Antisense Transcript Long Noncoding RNA (lncRNA) HOTAIR is Transcriptionally Induced by Estradiol

被引:224
作者
Bhan, Arunoday [1 ]
Hussain, Imran [1 ]
Ansari, Khairul I. [1 ]
Kasiri, Sahba [1 ]
Bashyal, Aarti [1 ]
Mandal, Subhrangsu S. [1 ]
机构
[1] Univ Texas Arlington, Dept Chem & Biochem, Arlington, TX 76019 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
long noncoding RNA; HOTAIR; estrogen receptors; epigenetics; MLL histone methylases; NUCLEAR RECEPTOR COREGULATORS; ESTROGEN-RECEPTOR; HISTONE METHYLASES; GENE-EXPRESSION; BREAST-CANCER; XIST GENE; CELL; APOPTOSIS; GROWTH; ROLES;
D O I
10.1016/j.jmb.2013.01.022
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
HOTAIR (HOX antisense intergenic RNA) is a long noncoding RNA (lncRNA) that is transcribed from the antisense strand of homeobox C gene locus in chromosome 12. HOTAIR coordinates with chromatin-modifying enzymes and regulates gene silencing. It is overexpressed in various carcinomas including breast cancer. Herein, we demonstrated that HOTAIR is crucial for cell growth and viability and its knockdown induced apoptosis in breast cancer cells. We also demonstrated that HOTAIR is transcriptionally induced by estradiol (E2). Its promoter contains multiple functional estrogen response elements (EREs). Estrogen receptors (ERs) along with various ER coregulators such as histone methylases MLL1 (mixed lineage leukemia 1) and MLL3 and CREB-binding protein/p300 bind to the promoter of HOTAIR in an E2-dependent manner. Level of histone H3 lysine-4 trimethylation, histone acetylation, and RNA polymerase II recruitment is enriched at the HOTAIR promoter in the presence of E2. Knockdown of ERs and MLLs downregulated the E2-induced HOTAIR expression. Thus, similar to protein-coding gene transcription, E2-induced transcription of antisense transcript HOTAIR is coordinated via ERs and ER coregulators, and this mechanism of HOTAIR overexpression potentially contributes towards breast cancer progression. Published by Elsevier Ltd.
引用
收藏
页码:3707 / 3722
页数:16
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