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本文引用的文献

1
Hox genes and their candidate downstream targets in the developing central nervous system.发育中的中枢神经系统中的Hox基因及其候选下游靶点。
Cell Mol Neurobiol. 2005 Jun;25(3-4):697-741. doi: 10.1007/s10571-005-3971-9.
2
Identification of pigment epithelium-derived factor as a direct target of the p53 family member genes.鉴定色素上皮衍生因子作为p53家族成员基因的直接靶点。
Oncogene. 2005 Jul 28;24(32):5131-6. doi: 10.1038/sj.onc.1208695.
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Expression of 11 HOX genes is deregulated in esophageal squamous cell carcinoma.11种HOX基因的表达在食管鳞状细胞癌中失调。
Clin Cancer Res. 2005 Feb 1;11(3):1044-9.
4
The identification of Hoxc8 target genes.Hoxc8靶基因的鉴定。
Proc Natl Acad Sci U S A. 2005 Feb 15;102(7):2420-4. doi: 10.1073/pnas.0409700102. Epub 2005 Feb 7.
5
Loss of HOXC6 expression induces apoptosis in prostate cancer cells.HOXC6表达缺失诱导前列腺癌细胞凋亡。
Oncogene. 2005 Jan 6;24(1):188-98. doi: 10.1038/sj.onc.1207906.
6
HOXB13 induces growth suppression of prostate cancer cells as a repressor of hormone-activated androgen receptor signaling.HOXB13作为激素激活的雄激素受体信号的抑制因子,可诱导前列腺癌细胞的生长抑制。
Cancer Res. 2004 Dec 15;64(24):9185-92. doi: 10.1158/0008-5472.CAN-04-1330.
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The role of Osteopontin in tumor metastasis.骨桥蛋白在肿瘤转移中的作用。
J Surg Res. 2004 Oct;121(2):228-41. doi: 10.1016/j.jss.2004.03.028.
8
Role of osteopontin in tumour progression.骨桥蛋白在肿瘤进展中的作用。
Br J Cancer. 2004 May 17;90(10):1877-81. doi: 10.1038/sj.bjc.6601839.
9
HOXB13 homeodomain protein suppresses the growth of prostate cancer cells by the negative regulation of T-cell factor 4.HOXB13 同源结构域蛋白通过负向调节 T 细胞因子 4 抑制前列腺癌细胞的生长。
Cancer Res. 2004 May 1;64(9):3046-51. doi: 10.1158/0008-5472.can-03-2614.
10
HOXA10 regulates p53 expression and matrigel invasion in human breast cancer cells.HOXA10调节人乳腺癌细胞中p53的表达和基质胶侵袭。
Cancer Biol Ther. 2004 Jun;3(6):568-72. doi: 10.4161/cbt.3.6.848. Epub 2004 Jun 15.

小鼠胚胎成纤维细胞中Hoxc8调控转录网络的鉴定。

Identification of a Hoxc8-regulated transcriptional network in mouse embryo fibroblast cells.

作者信息

Lei Haiyan, Juan Aster H, Kim Moo-Sang, Ruddle Frank H

机构信息

Department of Molecular, Cellular and Developmental Biology, Yale University, 266 Whitney Avenue, New Haven, CT 06511.

Department of Molecular, Cellular and Developmental Biology, Yale University, 266 Whitney Avenue, New Haven, CT 06511

出版信息

Proc Natl Acad Sci U S A. 2006 Jul 5;103(27):10305-10309. doi: 10.1073/pnas.0603552103. Epub 2006 Jun 22.

DOI:10.1073/pnas.0603552103
PMID:16793922
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1502453/
Abstract

The transcription factor, Hoxc8, is a member of the homeobox gene family that is vital for growth and differentiation. Previously, we identified 34 genes whose expression levels were changed at least 2-fold by forced expression of Hoxc8 in C57BL/6J mouse embryo fibroblast cells using a mouse 16,463-gene oligonucleotide microarray. In the present study, we used the combined power of microarray profiling, global Hoxc8 DNA-binding site analysis, and high-throughput chromatin immunoprecipitation assays to identify direct and biologically relevant targets of Hoxc8 in vivo. Here we show that 19 of the 34 responsive genes contain Hoxc8 consensus DNA-binding sequence(s) in their regulatory regions. Chromatin immunoprecipitation analysis indicated that Hoxc8-DNA interaction was detected in five of the 19 candidate genes. All of these five target genes have been implicated in oncogenesis, cell adhesion, proliferation, and apoptosis. Overall, the genes described here should aid in the understanding of global regulatory networks of Hox genes and to provide valuable insight into the molecular basis of Hoxc8 in development and carcinogenesis.

摘要

转录因子Hoxc8是同源盒基因家族的成员,对生长和分化至关重要。此前,我们使用小鼠16463基因寡核苷酸微阵列,在C57BL/6J小鼠胚胎成纤维细胞中通过强制表达Hoxc8,鉴定出34个表达水平至少改变2倍的基因。在本研究中,我们利用微阵列分析、全基因组Hoxc8 DNA结合位点分析和高通量染色质免疫沉淀分析的联合力量,在体内鉴定Hoxc8的直接和生物学相关靶点。在这里我们表明,34个反应基因中的19个在其调控区域含有Hoxc8共有DNA结合序列。染色质免疫沉淀分析表明,在19个候选基因中的5个中检测到Hoxc8与DNA的相互作用。所有这5个靶基因都与肿瘤发生、细胞黏附、增殖和凋亡有关。总体而言,这里描述的基因应有助于理解Hox基因的全局调控网络,并为Hoxc8在发育和致癌作用中的分子基础提供有价值的见解。