Literature DB >> 20506374

A functional NR4A nuclear receptor DNA-binding domain is required for organ development in Caenorhabditis elegans.

Melissa Heard, Claude V Maina, Benjamin E Morehead, Marius C Hoener, Tri Q Nguyen, Christopher C Williams, Brian G Rowan, Chris R Gissendanner.   

Abstract

NR4A nuclear receptors are a diverse group of orphan nuclear receptors with critical roles in regulating cell proliferation and cell differentiation. The ortholog of the NR4A nuclear receptor in Caenorhabditis elegans, NHR-6, also has a role in cell proliferation and cell differentiation during organogenesis of the spermatheca. Here we show that NHR-6 is able to bind the canonical NR4A monomer response element and can transactivate from this site in mammalian HEK293 cells. Using a functional GFP-tagged NHR-6 fusion, we also demonstrate that NHR-6 is nuclear localized during development of the spermatheca. Mutation of the DNA-binding domain of NHR-6 abolishes its activity in genetic rescue assays, demonstrating a requirement for the DNA-binding domain. This study represents the first genetic demonstration of an in vivo requirement for an NR4A nuclear receptor DNA-binding domain in a whole organism. (c) 2010 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20506374      PMCID: PMC2927863          DOI: 10.1002/dvg.20646

Source DB:  PubMed          Journal:  Genesis        ISSN: 1526-954X            Impact factor:   2.487


  22 in total

1.  Identification of Dlk1, Ptpru and Klhl1 as novel Nurr1 target genes in meso-diencephalic dopamine neurons.

Authors:  Frank M J Jacobs; Annemarie J A van der Linden; Yuhui Wang; Lars von Oerthel; Hei Sook Sul; J Peter H Burbach; Marten P Smidt
Journal:  Development       Date:  2009-06-10       Impact factor: 6.868

2.  DNA binding of the glucocorticoid receptor is not essential for survival.

Authors:  H M Reichardt; K H Kaestner; J Tuckermann; O Kretz; O Wessely; R Bock; P Gass; W Schmid; P Herrlich; P Angel; G Schütz
Journal:  Cell       Date:  1998-05-15       Impact factor: 41.582

3.  Induction of cell cycle arrest and morphological differentiation by Nurr1 and retinoids in dopamine MN9D cells.

Authors:  D S Castro; E Hermanson; B Joseph; A Wallén; P Aarnisalo; A Heller; T Perlmann
Journal:  J Biol Chem       Date:  2001-09-11       Impact factor: 5.157

4.  The AF-1 domain of the orphan nuclear receptor NOR-1 mediates trans-activation, coactivator recruitment, and activation by the purine anti-metabolite 6-mercaptopurine.

Authors:  K D Senali Abayratna Wansa; Jonathan M Harris; Grace Yan; Peter Ordentlich; George E O Muscat
Journal:  J Biol Chem       Date:  2003-04-22       Impact factor: 5.157

5.  The Caenorhabditis elegans NR4A nuclear receptor is required for spermatheca morphogenesis.

Authors:  Chris R Gissendanner; Kristopher Kelley; Tri Q Nguyen; Marius C Hoener; Ann E Sluder; Claude V Maina
Journal:  Dev Biol       Date:  2007-11-22       Impact factor: 3.582

6.  Abrogation of nuclear receptors Nr4a3 and Nr4a1 leads to development of acute myeloid leukemia.

Authors:  Shannon E Mullican; Shuo Zhang; Marina Konopleva; Vivian Ruvolo; Michael Andreeff; Jeffrey Milbrandt; Orla M Conneely
Journal:  Nat Med       Date:  2007-05-21       Impact factor: 53.440

7.  The genetics of Caenorhabditis elegans.

Authors:  S Brenner
Journal:  Genetics       Date:  1974-05       Impact factor: 4.562

8.  Mitogenic effect of orphan receptor TR3 and its regulation by MEKK1 in lung cancer cells.

Authors:  Siva Kumar Kolluri; Nathalie Bruey-Sedano; Xihua Cao; Bingzhen Lin; Feng Lin; Young-Hoon Han; Marcia I Dawson; Xiao-kun Zhang
Journal:  Mol Cell Biol       Date:  2003-12       Impact factor: 4.272

9.  The Drosophila orphan nuclear receptor DHR38 mediates an atypical ecdysteroid signaling pathway.

Authors:  Keith D Baker; Lisa M Shewchuk; Tatiana Kozlova; Makoto Makishima; Annie Hassell; Bruce Wisely; Justin A Caravella; Millard H Lambert; Jeffrey L Reinking; Henry Krause; Carl S Thummel; Timothy M Willson; David J Mangelsdorf
Journal:  Cell       Date:  2003-06-13       Impact factor: 41.582

10.  The NR4A subgroup: immediate early response genes with pleiotropic physiological roles.

Authors:  Megan A Maxwell; George E O Muscat
Journal:  Nucl Recept Signal       Date:  2006-02-08
View more
  7 in total

Review 1.  Transcriptional regulation of gene expression in C. elegans.

Authors:  Valerie Reinke; Michael Krause; Peter Okkema
Journal:  WormBook       Date:  2013-06-04

2.  C. elegans nuclear receptor NHR-6 functionally interacts with the jun-1 transcription factor during spermatheca development.

Authors:  Chris R Gissendanner; Derrick Cardin; Chris J Dubose; Moustafa El Sayed; Jeremy S Harmson; Brandon Praslicka; Brian G Rowan
Journal:  Genesis       Date:  2013-11-18       Impact factor: 2.487

3.  The C. elegans NR4A nuclear receptor gene nhr-6 promotes cell cycle progression in the spermatheca lineage.

Authors:  Brandon Praslicka; Chris R Gissendanner
Journal:  Dev Dyn       Date:  2015-01-24       Impact factor: 3.780

4.  BINDING SITE ANALYSIS OF THE CAENORHABDITIS ELEGANS NR4A NUCLEAR RECEPTOR NHR-6 DURING DEVELOPMENT.

Authors:  Brandon Praslicka; Jeremy S Harmson; Joohyun Kim; Vittobai Rashika Rangaraj; Aikseng Ooi; Chris R Gissendanner
Journal:  Nucl Receptor Res       Date:  2017-07-23

5.  Development of specialized sensory neurons engages a nuclear receptor required for functional plasticity.

Authors:  Mary Rossillo; Niels Ringstad
Journal:  Genes Dev       Date:  2020-11-12       Impact factor: 11.361

6.  The C. elegans gene pan-1 encodes novel transmembrane and cytoplasmic leucine-rich repeat proteins and promotes molting and the larva to adult transition.

Authors:  Chris R Gissendanner; Tram Do Kelley
Journal:  BMC Dev Biol       Date:  2013-05-17       Impact factor: 1.978

7.  HLH-29 regulates ovulation in C. elegans by targeting genes in the inositol triphosphate signaling pathway.

Authors:  Ana White; Abegail Fearon; Casonya M Johnson
Journal:  Biol Open       Date:  2012-02-08       Impact factor: 2.422

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.