Transcriptional regulation of tenascin genes

被引:86
作者
Chiovaro, Francesca [1 ,2 ]
Chiquet-Ehrismann, Ruth [1 ,2 ]
Chiquet, Matthias [3 ]
机构
[1] Friedrich Miescher Inst Biomed Res, Basel, Switzerland
[2] Univ Basel, Fac Sci, Basel, Switzerland
[3] Univ Bern, Sch Dent Med, Dept Orthodont & Dentofacial Orthoped, Bern, Switzerland
基金
瑞士国家科学基金会;
关键词
cytokine; cancer; development; extracellular matrix; glucocorticoid; growth factor; gene regulation; gene promoter; homeobox gene; matricellular; mechanical stress; tenascin; transcription factor; EHLERS-DANLOS-SYNDROME; EXTRACELLULAR-MATRIX GLYCOPROTEINS; HOMEODOMAIN PROTEIN OTX2; GROWTH-FACTOR-BETA; SMOOTH-MUSCLE; C EXPRESSION; BREAST-CANCER; R GENE; MOUSE TENASCIN; X DEFICIENCY;
D O I
10.1080/19336918.2015.1008333
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Extracellular matrix proteins of the tenascin family resemble each other in their domain structure, and also share functions in modulating cell adhesion and cellular responses to growth factors. Despite these common features, the 4 vertebrate tenascins exhibit vastly different expression patterns. Tenascin-R is specific to the central nervous system. Tenascin-C is an oncofetal protein controlled by many stimuli (growth factors, cytokines, mechanical stress), but with restricted occurrence in space and time. In contrast, tenascin-X is a constituitive component of connective tissues, and its level is barely affected by external factors. Finally, the expression of tenascin-W is similar to that of tenascin-C but even more limited. In accordance with their highly regulated expression, the promoters of the tenascin-C and -W genes contain TATA boxes, whereas those of the other 2 tenascins do not. This article summarizes what is currently known about the complex transcriptional regulation of the 4 tenascin genes in development and disease.
引用
收藏
页码:34 / 47
页数:14
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