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Aryl hydrocarbon receptor nuclear translocator-like 2
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| Identifiers | ||||||||||||||
| Symbols | ARNTL2; BMAL2; CLIF; MGC149671; MGC149672; MOP9; PASD9 | |||||||||||||
| External IDs | MGI: 2684845 HomoloGene: 10609 | |||||||||||||
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| RNA expression pattern | ||||||||||||||
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| Orthologs | ||||||||||||||
| Human | Mouse | |||||||||||||
| Entrez | 56938 | 272322 | ||||||||||||
| Ensembl | ENSG00000029153 | ENSMUSG00000040187 | ||||||||||||
| Uniprot | Q8WYA1 | Q1A3C9 | ||||||||||||
| Refseq | NM_020183 (mRNA) NP_064568 (protein) |
NM_172309 (mRNA) NP_758513 (protein) |
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| Location | Chr 12: 27.38 - 27.46 Mb | Chr 6: 146.76 - 146.79 Mb | ||||||||||||
| Pubmed search | [1] | [2] | ||||||||||||
Aryl hydrocarbon receptor nuclear translocator-like 2, also known as Mop9,1 Bmal2,2 CLIF,3, or ARNTL2, is a gene.
Arntl2 is a mammalian paralog (with ARNTL) of the Drosophila Cycle gene4. Homologs were isolated in fish5, birds6 and mammals such as mice7 and humans8. Based on phylogenetic analyses, it was proposed that Arntl2 arose from duplication of the Arntl gene early in the vertebrate lineage, followed by rapid divergence of the Arntl gene copy9. The protein product of the gene interacts with both Clock and NPAS2 to bind to E-box sequences in regulated promoters and activate their transcription.1 Although Arntl2 is not required for normal function of the mammalian circadian oscillator, it may play an important role in mediating the output of the circadian clock. Perhaps because of this, there is relatively little published literature on the role of Arntl2 in regulation of physiology.
Arntl2 is a candidate gene for human type 1 diabetes.10
In over expression studies, Arntl2 forms a heterodimer with Clock to regulate E-box sequences in the Pai-1 promoter.3 Recent work suggest that this interaction may be in concert with Arntl/Clock heterodimeric complexes.11
See also
References
- ^ a b Hogenesch JB, Gu YZ, Moran SM, et al (2000). "The basic helix-loop-helix-PAS protein MOP9 is a brain-specific heterodimeric partner of circadian and hypoxia factors". J. Neurosci. 20 (13): RC83. PMID 10864977.
- ^ Ikeda M, Yu W, Hirai M, et al (2000). "cDNA cloning of a novel bHLH-PAS transcription factor superfamily gene, BMAL2: its mRNA expression, subcellular distribution, and chromosomal localization". Biochem. Biophys. Res. Commun. 275 (2): 493–502. doi:. PMID 10964693.
- ^ a b Maemura K, de la Monte SM, Chin MT, et al (2000). "CLIF, a novel cycle-like factor, regulates the circadian oscillation of plasminogen activator inhibitor-1 gene expression". J. Biol. Chem. 275 (47): 36847–51. doi:. PMID 11018023.
- ^ Rutila JE, Suri V, Le M, So WV, Rosbash M, Hall JC (May 1998). "CYCLE is a second bHLH-PAS clock protein essential for circadian rhythmicity and transcription of Drosophila period and timeless". Cell 93 (5): 805–14. PMID 9630224, http://linkinghub.elsevier.com/retrieve/pii/S0092-8674(00)81441-5.
- ^ Cermakian N, Whitmore D, Foulkes NS, Sassone-Corsi P (April 2000). "Asynchronous oscillations of two zebrafish CLOCK partners reveal differential clock control and function". Proceedings of the National Academy of Sciences of the United States of America 97 (8): 4339–44. PMID 10760301. PMC: 18243, http://www.pnas.org/cgi/pmidlookup?view=long&pmid=10760301.
- ^ Okano T, Yamamoto K, Okano K, et al (September 2001). "Chicken pineal clock genes: implication of BMAL2 as a bidirectional regulator in circadian clock oscillation". Genes to cells : devoted to molecular & cellular mechanisms 6 (9): 825–36. PMID 11554928, http://www.blackwell-synergy.com/openurl?genre=article&sid=nlm:pubmed&issn=1356-9597&date=2001&volume=6&issue=9&spage=825.
- ^ Okano T, Sasaki M, Fukada Y (March 2001). "Cloning of mouse BMAL2 and its daily expression profile in the suprachiasmatic nucleus: a remarkable acceleration of Bmal2 sequence divergence after Bmal gene duplication". Neuroscience letters 300 (2): 111–4. PMID 11207387, http://linkinghub.elsevier.com/retrieve/pii/S0304394001015816.
- ^ Hogenesch JB, Gu YZ, Moran SM, et al (2000). "The basic helix-loop-helix-PAS protein MOP9 is a brain-specific heterodimeric partner of circadian and hypoxia factors". J. Neurosci. 20 (13): RC83. PMID 10864977.
- ^ Okano T, Sasaki M, Fukada Y (March 2001). "Cloning of mouse BMAL2 and its daily expression profile in the suprachiasmatic nucleus: a remarkable acceleration of Bmal2 sequence divergence after Bmal gene duplication". Neuroscience letters 300 (2): 111–4. PMID 11207387, http://linkinghub.elsevier.com/retrieve/pii/S0304394001015816.
- ^ Hung MS, Avner P, Rogner UC (2006). "Identification of the transcription factor ARNTL2 as a candidate gene for the type 1 diabetes locus Idd6". Hum. Mol. Genet. 15 (18): 2732–42. doi:. PMID 16893914.
- ^ Schoenhard JA, Smith LH, Painter CA, Eren M, Johnson CH, Vaughan DE (2003). "Regulation of the PAI-1 promoter by circadian clock components: differential activation by BMAL1 and BMAL2". J. Mol. Cell. Cardiol. 35 (5): 473–81. PMID 12738229.
External links
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