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Transcriptional regulation of tenascin genes

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BORIS DOI
10.7892/boris.76771
Date of Publication
2015
Publication Type
Article
Division/Institute

Zahnmedizinische Klin...

Author
Chiovaro, Francesca
Chiquet-Ehrismann, Ruth
Chiquet, Matthias
Zahnmedizinische Kliniken, Klinik für Kieferorthopädie
Subject(s)

600 - Technology::610...

Series
Cell adhesion & migration
ISSN or ISBN (if monograph)
1933-6918
Publisher
Landes Bioscience
Language
English
Publisher DOI
10.1080/19336918.2015.1008333
PubMed ID
25793574
Uncontrolled Keywords

AKT

v-akt murine thymoma ...

anaplastic lymphoma k...

activator protein-1 A...

activating transcript...

bone morphogenetic pr...

CREB binding protein ...

cAMP response element...

CREB-related protein ...

cytochrome P450 famil...

chromatin immunopreci...

Ets binding site ECM

extracellular matrix ...

epidermal growth fact...

extracellular signal-...

E26 transformation-sp...

Ewing sarcoma-Ets fus...

even skipped homeobox...

fibroblast growth fac...

homeodomain binding s...

interleukin ILK

integrin-linked kinas...

Janus kinase JNK

c-Jun N-terminal kina...

major histocompatibil...

megakaryoblastic leuk...

nuclear factor kappa ...

nerve growth factor; ...

nuclear factor of act...

orthodenticle homolog...

platelet-derived grow...

phosphatidylinositol ...

POU domain class 3 tr...

paired-related homeob...

recombining binding p...

Rho-associated

coiled-coil-containin...

ras homolog gene fami...

SAF-A/B

Acinus

and PIAS SCX

scleraxix SEAP

secreted alkaline pho...

small body size - mot...

sex determining regio...

serum response elemen...

serum response factor...

signal transducer and...

transforming growth f...

tenascin-C TNF-α

tumor necrosis factor...

tenascin-R TNW

tenascin-W TNX

tenascin-X TSS

transcription start s...

untranslated region W...

wingless-related inte...

micro RNA p38 MAPK

p38 mitogen activated...

Description
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.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/138636
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Transcriptional regulation of tenascin.pdftextAdobe PDF414.59 KBpublishedOpen
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