From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
Translation initiation factor eIF-2B subunit gamma is a
protein that in humans is encoded by the EIF2B3
gene .
[5]
[6]
References
^
a
b
c
GRCh38: Ensembl release 89: ENSG00000070785 –
Ensembl , May 2017
^
a
b
c
GRCm38: Ensembl release 89: ENSMUSG00000028683 –
Ensembl , May 2017
^
"Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^
"Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ Kruger M, Beger C, Li QX, Welch PJ, Tritz R, Leavitt M, Barber JR, Wong-Staal F (Aug 2000).
"Identification of eIF2Bgamma and eIF2gamma as cofactors of hepatitis C virus internal ribosome entry site-mediated translation using a functional genomics approach" . Proc Natl Acad Sci U S A . 97 (15): 8566–71.
Bibcode :
2000PNAS...97.8566K .
doi :
10.1073/pnas.97.15.8566 .
PMC
26988 .
PMID
10900014 .
^
"Entrez Gene: EIF2B3 eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa" .
Further reading
Welsh GI, Miyamoto S, Price NT, et al. (1996).
"T-cell activation leads to rapid stimulation of translation initiation factor eIF2B and inactivation of glycogen synthase kinase-3" . J. Biol. Chem . 271 (19): 11410–3.
doi :
10.1074/jbc.271.19.11410 .
PMID
8626696 .
Gomez E, Pavitt GD (2000).
"Identification of domains and residues within the epsilon subunit of eukaryotic translation initiation factor 2B (eIF2Bepsilon) required for guanine nucleotide exchange reveals a novel activation function promoted by eIF2B complex formation" . Mol. Cell. Biol . 20 (11): 3965–76.
doi :
10.1128/MCB.20.11.3965-3976.2000 .
PMC
85753 .
PMID
10805739 .
Anthony TG, Fabian JR, Kimball SR, Jefferson LS (2000). "Identification of domains within the epsilon-subunit of the translation initiation factor eIF2B that are necessary for guanine nucleotide exchange activity and eIF2B holoprotein formation". Biochim. Biophys. Acta . 1492 (1): 56–62.
doi :
10.1016/S0167-4781(00)00062-2 .
PMID
10858531 .
Hartley JL, Temple GF, Brasch MA (2001).
"DNA cloning using in vitro site-specific recombination" . Genome Res . 10 (11): 1788–95.
doi :
10.1101/gr.143000 .
PMC
310948 .
PMID
11076863 .
Wiemann S, Weil B, Wellenreuther R, et al. (2001).
"Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs" . Genome Res . 11 (3): 422–35.
doi :
10.1101/gr.GR1547R .
PMC
311072 .
PMID
11230166 .
Williams DD, Price NT, Loughlin AJ, Proud CG (2001).
"Characterization of the mammalian initiation factor eIF2B complex as a GDP dissociation stimulator protein" . J. Biol. Chem . 276 (27): 24697–703.
doi :
10.1074/jbc.M011788200 .
PMID
11323413 .
van der Knaap MS, Leegwater PA, Könst AA, et al. (2002). "Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter". Ann. Neurol . 51 (2): 264–70.
doi :
10.1002/ana.10112 .
PMID
11835386 .
S2CID
1849575 .
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.
Bibcode :
2002PNAS...9916899M .
doi :
10.1073/pnas.242603899 .
PMC
139241 .
PMID
12477932 .
Fogli A, Dionisi-Vici C, Deodato F, et al. (2003). "A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation". Neurology . 59 (12): 1966–8.
doi :
10.1212/01.wnl.0000041666.76863.47 .
PMID
12499492 .
S2CID
13129517 .
Fogli A, Rodriguez D, Eymard-Pierre E, et al. (2003).
"Ovarian failure related to eukaryotic initiation factor 2B mutations" . Am. J. Hum. Genet . 72 (6): 1544–50.
doi :
10.1086/375404 .
PMC
1180314 .
PMID
12707859 .
Ota T, Suzuki Y, Nishikawa T, et al. (2004).
"Complete sequencing and characterization of 21,243 full-length human cDNAs" . Nat. Genet . 36 (1): 40–5.
doi :
10.1038/ng1285 .
PMID
14702039 .
Fogli A, Schiffmann R, Hugendubler L, et al. (2005).
"Decreased guanine nucleotide exchange factor activity in eIF2B-mutated patients" . Eur. J. Hum. Genet . 12 (7): 561–6.
doi :
10.1038/sj.ejhg.5201189 .
PMID
15054402 .
Li W, Wang X, Van Der Knaap MS, Proud CG (2004).
"Mutations linked to leukoencephalopathy with vanishing white matter impair the function of the eukaryotic initiation factor 2B complex in diverse ways" . Mol. Cell. Biol . 24 (8): 3295–306.
doi :
10.1128/MCB.24.8.3295-3306.2004 .
PMC
381664 .
PMID
15060152 .
Van Haren K, van der Voorn JP, Peterson DR, et al. (2004).
"The life and death of oligodendrocytes in vanishing white matter disease" . J. Neuropathol. Exp. Neurol . 63 (6): 618–30.
doi :
10.1093/jnen/63.6.618 .
PMID
15217090 .
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 .
Wiemann S, Arlt D, Huber W, et al. (2004).
"From ORFeome to biology: a functional genomics pipeline" . Genome Res . 14 (10B): 2136–44.
doi :
10.1101/gr.2576704 .
PMC
528930 .
PMID
15489336 .
Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature . 437 (7062): 1173–8.
Bibcode :
2005Natur.437.1173R .
doi :
10.1038/nature04209 .
PMID
16189514 .
S2CID
4427026 .
Suragani RN, Kamindla R, Ehtesham NZ, Ramaiah KV (2006). "Interaction of recombinant human eIF2 subunits with eIF2B and eIF2alpha kinases". Biochem. Biophys. Res. Commun . 338 (4): 1766–72.
doi :
10.1016/j.bbrc.2005.10.150 .
PMID
16288713 .
Mikami S, Masutani M, Sonenberg N, et al. (2006).
"An efficient mammalian cell-free translation system supplemented with translation factors" . Protein Expr. Purif . 46 (2): 348–57.
doi :
10.1016/j.pep.2005.09.021 .
PMID
16289705 .