Biology:ZIC3

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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

ZIC3 is a member of the Zinc finger of the cerebellum (ZIC) protein family.[1][2]

ZIC3 is classified as a ZIC protein due to conservation of the five C2H2 zinc fingers, which enables the protein to interact with DNA and proteins. Correct function of this protein family in critical for early development, and as such mutations of the genes encoding these proteins is known to result in various congenital defects. For example, mutation of ZIC3 is associated with heterotaxy,[3][4] that is thought to occur due to the role of ZIC3 in initial left-right symmetry formation, which involves the maintaining redistributed Nodal after the asymmetry of the embryo is initially broken.[5] Mutation of ZIC3 is also associated with various heart defects, such as heart looping, however these are thought to represent a mild form of heterotaxy. Mouse based studies have linked defective ZIC3 with neural tube defects (spina bifida and exencephaly) and skeletal defects [6] as well indicated a role for Zic3 in neural crest specification. [7] Both the left-right defects and the neural tube defects caused by loss of Zic3 have been linked to defective planar cell polarity. [8]

ZIC3 is also of particular interest as it has been shown to be required for maintenance of embryonic stem cell pluripotency.[9]

Involvement in Wnt signalling

ZIC2, another member of the ZIC family, has recently been found to interact with TCF7L2, enabling it to act as a Wnt/β-catenin signalling inhibitor.[10] Further experiments have indicated that human ZIC3 is also able to inhibit Wnt signalling and that the Zinc finger domains are absolutely critical for this role.[11] Such a role is of critical importance, as not only is correct Wnt signalling critical for early development,[12] Wnt signalling has also been found to be upregulated to several cancers. In addition Zic3 inhibition of canonical Wnt has recently been shown to have a role in specification of the neural crest in mice.[13]

References

  1. "Zinc fingers of the cerebellum (Zic): transcription factors and co-factors". The International Journal of Biochemistry & Cell Biology 44 (11): 2065–2068. November 2012. doi:10.1016/j.biocel.2012.08.012. PMID 22964024. 
  2. "Entrez Gene: ZIC3 Zic family member 3 heterotaxy 1 (odd-paired homolog, Drosophila)". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7547. 
  3. "Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects". American Journal of Human Genetics 74 (1): 93–105. January 2004. doi:10.1086/380998. PMID 14681828. 
  4. "ZIC3 in Heterotaxy". Advances in Experimental Medicine and Biology 1046: 301–327. 2018. doi:10.1007/978-981-10-7311-3_15. ISBN 978-981-10-7310-6. PMID 29442328. 
  5. "Heart defects in X-linked heterotaxy: evidence for a genetic interaction of Zic3 with the nodal signaling pathway". Developmental Dynamics 235 (6): 1631–1637. June 2006. doi:10.1002/dvdy.20719. PMID 16496285. 
  6. "A complex syndrome of left-right axis, central nervous system and axial skeleton defects in Zic3 mutant mice". Development 129 (9): 2293–2302. May 2002. doi:10.1242/dev.129.9.2293. PMID 11959836. 
  7. "SUMOylation Potentiates ZIC Protein Activity to Influence Murine Neural Crest Cell Specification". International Journal of Molecular Sciences 22 (19): 10437. September 2021. doi:10.3390/ijms221910437. PMID 34638777. 
  8. "Loss of Zic3 impairs planar cell polarity leading to abnormal left-right signaling, heart defects and neural tube defects". Human Molecular Genetics 30 (24): 2402–2415. November 2021. doi:10.1093/hmg/ddab195. PMID 34274973. 
  9. "The pluripotency regulator Zic3 is a direct activator of the Nanog promoter in ESCs". Stem Cells 28 (11): 1961–1969. November 2010. doi:10.1002/stem.527. PMID 20872845. 
  10. "Transcription factor Zic2 inhibits Wnt/β-catenin protein signaling". The Journal of Biological Chemistry 286 (43): 37732–37740. October 2011. doi:10.1074/jbc.M111.242826. PMID 21908606. 
  11. "A murine Zic3 transcript with a premature termination codon evades nonsense-mediated decay during axis formation". Disease Models & Mechanisms 6 (3): 755–767. May 2013. doi:10.1242/dmm.011668. PMID 23471918. 
  12. "Stringent requirement of a proper level of canonical WNT signalling activity for head formation in mouse embryo". Development 138 (4): 667–676. February 2011. doi:10.1242/dev.052803. PMID 21228006. 
  13. "SUMOylation Potentiates ZIC Protein Activity to Influence Murine Neural Crest Cell Specification". International Journal of Molecular Sciences 22 (19): 10437. September 2021. doi:10.3390/ijms221910437. PMID 34638777. 

Further reading