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雄激素受体对初级靶基因的细胞和基因特异性调控。

Cell- and gene-specific regulation of primary target genes by the androgen receptor.

作者信息

Bolton Eric C, So Alex Y, Chaivorapol Christina, Haqq Christopher M, Li Hao, Yamamoto Keith R

机构信息

Department of Cellular and Molecular Pharmacology, University of California, San Francisco, California 94143, USA.

出版信息

Genes Dev. 2007 Aug 15;21(16):2005-17. doi: 10.1101/gad.1564207.

DOI:10.1101/gad.1564207
PMID:17699749
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1948856/
Abstract

The androgen receptor (AR) mediates the physiologic and pathophysiologic effects of androgens including sexual differentiation, prostate development, and cancer progression by binding to genomic androgen response elements (AREs), which influence transcription of AR target genes. The composition and context of AREs differ between genes, thus enabling AR to confer multiple regulatory functions within a single nucleus. We used expression profiling of an immortalized human prostate epithelial cell line to identify 205 androgen-responsive genes (ARGs), most of them novel. In addition, we performed chromatin immunoprecipitation to identify 524 AR binding regions and validated in reporter assays the ARE activities of several such regions. Interestingly, 67% of our AREs resided within approximately 50 kb of the transcription start sites of 84% of our ARGs. Indeed, most ARGs were associated with two or more AREs, and ARGs were sometimes themselves linked in gene clusters containing up to 13 AREs and 12 ARGs. AREs appeared typically to be composite elements, containing AR binding sequences adjacent to binding motifs for other transcriptional regulators. Functionally, ARGs were commonly involved in prostate cell proliferation, communication, differentiation, and possibly cancer progression. Our results provide new insights into cell- and gene-specific mechanisms of transcriptional regulation of androgen-responsive gene networks.

摘要

雄激素受体(AR)通过与基因组雄激素反应元件(AREs)结合来介导雄激素的生理和病理生理效应,包括性分化、前列腺发育和癌症进展,AREs会影响AR靶基因的转录。不同基因的AREs组成和背景存在差异,从而使AR能够在单个细胞核内发挥多种调节功能。我们利用永生化人前列腺上皮细胞系的表达谱分析来鉴定205个雄激素反应基因(ARG),其中大多数是新发现的。此外,我们进行了染色质免疫沉淀以鉴定524个AR结合区域,并在报告基因检测中验证了其中几个区域的ARE活性。有趣的是,我们鉴定的AREs中有67%位于84%的ARG转录起始位点约50 kb范围内。实际上,大多数ARG与两个或更多个ARE相关联,并且ARG有时自身也在包含多达13个ARE和12个ARG的基因簇中相连。AREs通常似乎是复合元件,包含与其他转录调节因子结合基序相邻的AR结合序列。在功能上,ARG通常参与前列腺细胞增殖、通讯、分化以及可能的癌症进展。我们的研究结果为雄激素反应基因网络转录调控的细胞和基因特异性机制提供了新的见解。

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本文引用的文献

1
Determinants of cell- and gene-specific transcriptional regulation by the glucocorticoid receptor.糖皮质激素受体对细胞和基因特异性转录调控的决定因素。
PLoS Genet. 2007 Jun;3(6):e94. doi: 10.1371/journal.pgen.0030094.
2
Identification of novel androgen response genes in prostate cancer cells by coupling chromatin immunoprecipitation and genomic microarray analysis.通过结合染色质免疫沉淀和基因组微阵列分析鉴定前列腺癌细胞中的新型雄激素反应基因。
Oncogene. 2007 Jun 28;26(30):4453-63. doi: 10.1038/sj.onc.1210229. Epub 2007 Feb 5.
3
Defects of cholesterol biosynthesis.胆固醇生物合成缺陷
FEBS Lett. 2006 Oct 9;580(23):5442-9. doi: 10.1016/j.febslet.2006.07.027. Epub 2006 Jul 20.
4
FOXO1A is a candidate for the 13q14 tumor suppressor gene inhibiting androgen receptor signaling in prostate cancer.FOXO1A是位于13q14的肿瘤抑制基因的候选基因,该基因可抑制前列腺癌中的雄激素受体信号传导。
Cancer Res. 2006 Jul 15;66(14):6998-7006. doi: 10.1158/0008-5472.CAN-06-0411.
5
c-Jun enhancement of androgen receptor transactivation is associated with prostate cancer cell proliferation.c-Jun增强雄激素受体反式激活与前列腺癌细胞增殖相关。
Oncogene. 2006 Nov 16;25(54):7212-23. doi: 10.1038/sj.onc.1209705. Epub 2006 May 29.
6
JHDM2A, a JmjC-containing H3K9 demethylase, facilitates transcription activation by androgen receptor.JHDM2A是一种含JmjC结构域的H3K9去甲基化酶,可促进雄激素受体介导的转录激活。
Cell. 2006 May 5;125(3):483-95. doi: 10.1016/j.cell.2006.03.027. Epub 2006 Apr 6.
7
Expression of c-jun oncogene in hyperplastic and carcinomatous human prostate.c-jun癌基因在人前列腺增生及癌组织中的表达
Urology. 2006 Jan;67(1):204-8. doi: 10.1016/j.urology.2005.07.045.
8
Direct, androgen receptor-mediated regulation of the FKBP5 gene via a distal enhancer element.雄激素受体通过远端增强子元件直接介导对FKBP5基因的调控。
Endocrinology. 2006 Jan;147(1):590-8. doi: 10.1210/en.2005-1001. Epub 2005 Oct 6.
9
Spatial and temporal recruitment of androgen receptor and its coactivators involves chromosomal looping and polymerase tracking.雄激素受体及其共激活因子的时空募集涉及染色体环化和聚合酶追踪。
Mol Cell. 2005 Sep 2;19(5):631-42. doi: 10.1016/j.molcel.2005.07.018.
10
Glucocorticoid receptor-dependent gene regulatory networks.糖皮质激素受体依赖性基因调控网络
PLoS Genet. 2005 Aug;1(2):e16. doi: 10.1371/journal.pgen.0010016. Epub 2005 Aug 5.