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Diseases associated with API5 include colon [[adenocarcinoma]], and [[cervical cancer]].
Diseases associated with API5 include colon [[adenocarcinoma]], and [[cervical cancer]].


API5 functions in nuclear export of mRNA.<ref>{{cite journal | vauthors = Bong SM, Bae SH, Song B, Gwak H, Yang SW, Kim S, Nam S, Rajalingam K, Oh SJ, Kim TW, Park S, Jang H, Lee BI | title = Regulation of mRNA Export Through API5 and Nuclear FGF2 Interaction. | journal = Nucleic Acids Res. | doi = 10.1093/nar/gkaa335 | pmid= 32383752 | year=2020| doi-access = free | volume = 48 | pmc = 7293033 | pages = 6340–6352 }} </ref>
API5 functions in nuclear export of mRNA.<ref>{{cite journal | vauthors = Bong SM, Bae SH, Song B, Gwak H, Yang SW, Kim S, Nam S, Rajalingam K, Oh SJ, Kim TW, Park S, Jang H, Lee BI | title = Regulation of mRNA Export Through API5 and Nuclear FGF2 Interaction. | journal = Nucleic Acids Res. | doi = 10.1093/nar/gkaa335 | pmid= 32383752 | year=2020| doi-access = free | volume = 48 | issue = 11 | pmc = 7293033 | pages = 6340–6352 }} </ref>


