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{{ | '''Cullin-7''' is a RING-E3 ligase [[protein]] that in humans is encoded by the ''CUL7'' [[gene]].<ref name="pmid12481031">{{cite journal | vauthors = Dias DC, Dolios G, Wang R, Pan ZQ | title = CUL7: A DOC domain-containing cullin selectively binds Skp1.Fbx29 to form an SCF-like complex | journal = Proc Natl Acad Sci U S A | volume = 99 | issue = 26 | pages = 16601–6 |date=Dec 2002 | pmid = 12481031 | pmc = 139190 | doi = 10.1073/pnas.252646399 }}</ref><ref name="pmid12904573">{{cite journal | vauthors = Arai T, Kasper JS, Skaar JR, Ali SH, Takahashi C, DeCaprio JA | title = Targeted disruption of p185/Cul7 gene results in abnormal vascular morphogenesis | journal = Proc Natl Acad Sci U S A | volume = 100 | issue = 17 | pages = 9855–60 |date=Aug 2003 | pmid = 12904573 | pmc = 187864 | doi = 10.1073/pnas.1733908100 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: CUL7 cullin 7| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=9820| accessdate = }}</ref> | ||
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== Clinical significance == | |||
It is associated with [[3-M syndrome]]. | |||
==Interactions== | |||
CUL7 has been shown to [[Protein-protein interaction|interact]] with [[RBX1]].<ref name=pmid12481031 /> | |||
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==References== | ==References== | ||
{{reflist | {{reflist}} | ||
==Further reading== | ==Further reading== | ||
{{refbegin | 2}} | {{refbegin | 2}} | ||
*{{cite journal | vauthors=Kim SS, Shago M, Kaustov L |title=CUL7 is a novel antiapoptotic oncogene. |journal=Cancer Res. |volume=67 |issue= 20 |pages= 9616–22 |year= 2007 |pmid= 17942889 |doi= 10.1158/0008-5472.CAN-07-0644 |display-authors=etal}} | |||
*{{cite journal | vauthors=Jung P, Verdoodt B, Bailey A |title=Induction of cullin 7 by DNA damage attenuates p53 function. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=104 |issue= 27 |pages= 11388–93 |year= 2007 |pmid= 17586686 |doi= 10.1073/pnas.0609467104 | pmc=2040908 |display-authors=etal}} | |||
*{{cite journal | | *{{cite journal | vauthors=Skaar JR, Florens L, Tsutsumi T |title=PARC and CUL7 form atypical cullin RING ligase complexes. |journal=Cancer Res. |volume=67 |issue= 5 |pages= 2006–14 |year= 2007 |pmid= 17332328 |doi= 10.1158/0008-5472.CAN-06-3241 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Kaustov L, Lukin J, Lemak A |title=The conserved CPH domains of Cul7 and PARC are protein-protein interaction modules that bind the tetramerization domain of p53. |journal=J. Biol. Chem. |volume=282 |issue= 15 |pages= 11300–7 |year= 2007 |pmid= 17298945 |doi= 10.1074/jbc.M611297200 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Kasper JS, Arai T, DeCaprio JA |title=A novel p53-binding domain in CUL7. |journal=Biochem. Biophys. Res. Commun. |volume=348 |issue= 1 |pages= 132–8 |year= 2006 |pmid= 16875676 |doi= 10.1016/j.bbrc.2006.07.013 }} | ||
*{{cite journal | | *{{cite journal | vauthors=Andrews P, He YJ, Xiong Y |title=Cytoplasmic localized ubiquitin ligase cullin 7 binds to p53 and promotes cell growth by antagonizing p53 function. |journal=Oncogene |volume=25 |issue= 33 |pages= 4534–48 |year= 2006 |pmid= 16547496 |doi= 10.1038/sj.onc.1209490 }} | ||
*{{cite journal | | *{{cite journal | vauthors=Huber C, Dias-Santagata D, Glaser A |title=Identification of mutations in CUL7 in 3-M syndrome. |journal=Nat. Genet. |volume=37 |issue= 10 |pages= 1119–24 |year= 2005 |pmid= 16142236 |doi= 10.1038/ng1628 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Gerhard DS, Wagner L, Feingold EA |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Mungall AJ, Palmer SA, Sims SK |title=The DNA sequence and analysis of human chromosome 6. |journal=Nature |volume=425 |issue= 6960 |pages= 805–11 |year= 2003 |pmid= 14574404 |doi= 10.1038/nature02055 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Strausberg RL, Feingold EA, Grouse LH |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Nakayama M, Kikuno R, Ohara O |title=Protein-protein interactions between large proteins: two-hybrid screening using a functionally classified library composed of long cDNAs. |journal=Genome Res. |volume=12 |issue= 11 |pages= 1773–84 |year= 2003 |pmid= 12421765 |doi= 10.1101/gr.406902 | pmc=187542 }} | ||
*{{cite journal | vauthors=Winston JT, Koepp DM, Zhu C |title=A family of mammalian F-box proteins. |journal=Curr. Biol. |volume=9 |issue= 20 |pages= 1180–2 |year= 1999 |pmid= 10531037 |doi= 10.1016/S0960-9822(00)80021-4 |display-authors=etal}} | |||
*{{cite journal | | *{{cite journal | vauthors=Nomura N, Nagase T, Miyajima N |title=Prediction of the coding sequences of unidentified human genes. II. The coding sequences of 40 new genes (KIAA0041-KIAA0080) deduced by analysis of cDNA clones from human cell line KG-1. |journal=DNA Res. |volume=1 |issue= 5 |pages= 223–9 |year= 1995 |pmid= 7584044 |doi=10.1093/dnares/1.5.223 |display-authors=etal}} | ||
*{{cite journal | | |||
*{{cite journal | | |||
*{{cite journal | | |||
}} | |||
{{refend}} | {{refend}} | ||
{{ | ==External links== | ||
{{ | * [https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=gr_3ms GeneReviews/NIH/NCBI/UW entry on 3-M syndrome] | ||
* [https://www.ncbi.nlm.nih.gov/omim/273750,609577,610991,612921,273750,609577,610991,612921 OMIM entries entry on 3-M syndrome] | |||
* {{UCSC gene info|CUL7}} | |||
{{PDB Gallery|geneid=9820}} | |||
{{Cell cycle proteins}} | |||
{{gene-6-stub}} |
Latest revision as of 10:11, 30 August 2017
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External IDs | GeneCards: [1] | ||||||
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Species | Human | Mouse | |||||
Entrez |
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Ensembl |
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UniProt |
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RefSeq (mRNA) |
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RefSeq (protein) |
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Location (UCSC) | n/a | n/a | |||||
PubMed search | n/a | n/a | |||||
Wikidata | |||||||
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Cullin-7 is a RING-E3 ligase protein that in humans is encoded by the CUL7 gene.[1][2][3]
Clinical significance
It is associated with 3-M syndrome.
