Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

The isoform‐specific functions of the c‐Jun N‐terminal Kinases (JNKs): differences revealed by gene targeting

View through CrossRef
AbstractThe c‐Jun N‐terminal kinases (JNKs) are members of the mitogen‐activated protein kinase (MAPK) family. In mammalian genomes, three genes encode the JNK family. To evaluate JNK function, mice have been created with deletions in one or more of three Jnk genes. Initial studies on jnk1−/− or jnk2−/− mice have shown roles for these JNKs in the immune system whereas studies on jnk3−/− mice have highlighted roles for JNK3 in the nervous system. Further studies have highlighted the contributions of JNK1 and/or JNK2 to a range of biological and pathological processes. These include bone remodelling and joint disease, inflammatory and autoimmune diseases, obesity, diabetes, cardiovascular disease, liver disease and tumorigenesis in addition to effects in neurons. These results emphasise the differences in the roles played by JNK isoforms in vivo and suggest that the design of JNK inhibitors for subsequent therapeutic uses may benefit from selective inhibition of individual JNK isoforms. BioEssays 28: 923–934, 2006. © 2006 Wiley periodicals, Inc.
Title: The isoform‐specific functions of the c‐Jun N‐terminal Kinases (JNKs): differences revealed by gene targeting
Description:
AbstractThe c‐Jun N‐terminal kinases (JNKs) are members of the mitogen‐activated protein kinase (MAPK) family.
In mammalian genomes, three genes encode the JNK family.
To evaluate JNK function, mice have been created with deletions in one or more of three Jnk genes.
Initial studies on jnk1−/− or jnk2−/− mice have shown roles for these JNKs in the immune system whereas studies on jnk3−/− mice have highlighted roles for JNK3 in the nervous system.
Further studies have highlighted the contributions of JNK1 and/or JNK2 to a range of biological and pathological processes.
These include bone remodelling and joint disease, inflammatory and autoimmune diseases, obesity, diabetes, cardiovascular disease, liver disease and tumorigenesis in addition to effects in neurons.
These results emphasise the differences in the roles played by JNK isoforms in vivo and suggest that the design of JNK inhibitors for subsequent therapeutic uses may benefit from selective inhibition of individual JNK isoforms.
BioEssays 28: 923–934, 2006.
© 2006 Wiley periodicals, Inc.

Related Results

The mTOR Pathway Regulates PKM2 to Affect Glycolysis in Esophageal Squamous Cell Carcinoma
The mTOR Pathway Regulates PKM2 to Affect Glycolysis in Esophageal Squamous Cell Carcinoma
Objectives: Esophageal squamous cell carcinoma is a highly prevalent cancer withpoor survival rate and prognosis. Increasing evidence suggests an important role for metabolic regul...
Expression and polymorphism of genes in gallstones
Expression and polymorphism of genes in gallstones
ABSTRACT Through the method of clinical case control study, to explore the expression and genetic polymorphism of KLF14 gene (rs4731702 and rs972283) and SR-B1 gene (rs...
Data from The Landscape of Isoform Switches in Human Cancers
Data from The Landscape of Isoform Switches in Human Cancers
<div>Abstract<p>Alternative usage of transcript isoforms from the same gene has been hypothesized as an important feature in cancers. However, differential usage of gen...
Data from The Landscape of Isoform Switches in Human Cancers
Data from The Landscape of Isoform Switches in Human Cancers
<div>Abstract<p>Alternative usage of transcript isoforms from the same gene has been hypothesized as an important feature in cancers. However, differential usage of gen...
The Need to Factor Asset Risk Into LNG Terminal Agreement Negotiations
The Need to Factor Asset Risk Into LNG Terminal Agreement Negotiations
Abstract As developers race around the globe building liquefied natural gas ("LNG") terminals, companies acquiring capacity at those terminals are analyzing their...
Abstract 1613: Characterization of the Src-regulated kinome by chemical proteomics
Abstract 1613: Characterization of the Src-regulated kinome by chemical proteomics
Abstract Enhanced Src activation has been implicated in many cancers, including those of breast, lung and pancreas. However single-agent therapies targeting Src have...
Expression pattern of an evolutionarily conserved splice variant in the rat Tacc2 gene
Expression pattern of an evolutionarily conserved splice variant in the rat Tacc2 gene
SummaryThe transforming acidic coiled‐coil containing protein 2 (Tacc2) gene and its paralogs, Tacc1 and Tacc3 encode proteins that are associated with the centrosome and involved ...

Back to Top