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Expression of Smad1 and Smad2 during embryogenesis suggests a role in organ development.
- Source :
-
Developmental dynamics : an official publication of the American Association of Anatomists [Dev Dyn] 1998 Apr; Vol. 211 (4), pp. 293-305. - Publication Year :
- 1998
-
Abstract
- Smad proteins are intracellular signalling molecules and putative transcription factors that transduce signals elicited by members of the transforming growth factor beta (TGF-beta) superfamily. By comparing the expression of Smad1 and Smad2 during embryonic development, we show that mRNAs of both Smad isoforms are present in a variety of tissues. The major sites of expression of both Smads can be correlated with the expression domains of several members of the TGF-beta superfamily. Our expression data suggest that Smad proteins are involved in organ development, particularly that of organs arising from mesenchymal-epithelial interactions. A second site of strong expression is the central nervous system. Transcriptional control mediated by Smad1 and Smad2, therefore, may exert an important function in differentiation processes of embryonic development that are controlled by ligands of the TGF-beta superfamily.
- Subjects :
- Animals
Cardiovascular System embryology
Cardiovascular System metabolism
Digestive System embryology
Digestive System metabolism
In Situ Hybridization
Kidney embryology
Kidney metabolism
Lung embryology
Lung metabolism
Mice
Mice, Inbred C57BL
Nervous System embryology
Nervous System metabolism
Polymerase Chain Reaction
Smad Proteins
Smad1 Protein
Smad2 Protein
Time Factors
Tissue Distribution
Tooth embryology
Tooth metabolism
Transcription, Genetic
DNA-Binding Proteins metabolism
Embryonic and Fetal Development
Gene Expression Regulation, Developmental
Signal Transduction
Trans-Activators
Subjects
Details
- Language :
- English
- ISSN :
- 1058-8388
- Volume :
- 211
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Developmental dynamics : an official publication of the American Association of Anatomists
- Publication Type :
- Academic Journal
- Accession number :
- 9566949
- Full Text :
- https://doi.org/10.1002/(SICI)1097-0177(199804)211:4<293::AID-AJA1>3.0.CO;2-C