LncRNA-dependent mechanisms of androgen-receptor-regulated gene activation programs

Liuqing Yang, Chunru Lin, Chunyu Jin, Joy C. Yang, Bogdan Tanasa, Wenbo Li, Daria Merkurjev, Kenneth A. Ohgi, Da Meng, Jie Zhang, Christopher P Evans, Michael G. Rosenfeld

Research output: Contribution to journalArticle

364 Citations (Scopus)

Abstract

Although recent studies have indicated roles of long non-coding RNAs (lncRNAs) in physiological aspects of cell-type determination and tissue homeostasis, their potential involvement in regulated gene transcription programs remains rather poorly understood. The androgen receptor regulates a large repertoire of genes central to the identity and behaviour of prostate cancer cells, and functions in a ligand-independent fashion in many prostate cancers when they become hormone refractory after initial androgen deprivation therapy. Here we report that two lncRNAs highly overexpressed in aggressive prostate cancer, PRNCR1 (also known as PCAT8) and PCGEM1, bind successively to the androgen receptor and strongly enhance both ligand-dependent and ligand-independent androgen-receptor-mediated gene activation programs and proliferation in prostate cancer cells. Binding of PRNCR1 to the carboxy-terminally acetylated androgen receptor on enhancers and its association with DOT1L appear to be required for recruitment of the second lncRNA, PCGEM1, to the androgen receptor amino terminus that is methylated by DOT1L. Unexpectedly, recognition of specific protein marks by PCGEM1-recruited pygopus 2 PHD domain enhances selective looping of androgen-receptor-bound enhancers to target gene promoters in these cells. In 'resistant' prostate cancer cells, these overexpressed lncRNAs can interact with, and are required for, the robust activation of both truncated and full-length androgen receptor, causing ligand-independent activation of the androgen receptor transcriptional program and cell proliferation. Conditionally expressed short hairpin RNA targeting these lncRNAs in castration-resistant prostate cancer cell lines strongly suppressed tumour xenograft growth in vivo. Together, these results indicate that these overexpressed lncRNAs can potentially serve as a required component of castration-resistance in prostatic tumours.

Original languageEnglish (US)
Pages (from-to)598-602
Number of pages5
JournalNature
Volume500
Issue number7464
DOIs
StatePublished - 2013

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Androgen Receptors
Long Noncoding RNA
Transcriptional Activation
Prostatic Neoplasms
Ligands
Castration
Genes
Heterografts
Small Interfering RNA
Androgens
Neoplasms
Homeostasis
Cell Proliferation
Hormones
Cell Line
Growth

ASJC Scopus subject areas

  • General

Cite this

Yang, L., Lin, C., Jin, C., Yang, J. C., Tanasa, B., Li, W., ... Rosenfeld, M. G. (2013). LncRNA-dependent mechanisms of androgen-receptor-regulated gene activation programs. Nature, 500(7464), 598-602. https://doi.org/10.1038/nature12451

LncRNA-dependent mechanisms of androgen-receptor-regulated gene activation programs. / Yang, Liuqing; Lin, Chunru; Jin, Chunyu; Yang, Joy C.; Tanasa, Bogdan; Li, Wenbo; Merkurjev, Daria; Ohgi, Kenneth A.; Meng, Da; Zhang, Jie; Evans, Christopher P; Rosenfeld, Michael G.

In: Nature, Vol. 500, No. 7464, 2013, p. 598-602.

Research output: Contribution to journalArticle

Yang, L, Lin, C, Jin, C, Yang, JC, Tanasa, B, Li, W, Merkurjev, D, Ohgi, KA, Meng, D, Zhang, J, Evans, CP & Rosenfeld, MG 2013, 'LncRNA-dependent mechanisms of androgen-receptor-regulated gene activation programs', Nature, vol. 500, no. 7464, pp. 598-602. https://doi.org/10.1038/nature12451
Yang, Liuqing ; Lin, Chunru ; Jin, Chunyu ; Yang, Joy C. ; Tanasa, Bogdan ; Li, Wenbo ; Merkurjev, Daria ; Ohgi, Kenneth A. ; Meng, Da ; Zhang, Jie ; Evans, Christopher P ; Rosenfeld, Michael G. / LncRNA-dependent mechanisms of androgen-receptor-regulated gene activation programs. In: Nature. 2013 ; Vol. 500, No. 7464. pp. 598-602.
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