Effects of histone H4 depletion on the cell cycle and transcription of Saccharomyces cerevisiae
- PMID: 3046933
- PMCID: PMC454562
- DOI: 10.1002/j.1460-2075.1988.tb03060.x
Effects of histone H4 depletion on the cell cycle and transcription of Saccharomyces cerevisiae
Abstract
We have constructed a yeast strain (UKY403) in which the sole histone H4 gene is under control of the GAL1 promoter. This allows the activation of H4 mRNA synthesis on galactose and its repression on glucose. UKY403 cells, pre-synchronized in G1 with alpha-mating factor, have been used to show that glucose treatment results in the loss of approximately half the chromosomal nucleosomes. This depletion is only partially reversible when the H4 gene is reactivated on galactose. It was found that the resultant lethality manifests itself first in S phase, the period of nucleosome assembly, but leads to highly synchronous arrest in G2 and a virtually complete block in chromosomal segregation. Histone H4-depleted chromatin was analyzed for its efficiency as a template for all three RNA polymerases. Using pulse-labeling, we find no evidence for altered transcription by RNA polymerase I (25S, 18S and 5.8S rRNAs) or RNA polymerase III (5S rRNA, tRNAs). Northern blot analysis was used to measure levels of RNA polymerase II transcripts. There was little effect on the activation or repression of the CUP1 chelatin gene. While there may be some decrease in the level of certain mRNAs (e.g. HIS4, ARG4) other message levels (HIS3, TRP1) show little change upon glucose repression. Therefore, nucleosome loss certainly does not have a general effect on transcription.
Similar articles
-
Depletion of histone H4 and nucleosomes activates the PHO5 gene in Saccharomyces cerevisiae.EMBO J. 1988 Jul;7(7):2221-8. doi: 10.1002/j.1460-2075.1988.tb03061.x. EMBO J. 1988. PMID: 3046934 Free PMC article.
-
In vivo effects of histone H3 depletion on nucleosome occupancy and position in Saccharomyces cerevisiae.PLoS Genet. 2012;8(6):e1002771. doi: 10.1371/journal.pgen.1002771. Epub 2012 Jun 21. PLoS Genet. 2012. PMID: 22737086 Free PMC article.
-
Nucleosome fractionation by mercury affinity chromatography. Contrasting distribution of transcriptionally active DNA sequences and acetylated histones in nucleosome fractions of wild-type yeast cells and cells expressing a histone H3 gene altered to encode a cysteine 110 residue.J Biol Chem. 1991 Apr 5;266(10):6489-98. J Biol Chem. 1991. PMID: 2007598
-
Primary Role of the Nucleosome.Mol Cell. 2020 Aug 6;79(3):371-375. doi: 10.1016/j.molcel.2020.07.020. Mol Cell. 2020. PMID: 32763226 Review.
-
Regulation of histone gene expression in budding yeast.Genetics. 2012 May;191(1):7-20. doi: 10.1534/genetics.112.140145. Genetics. 2012. PMID: 22555441 Free PMC article. Review.
Cited by
-
Beyond the tail: the consequence of context in histone post-translational modification and chromatin research.Biochem J. 2024 Feb 21;481(4):219-244. doi: 10.1042/BCJ20230342. Biochem J. 2024. PMID: 38353483 Free PMC article.
-
Glucocorticoids are required for establishment and maintenance of an alteration in chromatin structure: induction leads to a reversible disruption of nucleosomes over an enhancer.EMBO J. 1991 Sep;10(9):2569-76. doi: 10.1002/j.1460-2075.1991.tb07797.x. EMBO J. 1991. PMID: 1678348 Free PMC article.
-
Low dosage of histone H4 leads to growth defects and morphological changes in Candida albicans.PLoS One. 2010 May 13;5(5):e10629. doi: 10.1371/journal.pone.0010629. PLoS One. 2010. PMID: 20498713 Free PMC article.
-
Hir proteins are required for position-dependent gene silencing in Saccharomyces cerevisiae in the absence of chromatin assembly factor I.Mol Cell Biol. 1998 Aug;18(8):4793-806. doi: 10.1128/MCB.18.8.4793. Mol Cell Biol. 1998. PMID: 9671489 Free PMC article.
-
Nucleosome loss activates CUP1 and HIS3 promoters to fully induced levels in the yeast Saccharomyces cerevisiae.Mol Cell Biol. 1992 Apr;12(4):1621-9. doi: 10.1128/mcb.12.4.1621-1629.1992. Mol Cell Biol. 1992. PMID: 1549116 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases
Research Materials