Mutations in yeast Pcf11, a conserved protein essential for mRNA 3′ end processing and transcription termination, elicit the Environmental Stress Response

Author:

Graber Joel H1,Hoskinson Derick2,Liu Huiyun2,Kaczmarek Michaels Katarzyna2,Benson Peter S1ORCID,Maki Nathaniel J1,Wilson Christian L1,McGrath Caleb3,Puleo Franco2,Pearson Erika2,Kuehner Jason N3ORCID,Moore Claire2ORCID

Affiliation:

1. Mount Desert Island Biological Laboratory , Bar Harbor, ME 04609 , USA

2. Department of Development, Molecular, and Chemical Biology and School of Graduate Biomedical Science, Tufts University School of Medicine , Boston, MA 02111 , USA

3. Department of Biology, Emmanuel College , Boston, MA 02115 , USA

Abstract

Abstract The Pcf11 protein is an essential subunit of the large complex that cleaves and polyadenylates eukaryotic mRNA precursor. It has also been functionally linked to gene-looping, termination of RNA Polymerase II (Pol II) transcripts, and mRNA export. We have examined a poorly characterized but conserved domain (amino acids 142–225) of the Saccharomyces cerevisiae  Pcf11 and found that while it is not needed for mRNA 3′ end processing or termination downstream of the poly(A) sites of protein-coding genes, its presence improves the interaction with Pol II and the use of transcription terminators near gene promoters. Analysis of genome-wide Pol II occupancy in cells with Pcf11 missing this region, as well as Pcf11 mutated in the Pol II CTD Interacting Domain, indicates that systematic changes in mRNA expression are mediated primarily at the level of transcription. Global expression analysis also shows that a general stress response, involving both activation and suppression of specific gene sets known to be regulated in response to a wide variety of stresses, is induced in the two pcf11 mutants, even though cells are grown in optimal conditions. The mutants also cause an unbalanced expression of cell wall-related genes that does not activate the Cell Wall Integrity pathway but is associated with strong caffeine sensitivity. Based on these findings, we propose that Pcf11 can modulate the expression level of specific functional groups of genes in ways that do not involve its well-characterized role in mRNA 3′ end processing.

Funder

NSF

Institutional Development Award

National Institute of General Medical Sciences

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Genetics

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