WDR62

WDR62
Identifiers
Aliases	WDR62, C19orf14, MCPH2, WD repeat domain 62
External IDs	OMIM: 613583; MGI: 1923696; HomoloGene: 15927; GeneCards: WDR62; OMA:WDR62 - orthologs
Gene location (Human)
Chr.	Chromosome 19 (human)
End	36,105,108 bp
Gene location (Mouse)
Chr.	Chromosome 7 (mouse)
End	29,979,844 bp
RNA expression pattern
	Top expressed in
	left testis; ; right testis; ; apex of heart; ; thoracic diaphragm; ; triceps brachii muscle; ; vastus lateralis muscle; ; muscle of thigh; ; Skeletal muscle tissue of rectus abdominis; ; biceps brachii; ; glutes;
	Top expressed in
	seminiferous tubule; ; spermatocyte; ; spermatid; ; secondary oocyte; ; esophagus; ; genital tubercle; ; muscle of thigh; ; tail of embryo; ; zygote; ; morula;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	protein binding; RNA binding;
Cellular component	nucleus; centriole; cytoplasm; centrosome; spindle pole; cytoskeleton; U5 snRNP; precatalytic spliceosome; catalytic step 2 spliceosome; microtubule organizing center; cytosol;
Biological process	mitotic spindle organization; nervous system development; centriole replication; cerebral cortex development; neurogenesis; RNA splicing;
	Sources:Amigo / QuickGO
Orthologs
	284403
	233064
	ENSG00000075702
	ENSMUSG00000037020
	O43379
	Q3U3T8
	NM_001083961; NM_173636
	NM_146186
	NP_001077430; NP_775907
	n/a
	Wikidata
View/Edit Human	View/Edit Mouse

WD repeat-containing protein 62 is a protein that in humans is encoded by the WDR62 gene.^[5]^[6]

Function

WDR62 is a scaffold protein and interacts with different kinases. WDR62 plays a role in mediating activation of the JNK pathway in response to TNFα. This finding might have implications in the research of TNFα related diseases such as autoimmune diseases and cancer.^[7] It has been also shown that WDR62 upregulation can lead to overproliferation of glia cells and potentially glioma and this is coupled with an upregulation in AURKA, AKT, MYC and PI3K signalling.^[8]

WDR62 effect on neurogenesis is regulated by MEKK3 in coordination with FBW7 (F-box and WD repeat domain-containing protein 7).^[9]

WDR62 has been shown to have a regulatory role on hippocampus development and neurogenesis.^[10]

WDR62 is also involved in male spermatogenesis with an essential role in centriole duplication and manchette removal during the spermatogenesis process. The deficiency of WDR62 results in low sperm counts with defected motility, and abnormal morphology.^[11]

Clinical significance

Mutations in the WDR62 gene cause of a wide spectrum of severe cerebral cortical malformations including microcephaly,^[12] pachygyria with cortical thickening, hypoplasia of the corpus callosum,^[5] polymicrogyria as well as microlissencephaly.^[13]

Cortical malformation, associated with WDR62 point mutations occurring in humans (V65M and R438H) has been linked to ciliopathies. These WDR62 point mutations drive ciliary disruption in Radial glial cell via disrupting the cilia and centrosome localization of CENPJ and the Intraflagellar transport protein 88 (IFT88), which are required for tubulin requitment to centrosome and transport of tubulin to the cilia tip, respectively.^[14]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000075702 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000037020 – 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.
^ ^a ^b Bilgüvar K, Oztürk AK, Louvi A, Kwan KY, Choi M, Tatli B, et al. (September 2010). "Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations". Nature. 467 (7312): 207–210. Bibcode:2010Natur.467..207B. doi:10.1038/nature09327. PMC 3129007. PMID 20729831.
^ "Entrez Gene: WDR62 WD repeat domain 62".
^ Prinz E, Aviram S, Aronheim A (October 2018). "WDR62 mediates TNFα-dependent JNK activation via TRAF2-MLK3 axis". Molecular Biology of the Cell. 29 (20): 2470–2480. doi:10.1091/mbc.E17-08-0504. PMC 6233063. PMID 30091641.
^ Shohayeb B, Mitchell N, Millard SS, Quinn LM, Ng DC (July 2020). "Elevated levels of Drosophila Wdr62 promote glial cell growth and proliferation through AURKA signalling to AKT and MYC". Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1867 (7): 118713. doi:10.1016/j.bbamcr.2020.118713. PMID 32246948.
^ Xu D, Yao M, Wang Y, Yuan L, Hoeck JD, Yu J, et al. (December 2018). "MEKK3 coordinates with FBW7 to regulate WDR62 stability and neurogenesis". PLOS Biology. 16 (12): e2006613. doi:10.1371/journal.pbio.2006613. PMC 6347294. PMID 30566428.
^ Weiger WA, Bear DM (September 2020). "An approach to the neurology of aggression". Journal of Psychiatric Research. 22 (2): 85–98. doi:10.1016/0022-3956(88)90073-8. PMID 3042990.
^ Ho UY, Feng CA, Yeap YY, Bain AL, Wei Z, Shohayeb B, et al. (May 2021). "WDR62 is required for centriole duplication in spermatogenesis and manchette removal in spermiogenesis". Communications Biology. 4 (1): 645. doi:10.1038/s42003-021-02171-5. PMC 8167107. PMID 34059773.
^ Bhat V, Girimaji SC, Mohan G, Arvinda HR, Singhmar P, Duvvari MR, Kumar A (December 2011). "Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations". Clinical Genetics. 80 (6): 532–540. doi:10.1111/j.1399-0004.2011.01686.x. PMID 21496009. S2CID 45190332.
^ Murdock DR, Clark GD, Bainbridge MN, Newsham I, Wu YQ, Muzny DM, et al. (September 2011). "Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria". American Journal of Medical Genetics. Part A. 155A (9): 2071–2077. doi:10.1002/ajmg.a.34165. PMC 3616765. PMID 21834044.
^ Shohayeb B, Ho U, Yeap YY, Parton RG, Millard SS, Xu Z, et al. (January 2020). "The association of microcephaly protein WDR62 with CPAP/IFT88 is required for cilia formation and neocortical development". Human Molecular Genetics. 29 (2): 248–263. doi:10.1093/hmg/ddz281. PMID 31816041.

