Nudt21 Controls Cell Fate by Connecting Alternative Polyadenylation to Chromatin Signaling

被引:95
作者
Brumbaugh, Justin [1 ,2 ,3 ,4 ,5 ]
Di Stefano, Bruno [1 ,2 ,3 ,4 ,5 ]
Wang, Xiuye [6 ]
Borkent, Marti [1 ,2 ,3 ,4 ,5 ]
Forouzmand, Elmira [6 ]
Clowers, Katie J. [7 ]
Ji, Fei [1 ]
Schwarz, Benjamin A. [1 ,2 ,3 ,4 ,5 ]
Kalocsay, Marian [7 ]
Elledge, Stephen J. [8 ,9 ]
Chen, Yue [10 ]
Sadreyev, Ruslan I. [1 ,3 ]
Gygi, Steven P. [7 ]
Hu, Guang [11 ]
Shi, Yongsheng [6 ]
Hochedlinger, Konrad [1 ,2 ,3 ,4 ,5 ]
机构
[1] Massachusetts Gen Hosp, Dept Mol Biol, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Ctr Regenerat Med, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Canc Ctr, Boston, MA 02114 USA
[4] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
[5] Harvard Stem Cell Inst, Cambridge, MA 02138 USA
[6] Univ Calif Irvine, Sch Med, Dept Microbiol & Mol Genet, Irvine, CA 92697 USA
[7] Harvard Med Sch, Dept Cell Biol, Boston, MA 02115 USA
[8] Harvard Med Sch, Howard Hughes Med Inst, Brigham & Womens Hosp, Boston, MA 02115 USA
[9] Harvard Med Sch, Dept Genet, Boston, MA 02115 USA
[10] Univ Minnesota, Coll Biol Sci, Dept Biochem Mol Biol & Biophys, St Paul, MN 55018 USA
[11] NIEHS, Epigenet & Stem Cell Biol Lab, POB 12233, Res Triangle Pk, NC 27709 USA
关键词
CLEAVAGE FACTOR-I; 3' UNTRANSLATED REGIONS; ACUTE MYELOID-LEUKEMIA; EMBRYONIC STEM-CELLS; SELF-RENEWAL; MESSENGER-RNAS; DIFFERENTIAL EXPRESSION; BINDING PROTEINS; MOUSE; PLURIPOTENCY;
D O I
10.1016/j.cell.2017.11.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell fate transitions involve rapid gene expression changes and global chromatin remodeling, yet the underlying regulatory pathways remain incompletely understood. Here, we identified the RNA-processing factor Nudt21 as a novel regulator of cell fate change using transcription-factor-induced reprogramming as a screening assay. Suppression of Nudt21 enhanced the generation of induced pluripotent stem cells, facilitated transdifferentiation into trophoblast stem cells, and impaired differentiation of myeloid precursors and embryonic stem cells, suggesting a broader role for Nudt21 in cell fate change. We show that Nudt21 directs differential polyadenylation of over 1,500 transcripts in cells acquiring pluripotency, although only a fraction changed protein levels. Remarkably, these proteins were strongly enriched for chromatin regulators, and their suppression neutralized the effect of Nudt21 during reprogramming. Collectively, our data uncover Nudt21 as a novel post-transcriptional regulator of cell fate and establish a direct, previously unappreciated link between alternative polyadenylation and chromatin signaling.
引用
收藏
页码:106 / +
页数:36
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