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Biological Function of Nuclear Receptor Tyrosine Kinase Action
Author(s) -
Shen Song,
Kenneth M. Rosen,
Gabriel Corfas
Publication year - 2013
Publication title -
cold spring harbor perspectives in biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.011
H-Index - 173
ISSN - 1943-0264
DOI - 10.1101/cshperspect.a009001
Subject(s) - receptor tyrosine kinase , biology , microbiology and biotechnology , ror1 , receptor protein tyrosine kinases , sh2 domain , intracellular , signal transduction , tyrosine kinase , extracellular , receptor , platelet derived growth factor receptor , biochemistry , growth factor
Receptor tyrosine kinases (RTKs) were believed until recently to act at the cell membrane in a singular fashion (i.e., binding of ligands on the extracellular domain would activate the intrinsic tyrosine kinase activity in the intracellular domain), which would then start a cascade involving other intracellular signaling molecules that would act as effectors. However, new evidence indicates that some RTKs can signal through a different modality; they can move into the nucleus where they directly exert their actions. Although some studies have showed that the proteolytically released intracellular domain of several RTKs can move to the nucleus where they influence gene expression and cell function, others suggest that RTKs can also move to the nucleus as holoproteins. The identification of this novel signaling mechanism calls for a critical reevaluation of the mechanisms of action of RTKs and their biological roles.

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