Literature DB >> 23818495

Biological function of nuclear receptor tyrosine kinase action.

Sungmin Song1, Kenneth M Rosen, Gabriel Corfas.   

Abstract

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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Year:  2013        PMID: 23818495      PMCID: PMC3685897          DOI: 10.1101/cshperspect.a009001

Source DB:  PubMed          Journal:  Cold Spring Harb Perspect Biol        ISSN: 1943-0264            Impact factor:   10.005


  63 in total

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6.  Expression and nuclear localization of ErbB3 in prostate cancer.

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  14 in total

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Review 5.  Structure-function relationships of ErbB RTKs in the plasma membrane of living cells.

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Review 6.  The EGFR family: not so prototypical receptor tyrosine kinases.

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7.  Angulin proteins ILDR1 and ILDR2 regulate alternative pre-mRNA splicing through binding to splicing factors TRA2A, TRA2B, or SRSF1.

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Authors:  Míriam Javier-Torrent; Sergi Marco; Daniel Rocandio; Maria Pons-Vizcarra; Peter W Janes; Martin Lackmann; Joaquim Egea; Carlos A Saura
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