssDNA Binding Domain

Cells. 2022 Oct 21;11(20):3320. doi: 10.3390/cells11203320.

Abstract

Saccharomyces cerevisiae Sub1 (ScSub1) has been defined as a transcriptional stimulatory protein due to its homology to the ssDNA binding domain (ssDBD) of human PC4 (hPC4). Recently, PC4/Sub1 orthologues have been elucidated in eukaryotes, prokaryotes, and bacteriophages with functions related to DNA metabolism. Additionally, ScSub1 contains a unique carboxyl-terminal region (CT) of unknown function up to date. Specifically, it has been shown that Sub1 is required for transcription activation, as well as other processes, throughout the transcription cycle. Despite the progress that has been made in understanding the mechanism underlying Sub1's functions, some questions remain unanswered. As a case in point: whether Sub1's roles in initiation and elongation are differentially predicated on distinct regions of the protein or how Sub1's functions are regulated. Here, we uncover some residues that are key for DNA-ScSub1 interaction in vivo, localized in the ssDBD, and required for Sub1 recruitment to promoters. Furthermore, using an array of genetic and molecular techniques, we demonstrate that the CT region is required for transcription elongation by RNA polymerase II (RNAPII). Altogether, our data indicate that Sub1 plays a dual role during transcription-in initiation through the ssDBD and in elongation through the CT region.

Keywords: DNA binding proteins; PC4; RNA polymerase II; Saccharomyces cerevisiae; Sub1; transcription elongation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA-Binding Proteins / metabolism
  • Humans
  • RNA Polymerase II / metabolism
  • Saccharomyces cerevisiae Proteins* / genetics
  • Saccharomyces cerevisiae Proteins* / metabolism
  • Saccharomyces cerevisiae* / genetics
  • Saccharomyces cerevisiae* / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • DNA-Binding Proteins
  • RNA Polymerase II
  • Saccharomyces cerevisiae Proteins
  • Transcription Factors
  • SUB1 protein, S cerevisiae

Grants and funding

Funding was provided with the following grants conceded to O.C.: Project BFU2017-84694-P funded by MCIN/AEI/10.13039/501100011033/ and ERDF, a way to make Europe; and project PID2020-116396GB-I00 funded by MCIN/AEI/10.13039/501100011033. A.G.-J. was supported by a pre-doctoral contract from “Junta de Castilla y León” & co-funded by European Social Fund, and M.d.C.G.-J. with a “Margarita Salas” post-doctoral contract (UCOR01MS) from the University of Córdoba (grants to Public Universities for the requalification of the Spanish university system from the Ministry of Universities financed by the European Union (NexGenerationEU). The IBFG is supported in part by an institutional grant from the “Junta y Castilla y León” (Programa “Escalera de Excelencia” de la Junta de Castilla y León, Ref. CLU-2017-03 co-funded by P.O. FEDER de Castilla y León 14-20), and by the Project “CL-EI-2021-08-IBFG Unit of Excellence “ of the CSIC, funded by the Junta de Castilla y León and co-financed by the European Union (ERDF “Europe drives our growth”).