A novel domain in histone deacetylase 1 and 2 mediates repression of cartilage-specific genes in human chondrocytes

被引:94
作者
Hong, Sohee [1 ]
Derfoul, Assia [1 ]
Pereira-Mouries, Lucilia [1 ]
Hall, David J. [1 ]
机构
[1] NIAMSD, Cartilage Mol Genet Grp, Cartilage Biol & Orthopaed Branch, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
osteoarthritis; transcription; collagen 2(alpha 1); chromatin; II COLLAGEN; ARTICULAR-CARTILAGE; TRANSCRIPTIONAL CONTROL; EXTRACELLULAR-MATRIX; INDUCED ARTHRITIS; HDAC INHIBITORS; TRICHOSTATIN-A; EXPRESSION; CANCER; CELLS;
D O I
10.1096/fj.09-133215
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The role of histone deacetylase 1 and 2 (HDAC1 and HDAC2) in regulating cartilage-specific gene expression was explored in primary human chondrocytes. HDAC1 and HDAC2 protein levels were elevated in chondrocytes from osteoarthritic patients, consistent with a down-regulation of some cartilage marker genes. When expressed in these cells, HDAC1 and HDAC2 repressed aggrecan and collagen 2(alpha 1) expression but differed in their repression of collagen 9(alpha 1), collagen 11(alpha 1), dermatopontin, and cartilage oligomeric matrix protein (COMP). To identify the basis of these differences between HDAC1 and HDAC2, their carboxy-terminal domains (CTDs) were deleted, which led to proteins that retained enzymatic activity but were unable to repress cartilage gene expression. Further, exchange of the CTDs between HDAC1 and HDAC2 led to proteins that were enzymatically active but displayed altered target gene specificity, indicating that these CTDs can function independently of HDAC enzymatic activity, to target the HDACs to specific genes. The Snail transcription factor was identified as a mediator of HDAC1 and HDAC2 repression of the collagen 2(alpha 1) gene, via its interaction with the HDAC1 and 2 CTDs. The data indicate that the CTD serves a novel function within HDAC1 and HDAC2, to mediate repression of cartilage-specific gene expression in human chondrocytes.-Hong, S., Derfoul, A., Pereira-Mouries, L., Hall, D. J. A novel domain in histone deacetylase 1 and 2 mediates repression of cartilage-specific genes in human chondrocytes. FASEB J. 23, 3539-3552 (2009). www.fasebj.org
引用
收藏
页码:3539 / 3552
页数:14
相关论文
共 43 条
[1]
MEF2C transcription factor controls chondrocyte hypertrophy and bone development [J].
Arnold, Michael A. ;
Kim, Yuri ;
Czubryt, Michael P. ;
Phan, Dillon ;
McAnally, John ;
Qi, Xiaoxia ;
Shelton, John M. ;
Richardson, James A. ;
Bassel-Duby, Rhonda ;
Olson, Eric N. .
DEVELOPMENTAL CELL, 2007, 12 (03) :377-389
[2]
Cell growth inhibition and gene expression induced by the histone deacetylase inhibitor, trichostatin A, on human hepatoma cells [J].
Chiba, T ;
Yokosuka, O ;
Fukai, K ;
Kojima, H ;
Tada, M ;
Arai, M ;
Imazeki, F ;
Saisho, H .
ONCOLOGY, 2004, 66 (06) :481-491
[3]
A therapeutic strategy uses histone deacetylase inhibitors to modulate the expression of genes involved in the pathogenesis of rheumatoid arthritis [J].
Chung, YL ;
Lee, MY ;
Wang, AJ ;
Yao, LF .
MOLECULAR THERAPY, 2003, 8 (05) :707-717
[4]
Function of the zinc-finger transcription factor SNAI2 in cancer and development [J].
Cobaleda, Cesar ;
Perez-Caro, Maria ;
Vicente-Duenas, Carolina ;
Sanchez-Garcia, Isidro .
ANNUAL REVIEW OF GENETICS, 2007, 41 :41-61
[5]
Cress WD, 2000, J CELL PHYSIOL, V184, P1, DOI 10.1002/(SICI)1097-4652(200007)184:1<1::AID-JCP1>3.0.CO
[6]
2-7
[7]
Histone deacetylases (HDACs): characterization of the classical HDAC family [J].
De Ruijter, AJM ;
Van Gennip, AH ;
Caron, HN ;
Kemp, S ;
Van Kuilenburg, ABP .
BIOCHEMICAL JOURNAL, 2003, 370 :737-749
[8]
FRUTOS CA, 2007, DEV CELL, V13, P872
[9]
SP3 represses the SP1-mediated transactivation of the human COL2A1 gene in primary and de-differentiated chondrocytes [J].
Ghayor, C ;
Chadjichristos, C ;
Herrouin, JF ;
Ala-Kokko, L ;
Suske, G ;
Pujol, JP ;
Galéra, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (40) :36881-36895
[10]
Glaser KB, 2003, MOL CANCER THER, V2, P151