Literature DB >> 24104595

Gene regulatory network of renal primordium development.

Michael Marcotte1, Richa Sharma, Maxime Bouchard.   

Abstract

Animal development progresses through the stepwise deployment of gene regulatory networks (GRN) encoded in the genome. Comparative analyses in different species and organ systems have revealed that GRN blueprints are composed of subcircuits with stereotypical architectures that are often reused as modular units. In this review, we report the evidence for the GRN underlying renal primordium development. In vertebrates, renal development is initiated by the induction of a field of intermediate mesoderm cells competent to undergo lineage specification and nephric (Wolffian) duct formation. Definition of the renal field leads to the activation of a core regulatory subcircuit composed of the transcription factors Pax2/8, Gata3 and Lim1. These transcription factors turn on a second layer of transcriptional regulators while also activating effectors of tissue morphogenesis and cellular specialization. Elongation and connection of the nephric duct to the cloaca (bladder/urethra primordium) is followed by metanephric kidney induction through signals emanating from the metanephric mesenchyme. Central to this process is the activation and positioning of the glial cell line-derived neurotrophic factor (Gdnf)-Ret signaling pathway by network subcircuits located in the mesenchyme and epithelial tissues of the caudal trunk. Evidence shows that each step of the renal primordium developmental program is regulated by structured GRN subunits organized in a hierarchical manner. Understanding the structure and dynamics of the renal GRN will help us understand the intrinsic phenotypical variability of congenital anomalies of the kidney and urinary tract and guide our approaches to regenerative medicine.

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Year:  2013        PMID: 24104595     DOI: 10.1007/s00467-013-2635-0

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  85 in total

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Authors:  Eric H Davidson
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Authors:  David S Hains; Sunder Sims-Lucas; Ashley Carpenter; Monalee Saha; Inga Murawski; Kayle Kish; Indra Gupta; Kirk McHugh; Carlton M Bates
Journal:  J Urol       Date:  2010-03-19       Impact factor: 7.450

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Journal:  Dev Cell       Date:  2005-02       Impact factor: 12.270

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Authors:  M Taira; M Jamrich; P J Good; I B Dawid
Journal:  Genes Dev       Date:  1992-03       Impact factor: 11.361

8.  Renal agenesis and hypodysplasia in ret-k- mutant mice result from defects in ureteric bud development.

Authors:  A Schuchardt; V D'Agati; V Pachnis; F Costantini
Journal:  Development       Date:  1996-06       Impact factor: 6.868

9.  Characterization of three novel members of the zebrafish Pax2/5/8 family: dependency of Pax5 and Pax8 expression on the Pax2.1 (noi) function.

Authors:  P L Pfeffer; T Gerster; K Lun; M Brand; M Busslinger
Journal:  Development       Date:  1998-08       Impact factor: 6.868

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  13 in total

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Authors:  Débora M Cerqueira; Uyen Tran; Daniel Romaker; José G Abreu; Oliver Wessely
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Authors:  Carolyn A Morrison; Hao Chen; Tiffany Cook; Stuart Brown; Jessica E Treisman
Journal:  PLoS Genet       Date:  2018-01-11       Impact factor: 5.917

Review 5.  Developmental Origins of Chronic Kidney Disease: Should We Focus on Early Life?

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6.  Expression profiles of human epididymis epithelial cells reveal the functional diversity of caput, corpus and cauda regions.

Authors:  James A Browne; Rui Yang; Shih-Hsing Leir; Scott E Eggener; Ann Harris
Journal:  Mol Hum Reprod       Date:  2015-11-26       Impact factor: 4.025

7.  Renal Transcriptome Analysis of Programmed Hypertension Induced by Maternal Nutritional Insults.

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Journal:  Int J Mol Sci       Date:  2015-08-03       Impact factor: 5.923

8.  An Evaluation of Active Learning Causal Discovery Methods for Reverse-Engineering Local Causal Pathways of Gene Regulation.

Authors:  Sisi Ma; Patrick Kemmeren; Constantin F Aliferis; Alexander Statnikov
Journal:  Sci Rep       Date:  2016-03-04       Impact factor: 4.379

9.  Heterozygous p.S811F RET gene mutation associated with renal agenesis, oligomeganephronia and total colonic aganglionosis: a case report.

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10.  Glial-derived neurotrophic factor in human airway smooth muscle.

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