From Wikipedia, the free encyclopedia
HCFC1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
Aliases HCFC1, CFF, HCF-1, HCF1, HFC1, MRX3, PPP1R89, VCAF, HCF, Host cell factor C1, XLID3, MAHCX
External IDs OMIM: 300019; MGI: 105942; HomoloGene: 3898; GeneCards: HCFC1; OMA: HCFC1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005334

NM_008224

RefSeq (protein)

NP_005325

NP_032250

Location (UCSC) Chr X: 153.95 – 153.97 Mb Chr X: 72.99 – 73.01 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Host cell factor 1 (HCFC1, HCF1, or HCF-1), also known as VP16-accessory protein, [5] is a protein that in humans is encoded by the HCFC1 gene. [6] [7]

Structure

HCF1 is a member of the highly conserved host cell factor family and encodes a protein with five Kelch repeats, a fibronectin-like motif, and six HCF repeats, each of which contains a highly specific cleavage signal. This nuclear transcription coregulator is proteolytically cleaved at one or more of the six possible sites, resulting in the creation of an N-terminal chain and the corresponding C-terminal chain. The final form of this protein consists of noncovalently bound N- and C-terminal chains which interact through electrostatic forces.

Function

HCF1 is involved in control of the cell cycle as well as having regulatory roles in a multitude of processes related to transcription. Additionally, work in model organisms point to HCF1 as being a putative longevity determinant. [8] Alternatively spliced variants that encode different protein isoforms have been described; however, not all variants have been fully characterized. [7]

Mutations in this gene have been linked to disorders of the cobalamine metabolism. [9]

Interactions

Host cell factor C1 has been shown to interact with:

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000172534Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000031386Ensembl, 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.
  5. ^ GeneCards entry for HCFC1, http://genecards.org Archived 2013-10-14 at the Wayback Machine
  6. ^ Wilson AC, LaMarco K, Peterson MG, Herr W (Jul 1993). "The VP16 accessory protein HCF is a family of polypeptides processed from a large precursor protein". Cell. 74 (1): 115–25. doi: 10.1016/0092-8674(93)90299-6. PMID  8392914. S2CID  43569318.
  7. ^ a b "Entrez Gene: HCFC1 host cell factor C1 (VP16-accessory protein)".
  8. ^ Li J, Ebata A, Dong Y, Rizki G, Iwata T, Lee SS (Sep 2008). "Caenorhabditis elegans HCF-1 functions in longevity maintenance as a DAF-16 regulator". PLOS Biology. 6 (9): e233. doi: 10.1371/journal.pbio.0060233. PMC  2553839. PMID  18828672.
  9. ^ Yu HC, Sloan JL, Scharer G, Brebner A, Quintana AM, Achilly NP, Manoli I, Coughlin CR, Geiger EA, Schneck U, Watkins D, Suormala T, Van Hove JL, Fowler B, Baumgartner MR, Rosenblatt DS, Venditti CP, Shaikh TH (Sep 2013). "An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1". American Journal of Human Genetics. 93 (3): 506–14. doi: 10.1016/j.ajhg.2013.07.022. PMC  3769968. PMID  24011988.
  10. ^ Machida YJ, Machida Y, Vashisht AA, Wohlschlegel JA, Dutta A (Dec 2009). "The deubiquitinating enzyme BAP1 regulates cell growth via interaction with HCF-1". The Journal of Biological Chemistry. 284 (49): 34179–88. doi: 10.1074/jbc.M109.046755. PMC  2797188. PMID  19815555.
  11. ^ Lu R, Yang P, Padmakumar S, Misra V (Aug 1998). "The herpesvirus transactivator VP16 mimics a human basic domain leucine zipper protein, luman, in its interaction with HCF". Journal of Virology. 72 (8): 6291–7. doi: 10.1128/JVI.72.8.6291-6297.1998. PMC  109766. PMID  9658067.
  12. ^ Freiman RN, Herr W (Dec 1997). "Viral mimicry: common mode of association with HCF by VP16 and the cellular protein LZIP". Genes & Development. 11 (23): 3122–7. doi: 10.1101/gad.11.23.3122. PMC  316754. PMID  9389645.
  13. ^ Vogel JL, Kristie TM (Feb 2000). "The novel coactivator C1 (HCF) coordinates multiprotein enhancer formation and mediates transcription activation by GABP". The EMBO Journal. 19 (4): 683–90. doi: 10.1093/emboj/19.4.683. PMC  305606. PMID  10675337.
  14. ^ a b c d e f g Wysocka J, Myers MP, Laherty CD, Eisenman RN, Herr W (Apr 2003). "Human Sin3 deacetylase and trithorax-related Set1/Ash2 histone H3-K4 methyltransferase are tethered together selectively by the cell-proliferation factor HCF-1". Genes & Development. 17 (7): 896–911. doi: 10.1101/gad.252103. PMC  196026. PMID  12670868.
  15. ^ a b c Yokoyama A, Wang Z, Wysocka J, Sanyal M, Aufiero DJ, Kitabayashi I, Herr W, Cleary ML (Jul 2004). "Leukemia proto-oncoprotein MLL forms a SET1-like histone methyltransferase complex with menin to regulate Hox gene expression". Molecular and Cellular Biology. 24 (13): 5639–49. doi: 10.1128/MCB.24.13.5639-5649.2004. PMC  480881. PMID  15199122.
  16. ^ Scarr RB, Sharp PA (Aug 2002). "PDCD2 is a negative regulator of HCF-1 (C1)". Oncogene. 21 (34): 5245–54. doi: 10.1038/sj.onc.1205647. PMID  12149646.
  17. ^ La Boissière S, Hughes T, O'Hare P (Jan 1999). "HCF-dependent nuclear import of VP16". The EMBO Journal. 18 (2): 480–9. doi: 10.1093/emboj/18.2.480. PMC  1171141. PMID  9889203.
  18. ^ Kristie TM, Sharp PA (Mar 1993). "Purification of the cellular C1 factor required for the stable recognition of the Oct-1 homeodomain by the herpes simplex virus alpha-trans-induction factor (VP16)". The Journal of Biological Chemistry. 268 (9): 6525–34. doi: 10.1016/S0021-9258(18)53282-8. PMID  8454622.
  19. ^ Ajuh PM, Browne GJ, Hawkes NA, Cohen PT, Roberts SG, Lamond AI (Feb 2000). "Association of a protein phosphatase 1 activity with the human factor C1 (HCF) complex". Nucleic Acids Research. 28 (3): 678–86. doi: 10.1093/nar/28.3.678. PMC  102561. PMID  10637318.
  20. ^ Gunther M, Laithier M, Brison O (Jul 2000). "A set of proteins interacting with transcription factor Sp1 identified in a two-hybrid screening". Molecular and Cellular Biochemistry. 210 (1–2): 131–42. doi: 10.1023/A:1007177623283. PMID  10976766. S2CID  1339642.
  21. ^ Piluso D, Bilan P, Capone JP (Nov 2002). "Host cell factor-1 interacts with and antagonizes transactivation by the cell cycle regulatory factor Miz-1". The Journal of Biological Chemistry. 277 (48): 46799–808. doi: 10.1074/jbc.M206226200. PMID  12244100.

