A candidate enhancer element responsible for high-level expression of the aggrecan gene in chondrocytes

被引:6
作者
Ikeda, Yuichi [1 ]
Ito, Kazuo [2 ]
Izumi, Yuichi [1 ]
Shinomura, Tamayuki [1 ]
机构
[1] Tokyo Med & Dent Univ, Dept Biomatrix, Tokyo 1138549, Japan
[2] Tohoku Univ, Sch Med, Dept Orthopaed Surg, Sendai, Miyagi 9808574, Japan
关键词
Aggrecan; cartilage; extracellular matrix; transcriptional enhancer; type II collagen; CELL-LINE; COLLAGEN GENE; SOX9; PHENOTYPE; MOLECULES; SEQUENCES; CARTILAGE;
D O I
10.1093/jb/mvu014
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
Aggrecan is the most abundant proteoglycan in cartilage. It contains a lot of negatively charged glycosaminoglycan chains along the core protein, providing a large osmotic swelling pressure within the cartilage. Therefore, the biomechanical properties of cartilage, such as its compressive load-bearing capacity, are highly dependent on the presence of abundant aggrecan in the cartilage matrix. To elucidate the transcriptional mechanism that leads to abundant expression of aggrecan by chondrocytes, we screened for enhancer elements in 130 kb of the aggrecan gene, Agc1, using a reporter assay system that we previously developed. The system is based on co-transfection of candidate enhancer elements and reporter constructs into Swarm rat chondrosarcoma chondrocytes that retain a high level of aggrecan expression. We found an element that might be involved in high-level expression of Agc1 gene in chondrocytes in vivo. The element is located 30 kb upstream of the Agc1 transcription start site.
引用
收藏
页码:21 / 28
页数:8
相关论文
共 18 条
[1]
[Anonymous], BONE CARTILAGE DEV E
[2]
Construction and characterization of two bacterial artificial chromosome libraries of pea (Pisum sativum L.) for the isolation of economically important genes [J].
Coyne, C. J. ;
McClendon, M. T. ;
Walling, J. G. ;
Timmerman-Vaughan, G. M. ;
Murray, S. ;
Meksem, K. ;
Lightfoot, D. A. ;
Shultz, J. L. ;
Keller, K. E. ;
Martin, R. R. ;
Inglis, D. A. ;
Rajesh, P. N. ;
McPhee, K. E. ;
Weeden, N. F. ;
Grusak, M. A. ;
Li, C.-M. ;
Storlie, E. W. .
GENOME, 2007, 50 (09) :871-875
[3]
L-Sox5 and Sox6 drive expression of the aggrecan gene in cartilage by securing binding of Sox9 to a far-upstream enhancer [J].
Han, Yu ;
Lefebvre, Veronique .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (16) :4999-5013
[4]
Proteoglycans and more - from molecules to biology [J].
Heinegard, Dick .
INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, 2009, 90 (06) :575-586
[5]
The establishment and characterization of an immortal cell line with a stable chondrocytic phenotype [J].
King, KB ;
Kimura, JH .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2003, 89 (05) :992-1004
[6]
Kriegler M., 1990, GENE TRANSFER EXPRES, P165
[7]
SOX9 is a potent activator of the chondrocyte-specific enhancer of the pro alpha 1(II) collagen gene [J].
Lefebvre, V ;
Huang, WD ;
Harley, VR ;
Goodfellow, PN ;
deCrombrugghe, B .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (04) :2336-2346
[8]
Morris N., 2002, CONNECTIVE TISSUE IT, P41
[9]
Wwp2 is essential for palatogenesis mediated by the interaction between Sox9 and mediator subunit 25 [J].
Nakamura, Yukio ;
Yamamoto, Koji ;
He, Xinjun ;
Otsuki, Bungo ;
Kim, Youngwoo ;
Murao, Hiroki ;
Soeda, Tsunemitsu ;
Tsumaki, Noriyuki ;
Deng, Jian Min ;
Zhang, Zhaoping ;
Behringer, Richard R. ;
de Crombrugghe, Benoit ;
Postlethwait, John H. ;
Warman, Matthew L. ;
Nakamura, Takashi ;
Akiyama, Haruhiko .
NATURE COMMUNICATIONS, 2011, 2
[10]
An inhibitor of the stretch-activated cation receptor exerts a potent effect on chondrocyte phenotype [J].
Perkins, GL ;
Derfoul, A ;
Ast, A ;
Hall, DJ .
DIFFERENTIATION, 2005, 73 (05) :199-211