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Modulation of CREB activity by the Rho GTPase regulates cell and organism size during mouse embryonic development.
- Source :
-
Developmental cell [Dev Cell] 2002 May; Vol. 2 (5), pp. 553-65. - Publication Year :
- 2002
-
Abstract
- Rho GTPases regulate several aspects of tissue morphogenesis during animal development. We found that mice lacking the Rho-inhibitory protein, p190-B RhoGAP, are 30% reduced in size and exhibit developmental defects strikingly similar to those seen in mice lacking the CREB transcription factor. In p190-B RhoGAP-deficient mice, CREB phosphorylation is substantially reduced in embryonic tissues. Embryo-derived cells contain abnormally high levels of active Rho protein, are reduced in size, and exhibit defects in CREB activation upon exposure to insulin or IGF-1. The cell size defect is rescued by expression of constitutively activated CREB, and in wild-type cells, expression of activated Rho or dominant-negative CREB results in reduced cell size. Together, these results suggest that activity of the Rho GTPase modulates a signal from insulin/IGFs to CREB that determines cell size and animal size during embryogenesis.
- Subjects :
- Animals
Body Constitution
Cell Size
DNA-Binding Proteins
Embryonic and Fetal Development
GTPase-Activating Proteins
Guanine Nucleotide Exchange Factors deficiency
Guanine Nucleotide Exchange Factors genetics
Guanine Nucleotide Exchange Factors metabolism
Insulin metabolism
Insulin Receptor Substrate Proteins
Mice
Mice, Knockout
Mitogen-Activated Protein Kinases metabolism
Models, Biological
Nuclear Proteins deficiency
Nuclear Proteins genetics
Nuclear Proteins metabolism
Phenotype
Phosphoproteins metabolism
Phosphorylation
Repressor Proteins
Signal Transduction
Cyclic AMP Response Element-Binding Protein metabolism
rho GTP-Binding Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1534-5807
- Volume :
- 2
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Developmental cell
- Publication Type :
- Academic Journal
- Accession number :
- 12015964
- Full Text :
- https://doi.org/10.1016/s1534-5807(02)00162-4