Further reading

From Wikipedia, the free encyclopedia
HCFC1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
Aliases HCFC1, CFF, HCF-1, HCF1, HFC1, MRX3, PPP1R89, VCAF, HCF, Host cell factor C1, XLID3, MAHCX
External IDs OMIM: 300019; MGI: 105942; HomoloGene: 3898; GeneCards: HCFC1; OMA: HCFC1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005334

NM_008224

RefSeq (protein)

NP_005325

NP_032250

Location (UCSC) Chr X: 153.95 – 153.97 Mb Chr X: 72.99 – 73.01 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Host cell factor 1 (HCFC1, HCF1, or HCF-1), also known as VP16-accessory protein, [5] is a protein that in humans is encoded by the HCFC1 gene. [6] [7]

Structure

HCF1 is a member of the highly conserved host cell factor family and encodes a protein with five Kelch repeats, a fibronectin-like motif, and six HCF repeats, each of which contains a highly specific cleavage signal. This nuclear transcription coregulator is proteolytically cleaved at one or more of the six possible sites, resulting in the creation of an N-terminal chain and the corresponding C-terminal chain. The final form of this protein consists of noncovalently bound N- and C-terminal chains which interact through electrostatic forces.

Function

HCF1 is involved in control of the cell cycle as well as having regulatory roles in a multitude of processes related to transcription. Additionally, work in model organisms point to HCF1 as being a putative longevity determinant. [8] Alternatively spliced variants that encode different protein isoforms have been described; however, not all variants have been fully characterized. [7]

Mutations in this gene have been linked to disorders of the cobalamine metabolism. [9]

Interactions

Host cell factor C1 has been shown to interact with:

