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LITAF

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{{Short description|Protein-coding gene in the species Homo sapiens}}

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Lipopolysaccharide-induced tumor necrosis factor-alpha factor is a protein that in humans is encoded by the LITAF gene.{{cite journal |vauthors=Polyak K, Xia Y, Zweier JL, Kinzler KW, Vogelstein B | title = A model for p53-induced apoptosis | journal = Nature | volume = 389 | issue = 6648 | pages = 300–5 |date=Sep 1997 | pmid = 9305847 | doi = 10.1038/38525 | bibcode = 1997Natur.389..300P | s2cid = 4429638 }}{{cite journal |vauthors=Myokai F, Takashiba S, Lebo R, Amar S | title = A novel lipopolysaccharide-induced transcription factor regulating tumor necrosis factor alpha gene expression: molecular cloning, sequencing, characterization, and chromosomal assignment | journal = Proc Natl Acad Sci U S A | volume = 96 | issue = 8 | pages = 4518–23 |date=May 1999 | pmid = 10200294 | pmc = 16364 | doi =10.1073/pnas.96.8.4518 | bibcode = 1999PNAS...96.4518M | doi-access = free }}{{cite web | title = Entrez Gene: LITAF lipopolysaccharide-induced TNF factor| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=9516}}

It is associated with Charcot–Marie–Tooth disease 1C.

References

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External links

  • [https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=cmt1 GeneReviews/NCBI/NIH/UW entry on Charcot-Marie-Tooth Neuropathy Type 1]

