AMFR: Difference between revisions

Jump to navigation Jump to search
m (Bot: HTTP→HTTPS)
m (Adding 0 arxiv eprint(s), 4 bibcode(s) and 0 doi(s). Did it miss something? Report bugs, errors, and suggestions at User talk:Bibcode Bot)
Line 117: Line 117:
*{{cite journal  | vauthors=Hillier LD, Lennon G, Becker M |title=Generation and analysis of 280,000 human expressed sequence tags. |journal=Genome Res. |volume=6 |issue= 9 |pages= 807–28 |year= 1997 |pmid= 8889549 |doi=10.1101/gr.6.9.807  |display-authors=etal}}
*{{cite journal  | vauthors=Hillier LD, Lennon G, Becker M |title=Generation and analysis of 280,000 human expressed sequence tags. |journal=Genome Res. |volume=6 |issue= 9 |pages= 807–28 |year= 1997 |pmid= 8889549 |doi=10.1101/gr.6.9.807  |display-authors=etal}}
*{{cite journal  | vauthors=Shimizu K, Tani M, Watanabe H |title=The autocrine motility factor receptor gene encodes a novel type of seven transmembrane protein. |journal=FEBS Lett. |volume=456 |issue= 2 |pages= 295–300 |year= 1999 |pmid= 10456327 |doi=10.1016/S0014-5793(99)00966-7  |display-authors=etal}}
*{{cite journal  | vauthors=Shimizu K, Tani M, Watanabe H |title=The autocrine motility factor receptor gene encodes a novel type of seven transmembrane protein. |journal=FEBS Lett. |volume=456 |issue= 2 |pages= 295–300 |year= 1999 |pmid= 10456327 |doi=10.1016/S0014-5793(99)00966-7  |display-authors=etal}}
*{{cite journal  | vauthors=Fang S, Ferrone M, Yang C |title=The tumor autocrine motility factor receptor, gp78, is a ubiquitin protein ligase implicated in degradation from the endoplasmic reticulum. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=98 |issue= 25 |pages= 14422–7 |year= 2002 |pmid= 11724934 |doi= 10.1073/pnas.251401598  | pmc=64697 |display-authors=etal}}
*{{cite journal  | vauthors=Fang S, Ferrone M, Yang C |title=The tumor autocrine motility factor receptor, gp78, is a ubiquitin protein ligase implicated in degradation from the endoplasmic reticulum. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=98 |issue= 25 |pages= 14422–7 |year= 2002 |pmid= 11724934 |doi= 10.1073/pnas.251401598  | pmc=64697 |display-authors=etal|bibcode=2001PNAS...9814422F }}
*{{cite journal  | vauthors=Luo Y, Long JM, Lu C |title=A link between maze learning and hippocampal expression of neuroleukin and its receptor gp78. |journal=J. Neurochem. |volume=80 |issue= 2 |pages= 354–61 |year= 2002 |pmid= 11902125 |doi=10.1046/j.0022-3042.2001.00707.x  |display-authors=etal}}
*{{cite journal  | vauthors=Luo Y, Long JM, Lu C |title=A link between maze learning and hippocampal expression of neuroleukin and its receptor gp78. |journal=J. Neurochem. |volume=80 |issue= 2 |pages= 354–61 |year= 2002 |pmid= 11902125 |doi=10.1046/j.0022-3042.2001.00707.x  |display-authors=etal}}
*{{cite journal  | vauthors=Tímár J, Rásó E, Döme B |title=Expression and function of the AMF receptor by human melanoma in experimental and clinical systems. |journal=Clin. Exp. Metastasis |volume=19 |issue= 3 |pages= 225–32 |year= 2002 |pmid= 12067203 |doi=10.1023/A:1015595708241  |display-authors=etal}}
*{{cite journal  | vauthors=Tímár J, Rásó E, Döme B |title=Expression and function of the AMF receptor by human melanoma in experimental and clinical systems. |journal=Clin. Exp. Metastasis |volume=19 |issue= 3 |pages= 225–32 |year= 2002 |pmid= 12067203 |doi=10.1023/A:1015595708241  |display-authors=etal}}
*{{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  | 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|bibcode=2002PNAS...9916899M }}
*{{cite journal  | vauthors=Liang JS, Kim T, Fang S |title=Overexpression of the tumor autocrine motility factor receptor Gp78, a ubiquitin protein ligase, results in increased ubiquitinylation and decreased secretion of apolipoprotein B100 in HepG2 cells. |journal=J. Biol. Chem. |volume=278 |issue= 26 |pages= 23984–8 |year= 2003 |pmid= 12670940 |doi= 10.1074/jbc.M302683200 |display-authors=etal}}
*{{cite journal  | vauthors=Liang JS, Kim T, Fang S |title=Overexpression of the tumor autocrine motility factor receptor Gp78, a ubiquitin protein ligase, results in increased ubiquitinylation and decreased secretion of apolipoprotein B100 in HepG2 cells. |journal=J. Biol. Chem. |volume=278 |issue= 26 |pages= 23984–8 |year= 2003 |pmid= 12670940 |doi= 10.1074/jbc.M302683200 |display-authors=etal}}
*{{cite journal  | vauthors=Takanami I, Takeuchi K |title=Autocrine motility factor-receptor gene expression in lung cancer. |journal=Jpn. J. Thorac. Cardiovasc. Surg. |volume=51 |issue= 8 |pages= 368–73 |year= 2003 |pmid= 12962414 |doi=10.1007/BF02719469  }}