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000172534Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000031386Ensembl, 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.
  5. ^ GeneCards entry for HCFC1, http://genecards.org Archived 2013-10-14 at the Wayback Machine
  6. ^ Wilson AC, LaMarco K, Peterson MG, Herr W (Jul 1993). "The VP16 accessory protein HCF is a family of polypeptides processed from a large precursor protein". Cell. 74 (1): 115–25. doi: 10.1016/0092-8674(93)90299-6. PMID  8392914. S2CID  43569318.
  7. ^ a b "Entrez Gene: HCFC1 host cell factor C1 (VP16-accessory protein)".
  8. ^ Li J, Ebata A, Dong Y, Rizki G, Iwata T, Lee SS (Sep 2008). "Caenorhabditis elegans HCF-1 functions in longevity maintenance as a DAF-16 regulator". PLOS Biology. 6 (9): e233. doi: 10.1371/journal.pbio.0060233. PMC  2553839. PMID  18828672.
  9. ^ Yu HC, Sloan JL, Scharer G, Brebner A, Quintana AM, Achilly NP, Manoli I, Coughlin CR, Geiger EA, Schneck U, Watkins D, Suormala T, Van Hove JL, Fowler B, Baumgartner MR, Rosenblatt DS, Venditti CP, Shaikh TH (Sep 2013). "An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1". American Journal of Human Genetics. 93 (3): 506–14. doi: 10.1016/j.ajhg.2013.07.022. PMC  3769968. PMID  24011988.
  10. ^ Machida YJ, Machida Y, Vashisht AA, Wohlschlegel JA, Dutta A (Dec 2009). "The deubiquitinating enzyme BAP1 regulates cell growth via interaction with HCF-1". The Journal of Biological Chemistry. 284 (49): 34179–88. doi: 10.1074/jbc.M109.046755. PMC  2797188. PMID  19815555.
  11. ^ Lu R, Yang P, Padmakumar S, Misra V (Aug 1998). "The herpesvirus transactivator VP16 mimics a human basic domain leucine zipper protein, luman, in its interaction with HCF". Journal of Virology. 72 (8): 6291–7. doi: 10.1128/JVI.72.8.6291-6297.1998. PMC  109766. PMID  9658067.
  12. ^ Freiman RN, Herr W (Dec 1997). "Viral mimicry: common mode of association with HCF by VP16 and the cellular protein LZIP". Genes & Development. 11 (23): 3122–7. doi: 10.1101/gad.11.23.3122. PMC  316754. PMID  9389645.
  13. ^ Vogel JL, Kristie TM (Feb 2000). "The novel coactivator C1 (HCF) coordinates multiprotein enhancer formation and mediates transcription activation by GABP". The EMBO Journal. 19 (4): 683–90. doi: 10.1093/emboj/19.4.683. PMC  305606. PMID  10675337.
  14. ^ a b c d e f g Wysocka J, Myers MP, Laherty CD, Eisenman RN, Herr W (Apr 2003). "Human Sin3 deacetylase and trithorax-related Set1/Ash2 histone H3-K4 methyltransferase are tethered together selectively by the cell-proliferation factor HCF-1". Genes & Development. 17 (7): 896–911. doi: 10.1101/gad.252103. PMC  196026. PMID  12670868.
  15. ^ a b c Yokoyama A, Wang Z, Wysocka J, Sanyal M, Aufiero DJ, Kitabayashi I, Herr W, Cleary ML (Jul 2004). "Leukemia proto-oncoprotein MLL forms a SET1-like histone methyltransferase complex with menin to regulate Hox gene expression". Molecular and Cellular Biology. 24 (13): 5639–49. doi: 10.1128/MCB.24.13.5639-5649.2004. PMC  480881. PMID  15199122.
  16. ^ Scarr RB, Sharp PA (Aug 2002). "PDCD2 is a negative regulator of HCF-1 (C1)". Oncogene. 21 (34): 5245–54. doi: 10.1038/sj.onc.1205647. PMID  12149646.
  17. ^ La Boissière S, Hughes T, O'Hare P (Jan 1999). "HCF-dependent nuclear import of VP16". The EMBO Journal. 18 (2): 480–9. doi: 10.1093/emboj/18.2.480. PMC  1171141. PMID  9889203.
  18. ^ Kristie TM, Sharp PA (Mar 1993). "Purification of the cellular C1 factor required for the stable recognition of the Oct-1 homeodomain by the herpes simplex virus alpha-trans-induction factor (VP16)". The Journal of Biological Chemistry. 268 (9): 6525–34. doi: 10.1016/S0021-9258(18)53282-8. PMID  8454622.
  19. ^ Ajuh PM, Browne GJ, Hawkes NA, Cohen PT, Roberts SG, Lamond AI (Feb 2000). "Association of a protein phosphatase 1 activity with the human factor C1 (HCF) complex". Nucleic Acids Research. 28 (3): 678–86. doi: 10.1093/nar/28.3.678. PMC  102561. PMID  10637318.
  20. ^ Gunther M, Laithier M, Brison O (Jul 2000). "A set of proteins interacting with transcription factor Sp1 identified in a two-hybrid screening". Molecular and Cellular Biochemistry. 210 (1–2): 131–42. doi: 10.1023/A:1007177623283. PMID  10976766. S2CID  1339642.
  21. ^ Piluso D, Bilan P, Capone JP (Nov 2002). "Host cell factor-1 interacts with and antagonizes transactivation by the cell cycle regulatory factor Miz-1". The Journal of Biological Chemistry. 277 (48): 46799–808. doi: 10.1074/jbc.M206226200. PMID  12244100.

Further reading


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