INCENP

INCENP
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesINCENP, inner centromere protein
External IDsMGI: 1313288 HomoloGene: 9624 GeneCards: INCENP
Gene location (Human)
Chr.Chromosome 11 (human)[1]
BandNo data availableStart62,123,973 bp[1]
End62,153,163 bp[1]
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

3619

16319

Ensembl

ENSG00000149503

ENSMUSG00000024660

UniProt

Q9NQS7

Q9WU62

RefSeq (mRNA)

NM_001040694
NM_020238

NM_016692

RefSeq (protein)

NP_001035784
NP_064623

NP_057901

Location (UCSC)Chr 11: 62.12 – 62.15 MbChr 19: 9.87 – 9.9 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
Chromosome passenger complex (CPC) protein INCENP N terminal
Identifiers
Symbol INCENP_N
Pfam PF12178
InterPro IPR022006
Inner centromere protein, ARK binding region
Identifiers
Symbol INCENP_ARK-bind
Pfam PF03941
InterPro IPR005635

Inner centromere protein is a protein that in humans is encoded by the INCENP gene.[5][6][7]

In mammalian cells, two broad groups of centromere-interacting proteins have been described: constitutively binding centromere proteins and 'passenger' (or transiently interacting) proteins.[8] The constitutive proteins include CENPA (centromere protein A), CENPB, CENPC1, and CENPD.

The term 'passenger proteins' encompasses a broad collection of proteins that localize to the centromere during specific stages of the cell cycle.[9] These include CENPE; MCAK; KID; cytoplasmic dynein (e.g., DYNC1H1); CliPs (e.g. CLIP1); and CENPF/mitosin (CENPF). The inner centromere proteins (INCENPs),[5] the initial members of the passenger protein group, display a broad localization along chromosomes in the early stages of mitosis but gradually become concentrated at centromeres as the cell cycle progresses into mid-metaphase. During telophase, the proteins are located within the midbody in the intercellular bridge, where they are discarded after cytokinesis.[7][10]

INCENP is a regulatory protein in the chromosome passenger complex. It is involved in regulation of the catalytic protein Aurora B. It performs this function in association with two other proteins - Survivin and Borealin. These proteins form a tight three-helical bundle. The N-terminal domain of INCENP is the domain involved in formation of this three-helical bundle.[11]

Interactions

INCENP has been shown to interact with H2AFZ,[12] Survivin[13] and CDCA8.[14] The ARK binding region has been found to be necessary and sufficient for binding to aurora-related kinase. This interaction has been implicated in the coordination of chromosome segregation with cell division in yeast.[15]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000149503 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000024660 - Ensembl, May 2017
  3. ↑ "Human PubMed Reference:".
  4. ↑ "Mouse PubMed Reference:".
  5. 1 2 Earnshaw WC, Cooke CA (Sep 1991). "Analysis of the distribution of the INCENPs throughout mitosis reveals the existence of a pathway of structural changes in the chromosomes during metaphase and early events in cleavage furrow formation". J Cell Sci. 98 (4): 443–61. PMID 1860899.
  6. ↑ Adams RR, Eckley DM, Vagnarelli P, Wheatley SP, Gerloff DL, Mackay AM, Svingen PA, Kaufmann SH, Earnshaw WC (Jul 2001). "Human INCENP colocalizes with the Aurora-B/AIRK2 kinase on chromosomes and is overexpressed in tumour cells". Chromosoma. 110 (2): 65–74. PMID 11453556. doi:10.1007/s004120100130.
  7. 1 2 "Entrez Gene: INCENP inner centromere protein antigens 135/155kDa".
  8. ↑ Choo, K. H. Andy (1997). The centromere. Oxford [Oxfordshire]: Oxford University Press. ISBN 0-19-857780-X.
  9. ↑ Earnshaw WC, Mackay AM (September 1994). "Role of nonhistone proteins in the chromosomal events of mitosis". FASEB J. 8 (12): 947–56. PMID 8088460.
  10. ↑ Cutts SM, Fowler KJ, Kile BT, Hii LL, O'Dowd RA, Hudson DF, Saffery R, Kalitsis P, Earle E, Choo KH (July 1999). "Defective chromosome segregation, microtubule bundling and nuclear bridging in inner centromere protein gene (Incenp)-disrupted mice". Hum. Mol. Genet. 8 (7): 1145–55. PMID 10369859. doi:10.1093/hmg/8.7.1145.
  11. ↑ Jeyaprakash, A. A.; Klein, U. R.; Lindner, D.; Ebert, J.; Nigg, E. A.; Conti, E. (2007). "Structure of a Survivin–Borealin–INCENP Core Complex Reveals How Chromosomal Passengers Travel Together". Cell. 131 (2): 271–285. PMID 17956729. doi:10.1016/j.cell.2007.07.045.
  12. ↑ Rangasamy D, Berven L, Ridgway P, Tremethick DJ (April 2003). "Pericentric heterochromatin becomes enriched with H2A.Z during early mammalian development". EMBO J. 22 (7): 1599–607. PMC 152904 Freely accessible. PMID 12660166. doi:10.1093/emboj/cdg160.
  13. ↑ Wheatley SP, Carvalho A, Vagnarelli P, Earnshaw WC (June 2001). "INCENP is required for proper targeting of Survivin to the centromeres and the anaphase spindle during mitosis". Curr. Biol. 11 (11): 886–90. PMID 11516652. doi:10.1016/S0960-9822(01)00238-X.
  14. ↑ Gassmann R, Carvalho A, Henzing AJ, Ruchaud S, Hudson DF, Honda R, Nigg EA, Gerloff DL, Earnshaw WC (July 2004). "Borealin: a novel chromosomal passenger required for stability of the bipolar mitotic spindle". J. Cell Biol. 166 (2): 179–91. PMC 2172304 Freely accessible. PMID 15249581. doi:10.1083/jcb.200404001.
  15. ↑ Leverson JD, Huang HK, Forsburg SL, Hunter T (April 2002). "The Schizosaccharomyces pombe aurora-related kinase Ark1 interacts with the inner centromere protein Pic1 and mediates chromosome segregation and cytokinesis". Mol. Biol. Cell. 13 (4): 1132–43. PMC 102257 Freely accessible. PMID 11950927. doi:10.1091/mbc.01-07-0330.

Further reading

This article incorporates text from the public domain Pfam and InterPro IPR005635

This article incorporates text from the public domain Pfam and InterPro IPR022006

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