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Publication : Cyclin D1 acts as a barrier to pluripotent reprogramming by promoting neural progenitor fate commitment.

First Author  Chen CL Year  2014
Journal  FEBS Lett Volume  588
Issue  21 Pages  4008-17
PubMed ID  25261251 Mgi Jnum  J:216454
Mgi Id  MGI:5608830 Doi  10.1016/j.febslet.2014.08.039
Citation  Chen CL, et al. (2014) Cyclin D1 acts as a barrier to pluripotent reprogramming by promoting neural progenitor fate commitment. FEBS Lett 588(21):4008-17
abstractText  A short G1 phase is a characteristic feature of the cell cycle structure of pluripotent cells, and is reestablished during Yamanaka factor-mediated pluripotent reprogramming. How cell cycle control is adjusted to meet the requirements of pluripotent cell fate commitment during reprogramming is less well understood. Elevated levels of cyclin D1 were initially found to impair pluripotency maintenance. The current work further identified Cyclin D1 to be capable of transcriptionally upregulating Pax6, which promoted reprogramming cells to commit to a neural progenitor fate rather than a pluripotent cell fate. These findings explain the importance of reestablishment of G1-phase restriction in pluripotent reprogramming.
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