*{{cite journal  | vauthors=Takanami I, Takeuchi K |title=Autocrine motility factor-receptor gene expression in lung cancer. |journal=Jpn. J. Thorac. Cardiovasc. Surg. |volume=51 |issue= 8 |pages= 368–73 |year= 2003 |pmid= 12962414 |doi=10.1007/BF02719469  }}
Line 129: Line 129:
*{{cite journal  | vauthors=Song BL, Sever N, DeBose-Boyd RA |title=Gp78, a membrane-anchored ubiquitin ligase, associates with Insig-1 and couples sterol-regulated ubiquitination to degradation of HMG CoA reductase. |journal=Mol. Cell |volume=19 |issue= 6 |pages= 829–40 |year= 2005 |pmid= 16168377 |doi= 10.1016/j.molcel.2005.08.009 }}
*{{cite journal  | vauthors=Song BL, Sever N, DeBose-Boyd RA |title=Gp78, a membrane-anchored ubiquitin ligase, associates with Insig-1 and couples sterol-regulated ubiquitination to degradation of HMG CoA reductase. |journal=Mol. Cell |volume=19 |issue= 6 |pages= 829–40 |year= 2005 |pmid= 16168377 |doi= 10.1016/j.molcel.2005.08.009 }}
*{{cite journal  | vauthors=Kaynak K, Kara M, Oz B |title=Autocrine motility factor receptor expression implies an unfavourable prognosis in resected stage I pulmonary adenocarcinomas. |journal=Acta Chir. Belg. |volume=105 |issue= 4 |pages= 378–82 |year= 2006 |pmid= 16184720 |doi=  |display-authors=etal}}
*{{cite journal  | vauthors=Kaynak K, Kara M, Oz B |title=Autocrine motility factor receptor expression implies an unfavourable prognosis in resected stage I pulmonary adenocarcinomas. |journal=Acta Chir. Belg. |volume=105 |issue= 4 |pages= 378–82 |year= 2006 |pmid= 16184720 |doi=  |display-authors=etal}}
*{{cite journal  | vauthors=Ye Y, Shibata Y, Kikkert M |title=Inaugural Article: Recruitment of the p97 ATPase and ubiquitin ligases to the site of retrotranslocation at the endoplasmic reticulum membrane. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=102 |issue= 40 |pages= 14132–8 |year= 2006 |pmid= 16186510 |doi= 10.1073/pnas.0505006102  | pmc=1242302 |display-authors=etal}}
*{{cite journal  | vauthors=Ye Y, Shibata Y, Kikkert M |title=Inaugural Article: Recruitment of the p97 ATPase and ubiquitin ligases to the site of retrotranslocation at the endoplasmic reticulum membrane. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=102 |issue= 40 |pages= 14132–8 |year= 2006 |pmid= 16186510 |doi= 10.1073/pnas.0505006102  | pmc=1242302 |display-authors=etal|bibcode=2005PNAS..10214132Y }}
*{{cite journal  | vauthors=Chen B, Mariano J, Tsai YC |title=The activity of a human endoplasmic reticulum-associated degradation E3, gp78, requires its Cue domain, RING finger, and an E2-binding site. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=103 |issue= 2 |pages= 341–6 |year= 2006 |pmid= 16407162 |doi= 10.1073/pnas.0506618103  | pmc=1326157 |display-authors=etal}}
*{{cite journal  | vauthors=Chen B, Mariano J, Tsai YC |title=The activity of a human endoplasmic reticulum-associated degradation E3, gp78, requires its Cue domain, RING finger, and an E2-binding site. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=103 |issue= 2 |pages= 341–6 |year= 2006 |pmid= 16407162 |doi= 10.1073/pnas.0506618103  | pmc=1326157 |display-authors=etal|bibcode=2006PNAS..103..341C }}
*{{cite journal  | vauthors=Haga A, Tanaka N, Funasaka T |title=The autocrine motility factor (AMF) and AMF-receptor combination needs sugar chain recognition ability and interaction using the C-terminal region of AMF. |journal=J. Mol. Biol. |volume=358 |issue= 3 |pages= 741–53 |year= 2006 |pmid= 16563432 |doi= 10.1016/j.jmb.2006.02.046 |display-authors=etal}}
*{{cite journal  | vauthors=Haga A, Tanaka N, Funasaka T |title=The autocrine motility factor (AMF) and AMF-receptor combination needs sugar chain recognition ability and interaction using the C-terminal region of AMF. |journal=J. Mol. Biol. |volume=358 |issue= 3 |pages= 741–53 |year= 2006 |pmid= 16563432 |doi= 10.1016/j.jmb.2006.02.046 |display-authors=etal}}
*{{cite journal  | vauthors=Shen Y, Ballar P, Fang S |title=Ubiquitin ligase gp78 increases solubility and facilitates degradation of the Z variant of alpha-1-antitrypsin. |journal=Biochem. Biophys. Res. Commun. |volume=349 |issue= 4 |pages= 1285–93 |year= 2006 |pmid= 16979136 |doi= 10.1016/j.bbrc.2006.08.173 }}
*{{cite journal  | vauthors=Shen Y, Ballar P, Fang S |title=Ubiquitin ligase gp78 increases solubility and facilitates degradation of the Z variant of alpha-1-antitrypsin. |journal=Biochem. Biophys. Res. Commun. |volume=349 |issue= 4 |pages= 1285–93 |year= 2006 |pmid= 16979136 |doi= 10.1016/j.bbrc.2006.08.173 }}

