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Genetic regulatory networks of nephrogenesis: deregulation of WT1 splicing by benzo(a)pyrene.
- Source :
-
Birth defects research. Part C, Embryo today : reviews [Birth Defects Res C Embryo Today] 2009 Jun; Vol. 87 (2), pp. 192-7. - Publication Year :
- 2009
-
Abstract
- Recent studies have identified AHR as a master regulator of Wilms' tumor suppressor gene (WT1) signaling in the developing kidney. Activation of AHR signaling by environmental chemical is associated with proteasome-mediated degradation of AHR protein, disruption of WT1 alternative splicing, and marked alterations in the regulation of genetic programs of developmental progression in the developing kidney. The complexity of genetic regulatory networks of nephrogenesis controlled by AHR-WT1 interactions will be discussed here with particular emphasis given to the biological and medical consequences that may result from deficits in nephrogenesis that compromise reserve capacity and renal function later in life. Understanding the impact of early-life environmental exposures to chemicals that disrupt AHR signaling can help minimize negative health consequences to pregnant women and their offspring.
- Subjects :
- Adult
Alternative Splicing drug effects
Alternative Splicing genetics
Animals
Female
Gene Expression Regulation, Developmental drug effects
Humans
Kidney drug effects
Mice
Mice, Knockout
Morphogenesis
Pregnancy
Rats
Receptor Cross-Talk drug effects
Receptor Cross-Talk physiology
Receptors, Aryl Hydrocarbon drug effects
Receptors, Aryl Hydrocarbon genetics
Receptors, Aryl Hydrocarbon metabolism
Signal Transduction drug effects
Signal Transduction physiology
WT1 Proteins drug effects
Young Adult
Benzo(a)pyrene toxicity
Carcinogens toxicity
Gene Expression Regulation, Developmental genetics
Gene Regulatory Networks
Kidney embryology
WT1 Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1542-9768
- Volume :
- 87
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Birth defects research. Part C, Embryo today : reviews
- Publication Type :
- Academic Journal
- Accession number :
- 19530133
- Full Text :
- https://doi.org/10.1002/bdrc.20148