Journal article
Repression of organizer genes in dorsal and ventral Xenopus cells mediated by maternal XTcf3
Development (Cambridge), Vol.129(17), pp.4015-4025
09/2002
PMID: 12163405
Abstract
In the early Xenopus embryo, the dorsal axis is specified by a Wnt signal transduction pathway, involving the movement of beta-catenin into dorsal cell nuclei and its functional association with the LEF-type transcription factor XTcf3. The subsequent function of XTcf3 is uncertain. Overexpression data has suggested that it can be both an activator and repressor of downstream genes. XTcf3 mRNA is synthesized during oogenesis in Xenopus and is stored in the egg. To identify its role in dorsal axis specification, we depleted this maternal store in full-grown oocytes using antisense deoxyoligonucleotides, and fertilized them. The developmental effects of XTcf3 depletion, both on morphogenesis and the expression of marker genes, show that primarily, XTcf3 is an inhibitor, preventing both dorsal and ventral cells of the late blastula from expressing dorsal genes. We also show that simple relief from the repression is not the only factor required for dorsal gene expression. To demonstrate this, we fertilized eggs that had been depleted of both XTcf3 and the maternal transcription factor VegT. Dorsal genes normally repressed by XTcf3 are not activated in these embryos. These data show that normal dorsal gene expression in the embryo requires the transcriptional activator VegT, whilst XTcf3 prevents their inappropriate expression on the ventral side of the embryo.
Details
- Title: Subtitle
- Repression of organizer genes in dorsal and ventral Xenopus cells mediated by maternal XTcf3
- Creators
- Douglas W Houston - Division of Developmental Biology, Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229-3039, USAMatt KofronErnesto ResnikRachel LanglandOlivier DestreeChristopher WylieJanet Heasman
- Resource Type
- Journal article
- Publication Details
- Development (Cambridge), Vol.129(17), pp.4015-4025
- Publisher
- England
- PMID
- 12163405
- ISSN
- 0950-1991
- eISSN
- 1477-9129
- Grant note
- R01 HD33002 / NICHD NIH HHS F32 HD40716-01 / NICHD NIH HHS
- Language
- English
- Date published
- 09/2002
- Academic Unit
- Biology
- Record Identifier
- 9983992055602771
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