Cargando…

The Fkh1 Forkhead associated domain promotes ORC binding to a subset of DNA replication origins in budding yeast

The pioneer event in eukaryotic DNA replication is binding of chromosomal DNA by the origin recognitioncomplex (ORC). The ORC-DNA complex directs the formation of origins, the specific chromosomal regions where DNA synthesis initiates. In all eukaryotes, incompletely understood features of chromatin...

Descripción completa

Detalles Bibliográficos
Autores principales: Hoggard, Timothy, Hollatz, Allison J, Cherney, Rachel E, Seman, Melissa R, Fox, Catherine A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501964/
https://www.ncbi.nlm.nih.gov/pubmed/34095951
http://dx.doi.org/10.1093/nar/gkab450
_version_ 1784580782781628416
author Hoggard, Timothy
Hollatz, Allison J
Cherney, Rachel E
Seman, Melissa R
Fox, Catherine A
author_facet Hoggard, Timothy
Hollatz, Allison J
Cherney, Rachel E
Seman, Melissa R
Fox, Catherine A
author_sort Hoggard, Timothy
collection PubMed
description The pioneer event in eukaryotic DNA replication is binding of chromosomal DNA by the origin recognitioncomplex (ORC). The ORC-DNA complex directs the formation of origins, the specific chromosomal regions where DNA synthesis initiates. In all eukaryotes, incompletely understood features of chromatin promote ORC-DNA binding. Here, we uncover a role for the Fkh1 (Forkhead homolog) protein and its forkhead associated (FHA) domain in promoting ORC-origin binding and origin activity at a subset of origins in Saccharomyces cerevisiae. Several of the FHA-dependent origins examined required a distinct Fkh1 binding site located 5′ of and proximal to their ORC sites (5′-FKH-T site). Genetic and molecular experiments provided evidence that the Fkh1-FHA domain promoted origin activity directly through Fkh1 binding to this 5′ FKH-T site. Nucleotide substitutions within two relevant origins that enhanced their ORC-DNA affinity bypassed the requirement for their 5′ FKH-T sites and for the Fkh1-FHA domain. Significantly, assessment of ORC-origin binding by ChIPSeq provided evidence that this mechanism was relevant at ∼25% of yeast origins. Thus, the FHA domain of the conserved cell-cycle transcription factor Fkh1 enhanced origin selection in yeast at the level of ORC-origin binding.
format Online
Article
Text
id pubmed-8501964
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-85019642021-10-12 The Fkh1 Forkhead associated domain promotes ORC binding to a subset of DNA replication origins in budding yeast Hoggard, Timothy Hollatz, Allison J Cherney, Rachel E Seman, Melissa R Fox, Catherine A Nucleic Acids Res NAR Breakthrough Article The pioneer event in eukaryotic DNA replication is binding of chromosomal DNA by the origin recognitioncomplex (ORC). The ORC-DNA complex directs the formation of origins, the specific chromosomal regions where DNA synthesis initiates. In all eukaryotes, incompletely understood features of chromatin promote ORC-DNA binding. Here, we uncover a role for the Fkh1 (Forkhead homolog) protein and its forkhead associated (FHA) domain in promoting ORC-origin binding and origin activity at a subset of origins in Saccharomyces cerevisiae. Several of the FHA-dependent origins examined required a distinct Fkh1 binding site located 5′ of and proximal to their ORC sites (5′-FKH-T site). Genetic and molecular experiments provided evidence that the Fkh1-FHA domain promoted origin activity directly through Fkh1 binding to this 5′ FKH-T site. Nucleotide substitutions within two relevant origins that enhanced their ORC-DNA affinity bypassed the requirement for their 5′ FKH-T sites and for the Fkh1-FHA domain. Significantly, assessment of ORC-origin binding by ChIPSeq provided evidence that this mechanism was relevant at ∼25% of yeast origins. Thus, the FHA domain of the conserved cell-cycle transcription factor Fkh1 enhanced origin selection in yeast at the level of ORC-origin binding. Oxford University Press 2021-06-07 /pmc/articles/PMC8501964/ /pubmed/34095951 http://dx.doi.org/10.1093/nar/gkab450 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle NAR Breakthrough Article
Hoggard, Timothy
Hollatz, Allison J
Cherney, Rachel E
Seman, Melissa R
Fox, Catherine A
The Fkh1 Forkhead associated domain promotes ORC binding to a subset of DNA replication origins in budding yeast
title The Fkh1 Forkhead associated domain promotes ORC binding to a subset of DNA replication origins in budding yeast
title_full The Fkh1 Forkhead associated domain promotes ORC binding to a subset of DNA replication origins in budding yeast
title_fullStr The Fkh1 Forkhead associated domain promotes ORC binding to a subset of DNA replication origins in budding yeast
title_full_unstemmed The Fkh1 Forkhead associated domain promotes ORC binding to a subset of DNA replication origins in budding yeast
title_short The Fkh1 Forkhead associated domain promotes ORC binding to a subset of DNA replication origins in budding yeast
title_sort fkh1 forkhead associated domain promotes orc binding to a subset of dna replication origins in budding yeast
topic NAR Breakthrough Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501964/
https://www.ncbi.nlm.nih.gov/pubmed/34095951
http://dx.doi.org/10.1093/nar/gkab450
work_keys_str_mv AT hoggardtimothy thefkh1forkheadassociateddomainpromotesorcbindingtoasubsetofdnareplicationoriginsinbuddingyeast
AT hollatzallisonj thefkh1forkheadassociateddomainpromotesorcbindingtoasubsetofdnareplicationoriginsinbuddingyeast
AT cherneyrachele thefkh1forkheadassociateddomainpromotesorcbindingtoasubsetofdnareplicationoriginsinbuddingyeast
AT semanmelissar thefkh1forkheadassociateddomainpromotesorcbindingtoasubsetofdnareplicationoriginsinbuddingyeast
AT foxcatherinea thefkh1forkheadassociateddomainpromotesorcbindingtoasubsetofdnareplicationoriginsinbuddingyeast
AT hoggardtimothy fkh1forkheadassociateddomainpromotesorcbindingtoasubsetofdnareplicationoriginsinbuddingyeast
AT hollatzallisonj fkh1forkheadassociateddomainpromotesorcbindingtoasubsetofdnareplicationoriginsinbuddingyeast
AT cherneyrachele fkh1forkheadassociateddomainpromotesorcbindingtoasubsetofdnareplicationoriginsinbuddingyeast
AT semanmelissar fkh1forkheadassociateddomainpromotesorcbindingtoasubsetofdnareplicationoriginsinbuddingyeast
AT foxcatherinea fkh1forkheadassociateddomainpromotesorcbindingtoasubsetofdnareplicationoriginsinbuddingyeast