Bonaldo MF, Lennon G, Soares MB (September 1996). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Research. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
Beausoleil SA, Jedrychowski M, Schwartz D, Elias JE, Villén J, Li J, et al. (August 2004). "Large-scale characterization of HeLa cell nuclear phosphoproteins". Proceedings of the National Academy of Sciences of the United States of America. 101 (33): 12130–12135. Bibcode:2004PNAS..10112130B. doi:10.1073/pnas.0404720101. PMC 514446. PMID 15302935.
Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, et al. (October 2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–1178. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID 16189514. S2CID 4427026.
Nousiainen M, Silljé HH, Sauer G, Nigg EA, Körner R (April 2006). "Phosphoproteome analysis of the human mitotic spindle". Proceedings of the National Academy of Sciences of the United States of America. 103 (14): 5391–5396. Bibcode:2006PNAS..103.5391N. doi:10.1073/pnas.0507066103. PMC 1459365. PMID 16565220.
Olsen JV, Blagoev B, Gnad F, Macek B, Kumar C, Mortensen P, Mann M (November 2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks". Cell. 127 (3): 635–648. doi:10.1016/j.cell.2006.09.026. PMID 17081983. S2CID 7827573.

This article on a gene on human chromosome 19 is a stub. You can help Wikipedia by expanding it.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000075702 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000037020 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid20729831-5] Bilgüvar K, Oztürk AK, Louvi A, Kwan KY, Choi M, Tatli B, et al. (September 2010). "Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations". Nature. 467 (7312): 207–210. Bibcode:2010Natur.467..207B. doi:10.1038/nature09327. PMC 3129007. PMID 20729831.

[entrez-6] "Entrez Gene: WDR62 WD repeat domain 62".

[7] Prinz E, Aviram S, Aronheim A (October 2018). "WDR62 mediates TNFα-dependent JNK activation via TRAF2-MLK3 axis". Molecular Biology of the Cell. 29 (20): 2470–2480. doi:10.1091/mbc.E17-08-0504. PMC 6233063. PMID 30091641.

[8] Shohayeb B, Mitchell N, Millard SS, Quinn LM, Ng DC (July 2020). "Elevated levels of Drosophila Wdr62 promote glial cell growth and proliferation through AURKA signalling to AKT and MYC". Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1867 (7): 118713. doi:10.1016/j.bbamcr.2020.118713. PMID 32246948.

[9] Xu D, Yao M, Wang Y, Yuan L, Hoeck JD, Yu J, et al. (December 2018). "MEKK3 coordinates with FBW7 to regulate WDR62 stability and neurogenesis". PLOS Biology. 16 (12): e2006613. doi:10.1371/journal.pbio.2006613. PMC 6347294. PMID 30566428.

[10] Weiger WA, Bear DM (September 2020). "An approach to the neurology of aggression". Journal of Psychiatric Research. 22 (2): 85–98. doi:10.1016/0022-3956(88)90073-8. PMID 3042990.

[11] Ho UY, Feng CA, Yeap YY, Bain AL, Wei Z, Shohayeb B, et al. (May 2021). "WDR62 is required for centriole duplication in spermatogenesis and manchette removal in spermiogenesis". Communications Biology. 4 (1): 645. doi:10.1038/s42003-021-02171-5. PMC 8167107. PMID 34059773.

[pmid21496009-12] Bhat V, Girimaji SC, Mohan G, Arvinda HR, Singhmar P, Duvvari MR, Kumar A (December 2011). "Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations". Clinical Genetics. 80 (6): 532–540. doi:10.1111/j.1399-0004.2011.01686.x. PMID 21496009. S2CID 45190332.

[pmid21834044-13] Murdock DR, Clark GD, Bainbridge MN, Newsham I, Wu YQ, Muzny DM, et al. (September 2011). "Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria". American Journal of Medical Genetics. Part A. 155A (9): 2071–2077. doi:10.1002/ajmg.a.34165. PMC 3616765. PMID 21834044.

[14] Shohayeb B, Ho U, Yeap YY, Parton RG, Millard SS, Xu Z, et al. (January 2020). "The association of microcephaly protein WDR62 with CPAP/IFT88 is required for cilia formation and neocortical development". Human Molecular Genetics. 29 (2): 248–263. doi:10.1093/hmg/ddz281. PMID 31816041.

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Function

Clinical significance

References

Further reading