Cooperativity of co-factor NR2F2 with Pioneer Factors GATA3, FOXA1 in promoting ERα function

• Published in: Theranostics 2019-01, Vol.9 (22), p.6501-6516
• Main Authors: Jiang, Guojuan, Wang, Xinrui, Sheng, Dandan, Zhou, Lei, Liu, Yang, Xu, Congling, Liu, Suling, Zhang, Ji
• Format: Article
• Language: English
• Subjects: Binding sites; Breast cancer; Breast Neoplasms - genetics; Breast Neoplasms - metabolism; Breast Neoplasms - pathology; Cell culture; Cell Line, Tumor; Chromatin - genetics; Chromatin - metabolism; Chromatin Immunoprecipitation; COUP Transcription Factor II - genetics; COUP Transcription Factor II - metabolism; Enhancer Elements, Genetic; Estrogen Receptor alpha - genetics; Estrogen Receptor alpha - metabolism; Estrogens; Female; GATA3 Transcription Factor - metabolism; Gene Expression Regulation, Neoplastic; Genomes; Hepatocyte Nuclear Factor 3-alpha - metabolism; Humans; MCF-7 Cells; Metastasis; Promoter Regions, Genetic; Prostate cancer; Proteins; Research Paper; Stem cells; Transcription factors
• ISSN: 1838-7640; 1838-7640
• DOI: 10.7150/thno.34874

Estrogen receptor α (ERα) drives growth in the majority of human breast cancers by binding to regulatory elements and inducing transcriptional events that promote tumor growth. ERα binding activity largely depends on access to binding sites on chromatin, which is facilitated in part by Pioneer Factors (PFs). Transcription factors operate in complexes through thousands of genomic binding sites in a combinatorial fashion to control the expression of genes. However, the extent of crosstalk and cooperation between ERα pioneer factors and more collaborative transcription factors in breast cancer still remains to be elucidated systematically. : Here, we determined the genomic binding information of 40 transcription-related factors and histone modifications with ChIP-seq in ENCODE and integrated it with other genomic information (RNA-seq, ATAC-seq, Gene microarray, 450k methylation chip, GRO-seq), forming a multi-dimension network to illuminate ERα associated transcription. : We show that transcription factor, NR2F2 binds to most sites independently of estrogen. Perturbation of NR2F2 expression decreases ERα DNA binding, chromatin openning, and estrogen-dependent cell growth. In the genome-wide analysis, we show that most binding events of NR2F2 and known pioneer factors FOXA1, GATA3 occur together, covering 85% of the ERα binding sites. Regions bound by all the three TFs appeared to be the most active, to have the strongest ERα binding and to be enriched for the super enhancers. : The ERα binds to pre-accessible sites containing ERE elements bound by the three transcription factors (NR2F2, FOXA1 and GATA3).The three genes were also identified to correlate with decreased metastatic potential in patient cohorts and co-regulate each other. Together, our results suggest that NR2F2 is a cofactor with FOXA1 and GATA3 in ERα-mediated transcription.