Interactions
CUL7 has been shown to interact with RBX1.[1]
References
- ↑ 1.0 1.1 Dias DC, Dolios G, Wang R, Pan ZQ (Dec 2002). "CUL7: A DOC domain-containing cullin selectively binds Skp1.Fbx29 to form an SCF-like complex". Proc Natl Acad Sci U S A. 99 (26): 16601–6. doi:10.1073/pnas.252646399. PMC 139190. PMID 12481031.
- ↑ Arai T, Kasper JS, Skaar JR, Ali SH, Takahashi C, DeCaprio JA (Aug 2003). "Targeted disruption of p185/Cul7 gene results in abnormal vascular morphogenesis". Proc Natl Acad Sci U S A. 100 (17): 9855–60. doi:10.1073/pnas.1733908100. PMC 187864. PMID 12904573.
- ↑ "Entrez Gene: CUL7 cullin 7".
Further reading
- Kim SS, Shago M, Kaustov L, et al. (2007). "CUL7 is a novel antiapoptotic oncogene". Cancer Res. 67 (20): 9616–22. doi:10.1158/0008-5472.CAN-07-0644. PMID 17942889.
- Jung P, Verdoodt B, Bailey A, et al. (2007). "Induction of cullin 7 by DNA damage attenuates p53 function". Proc. Natl. Acad. Sci. U.S.A. 104 (27): 11388–93. doi:10.1073/pnas.0609467104. PMC 2040908. PMID 17586686.
- Skaar JR, Florens L, Tsutsumi T, et al. (2007). "PARC and CUL7 form atypical cullin RING ligase complexes". Cancer Res. 67 (5): 2006–14. doi:10.1158/0008-5472.CAN-06-3241. PMID 17332328.
- Kaustov L, Lukin J, Lemak A, et al. (2007). "The conserved CPH domains of Cul7 and PARC are protein-protein interaction modules that bind the tetramerization domain of p53". J. Biol. Chem. 282 (15): 11300–7. doi:10.1074/jbc.M611297200. PMID 17298945.
- Kasper JS, Arai T, DeCaprio JA (2006). "A novel p53-binding domain in CUL7". Biochem. Biophys. Res. Commun. 348 (1): 132–8. doi:10.1016/j.bbrc.2006.07.013. PMID 16875676.
- Andrews P, He YJ, Xiong Y (2006). "Cytoplasmic localized ubiquitin ligase cullin 7 binds to p53 and promotes cell growth by antagonizing p53 function". Oncogene. 25 (33): 4534–48. doi:10.1038/sj.onc.1209490. PMID 16547496.
- Huber C, Dias-Santagata D, Glaser A, et al. (2005). "Identification of mutations in CUL7 in 3-M syndrome". Nat. Genet. 37 (10): 1119–24. doi:10.1038/ng1628. PMID 16142236.
- 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.
- Mungall AJ, Palmer SA, Sims SK, et al. (2003). "The DNA sequence and analysis of human chromosome 6". Nature. 425 (6960): 805–11. doi:10.1038/nature02055. PMID 14574404.
- 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.
- Nakayama M, Kikuno R, Ohara O (2003). "Protein-protein interactions between large proteins: two-hybrid screening using a functionally classified library composed of long cDNAs". Genome Res. 12 (11): 1773–84. doi:10.1101/gr.406902. PMC 187542. PMID 12421765.
- Winston JT, Koepp DM, Zhu C, et al. (1999). "A family of mammalian F-box proteins". Curr. Biol. 9 (20): 1180–2. doi:10.1016/S0960-9822(00)80021-4. PMID 10531037.
- Nomura N, Nagase T, Miyajima N, et al. (1995). "Prediction of the coding sequences of unidentified human genes. II. The coding sequences of 40 new genes (KIAA0041-KIAA0080) deduced by analysis of cDNA clones from human cell line KG-1". DNA Res. 1 (5): 223–9. doi:10.1093/dnares/1.5.223. PMID 7584044.
External links
- GeneReviews/NIH/NCBI/UW entry on 3-M syndrome
- OMIM entries entry on 3-M syndrome
- Human CUL7 genome location and CUL7 gene details page in the UCSC Genome Browser.
This article on a gene on human chromosome 6 is a stub. You can help Wikipedia by expanding it. |