NDE1

NDE1
Identifiers
Aliases	NDE1, HOM-TES-87, LIS4, MHAC, NDE, NUDE, NUDE1, nudE neurodevelopment protein 1
External IDs	OMIM: 609449 MGI: 1914453 HomoloGene: 32354 GeneCards: NDE1
Gene location (Human)
Chr.	Chromosome 16 (human)[1]
End	15,726,353 bp[1]
Gene location (Mouse)
Chr.	Chromosome 16 (mouse)[2]
End	14,192,928 bp[2]
RNA expression pattern
	More reference expression data
Gene ontology
Molecular function	• protein domain specific binding; • GO:0001948 protein binding; • identical protein binding; • microtubule binding;
Cellular component	• cytoplasm; • condensed chromosome kinetochore; • cytosol; • centrosome; • membrane; • spindle; • spindle pole centrosome; • synapse; • chromosome; • microtubule organizing center; • cleavage furrow; • microtubule; • chromosome, centromeric region; • cytoskeleton; • kinetochore; • kinesin complex;
Biological process	• cell differentiation; • centrosome duplication; • establishment of chromosome localization; • neuron migration; • nervous system development; • cell division; • multicellular organism development; • G2/M transition of mitotic cell cycle; • establishment of mitotic spindle orientation; • cerebral cortex development; • neuroblast proliferation; • cell cycle; • forebrain development; • microtubule organizing center organization; • regulation of microtubule motor activity; • sister chromatid cohesion; • ciliary basal body docking; • microtubule nucleation; • chromosome segregation; • mitotic centrosome separation; • cell migration; • vesicle transport along microtubule; • centrosome localization; • regulation of G2/M transition of mitotic cell cycle;
	Sources:Amigo / QuickGO
Orthologs
	54820
	67203
	ENSG00000072864; ENSG00000275911
	ENSMUSG00000022678
	Q9NXR1
	Q9CZA6
	NM_001143979; NM_017668
	NM_001114085; NM_001285503; NM_001285504; NM_023317
	NP_001137451; NP_060138
	NP_001107557; NP_001272432; NP_001272433; NP_075806
	Wikidata
View/Edit Human	View/Edit Mouse

Nuclear distribution protein nudE homolog 1 is a protein that in humans is encoded by the NDE1 gene.[5][6][7]

Clinical significance

Mutations in both copies of NDE1 cause microlissencephaly type 4.[8]

References

ENSG00000275911 GRCh38: Ensembl release 89: ENSG00000072864, ENSG00000275911 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000022678 - 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.
Kitagawa M, Umezu M, Aoki J, Koizumi H, Arai H, Inoue K (Sep 2000). "Direct association of LIS1, the lissencephaly gene product, with a mammalian homologue of a fungal nuclear distribution protein, rNUDE". FEBS Lett. 479 (1–2): 57–62. doi:10.1016/S0014-5793(00)01856-1. PMID 10940388.
Meyer G, Perez-Garcia CG, Gleeson JG (Nov 2002). "Selective expression of doublecortin and LIS1 in developing human cortex suggests unique modes of neuronal movement". Cereb Cortex. 12 (12): 1225–36. doi:10.1093/cercor/12.12.1225. PMID 12427674.
"Entrez Gene: NDE1 nudE nuclear distribution gene E homolog 1 (A. nidulans)".
"OMIM Entry - # 614019 - LISSENCEPHALY 4; LIS4". omim.org. Retrieved 2019-12-10.

