SOX9 overexpression plays a potential role in idiopathic congenital talipes equinovarus

被引:11
作者
Wang, Zhengdong [1 ,2 ]
Yan, Nan [2 ]
Liu, Liying [1 ,3 ]
Cao, Donghua [1 ]
Gao, Ming [1 ]
Lin, Changkun [1 ]
Jin, Chunlian [1 ]
机构
[1] China Med Univ, Dept Med Genet, Shenyang 110001, Peoples R China
[2] Shenyang Med Coll, Dept Anat, Shenyang 110034, Peoples R China
[3] Shenyang Womens & Childrens Hosp, Shenyang 110001, Peoples R China
关键词
clubfoot; congenital; gene expression; SRY (sex-determining region Y)-box 9; CLUB FOOT; COL9A1; GENE; EXPRESSION; COLLAGEN; TRANSCRIPTION; CHONDROGENESIS; DIMERIZATION; DYSPLASIA; CELLS; DNA;
D O I
10.3892/mmr.2012.1245
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The collagen, type IX, alpha 1 (COL9A1) gene was previously identified as a candidate gene for idiopathic congenital talipes equinovarus (ICTEV), a congenital lower limb deformity in humans. In the present study, increased expression levels of COL9A1 were identified in the abductor hallucis muscle of ICTEV patients compared with those in control samples. The COL9A1 gene is regulated by SRY (sex-determining region Y)-box 9 (S0X9). Immunofluorescence analysis of SOX9 and COL9A1 proteins identified colocalization to the sarcolemma, endomysium and muscle membrane in muscle samples of ICTEV. No mutations in the exons and promoters of SOX9 were detected in blood samples of 84 ICTEV patients by denaturing gradient gel electrophoresis. mRNA and protein expression levels of SOX9 were detected by real-time polymerase chain reaction and western blot analysis, respectively and were found to be significantly higher in ICTEV muscle samples compared with those in control samples. Based on present observations, we hypothesize that overexpression of the SOX9 gene may play a role in the genetic etiology of ICTEV.
引用
收藏
页码:821 / 825
页数:5
相关论文
共 29 条
[1]   Dimerization of SOX9 is required for chondrogenesis, but not for sex determination [J].
Bernard, P ;
Tang, PY ;
Dewing, P ;
Harley, VR ;
Vilain, E .
HUMAN MOLECULAR GENETICS, 2003, 12 (14) :1755-1765
[2]   The expression of Gli3, regulated by HOXDI3, may play a role in idiopathic congenital talipes equinovarus [J].
Cao, DongHua ;
Jin, ChunLian ;
Ren, MeiHong ;
Lin, ChangKun ;
Zhang, Xuan ;
Zhao, Ning .
BMC MUSCULOSKELETAL DISORDERS, 2009, 10
[3]   Pedigree analysis and epidemiological features of idiopathic congenital talipes equinovarus in the United Kingdom: a case-control study [J].
Cardy, A. H. ;
Barker, S. ;
Chesney, D. ;
Sharp, L. ;
Maffulli, N. ;
Miedzybrodzka, Z. .
BMC MUSCULOSKELETAL DISORDERS, 2007, 8 (1)
[4]   Genetics of club foot in Maori and Pacific people [J].
Chapman, C ;
Stott, NS ;
Port, RV ;
Nicol, RO .
JOURNAL OF MEDICAL GENETICS, 2000, 37 (09) :680-683
[5]   The genetics of idiopathic clubfoot [J].
Dietz, F .
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 2002, (401) :39-48
[6]   Basic Helix-Loop-Helix Transcription Factor Twist1 Inhibits Transactivator Function of Master Chondrogenic Regulator Sox9 [J].
Gu, Shoujun ;
Boyer, Thomas G. ;
Naski, Michael C. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (25) :21082-21092
[7]  
IONASESCU V, 1974, HELV PAEDIATR ACTA, V29, P305
[8]   UPDATE ON PATHOLOGICAL ANATOMY OF CLUBFOOT [J].
IPPOLITO, E .
JOURNAL OF PEDIATRIC ORTHOPAEDICS-PART B, 1995, 4 (01) :17-24
[9]   Long-term comparative results in patients with congenital club foot treated with two different protocols [J].
Ippolito, E ;
Farsetti, P ;
Caterini, R ;
Tudisco, C .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2003, 85A (07) :1286-1294
[10]   CONGENITAL CLUB FOOT IN THE HUMAN-FETUS - HISTOLOGICAL STUDY [J].
IPPOLITO, E ;
PONSETI, IV .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1980, 62 (01) :8-22