Literature DB >> 15805112

Spatiotemporal switch from DeltaNp73 to TAp73 isoforms during nephrogenesis: impact on differentiation gene expression.

Zubaida Saifudeen1, Virginia Diavolitsis, Jana Stefkova, Susana Dipp, Hao Fan, Samir S El-Dahr.   

Abstract

p73 is a member of the p53 gene family, which also includes p53 and p63. These proteins share sequence similarity and target genes but also have divergent roles in cancer and development. Unlike p53, transcription of the p73 gene yields multiple full-length (transactivation (TA) domain) and amino terminus-truncated (DeltaN) isoforms. DeltaNp73 acts in a dominant negative fashion to inhibit the actions of TAp73 and p53 on their target genes, promoting cell survival and proliferation and suppressing apoptosis. The balance between TAp73 and its negative regulator, DeltaNp73, may therefore represent an important determinant of developmental cell fate. There is little if anything known regarding the developmental regulation of the p73 gene. In this study, we showed that TAp73 and DeltaNp73 exhibit reciprocal spatiotemporal expression and functions during nephrogenesis. TAp73 was predominantly expressed in the differentiation domain of the renal cortex in an overlapping manner with the vasopressin-sensitive water channel aquaporin-2 (AQP-2). Chromatin immunoprecipitation assays demonstrated that the endogenous AQP-2 promoter was occupied by TAp73 in a developmentally regulated manner. Furthermore TAp73 stimulated AQP-2 promoter-driven reporter expression. TAp73 also activated the bradykinin B2 receptor (B2R) promoter, a developmentally regulated gene involved in regulation of sodium excretion. The transcriptional effects of TAp73 on AQP-2 and B2R were independent of p53. In marked contrast to TAp73, DeltaNp73 isoforms were induced early in development and were preferentially expressed in proliferating nephron precursors. Moreover DeltaNp73 was a potent repressor of B2R gene transcription. We conclude that the p73 gene is developmentally regulated during kidney organogenesis. The spatiotemporal switch from DeltaNp73 to TAp73 may play an important role in the terminal differentiation program of the developing nephron.

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Year:  2005        PMID: 15805112     DOI: 10.1074/jbc.M414575200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  13 in total

1.  Mechanisms of p53 activation and physiological relevance in the developing kidney.

Authors:  Karam Aboudehen; Sylvia Hilliard; Zubaida Saifudeen; Samir S El-Dahr
Journal:  Am J Physiol Renal Physiol       Date:  2012-01-11

Review 2.  Transcriptional control of terminal nephron differentiation.

Authors:  Samir S El-Dahr; Karam Aboudehen; Zubaida Saifudeen
Journal:  Am J Physiol Renal Physiol       Date:  2008-02-20

3.  Histone signature of metanephric mesenchyme cell lines.

Authors:  Nathan McLaughlin; Xiao Yao; Yuwen Li; Zubaida Saifudeen; Samir S El-Dahr
Journal:  Epigenetics       Date:  2013-07-18       Impact factor: 4.528

4.  G Protein-Coupled Receptor 87: a Promising Opportunity for Cancer Drug Discovery.

Authors:  Yanhong Zhang; Ariane Scoumanne; Xinbin Chen
Journal:  Mol Cell Pharmacol       Date:  2010-01-01

Review 5.  The MDM2-p53 pathway: multiple roles in kidney development.

Authors:  Samir El-Dahr; Sylvia Hilliard; Karam Aboudehen; Zubaida Saifudeen
Journal:  Pediatr Nephrol       Date:  2014-04       Impact factor: 3.714

6.  DeltaNp73 modulates nerve growth factor-mediated neuronal differentiation through repression of TrkA.

Authors:  Jin Zhang; Xinbin Chen
Journal:  Mol Cell Biol       Date:  2007-03-12       Impact factor: 4.272

Review 7.  Mechanisms, function and clinical applications of DNp73.

Authors:  Cuixia Di; Lina Yang; Hong Zhang; Xiaofei Ma; Xin Zhang; Chao Sun; Hongyan Li; Shuai Xu; Lizhe An; Xun Li; Zhongtian Bai
Journal:  Cell Cycle       Date:  2013-06-13       Impact factor: 4.534

8.  Ontogeny of bradykinin B1 receptors in the mouse kidney.

Authors:  Ozlem Pinar Bulut; Susana Dipp; Samir El-Dahr
Journal:  Pediatr Res       Date:  2009-11       Impact factor: 3.756

9.  A p53-Pax2 pathway in kidney development: implications for nephrogenesis.

Authors:  Zubaida Saifudeen; Jiao Liu; Susana Dipp; Xiao Yao; Yuwen Li; Nathaniel McLaughlin; Karam Aboudehen; Samir S El-Dahr
Journal:  PLoS One       Date:  2012-09-12       Impact factor: 3.240

10.  Tissue-specific expression of p73 C-terminal isoforms in mice.

Authors:  Francesca Grespi; Ivano Amelio; Paola Tucci; Margherita Annicchiarico-Petruzzelli; Gerry Melino
Journal:  Cell Cycle       Date:  2012-11-16       Impact factor: 4.534

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