Document Detail


XPteg (Xenopus proximal tubules-expressed gene) is essential for pronephric mesoderm specification and tubulogenesis.
MedLine Citation:
PMID:  19909807     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Retinoic acid (RA) signaling is important for the early steps of nephrogenic cell fate specification. Here, we report a novel target gene of RA signaling named XPteg (Xenopus proximal tubules-expressed gene) which is critical for pronephric development. XPteg starts to be expressed at the earliest stage of embryonic kidney specification and was restricted to the pronephric proximal tubules during kidney development. Anti-sense morpholino (MO)-mediated knockdown of XPteg perturbed formation of pronephros as demonstrated by reduced expression of pronephric tubule markers. Conversely, overexpression of XPteg promoted endogenous and ectopic expression of those markers and expanded pronephric tubules. Treatment of retinoic acid induced the expression of XPteg in the pronephric field without protein synthesis. Furthermore, we found that the pronephric defects caused by a dominant negative RA receptor could be rescued by coexpression of XPteg. Taken together, these results suggest that XPteg functions as a direct transcriptional target of RA signaling to regulate pronephric tubulogenesis in Xenopus early development.
Authors:
Seung Joon Lee; Sanghee Kim; Sun-Cheol Choi; Jin-Kwan Han
Related Documents :
3591957 - Adp activates protooncogene expression in renal epithelial cells.
12697807 - Increased expression of tata-binding protein, the central transcription factor, can con...
2657577 - Elevation of 1,2-diacylglycerol in ras-transformed neonatal liver and pancreas of trans...
10679397 - Integration of positive and negative growth signals during ras pathway activation in vivo.
1995637 - Structural and functional studies on the human interleukin-6 receptor. binding, cross-l...
21791387 - Proteasome affects the expression of aryl hydrocarbon receptor-regulated proteins.
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2009-11-10
Journal Detail:
Title:  Mechanisms of development     Volume:  127     ISSN:  1872-6356     ISO Abbreviation:  Mech. Dev.     Publication Date:    2010 Jan-Feb
Date Detail:
Created Date:  2010-02-03     Completed Date:  2010-05-06     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9101218     Medline TA:  Mech Dev     Country:  Ireland    
Other Details:
Languages:  eng     Pagination:  49-61     Citation Subset:  IM    
Copyright Information:
Copyright 2009 Elsevier Ireland Ltd. All rights reserved.
Affiliation:
Department of Life Science, Division of Molecular and Life Sciences, Pohang University of Science and Technology, Pohang, Kyungbuk, South Korea.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Amino Acid Sequence
Animals
Gene Expression Regulation, Developmental
Homeodomain Proteins / metabolism
In Situ Hybridization
Intracellular Signaling Peptides and Proteins / metabolism,  physiology*
Kidney Tubules / embryology*
Mesoderm / metabolism*
Molecular Sequence Data
Nephrons / embryology*
Oligonucleotides, Antisense / genetics
Paired Box Transcription Factors / metabolism
Protein Structure, Tertiary
Sequence Homology, Amino Acid
Tretinoin / metabolism
Xenopus Proteins / metabolism,  physiology*
Xenopus laevis / metabolism*
Chemical
Reg. No./Substance:
0/Homeodomain Proteins; 0/Intracellular Signaling Peptides and Proteins; 0/Lim-1 protein, Xenopus; 0/Oligonucleotides, Antisense; 0/Paired Box Transcription Factors; 0/Pax8 protein, Xenopus; 0/Pteg protein, Xenopus; 0/Xenopus Proteins; 302-79-4/Tretinoin

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  The role of 11?-hydroxysteroid dehydrogenase type 2 in human hypertension.
Next Document:  Modelling honeybee visual guidance in a 3-D environment.