Biology:GLI3

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Short description: Protein-coding gene in the species Homo sapiens


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

Zinc finger protein GLI3 is a protein that in humans is encoded by the GLI3 gene.[1][2]

This gene encodes a protein that belongs to the C2H2-type zinc finger proteins subclass of the Gli family. They are characterized as DNA-binding transcription factors and are mediators of Sonic hedgehog (Shh) signaling. The protein encoded by this gene localizes in the cytoplasm and activates patched Drosophila homolog (PTCH1) gene expression. It is also thought to play a role during embryogenesis.[2]

Role in development

Gli3 is a known transcriptional repressor but may also have a positive transcriptional function.[3][4] Gli3 represses dHand and Gremlin, which are involved in developing digits.[5] There is evidence that Shh-controlled processing (e.g., cleavage) regulates transcriptional activity of Gli3 similarly to that of Ci.[4] Gli3 mutant mice have many abnormalities including CNS and lung defects and limb polydactyly.[6][7][8][9][10] In the developing mouse limb bud, Gli3 derepression predominantly regulates Shh target genes.[11]

Disease association

Mutations in this gene have been associated with several diseases, including Greig cephalopolysyndactyly syndrome, Pallister–Hall syndrome, preaxial polydactyly type IV, and postaxial polydactyly types A1 and B.[2] DNA copy-number alterations that contribute to increased conversion of the oncogenes Gli1–3 into transcriptional activators by the Hedgehog signaling pathway are included in a genome-wide pattern, which was found to be correlated with an astrocytoma patient's outcome.[12][13]

There is evidence that the autosomal dominant disorder Greig cephalopolysyndactyly syndrome (GCPS) that affects limb and craniofacial development in humans is caused by a translocations within the GLI3 gene.[14]

Interactions with Gli1 and Gli2

The independent overexpression Gli1 and Gli2 in mice models to lead to formation of basal cell carcinoma (BCC). Gli1 knockout is shown to lead to similar embryonic malformations as Gli1 overexpressions but not the formation of BCCs. Overexpression of Gli3 in transgenic mice and frogs does not lead to the development of BCC-like tumors and is not thought to play a role in tumor BCC formation.[15]

Gli1 and Gli2 overexpression leads to BCC formation in mouse models and a one step model for tumour formation has been suggested in both cases. This also indicates that Gli1 and/or Gli2 overexpression is vital in BCC formation. Co-overexpression of Gli1 with Gli2 and Gli2 with Gli3 leads to transgenic mice malformations and death, respectively, but not the formation of BCC. This suggests that overexpression of more than one Gli protein is not necessary for BCC formation.

Interactions

GLI3 has been shown to interact with CREBBP[16] SUFU,[17] ZIC1,[18] and ZIC2.[18]

References

  1. ↑ "GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity". Molecular and Cellular Biology 10 (10): 5408–15. October 1990. doi:10.1128/mcb.10.10.5408. PMID 2118997. 
  2. ↑ 2.0 2.1 2.2 "Entrez Gene: GLI3 GLI-Kruppel family member GLI3 (Greig cephalopolysyndactyly syndrome)". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2737. 
  3. ↑ "The Hedgehog and Wnt signalling pathways in cancer". Nature 411 (6835): 349–54. May 2001. doi:10.1038/35077219. PMID 11357142. Bibcode: 2001Natur.411..349T. 
  4. ↑ 4.0 4.1 "Gli proteins and the control of spinal-cord patterning". EMBO Reports 4 (8): 761–5. August 2003. doi:10.1038/sj.embor.embor896. PMID 12897799. 
  5. ↑ "Mutual genetic antagonism involving GLI3 and dHAND prepatterns the vertebrate limb bud mesenchyme prior to SHH signaling". Genes & Development 16 (4): 421–6. February 2002. doi:10.1101/gad.219202. PMID 11850405. 
  6. ↑ "Patterning the dorsal telencephalon: a role for sonic hedgehog?". The Journal of Neuroscience 27 (43): 11595–603. October 2007. doi:10.1523/jneurosci.3204-07.2007. PMID 17959802. 
  7. ↑ "Extra-toes (Xt) homozygous mutant mice demonstrate a role for the Gli-3 gene in the development of the forebrain". Acta Anatomica 150 (1): 38–44. 1994. doi:10.1159/000147600. PMID 7976186. 
  8. ↑ "The hem of the embryonic cerebral cortex is defined by the expression of multiple Wnt genes and is compromised in Gli3-deficient mice". Development 125 (12): 2315–25. June 1998. doi:10.1242/dev.125.12.2315. PMID 9584130. 
  9. ↑ "A mouse model of greig cephalopolysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 gene". Nature Genetics 3 (3): 241–6. March 1993. doi:10.1038/ng0393-241. PMID 8387379. 
  10. ↑ "Expression of the zinc finger gene Gli3 is affected in the morphogenetic mouse mutant extra-toes (Xt)". Development 116 (3): 799–804. November 1992. doi:10.1242/dev.116.3.799. PMID 1289066. 
  11. ↑ "Spatiotemporal regulation of GLI target genes in the mammalian limb bud". Dev. Biol. 406 (1): 92–103. Oct 2015. doi:10.1016/j.ydbio.2015.07.022. PMID 26238476. 
  12. ↑ "Mathematically universal and biologically consistent astrocytoma genotype encodes for transformation and predicts survival phenotype". APL Bioengineering 2 (3): 031909. September 2018. doi:10.1063/1.5037882. PMID 30397684. 
  13. ↑ "Platform-Independent Genome-Wide Pattern of DNA Copy-Number Alterations Predicting Astrocytoma Survival and Response to Treatment Revealed by the GSVD Formulated as a Comparative Spectral Decomposition". PLOS ONE 11 (10): e0164546. October 2016. doi:10.1371/journal.pone.0164546. PMID 27798635. Bibcode: 2016PLoSO..1164546A. 
  14. ↑ "Pallister-Hall syndrome phenotype in mice mutant for Gli3". Human Molecular Genetics 11 (9): 1129–35. May 2002. doi:10.1093/hmg/11.9.1129. PMID 11978771. 
  15. ↑ "Activation of the transcription factor Gli1 and the Sonic hedgehog signalling pathway in skin tumours". Nature 389 (6653): 876–81. October 1997. doi:10.1038/39918. PMID 9349822. Bibcode: 1997Natur.389..876D. 
  16. ↑ "Sonic Hedgehog-induced activation of the Gli1 promoter is mediated by GLI3". The Journal of Biological Chemistry 274 (12): 8143–52. March 1999. doi:10.1074/jbc.274.12.8143. PMID 10075717. 
  17. ↑ "The output of Hedgehog signaling is controlled by the dynamic association between Suppressor of Fused and the Gli proteins". Genes & Development 24 (7): 670–82. April 2010. doi:10.1101/gad.1902910. PMID 20360384. 
  18. ↑ 18.0 18.1 "Physical and functional interactions between Zic and Gli proteins". The Journal of Biological Chemistry 276 (10): 6889–92. March 2001. doi:10.1074/jbc.C000773200. PMID 11238441. 

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.



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