Down-regulation of nucleosomal binding protein HMGN1 expression during embryogenesis modulates Sox9 expression in chondrocytes

被引:56
作者
Furusawa, T
Lim, JH
Catez, F
Birger, Y
Mackem, S
Bustin, M
机构
[1] NCI, Prot Sect, Lab Metab, NIH, Bethesda, MD 20892 USA
[2] NCI, Pathol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[3] Andong Natl Univ, Dept Biol, Andong 760749, Gyungsangbuk, South Korea
关键词
D O I
10.1128/MCB.26.2.592-604.2006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We find that during embryogenesis the expression of HMGN1, a nuclear protein that binds to nucleosomes and reduces the compaction of the chromatin fiber, is progressively down-regulated throughout the entire embryo, except in committed but continuously renewing cell types, such as the basal layer of the epithelium. In the developing limb bud, the expression of HMGN1 is complementary to Sox9, a master regulator of the chondrocyte lineage. In limb bud micromass cultures, which faithfully mimic in vivo chondrogenic differentiation, loss of HMGN1 accelerates differentiation. Expression of wild-type HMGN1, but not of a mutant HMGN1 that does not bind to chromatin, in Hmgn1(-/-) micromass cultures inhibits Sox9 expression and retards differentiation. Chromatin immunoprecipitation analysis reveals that HMGN1 binds to Sox9 chromatin in cells that are poised to express Sox9. Loss of HMGN1 elevates the amount of HMGN2 bound to Sox9, suggesting functional redundancy among these proteins. These findings suggest a role for HMGN1 in chromatin remodeling during embryogenesis and in the activation of Sox9 during chondrogenesis.
引用
收藏
页码:592 / 604
页数:13
相关论文
共 36 条
[1]  
BEGUM N, 1990, J BIOL CHEM, V265, P11936
[2]   Increased tumorigenicity and sensitivity to ionizing radiation upon loss of chromosomal protein HMGN1 [J].
Birger, Y ;
Catez, F ;
Furusawa, T ;
Lim, JH ;
Prymakowska-Bosak, M ;
West, KL ;
Postnikov, YV ;
Haines, DC ;
Bustin, M .
CANCER RESEARCH, 2005, 65 (15) :6711-6718
[3]   Chromosomal protein HMGN1 enhances the rate of DNA repair in chromatin [J].
Birger, Y ;
West, KL ;
Postnikov, YV ;
Lim, JH ;
Furusawa, T ;
Wagner, JP ;
Laufer, CS ;
Kraemer, KH ;
Bustin, M .
EMBO JOURNAL, 2003, 22 (07) :1665-1675
[4]   The dynamics of histone H1 function in chromatin [J].
Bustin, M ;
Catez, F ;
Lim, JH .
MOLECULAR CELL, 2005, 17 (05) :617-620
[5]   Chromatin unfolding and activation by HMGN chromosomal proteins [J].
Bustin, M .
TRENDS IN BIOCHEMICAL SCIENCES, 2001, 26 (07) :431-437
[6]  
Bustin M, 1999, MOL CELL BIOL, V19, P5237
[7]   Network of dynamic interactions between histone H1 and high-mobility-group proteins in chromatin [J].
Catez, F ;
Yang, H ;
Tracey, KJ ;
Reeves, R ;
Misteli, T ;
Bustin, M .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (10) :4321-4328
[8]  
CRIPPA MP, 1991, J BIOL CHEM, V266, P2712
[9]   DIFFERENTIATION-DEPENDENT ALTERATION IN THE CHROMATIN STRUCTURE OF CHROMOSOMAL PROTEIN HMG-17 GENE DURING ERYTHROPOIESIS [J].
CRIPPA, MP ;
NICKOL, JM ;
BUSTIN, M .
JOURNAL OF MOLECULAR BIOLOGY, 1991, 217 (01) :75-84
[10]   Regulatory mechanisms in the pathways of cartilage and bone formation [J].
de Crombrugghe, B ;
Lefebvre, W .
CURRENT OPINION IN CELL BIOLOGY, 2001, 13 (06) :721-727