Further reading

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  • {{cite journal |vauthors=Jolliffe CN, Harvey KF, Haines BP, etal |title=Identification of multiple proteins expressed in murine embryos as binding partners for the WW domains of the ubiquitin-protein ligase Nedd4. |journal=Biochem. J. |volume=351 |issue= 3|pages= 557–65 |year= 2001 |pmid= 11042109 |doi= 10.1042/0264-6021:3510557| pmc=1221394 }}
  • {{cite journal |vauthors=Moriwaki Y, Begum NA, Kobayashi M, etal |title=Mycobacterium bovis Bacillus Calmette-Guerin and its cell wall complex induce a novel lysosomal membrane protein, SIMPLE, that bridges the missing link between lipopolysaccharide and p53-inducible gene, LITAF(PIG7), and estrogen-inducible gene, EET-1. |journal=J. Biol. Chem. |volume=276 |issue= 25 |pages= 23065–76 |year= 2001 |pmid= 11274176 |doi= 10.1074/jbc.M011660200 |doi-access= free }}
  • {{cite journal |vauthors=Street VA, Goldy JD, Golden AS, etal |title=Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathies. |journal=Am. J. Hum. Genet. |volume=70 |issue= 1 |pages= 244–50 |year= 2002 |pmid= 11713717 |doi=10.1086/337943 | pmc=384893 }}
  • {{cite journal |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |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 |bibcode=2002PNAS...9916899M |doi-access=free }}
  • {{cite journal |vauthors=Street VA, Bennett CL, Goldy JD, etal |title=Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C. |journal=Neurology |volume=60 |issue= 1 |pages= 22–6 |year= 2003 |pmid= 12525712 |doi= 10.1212/wnl.60.1.22|s2cid=7495837 }}
  • {{cite journal |vauthors=Matsuda A, Suzuki Y, Honda G, etal |title=Large-scale identification and characterization of human genes that activate NF-kappaB and MAPK signaling pathways. |journal=Oncogene |volume=22 |issue= 21 |pages= 3307–18 |year= 2003 |pmid= 12761501 |doi= 10.1038/sj.onc.1206406 |s2cid=38880905 |doi-access= }}
  • {{cite journal |vauthors=Street VA, Bennett CL, Bird TD, Chance PF |title=New gene for CMT. |journal=J. Peripher. Nerv. Syst. |volume=8 |issue= 4 |pages= 206 |year= 2004 |pmid= 14641644 |doi=10.1111/j.1085-9489.2003.03025.x |s2cid=12117063 }}
  • {{cite journal |vauthors=Ota T, Suzuki Y, Nishikawa T, etal |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 |doi-access= free }}
  • {{cite journal |vauthors=Ludes-Meyers JH, Kil H, Bednarek AK, etal |title=WWOX binds the specific proline-rich ligand PPXY: identification of candidate interacting proteins. |journal=Oncogene |volume=23 |issue= 29 |pages= 5049–55 |year= 2004 |pmid= 15064722 |doi= 10.1038/sj.onc.1207680 |pmc=4143251 }}
  • {{cite journal |vauthors=Bennett CL, Shirk AJ, Huynh HM, etal |title=SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve. |journal=Ann. Neurol. |volume=55 |issue= 5 |pages= 713–20 |year= 2004 |pmid= 15122712 |doi= 10.1002/ana.20094 |s2cid=7719672 }}
  • {{cite journal |vauthors=Matsumura Y, Matsumura Y, Nishigori C, etal |title=PIG7/LITAF gene mutation and overexpression of its gene product in extramammary Paget's disease. |journal=Int. J. Cancer |volume=111 |issue= 2 |pages= 218–23 |year= 2004 |pmid= 15197774 |doi= 10.1002/ijc.20251 |s2cid=27155753 }}
  • {{cite journal |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |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 }}
  • {{cite journal |vauthors=Saifi GM, Szigeti K, Wiszniewski W, etal |title=SIMPLE mutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation. |journal=Hum. Mutat. |volume=25 |issue= 4 |pages= 372–83 |year= 2006 |pmid= 15776429 |doi= 10.1002/humu.20153 |s2cid=20127440 }}
  • {{cite journal |vauthors=Meggouh F, de Visser M, Arts WF, etal |title=Early onset neuropathy in a compound form of Charcot-Marie-Tooth disease. |journal=Ann. Neurol. |volume=57 |issue= 4 |pages= 589–91 |year= 2005 |pmid= 15786462 |doi= 10.1002/ana.20434 |s2cid=32014135 }}
  • {{cite journal |vauthors=Tang X, Marciano DL, Leeman SE, Amar S |title=LPS induces the interaction of a transcription factor, LPS-induced TNF-alpha factor, and STAT6(B) with effects on multiple cytokines. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=102 |issue= 14 |pages= 5132–7 |year= 2005 |pmid= 15793005 |doi= 10.1073/pnas.0501159102 | pmc=555602 |bibcode=2005PNAS..102.5132T |doi-access=free }}
  • {{cite journal |vauthors=Beauvais K, Furby A, Latour P |title=Clinical, electrophysiological and molecular genetic studies in a family with X-linked dominant Charcot-Marie-Tooth neuropathy presenting a novel mutation in GJB1 Promoter and a rare polymorphism in LITAF/SIMPLE. |journal=Neuromuscul. Disord. |volume=16 |issue= 1 |pages= 14–8 |year= 2006 |pmid= 16373087 |doi= 10.1016/j.nmd.2005.09.008 |s2cid=32730191 }}
  • {{cite journal |vauthors=Latour P, Gonnaud PM, Ollagnon E, etal |title=SIMPLE mutation analysis in dominant demyelinating Charcot-Marie-Tooth disease: three novel mutations. |journal=J. Peripher. Nerv. Syst. |volume=11 |issue= 2 |pages= 148–55 |year= 2006 |pmid= 16787513 |doi= 10.1111/j.1085-9489.2006.00080.x |s2cid=24702162 |doi-access=free }}
  • {{cite journal |vauthors=Stucchi A, Reed K, O'Brien M, etal |title=A new transcription factor that regulates TNF-alpha gene expression, LITAF, is increased in intestinal tissues from patients with CD and UC. |journal=Inflamm. Bowel Dis. |volume=12 |issue= 7 |pages= 581–7 |year= 2007 |pmid= 16804395 |doi= 10.1097/01.MIB.0000225338.14356.d5 |s2cid=28836872 |doi-access=free }}

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