| Literature DB >> 16292775 |
Frank Bollig1, Rebecca Mehringer, Birgit Perner, Christina Hartung, Matthias Schäfer, Manfred Schartl, Jean-Nicolas Volff, Christoph Winkler, Christoph Englert.
Abstract
The Wilms' tumor suppressor gene wt1 encodes a zinc-finger transcription factor that plays an important role in the development of the mammalian genitourinary system. Mutations in WT1 in humans lead to anomalies of kidney and gonad development and cause Wilms' tumor, a pediatric kidney cancer. The inactivation of both wt1 alleles in mice gives rise to multiple organ defects, among them agenesis of kidney, spleen, and gonads. In zebrafish, an ortholog of wt1 has been described that is expressed in the pronephric field and is later restricted to the podocytes. Here, we report the existence of a second wt1 gene in zebrafish, which we have named wt1b (we named the initial gene wt1a). The overall sequence identity of the two Wt1 proteins is 70% and 92% between the zinc-finger regions, respectively. In contrast to wt1a, wt1b is expressed from the earliest stages of development onward, albeit at low levels. Both wt1a and wt1b are expressed in the intermediate mesoderm, with wt1b being restricted to a smaller area lying at the caudal end of the wt1a expression domain. In adult fish, high expression levels for both genes can be found in gonads, kidney, heart, spleen, and muscle. Copyright 2005 Wiley-Liss, Inc.Entities:
Mesh:
Substances:
Year: 2006 PMID: 16292775 DOI: 10.1002/dvdy.20645
Source DB: PubMed Journal: Dev Dyn ISSN: 1058-8388 Impact factor: 3.780