Presentation is loading. Please wait.

Presentation is loading. Please wait.

Lsh does not regulate global histone methylation levels.

Published byViolette Goulet Modified over 5 years ago

Similar presentations

Presentation on theme: "Lsh does not regulate global histone methylation levels."— Presentation transcript:

1 Lsh does not regulate global histone methylation levels.
Lsh does not regulate global histone methylation levels. (A) Loss of Lsh does not alter H3‐K9me, H3‐K4me or Hp1 protein levels. Western analysis of nuclear extracts derived from four Lsh‐deficient embryos (gestation day 14) and their wild‐type littermates. (B) Titration of nuclear extracts of one wild‐type and one Lsh‐deficient embryo. (C) Loss of Lsh does not alter Hp1 binding to chromatin. Lsh‐deficient and Lsh wild‐type MEFs are compared for resistance to Triton X‐100 washes followed by western analysis to detect HP1 or PCNA and Vimentin as control. Qingsheng Yan et al. EMBO J. 2003;22: © as stated in the article, figure or figure legend

Download ppt "Lsh does not regulate global histone methylation levels."

Similar presentations

Chromatin Regulation in the C. elegans Germ Line

Chromatin Regulation in the C. elegans Germ Line
Lsh, DNA methylation and aging 报告人 : 周瑞. Normal DNA methylation In mammals, DNA methylation patterns: an initial wave of global demethylation; the rapid.

Lsh, DNA methylation and aging 报告人 : 周瑞. Normal DNA methylation In mammals, DNA methylation patterns: an initial wave of global demethylation; the rapid.
Validating Cdk‐dependent chromatin association changes of selected outliers A–EValidation of changes in chromatin affinity following Cdk inhibition of.

Validating Cdk‐dependent chromatin association changes of selected outliers A–EValidation of changes in chromatin affinity following Cdk inhibition of.
Protection of HIF‐1α against VHL‐mediated degradation requires nuclear translocation of HIF‐1α and a hypoxia‐dependent intranuclear signal. Protection.

Protection of HIF‐1α against VHL‐mediated degradation requires nuclear translocation of HIF‐1α and a hypoxia‐dependent intranuclear signal. Protection.
HIF predominantly regulates transcription through release of promoter‐paused RNA‐pol2 A–CMean distribution of normoxic (red) and hypoxic (blue) RNApol2.

HIF predominantly regulates transcription through release of promoter‐paused RNA‐pol2 A–CMean distribution of normoxic (red) and hypoxic (blue) RNApol2.
Loss of Hdac3 impairs Ar signaling in mouse prostate tissues and has no effect on apoptosis Loss of Hdac3 impairs Ar signaling in mouse prostate tissues.

Loss of Hdac3 impairs Ar signaling in mouse prostate tissues and has no effect on apoptosis Loss of Hdac3 impairs Ar signaling in mouse prostate tissues.
Mba1 cofractionates with mitochondrial ribosomes on sucrose gradients.

Mba1 cofractionates with mitochondrial ribosomes on sucrose gradients.
Post‐translational modifications (PTMs) involved in the context of infection Post‐translational modifications (PTMs) involved in the context of infection.

Post‐translational modifications (PTMs) involved in the context of infection Post‐translational modifications (PTMs) involved in the context of infection.
Mitochondrial ribosomes remain associated with the inner membrane in the absence of the ribosome‐binding domain of Oxa1 and of Mba1. Mitochondrial ribosomes.

Mitochondrial ribosomes remain associated with the inner membrane in the absence of the ribosome‐binding domain of Oxa1 and of Mba1. Mitochondrial ribosomes.
Analysis of the effect of loss of Brca2 on in vivo somatic mutation frequency and mutation type. Analysis of the effect of loss of Brca2 on in vivo somatic.

Analysis of the effect of loss of Brca2 on in vivo somatic mutation frequency and mutation type. Analysis of the effect of loss of Brca2 on in vivo somatic.
Expression of adenylyl cyclases and miR‐142‐3p in CD4+CD25− T cells and CD4+CD25+ regulatory T cells. Expression of adenylyl cyclases and miR‐142‐3p in.

Expression of adenylyl cyclases and miR‐142‐3p in CD4+CD25− T cells and CD4+CD25+ regulatory T cells. Expression of adenylyl cyclases and miR‐142‐3p in.
Abundance of proteins matching selected subcellular locations and functions in CaCo‐2 cells. Abundance of proteins matching selected subcellular locations.

Abundance of proteins matching selected subcellular locations and functions in CaCo‐2 cells. Abundance of proteins matching selected subcellular locations.
Mechanisms of lncRNA function.

Mechanisms of lncRNA function.
H3K9me2 and G9a levels decrease during adipogenesis.

H3K9me2 and G9a levels decrease during adipogenesis.
Accumulation of 2,4‐dienoyl‐CoA ester (C22:7) during β‐oxidation of docosahexaenoic acid (C22:6). Accumulation of 2,4‐dienoyl‐CoA ester (C22:7) during.

Accumulation of 2,4‐dienoyl‐CoA ester (C22:7) during β‐oxidation of docosahexaenoic acid (C22:6). Accumulation of 2,4‐dienoyl‐CoA ester (C22:7) during.
1,25‐dihydroxyvitamin D3 and retinoic acid induce p19ink4d expression.

1,25‐dihydroxyvitamin D3 and retinoic acid induce p19ink4d expression.
Cooperative formation of a higher‐order complex containing AP1 and HMG‐I(Y). Cooperative formation of a higher‐order complex containing AP1 and HMG‐I(Y).

Cooperative formation of a higher‐order complex containing AP1 and HMG‐I(Y). Cooperative formation of a higher‐order complex containing AP1 and HMG‐I(Y).
Calcium regulates ERK nuclear association, but not its activation.

Calcium regulates ERK nuclear association, but not its activation.
mTORC1 regulates TFEB. (A) Lysosomal stress inhibits mTOR signalling.

mTORC1 regulates TFEB. (A) Lysosomal stress inhibits mTOR signalling.
Cytochrome c and ATP hydrolysis are required for Apaf‐1 to interact with procaspase‐9. Cytochrome c and ATP hydrolysis are required for Apaf‐1 to interact.

Cytochrome c and ATP hydrolysis are required for Apaf‐1 to interact with procaspase‐9. Cytochrome c and ATP hydrolysis are required for Apaf‐1 to interact.

Similar presentations

Ads by Google