Affiliation:
1. Program in Molecular Medicine, University of Massachusetts Medical School
2. Howard Hughes Medical Institute, Worcester, Massachusetts 01605
Abstract
ABSTRACT
The c-Jun NH
2
-terminal kinase (JNK) is implicated in proliferation. Mice with a deficiency of either the
Jnk1
or the
Jnk2
genes are viable, but a compound deficiency of both
Jnk1
and
Jnk2
causes early embryonic lethality. Studies using conditional gene ablation and chemical genetic approaches demonstrate that the combined loss of JNK1 and JNK2 protein kinase function results in rapid senescence. To test whether this role of JNK was required for stem cell proliferation, we isolated embryonic stem (ES) cells from wild-type and JNK-deficient mice. We found that
Jnk1
−/−
Jnk2
−/−
ES cells underwent self-renewal, but these cells proliferated more rapidly than wild-type ES cells and exhibited major defects in lineage-specific differentiation. Together, these data demonstrate that JNK is not required for proliferation or self-renewal of ES cells, but JNK plays a key role in the differentiation of ES cells.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
38 articles.
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