| Chapter title |
Epigenomic Regulation of Smad1 Signaling During Cellular Senescence Induced by Ras Activation.
|
|---|---|
| Chapter number | 22 |
| Book title |
TGF-β Signaling
|
| Published in |
Methods in molecular biology, January 2016
|
| DOI | 10.1007/978-1-4939-2966-5_22 |
| Pubmed ID | |
| Book ISBNs |
978-1-4939-2965-8, 978-1-4939-2966-5
|
| Authors |
Kaneda, Atsushi, Nonaka, Aya, Fujita, Takanori, Yamanaka, Ryota, Fujimoto, Mai, Miyazono, Kohei, Aburatani, Hiroyuki, Atsushi Kaneda, Aya Nonaka, Takanori Fujita, Ryota Yamanaka, Mai Fujimoto, Kohei Miyazono, Hiroyuki Aburatani |
| Abstract |
Epigenomic modification plays important roles in regulating gene expression during development, differentiation, and cellular senescence. When oncogenes are activated, cells fall into stable growth arrest to block cellular proliferation, which is called oncogene-induced senescence. We recently identified through genome-wide analyses that Bmp2-Smad1 signal and its regulation by harmonized epigenomic alteration play an important role in Ras-induced senescence of mouse embryonic fibroblasts. We describe in this chapter the methods for analyses of epigenomic alteration and Smad1 targets on genome-wide scale. |
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| Unknown | 2 | 50% |
Demographic breakdown
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Mendeley readers
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Demographic breakdown
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|---|---|---|
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| Student > Ph. D. Student | 1 | 33% |
| Readers by discipline | Count | As % |
|---|---|---|
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