Feng Y, Olson EC, Stukenberg PT, et al. (2001). "LIS1 regulates CNS lamination by interacting with mNudE, a central component of the centrosome". Neuron. 28 (3): 665–79. doi:10.1016/S0896-6273(00)00145-8. PMID 11163258.
Türeci O, Sahin U, Koslowski M, et al. (2002). "A novel tumour associated leucine zipper protein targeting to sites of gene transcription and splicing". Oncogene. 21 (24): 3879–88. doi:10.1038/sj.onc.1205481. PMID 12032826.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
Yan X, Li F, Liang Y, et al. (2003). "Human Nudel and NudE as regulators of cytoplasmic dynein in poleward protein transport along the mitotic spindle". Mol. Cell. Biol. 23 (4): 1239–50. doi:10.1128/MCB.23.4.1239-1250.2003. PMC 141156. PMID 12556484.
Millar JK, Christie S, Porteous DJ (2004). "Yeast two-hybrid screens implicate DISC1 in brain development and function". Biochem. Biophys. Res. Commun. 311 (4): 1019–25. doi:10.1016/j.bbrc.2003.10.101. PMID 14623284.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
Jin J, Smith FD, Stark C, et al. (2004). "Proteomic, functional, and domain-based analysis of in vivo 14-3-3 binding proteins involved in cytoskeletal regulation and cellular organization". Curr. Biol. 14 (16): 1436–50. doi:10.1016/j.cub.2004.07.051. PMID 15324660.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
Rush J, Moritz A, Lee KA, et al. (2005). "Immunoaffinity profiling of tyrosine phosphorylation in cancer cells". Nat. Biotechnol. 23 (1): 94–101. doi:10.1038/nbt1046. PMID 15592455.
Martin J, Han C, Gordon LA, et al. (2005). "The sequence and analysis of duplication-rich human chromosome 16" (PDF). Nature. 432 (7020): 988–94. doi:10.1038/nature03187. PMID 15616553.
Brandon NJ, Schurov I, Camargo LM, et al. (2005). "Subcellular targeting of DISC1 is dependent on a domain independent from the Nudel binding site". Mol. Cell. Neurosci. 28 (4): 613–24. doi:10.1016/j.mcn.2004.11.003. PMID 15797709.
Guo J, Yang Z, Song W, et al. (2006). "Nudel contributes to microtubule anchoring at the mother centriole and is involved in both dynein-dependent and -independent centrosomal protein assembly". Mol. Biol. Cell. 17 (2): 680–9. doi:10.1091/mbc.E05-04-0360. PMC 1356579. PMID 16291865.
Hirohashi Y, Wang Q, Liu Q, et al. (2006). "Centrosomal proteins Nde1 and Su48 form a complex regulated by phosphorylation". Oncogene. 25 (45): 6048–55. doi:10.1038/sj.onc.1209637. PMID 16682949.
Beausoleil SA, Villén J, Gerber SA, et al. (2006). "A probability-based approach for high-throughput protein phosphorylation analysis and site localization". Nat. Biotechnol. 24 (10): 1285–92. doi:10.1038/nbt1240. PMID 16964243.
Hennah W, Tomppo L, Hiekkalinna T, et al. (2007). "Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1". Hum. Mol. Genet. 16 (5): 453–62. doi:10.1093/hmg/ddl462. PMID 17185386.

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[refGRCh38Ensembl-1] ENSG00000275911 GRCh38: Ensembl release 89: ENSG00000072864, ENSG00000275911 - Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000022678 - 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.

[pmid10940388-5] Kitagawa M, Umezu M, Aoki J, Koizumi H, Arai H, Inoue K (Sep 2000). "Direct association of LIS1, the lissencephaly gene product, with a mammalian homologue of a fungal nuclear distribution protein, rNUDE". FEBS Lett. 479 (1–2): 57–62. doi:10.1016/S0014-5793(00)01856-1. PMID 10940388.

[pmid12427674-6] Meyer G, Perez-Garcia CG, Gleeson JG (Nov 2002). "Selective expression of doublecortin and LIS1 in developing human cortex suggests unique modes of neuronal movement". Cereb Cortex. 12 (12): 1225–36. doi:10.1093/cercor/12.12.1225. PMID 12427674.

[entrez-7] "Entrez Gene: NDE1 nudE nuclear distribution gene E homolog 1 (A. nidulans)".

[8] "OMIM Entry - # 614019 - LISSENCEPHALY 4; LIS4". omim.org. Retrieved 2019-12-10.

NDE1

Clinical significance

References

Further reading