Identification and characterization of a novel Schwann and outflow tract endocardial cushion lineage-restricted periostin enhancer

被引:97
作者
Lindsley, Andrew
Snider, Paige
Zhou, Hongming
Rogers, Rhonda
Wang, Jian
Olaopa, Michael
Kruzynska-Frejtag, Agnieszka
Koushik, Shrinagesh V.
Lilly, Brenda
Burch, John B. E.
Firulli, Anthony B.
Conway, Simon J.
机构
[1] Indiana Univ, Sch Med, Riley Hosp Children, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Herman B Wells Ctr Pediat Res, Cardiovasc Dev Grp, Indianapolis, IN 46202 USA
[3] Wroclaw Med Univ, PL-50367 Wroclaw, Poland
[4] Med Coll Georgia, Vasc Biol Ctr, Augusta, GA 30912 USA
[5] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
关键词
Periostin; mouse embryo; Schwann cells; heart development; endocardial cushions; peripheral nervous system; lineage restricted promoter; lacZ; reporter mice;
D O I
10.1016/j.ydbio.2007.04.041
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Periostin is a fasciclin-containing adhesive glycoprotein that facilitates the migration and differentiation of cells that have undergone epithelial-mesenchymal transformation during embryogenesis and in pathological conditions. Despite the importance of post-transformational differentiation as a general developmental mechanism, little is known how periostin's embryonic expression is regulated. To help resolve this deficiency, a 3.9-kb periostin proximal promoter was isolated and shown to drive tissue-specific expression in the neural crest-derived Schwann cell lineage and in a subpopulation of periostin-expressing cells in the cardiac outflow tract endocardial cushions. In order to identify the enhancer and associated DNA binding factor(s) responsible, in vitro promoter dissection was undertaken in a Schwannoma line. Ultimately a 304-bp(peri) enhancer was identified and shown to be capable of recapitulating 3.9 kb(peri-lacZ) in vivo spatiotemporal patterns. Further mutational and EMSA analysis helped identify a minimal 37-bp region that is bound by the YY1 transcription factor. The 37-bp enhancer was subsequently shown to be essential for in vivo 3.9 kb(peri-lacZ) promoter activity. Taken together, these studies identify an evolutionary-con served YY1-binding 37-bp region within a 304-bp periostin core enhancer that is capable of regulating simultaneous novel tissue-specific periostin expression in the cardiac outflow-tract cushion mesenchyme and Schwann cell lineages. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:340 / 355
页数:16
相关论文
共 73 条
[1]   Essential dosage-dependent functions of the transcription factor Yin Yang 1 in late embryonic development and cell cycle progression [J].
Affar, E ;
Gay, F ;
Shi, YJ ;
Liu, HF ;
Huarte, M ;
Wu, S ;
Collins, T ;
Li, E ;
Shi, Y .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (09) :3565-3581
[2]   Periostin potently promotes metastatic growth of colon cancer by augmenting cell survival via the Akt/PKB pathway [J].
Bao, SD ;
Ouyang, G ;
Bai, XF ;
Huang, Z ;
Ma, CY ;
Liu, M ;
Shoo, R ;
Anderson, RM ;
Rich, JN ;
Wang, XF .
CANCER CELL, 2004, 5 (04) :329-339
[3]   Yin-yang 1 and glucocorticoid receptor participate in the Stat5-mediated growth hormone response of the serine protease inhibitor 2.1 gene [J].
Bergad, PL ;
Towle, HC ;
Berry, SA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (11) :8114-8120
[4]   The transcription factor Sox10 is a key regulator of peripheral glial development [J].
Britsch, S ;
Goerich, DE ;
Riethmacher, D ;
Peirano, RI ;
Rossner, M ;
Nave, KA ;
Birchmeier, C ;
Wegner, M .
GENES & DEVELOPMENT, 2001, 15 (01) :66-78
[5]   Heart-valve mesenchyme formation is dependent on hyaluronan-augmented activation of ErbB2-ErbB3 receptors [J].
Camenisch, TD ;
Schroeder, JA ;
Bradley, J ;
Klewer, SE ;
McDonald, JA .
NATURE MEDICINE, 2002, 8 (08) :850-855
[6]   Decreased neural crest stem cell expansion is responsible for the conotruncal heart defects within the Splotch (Sp2H)/Pax3 mouse mutant [J].
Conway, SJ ;
Bundy, J ;
Chen, JW ;
Dickman, E ;
Rogers, R ;
Will, BM .
CARDIOVASCULAR RESEARCH, 2000, 47 (02) :314-328
[7]   What cardiovascular defect does my prenatal mouse mutant have, and why? [J].
Conway, SJ ;
Kruzynska-Frejtag, A ;
Kneer, PL ;
Machnicki, M ;
Koushik, SV .
GENESIS, 2003, 35 (01) :1-21
[8]  
DIGNAM JD, 1983, METHOD ENZYMOL, V101, P582
[9]  
Donohoe ME, 1999, MOL CELL BIOL, V19, P7237
[10]   ULTRASTRUCTURAL-LOCALIZATION OF HYALURONAN IN MYELIN SHEATHS OF THE RAT CENTRAL AND RAT AND HUMAN PERIPHERAL NERVOUS SYSTEMS USING HYALURONAN-BINDING PROTEIN GOLD AND LINK PROTEIN GOLD [J].
EGGLI, PS ;
LUCOCQ, J ;
OTT, P ;
GRABER, W ;
VANDERZYPEN, E .
NEUROSCIENCE, 1992, 48 (03) :737-744