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PMID |
Sentence |
1 |
23629948
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Affinity purification also was used to identify the distinct composition of the h-CDYLa or h-CDYLb protein complex. h-CDYLb was found in a multiprotein complex with G9a and GLP, while the h-CDYLa complex did not contain these two enzymes.
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2 |
25637356
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GLP and G9a are major H3K9 dimethylases and are essential for mouse early embryonic development.
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3 |
25637356
|
GLP and G9a both harbor ankyrin repeat domains that are capable of binding H3K9 methylation.
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4 |
25637356
|
Here, we report that the histone methyltransferase activities of GLP and G9a are stimulated by neighboring nucleosomes that are premethylated at H3K9.
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5 |
25637356
|
These stimulation events function in cis and are dependent on the H3K9 methylation binding activities of ankyrin repeat domains of GLP and G9a.
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6 |
25637356
|
In mouse embryonic stem cells (ESCs) harboring a mutant GLP that lacks H3K9me1-binding activity, critical pluripotent genes, including Oct4 and Nanog, display inefficient establishment of H3K9me2 and delayed gene silencing during differentiation.
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7 |
25637356
|
Collectively, our study reveals a new activation mechanism for GLP and G9a that plays an important role in ESC differentiation and mouse viability.
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8 |
25637356
|
GLP and G9a are major H3K9 dimethylases and are essential for mouse early embryonic development.
|
9 |
25637356
|
GLP and G9a both harbor ankyrin repeat domains that are capable of binding H3K9 methylation.
|
10 |
25637356
|
Here, we report that the histone methyltransferase activities of GLP and G9a are stimulated by neighboring nucleosomes that are premethylated at H3K9.
|
11 |
25637356
|
These stimulation events function in cis and are dependent on the H3K9 methylation binding activities of ankyrin repeat domains of GLP and G9a.
|
12 |
25637356
|
In mouse embryonic stem cells (ESCs) harboring a mutant GLP that lacks H3K9me1-binding activity, critical pluripotent genes, including Oct4 and Nanog, display inefficient establishment of H3K9me2 and delayed gene silencing during differentiation.
|
13 |
25637356
|
Collectively, our study reveals a new activation mechanism for GLP and G9a that plays an important role in ESC differentiation and mouse viability.
|
14 |
25637356
|
GLP and G9a are major H3K9 dimethylases and are essential for mouse early embryonic development.
|
15 |
25637356
|
GLP and G9a both harbor ankyrin repeat domains that are capable of binding H3K9 methylation.
|
16 |
25637356
|
Here, we report that the histone methyltransferase activities of GLP and G9a are stimulated by neighboring nucleosomes that are premethylated at H3K9.
|
17 |
25637356
|
These stimulation events function in cis and are dependent on the H3K9 methylation binding activities of ankyrin repeat domains of GLP and G9a.
|
18 |
25637356
|
In mouse embryonic stem cells (ESCs) harboring a mutant GLP that lacks H3K9me1-binding activity, critical pluripotent genes, including Oct4 and Nanog, display inefficient establishment of H3K9me2 and delayed gene silencing during differentiation.
|
19 |
25637356
|
Collectively, our study reveals a new activation mechanism for GLP and G9a that plays an important role in ESC differentiation and mouse viability.
|
20 |
25637356
|
GLP and G9a are major H3K9 dimethylases and are essential for mouse early embryonic development.
|
21 |
25637356
|
GLP and G9a both harbor ankyrin repeat domains that are capable of binding H3K9 methylation.
|
22 |
25637356
|
Here, we report that the histone methyltransferase activities of GLP and G9a are stimulated by neighboring nucleosomes that are premethylated at H3K9.
|
23 |
25637356
|
These stimulation events function in cis and are dependent on the H3K9 methylation binding activities of ankyrin repeat domains of GLP and G9a.
|
24 |
25637356
|
In mouse embryonic stem cells (ESCs) harboring a mutant GLP that lacks H3K9me1-binding activity, critical pluripotent genes, including Oct4 and Nanog, display inefficient establishment of H3K9me2 and delayed gene silencing during differentiation.
|
25 |
25637356
|
Collectively, our study reveals a new activation mechanism for GLP and G9a that plays an important role in ESC differentiation and mouse viability.
|
26 |
25637356
|
GLP and G9a are major H3K9 dimethylases and are essential for mouse early embryonic development.
|
27 |
25637356
|
GLP and G9a both harbor ankyrin repeat domains that are capable of binding H3K9 methylation.
|
28 |
25637356
|
Here, we report that the histone methyltransferase activities of GLP and G9a are stimulated by neighboring nucleosomes that are premethylated at H3K9.
|
29 |
25637356
|
These stimulation events function in cis and are dependent on the H3K9 methylation binding activities of ankyrin repeat domains of GLP and G9a.
|
30 |
25637356
|
In mouse embryonic stem cells (ESCs) harboring a mutant GLP that lacks H3K9me1-binding activity, critical pluripotent genes, including Oct4 and Nanog, display inefficient establishment of H3K9me2 and delayed gene silencing during differentiation.
|
31 |
25637356
|
Collectively, our study reveals a new activation mechanism for GLP and G9a that plays an important role in ESC differentiation and mouse viability.
|