twenty-five years of the nucleosome kornberg and lorch 1998, cell 98: 285
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Twenty-five years of the nucleosome Kornberg and Lorch 1998, Cell 98: 285. HATs. HDACs. Important point-. P289- Although acetylation of histone tails may counteract condensation of nucleosomes in chromatin fibers, it is unlikely to disrupt the structure of the core particle for transcription - PowerPoint PPT PresentationTRANSCRIPT
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Twenty-five years of the nucleosome
Kornberg and Lorch 1998, Cell 98: 285.
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HATs
HDACs
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Important point-• P289- Although acetylation of histone tails
may counteract condensation of nucleosomes in chromatin fibers, it is unlikely to disrupt the structure of the core particle for transcription
• Why? Tails are outside of the core, make little contribution to overall structure
• Chromatin remodeling enzymes are likely responsible for nucleosome disruption
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Chromatin remodeling
• SWI/SNF proteins are chromatin remodelers
• These disrupt nucleosome in an ATP-dependent fashion (ATPase activity)
• Models- – displacement– octamer sliding
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Histones- modifications and function
Michael Hagmann 1999 Science 285:1203
• A. Phosphorylation of histones• two opposing functions reported
» opening chromatin» condensing chromatin (cell division)
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I. Phosphorylation
Cellular and Molecular Genetics BLA510 Spring 2001Gary A. Bulla, PhD
• Immunocytochemistry with anti-phosphoH3 antibody
• Phosphorylation of H3 observed during mitosis
• Growth factor stimulation- observe ~100 speckels in cells, randomly distributed
– correlates with # of genes that respond to growth factor stimuli.
– Identify a 90 Kd protein
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B. Coffin Lowry syndrome- mental retardation and a defect in growth factor response
• mutation identified in in Rsk-2 gene •Immunocytochemistry with anti-phosphoH3 Ab -no speckles observed
Growth factor
Receptor Ras
Raf (MAPKKK)
MEK (MAPKK)
ERK ( MAPK)
RSK-2H3 H3
P
MAP kinase signal transduction
pathway
Thus, Rsk-2 mutation prevented H3 phosphorylation
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Experiment-Induce cells with growth factors,Crosslink DNA+ proteins, then immunoprecipitate with anti-Phospho-H3 Ab
Immunoprecipitatewith anti-Phospho-H3
DNA
Crosslink, nuclease
H3 P H3
P H3H3
Most genes c-fos
SouthernAgarose gel Probe with labeled c-fos DNA
Thus, known growth-response genes are bound by histones with phosphorylated H3
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C. Role in phosphorylation in cell division
1. Tetrahymena
# copies of chromosomes
Mode of replication in cell division
macronucleus
micronucleus
90
2
Pinching off none
Normal mitosis abnormal condensation chromosome loss
Affect of H3 mutation at phosphorylation site
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Genetics, Russell, p6.
Tetrahymena(a protozoan)
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Macronuclei
Tetrahymena- Histone H3 phosphorylation occurs only in mitotic micronuclei
Micronuclei Mitotic (football shape)
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2. Immunocytochemistry- observe phospho-H3 throughout chromosomes during cell divisionThus, this must play a role is chromosome condensation during mitosis
3. Models- 1. Phosphorylation + acetylation allows activation of gene expression, depending on context 2. Phospho-H3 loosens chromatin, enhancing transcription factor binding or mitotic factor binding
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II. Methylation
CARM-1 -
p160CARM-1
TATAA
Steroid hormone receptor+1
coactivator
• activates transcription (coactivator)
• methylates proteins
• inactivation of methylation activity - lose transcriptional activation
• methylates histone H3 in vitro
• what are CARM-1 targets??
Me H3
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III. Acetylation- Bromodomain -100 AA found in ~30 chromatin associated proteins (inc. HATs)
- may be binding motif for actetylated histones
IV. Other modifications- ubiquitination, glycosylation
Acetylated lysine
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OFF
ON
Histone H3
Bromodomain of a HAT
Chromodomain of a chromatin remodeler
Methylation, phosphorylation and acetylation of histones
Science 292:65, 2001
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Is there a “Histone Code”?
• Definition- “Covalent modifications of histones constitute an intricate pattern that creates a docking surface with which the modules of other proteins can interact”
Science 292:65, 2001
Shelley Berger, Wistar Institute
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