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Rev-ErbA beta: Wikis

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Nuclear receptor subfamily 1, group D, member 2

Structure of the ligand binding domain (LBD) of the Rev-erbβ receptor based on PDB 2v0v. Depicted here is a dimer of comprising two LBD protein molecules.
Available structures
2v0v, 2v7c, 3cqv
Identifiers
Symbols NR1D2; HZF2; BD73; EAR-1r; Hs.37288; RVR
External IDs OMIM602304 MGI2449205 HomoloGene3763 GeneCards: NR1D2 Gene
RNA expression pattern
PBB GE NR1D2 209750 at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez 9975 353187
Ensembl ENSG00000174738 ENSMUSG00000021775
UniProt Q14995 Q4VAB7
RefSeq (mRNA) XM_001130839 NM_011584
RefSeq (protein) XP_001130839 NP_035714
Location (UCSC) Chr 3:
23.96 - 24 Mb
Chr 14:
17 - 17.03 Mb
PubMed search [1] [2]

Rev-ErbA beta (Rev-erbβ) also known as NR1D2 (nuclear receptor subfamily 1, group D, member 2) is a member of the Rev-ErbA family of transcription factors. Rev-erbβ, like Rev-erbα, belongs to the nuclear receptor superfamily and can modulate gene expression by directly binding to their promoters.[1][2]

Contents

Structure

Cartoon diagram of the ligand binding domain of Rev-ErbA beta (rainbow colored, N-terminus = blue, C-terminus = red) complexed with heme (space-filling model, carbon atoms = white, nitrogen = blue, oxygen = red, iron = magenta) based on the PDB 3CQV crystallographic coordinates.

Rev-erbβ is similar to Rev-erbα in its protein structure and function as a transcriptional repressor. The crystal structure of an unliganded Rev-erbβ ligand-binding domain (LBD) has been resolved (see figure to the right) and shows an extremely small ligand-binding pocket.[3] However, Rev-erbβ has been shown to interact with heme, which appears important for its function.[4]

The structure of Rev-erbβ complexed with heme (see figure to the left) shows a substantial movement of helices 1 (N-terminus ) and 11 (C-terminus ) which opens up a large binding pocket in the interior of the protein that is able to accommodate this ligand.[5]

Function

Rev-erbβ has been implicated in the control of lipid and energy homoeostasis in skeletal muscle.[6]

Rev-erbβ is also a circadian regulated gene; its mRNA displays rhythmic expression in vivo and in serum-synchronized cell cultures. However, it is currently unknown to what extent Rev-erbβ contributes to oscillations of the core circadian clock. However it has been shown heme suppresses hepatic gluconeogenic gene expression and glucose output through the related Rev-erbα receptor which mediates gene repression. Hence, the Rev-erbα receptor detects heme and thereby coordinates the cellular clock, glucose homeostasis, and energy metabolism.[7]

References

  1. ^ Bonnelye E, Vanacker JM, Desbiens X, Begue A, Stehelin D, Laudet V (1994). "Rev-erbβ, a new member of the nuclear receptor superfamily, is expressed in the nervous system during chicken development". Cell Growth Differ. 5 (12): 1357–65. PMID 7696184. http://cgd.aacrjournals.org/cgi/content/abstract/5/12/1357.  
  2. ^ Giambiagi N, Cassia R, Petropoulos I, Part D, Cereghini S, Zakin MM, Ochoa A (1995). "Rev-erb β 2, a novel isoform of the Rev-erb family of orphan nuclear receptors". Biochem. Mol. Biol. Int. 37 (6): 1091–1102. PMID 8747539.  
  3. ^ Woo EJ, Jeong DG, Lim MY, Jun Kim S, Kim KJ, Yoon SM, Park BC, Eon Ryu S (2007). "Structural Insight into the Constitutive Repression Function of the Nuclear Receptor Rev-erbβ". J. Mol. Biol. 373 (3): 735–44. doi:10.1016/j.jmb.2007.08.037. PMID 17870090.  
  4. ^ Raghuram S, Stayrook KR, Huang P, Rogers PM, Nosie AK, McClure DB, Burris LL, Khorasanizadeh S, Burris TP, Rastinejad F (December 2007). "Identification of heme as the ligand for the orphan nuclear receptors REV-Erbα and REV-Erbβ". Nat. Struct. Mol. Biol. 14 (12): 1207–13. doi:10.1038/nsmb1344. PMID 18037887.  
  5. ^ PDB 3CQV; "Human nuclear receptor subfamily 1, group D, member 2 in complex with heme". The Structural Genomics Consortium (SGC). http://www.thesgc.com/SGC-WebPages/StructureDescription/3CQV.php. Retrieved 2008-08-09.  ; Pardee K, Xu X, Dong A, Reinking J, Krause H, Schuetz A, Zhang R, Cui H, Arrowsmith CH, Weigelt J, Bountra C, Savchenko A, Bochkarev A, Edwards AM (2008). "Crystal structure of Reverb beta in complex with heme". To be Published.  
  6. ^ Ramakrishnan SN, Lau P, Burke LJ, Muscat GE (2005). "Rev-erbβ regulates the expression of genes involved in lipid absorption in skeletal muscle cells: evidence for cross-talk between orphan nuclear receptors and myokines". J. Biol. Chem. 280 (10): 8651–9. doi:10.1074/jbc.M413949200. PMID 15623503.  
  7. ^ Yin L, Wu N, Curtin JC, Qatanani M, Szwergold NR, Reid RA, Waitt GM, Parks DJ, Pearce KH, Wisely GB, Lazar MA (December 2007). "Rev-erbα, a heme sensor that coordinates metabolic and circadian pathways". Science (journal) 318 (5857): 1786–9. doi:10.1126/science.1150179. PMID 18006707.  

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