== References==
== References==
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== Further reading ==
== Further reading ==
{{refbegin | 2}}
{{refbegin | 2}}
* {{cite journal | vauthors = Gianfrancesco F, Esposito T, Ciccodicola A, D'Esposito M, Mazzarella R, D'Urso M, Forabosco A | title = Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene | journal = Cytogenetics and Cell Genetics | volume = 84 | issue = 3–4 | pages = 164–6 | year = 1999 | pmid = 10393420 | doi = 10.1159/000015247 }}
* {{cite journal | vauthors = Gianfrancesco F, Esposito T, Ciccodicola A, D'Esposito M, Mazzarella R, D'Urso M, Forabosco A | title = Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene | journal = Cytogenetics and Cell Genetics | volume = 84 | issue = 3–4 | pages = 164–6 | year = 1999 | pmid = 10393420 | doi = 10.1159/000015247 | s2cid = 44601647 }}
* {{cite journal | vauthors = Kim JW, Cho HS, Kim JH, Hur SY, Kim TE, Lee JM, Kim IK, Namkoong SE | title = AAC-11 overexpression induces invasion and protects cervical cancer cells from apoptosis | journal = Laboratory Investigation; A Journal of Technical Methods and Pathology | volume = 80 | issue = 4 | pages = 587–94 | date = April 2000 | pmid = 10780674 | doi = 10.1038/labinvest.3780008 | doi-access = free }}
* {{cite journal | vauthors = Kim JW, Cho HS, Kim JH, Hur SY, Kim TE, Lee JM, Kim IK, Namkoong SE | title = AAC-11 overexpression induces invasion and protects cervical cancer cells from apoptosis | journal = Laboratory Investigation; A Journal of Technical Methods and Pathology | volume = 80 | issue = 4 | pages = 587–94 | date = April 2000 | pmid = 10780674 | doi = 10.1038/labinvest.3780008 | doi-access = free }}
* {{cite journal | vauthors = Van den Berghe L, Laurell H, Huez I, Zanibellato C, Prats H, Bugler B | title = FIF [fibroblast growth factor-2 (FGF-2)-interacting-factor], a nuclear putatively antiapoptotic factor, interacts specifically with FGF-2 | journal = Molecular Endocrinology | volume = 14 | issue = 11 | pages = 1709–24 | date = November 2000 | pmid = 11075807 | doi = 10.1210/me.14.11.1709 | doi-access = free }}
* {{cite journal | vauthors = Van den Berghe L, Laurell H, Huez I, Zanibellato C, Prats H, Bugler B | title = FIF [fibroblast growth factor-2 (FGF-2)-interacting-factor], a nuclear putatively antiapoptotic factor, interacts specifically with FGF-2 | journal = Molecular Endocrinology | volume = 14 | issue = 11 | pages = 1709–24 | date = November 2000 | pmid = 11075807 | doi = 10.1210/me.14.11.1709 | doi-access = free }}
* {{cite journal | vauthors = Sutherland HG, Mumford GK, Newton K, Ford LV, Farrall R, Dellaire G, Cáceres JF, Bickmore WA | title = Large-scale identification of mammalian proteins localized to nuclear sub-compartments | journal = Human Molecular Genetics | volume = 10 | issue = 18 | pages = 1995–2011 | date = September 2001 | pmid = 11555636 | doi = 10.1093/hmg/10.18.1995 | doi-access = free }}
* {{cite journal | vauthors = Sutherland HG, Mumford GK, Newton K, Ford LV, Farrall R, Dellaire G, Cáceres JF, Bickmore WA | title = Large-scale identification of mammalian proteins localized to nuclear sub-compartments | journal = Human Molecular Genetics | volume = 10 | issue = 18 | pages = 1995–2011 | date = September 2001 | pmid = 11555636 | doi = 10.1093/hmg/10.18.1995 | doi-access = free }}
* {{cite journal | vauthors = Li Z, Hu CY, Mo BQ, Xu JD, Zhao Y | title = [Effect of beta-carotene on gene expression of breast cancer cells] | journal = Ai Zheng = Aizheng = Chinese Journal of Cancer | volume = 22 | issue = 4 | pages = 380–4 | date = April 2003 | pmid = 12703993 | doi = }}
* {{cite journal | vauthors = Li Z, Hu CY, Mo BQ, Xu JD, Zhao Y | title = [Effect of beta-carotene on gene expression of breast cancer cells] | journal = AI Zheng = Aizheng = Chinese Journal of Cancer | volume = 22 | issue = 4 | pages = 380–4 | date = April 2003 | pmid = 12703993 | doi = }}
* {{cite journal | vauthors = Andersen JS, Lam YW, Leung AK, Ong SE, Lyon CE, Lamond AI, Mann M | title = Nucleolar proteome dynamics | journal = Nature | volume = 433 | issue = 7021 | pages = 77–83 | date = January 2005 | pmid = 15635413 | doi = 10.1038/nature03207 | bibcode = 2005Natur.433...77A }}
* {{cite journal | vauthors = Andersen JS, Lam YW, Leung AK, Ong SE, Lyon CE, Lamond AI, Mann M | title = Nucleolar proteome dynamics | journal = Nature | volume = 433 | issue = 7021 | pages = 77–83 | date = January 2005 | pmid = 15635413 | doi = 10.1038/nature03207 | bibcode = 2005Natur.433...77A | s2cid = 4344740 }}
* {{cite journal | vauthors = Kim JE, Tannenbaum SR, White FM | title = Global phosphoproteome of HT-29 human colon adenocarcinoma cells | journal = Journal of Proteome Research | volume = 4 | issue = 4 | pages = 1339–46 | year = 2005 | pmid = 16083285 | doi = 10.1021/pr050048h }}
* {{cite journal | vauthors = Kim JE, Tannenbaum SR, White FM | title = Global phosphoproteome of HT-29 human colon adenocarcinoma cells | journal = Journal of Proteome Research | volume = 4 | issue = 4 | pages = 1339–46 | year = 2005 | pmid = 16083285 | doi = 10.1021/pr050048h }}
* {{cite journal | vauthors = Olsen JV, Blagoev B, Gnad F, Macek B, Kumar C, Mortensen P, Mann M | title = Global, in vivo, and site-specific phosphorylation dynamics in signaling networks | journal = Cell | volume = 127 | issue = 3 | pages = 635–48 | date = November 2006 | pmid = 17081983 | doi = 10.1016/j.cell.2006.09.026 }}
* {{cite journal | vauthors = Olsen JV, Blagoev B, Gnad F, Macek B, Kumar C, Mortensen P, Mann M | title = Global, in vivo, and site-specific phosphorylation dynamics in signaling networks | journal = Cell | volume = 127 | issue = 3 | pages = 635–48 | date = November 2006 | pmid = 17081983 | doi = 10.1016/j.cell.2006.09.026 | s2cid = 7827573 }}
* {{cite journal | vauthors = Morris EJ, Michaud WA, Ji JY, Moon NS, Rocco JW, Dyson NJ | title = Functional identification of Api5 as a suppressor of E2F-dependent apoptosis in vivo | journal = PLoS Genetics | volume = 2 | issue = 11 | pages = e196 | date = November 2006 | pmid = 17112319 | pmc = 1636698 | doi = 10.1371/journal.pgen.0020196 }} {{open access}}
* {{cite journal | vauthors = Morris EJ, Michaud WA, Ji JY, Moon NS, Rocco JW, Dyson NJ | title = Functional identification of Api5 as a suppressor of E2F-dependent apoptosis in vivo | journal = PLOS Genetics | volume = 2 | issue = 11 | pages = e196 | date = November 2006 | pmid = 17112319 | pmc = 1636698 | doi = 10.1371/journal.pgen.0020196 }} {{open access}}
* {{cite journal | vauthors = Han BG, Kim KH, Lee SJ, Jeong KC, Cho JW, Noh KH, Kim TW, Kim SJ, Yoon HJ, Suh SW, Lee S, Lee BI | title = Helical repeat structure of apoptosis inhibitor 5 reveals protein-protein interaction modules | journal = J Biol Chem | volume = 287 | pages = 10727-37 | doi = 10.1074/jbc.M111.317594 | pmc = 3322819 | pmid=22334682 | year=2012}}
* {{cite journal | vauthors = Han BG, Kim KH, Lee SJ, Jeong KC, Cho JW, Noh KH, Kim TW, Kim SJ, Yoon HJ, Suh SW, Lee S, Lee BI | title = Helical repeat structure of apoptosis inhibitor 5 reveals protein-protein interaction modules | journal = J Biol Chem | volume = 287 | pages = 10727–37 | doi = 10.1074/jbc.M111.317594 | pmc = 3322819 | pmid=22334682 | year=2012| issue = 14 }}
* {{cite journal | vauthors = Bong SM, Bae SH, Song B, Gwak H, Yang SW, Kim S, Nam S, Rajalingam K, Oh SJ, Kim TW, Park S, Jang H, Lee BI | title = Regulation of mRNA Export Through API5 and Nuclear FGF2 Interaction. | journal = Nucleic Acids Res. | doi = 10.1093/nar/gkaa335 | pmid= 32383752 | year=2020| doi-access = free | volume = 48 | pmc = 7293033 | pages = 6340–6352 }}
* {{cite journal | vauthors = Bong SM, Bae SH, Song B, Gwak H, Yang SW, Kim S, Nam S, Rajalingam K, Oh SJ, Kim TW, Park S, Jang H, Lee BI | title = Regulation of mRNA Export Through API5 and Nuclear FGF2 Interaction. | journal = Nucleic Acids Res. | doi = 10.1093/nar/gkaa335 | pmid= 32383752 | year=2020| doi-access = free | volume = 48 | issue = 11 | pmc = 7293033 | pages = 6340–6352 }}
{{refend}}
{{refend}}