Revision as of 16:33, 22 June 2018

VALUE_ERROR (nil)
Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Autocrine motility factor receptor, isoform 2 is a protein that in humans is encoded by the AMFR gene.[1][2]

Autocrine motility factor is a tumor motility-stimulating protein secreted by tumor cells. The protein encoded by this gene is a glycosylated transmembrane protein and a receptor for autocrine motility factor. The receptor, which shows some sequence similarity to tumor protein p53, is localized to the leading and trailing edges of carcinoma cells.[2]

Model organisms

Model organisms have been used in the study of AMFR function. A conditional knockout mouse line, called Amfrtm1a(KOMP)Wtsi[7][8] was generated as part of the International Knockout Mouse Consortium program — a high-throughput mutagenesis project to generate and distribute animal models of disease to interested scientists.[9][10][11]

Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion.[5][12] Twenty six tests were carried out on mutant mice and one significant abnormality was observed: Fewer than expected homozygous mutant mice survived until weaning.[5]

Interactions

AMFR has been shown to interact with Valosin-containing protein.[13][14]

References

  1. Watanabe H, Carmi P, Hogan V, Raz T, Silletti S, Nabi IR, Raz A (Aug 1991). "Purification of human tumor cell autocrine motility factor and molecular cloning of its receptor". J Biol Chem. 266 (20): 13442–8. PMID 1649192.
  2. 2.0 2.1 "Entrez Gene: AMFR autocrine motility factor receptor".
  3. "Salmonella infection data for Amfr". Wellcome Trust Sanger Institute.
  4. "Citrobacter infection data for Amfr". Wellcome Trust Sanger Institute.
  5. 5.0 5.1 5.2 Gerdin AK (2010). "The Sanger Mouse Genetics Programme: High throughput characterisation of knockout mice". Acta Ophthalmologica. 88: 925–7. doi:10.1111/j.1755-3768.2010.4142.x.
  6. Mouse Resources Portal, Wellcome Trust Sanger Institute.
  7. "International Knockout Mouse Consortium".
  8. "Mouse Genome Informatics".
  9. Skarnes, W. C.; Rosen, B.; West, A. P.; Koutsourakis, M.; Bushell, W.; Iyer, V.; Mujica, A. O.; Thomas, M.; Harrow, J.; Cox, T.; Jackson, D.; Severin, J.; Biggs, P.; Fu, J.; Nefedov, M.; De Jong, P. J.; Stewart, A. F.; Bradley, A. (2011). "A conditional knockout resource for the genome-wide study of mouse gene function". Nature. 474 (7351): 337–342. doi:10.1038/nature10163. PMC 3572410. PMID 21677750.
  10. Dolgin E (2011). "Mouse library set to be knockout". Nature. 474 (7351): 262–3. doi:10.1038/474262a. PMID 21677718.
  11. Collins FS, Rossant J, Wurst W (2007). "A Mouse for All Reasons". Cell. 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMID 17218247.
  12. van der Weyden L, White JK, Adams DJ, Logan DW (2011). "The mouse genetics toolkit: revealing function and mechanism". Genome Biol. 12 (6): 224. doi:10.1186/gb-2011-12-6-224. PMC 3218837. PMID 21722353.
  13. Zhong, Xiaoyan; Shen Yuxian; Ballar Petek; Apostolou Andria; Agami Reuven; Fang Shengyun (Oct 2004). "AAA ATPase p97/valosin-containing protein interacts with gp78, a ubiquitin ligase for endoplasmic reticulum-associated degradation". J. Biol. Chem. United States. 279 (44): 45676–84. doi:10.1074/jbc.M409034200. ISSN 0021-9258. PMID 15331598.
  14. Lee, Joon No; Zhang Xiangyu; Feramisco Jamison D; Gong Yi; Ye Jin (Nov 2008). "Unsaturated fatty acids inhibit proteasomal degradation of Insig-1 at a postubiquitination step". J. Biol. Chem. United States. 283 (48): 33772–83. doi:10.1074/jbc.M806108200. ISSN 0021-9258. PMC 2586246. PMID 18835813.

External links

Further reading