Literature DB >> 27912097

LncPRESS1 Is a p53-Regulated LncRNA that Safeguards Pluripotency by Disrupting SIRT6-Mediated De-acetylation of Histone H3K56.

Abhinav K Jain1, Yuanxin Xi2, Ryan McCarthy3, Kendra Allton3, Kadir C Akdemir4, Lalit R Patel5, Bruce Aronow6, Chunru Lin7, Wei Li2, Liuqing Yang7, Michelle C Barton8.   

Abstract

Recent evidence suggests that lncRNAs play an integral regulatory role in numerous functions, including determination of cellular identity. We determined global expression (RNA-seq) and genome-wide profiles (ChIP-seq) of histone post-translational modifications and p53 binding in human embryonic stem cells (hESCs) undergoing differentiation to define a high-confidence set of 40 lncRNAs, which are p53 transcriptional targets. We focused on lncRNAs highly expressed in pluripotent hESCs and repressed by p53 during differentiation to identify lncPRESS1 as a p53-regulated transcript that maintains hESC pluripotency in concert with core pluripotency factors. RNA-seq of hESCs depleted of lncPRESS1 revealed that lncPRESS1 controls a gene network that promotes pluripotency. Further, we found that lncPRESS1 physically interacts with SIRT6 and prevents SIRT6 chromatin localization, which maintains high levels of histone H3K56 and H3K9 acetylation at promoters of pluripotency genes. In summary, we describe a p53-regulated, pluripotency-specific lncRNA that safeguards the hESC state by disrupting SIRT6 activity. Copyright Â
© 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  H3K56ac; H3K9ac; SIRT6; chromatin; differentiation; genome-wide; hESC; lncRNA; p53; pluripotency

Mesh:

Substances:

Year:  2016        PMID: 27912097      PMCID: PMC5137794          DOI: 10.1016/j.molcel.2016.10.039

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


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10.  Genome-wide profiling reveals stimulus-specific functions of p53 during differentiation and DNA damage of human embryonic stem cells.

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Review 10.  G1-phase progression in pluripotent stem cells.

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