TLX
Nuclear receptor TLX (homologue of the Drosophila tailless gene) also known as NR2E1 (Nuclear receptor subfamily 2 group E member 1) is a
Function
TLX regulates the expression of another nuclear receptor, RAR.[6]
TLX also is essential for normal brain-eye coordination and appears to play a role in control of aggressive behavior.[7]
Adult neural stem cells are nuclear receptor TLX-positive and TLX expression in these cells is crucial in maintaining their undifferentiated state.[8] Furthermore, TLX regulates adult neural stem cell proliferation. Removal of TLX from the adult mouse brain resulted in a reduction of stem cell proliferation and spatial learning.[9]
Tlx-positive cells of the
Ligands
TLX belongs to a small family of NRs that lack two helices in the ligand-binding domain, forming an enlarged binding pocket. Three compounds, termed ccrp1–3 (famprofazone, 1-(1,5-dimethylpyrazole-3-carbonyl)-4-(diphenylmethyl)piperazine, dydrogesterone), have been discovered in high-throughput screening that enhance TLX's ability of transcription repression with high potency.[11]
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000112333 - Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000019803 - Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- PMID 9628820.
- PMID 11073974.
- PMID 16000615.
- S2CID 6495861.
- S2CID 14445703.
- PMID 18794344.
- PMID 24936658.
Further reading
- Yu RT, McKeown M, Evans RM, Umesono K (August 1994). "Relationship between Drosophila gap gene tailless and a vertebrate nuclear receptor Tlx". Nature. 370 (6488): 375–9. S2CID 4326071.
- Kobayashi M, Yu RT, Yasuda K, Umesono K (December 2000). "Cell-type-specific regulation of the retinoic acid receptor mediated by the orphan nuclear receptor TLX". Molecular and Cellular Biology. 20 (23): 8731–9. PMID 11073974.
- Abrahams BS, Mak GM, Berry ML, Palmquist DL, Saionz JR, Tay A, et al. (July 2002). "Novel vertebrate genes and putative regulatory elements identified at kidney disease and NR2E1/fierce loci". Genomics. 80 (1): 45–53. PMID 12079282.
- Abrahams BS, Kwok MC, Trinh E, Budaghzadeh S, Hossain SM, Simpson EM (July 2005). "Pathological aggression in "fierce" mice corrected by human nuclear receptor 2E1". The Journal of Neuroscience. 25 (27): 6263–70. PMID 16000615.
- Kumar RA, Leach S, Bonaguro R, Chen J, Yokom DW, Abrahams BS, et al. (August 2007). "Mutation and evolutionary analyses identify NR2E1-candidate-regulatory mutations in humans with severe cortical malformations". Genes, Brain and Behavior. 6 (6): 503–16. PMID 17054721.
- Kumar RA, Everman DB, Morgan CT, Slavotinek A, Schwartz CE, Simpson EM (July 2007). "Absence of mutations in NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes". BMC Medical Genetics. 8: 48. PMID 17655765.
- Sun G, Yu RT, Evans RM, Shi Y (September 2007). "Orphan nuclear receptor TLX recruits histone deacetylases to repress transcription and regulate neural stem cell proliferation". Proceedings of the National Academy of Sciences of the United States of America. 104 (39): 15282–7. PMID 17873065.
External links
- NR2E1+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
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