Revision as of 08:32, 11 October 2020

API5
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesAPI5, AAC-11, AAC11, apoptosis inhibitor 5
External IDsOMIM: 609774; MGI: 1888993; HomoloGene: 4809; GeneCards: API5; OMA:API5 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001142930
NM_001142931
NM_001243747
NM_006595

NM_007466
NM_001305258
NM_001349003

RefSeq (protein)

NP_001136402
NP_001136403
NP_001230676
NP_006586

NP_001292187
NP_031492
NP_001335932

Location (UCSC)Chr 11: 43.31 – 43.34 MbChr 2: 94.24 – 94.27 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

The human gene API5 encodes the protein Apoptosis inhibitor 5.[5][6]

This gene encodes an apoptosis inhibitory protein whose expression prevents apoptosis after growth factor deprivation. This protein suppresses the transcription factor E2F1-induced apoptosis and also interacts with, and negatively regulates acinus, a nuclear factor involved in apoptotic DNA fragmentation. Its depletion enhances the cytotoxic action of chemotherapeutic drugs. Crystal structure of API5 exhibited the function for protein-protein interaction [7]

Diseases associated with API5 include colon adenocarcinoma, and cervical cancer.

API5 functions in nuclear export of mRNA.[8]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000166181Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000027193Ensembl, 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. ^ Tewari M, Yu M, Ross B, Dean C, Giordano A, Rubin R (September 1997). "AAC-11, a novel cDNA that inhibits apoptosis after growth factor withdrawal". Cancer Research. 57 (18): 4063–9. PMID 9307294.
  6. ^ "Entrez Gene: API5 apoptosis inhibitor 5".
  7. ^ Han BG, Kim KH, Lee SJ, Jeong KC, Cho JW, Noh KH, Kim TW, Kim SJ, Yoon HJ, Suh SW, Lee S, Lee BI (March 2012). "Helical repeat structure of apoptosis inhibitor 5 reveals protein-protein interaction modules". The Journal of Biological Chemistry. 287 (14): 10727–37. doi:10.1074/jbc.M111.317594. PMC 3322819. PMID 22334682.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  8. ^ Bong SM, Bae SH, Song B, Gwak H, Yang SW, Kim S, Nam S, Rajalingam K, Oh SJ, Kim TW, Park S, Jang H, Lee BI (2020). "Regulation of mRNA Export Through API5 and Nuclear FGF2 Interaction". Nucleic Acids Res. 48 (11): 6340–6352. doi:10.1093/nar/gkaa335. PMC 7293033. PMID 32383752.

Further reading