LITAF

LITAF
Identifiers
Aliases	LITAF, PIG7, SIMPLE, TP53I7, lipopolysaccharide induced TNF factor
External IDs	OMIM: 603795; MGI: 1929512; HomoloGene: 37974; GeneCards: LITAF; OMA:LITAF - orthologs
Gene location (Human) Chr. Chromosome 16 (human) Band 16p13.13 Start 11,547,722 bp End 11,636,381 bp
Gene location (Mouse) Chr. Chromosome 16 (mouse) Band 16|16 A1 Start 10,777,139 bp End 10,884,021 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in blood palpebral conjunctiva periodontal fiber visceral pleura mucosa of urinary bladder appendix tibia granulocyte canal of the cervix gallbladder Top expressed in granulocyte endothelial cell of lymphatic vessel stroma of bone marrow blood decidua vestibular sensory epithelium left colon gastrula vestibular membrane of cochlear duct skin of external ear More reference expression data BioGPS More reference expression data
Gene ontology Molecular function signal transducer activity protein binding WW domain binding zinc ion binding RNA polymerase II cis-regulatory region sequence-specific DNA binding DNA-binding transcription activator activity, RNA polymerase II-specific DNA binding metal ion binding Cellular component membrane nucleoplasm lysosomal membrane lysosome cytosol cytoplasmic side of plasma membrane cytoplasmic side of early endosome membrane cytoplasmic side of late endosome membrane cytoplasmic side of lysosomal membrane Golgi membrane nucleus cytoplasm endosome Golgi apparatus plasma membrane endosome membrane early endosome membrane late endosome membrane intracellular membrane-bounded organelle integral component of membrane Biological process regulation of transcription, DNA-templated regulation of transcription by RNA polymerase II ageing transcription, DNA-templated regulation of cytokine production response to lipopolysaccharide positive regulation of I-kappaB kinase/NF-kappaB signaling cellular response to lipopolysaccharide signal transduction transcription by RNA polymerase II positive regulation of transcription by RNA polymerase II Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 9516 56722 Ensembl ENSG00000189067 ENSMUSG00000022500 UniProt Q99732 Q9JLJ0 RefSeq (mRNA) NM_001136472 NM_001136473 NM_004862 NM_019980 RefSeq (protein) NP_001129944 NP_001129945 NP_004853 NP_064364 Location (UCSC) Chr 16: 11.55 – 11.64 Mb Chr 16: 10.78 – 10.88 Mb PubMed search
Wikidata
View/Edit Human View/Edit Mouse

Lipopolysaccharide-induced tumor necrosis factor-alpha factor is a protein that in humans is encoded by the LITAF gene.

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

External links

• GeneReviews/NCBI/NIH/UW entry on Charcot-Marie-Tooth Neuropathy Type 1

Further reading

• Jolliffe CN, Harvey KF, Haines BP, et al. (2001). "Identification of multiple proteins expressed in murine embryos as binding partners for the WW domains of the ubiquitin-protein ligase Nedd4". Biochem. J. 351 (3): 557–65. doi:10.1042/0264-6021:3510557. PMC 1221394. PMID 11042109.
• Moriwaki Y, Begum NA, Kobayashi M, et al. (2001). "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". J. Biol. Chem. 276 (25): 23065–76. doi:10.1074/jbc.M011660200. PMID 11274176.
• Street VA, Goldy JD, Golden AS, et al. (2002). "Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathies". Am. J. Hum. Genet. 70 (1): 244–50. doi:10.1086/337943. PMC 384893. PMID 11713717.
• 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.
• Street VA, Bennett CL, Goldy JD, et al. (2003). "Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C". Neurology. 60 (1): 22–6. doi:10.1212/wnl.60.1.22. PMID 12525712.
• Matsuda A, Suzuki Y, Honda G, et al. (2003). "Large-scale identification and characterization of human genes that activate NF-kappaB and MAPK signaling pathways". Oncogene. 22 (21): 3307–18. doi:10.1038/sj.onc.1206406. PMID 12761501.
• Street VA, Bennett CL, Bird TD, Chance PF (2004). "New gene for CMT". J. Peripher. Nerv. Syst. 8 (4): 206. doi:10.1111/j.1085-9489.2003.03025.x. PMID 14641644.
• 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.
• Ludes-Meyers JH, Kil H, Bednarek AK, et al. (2004). "WWOX binds the specific proline-rich ligand PPXY: identification of candidate interacting proteins". Oncogene. 23 (29): 5049–55. doi:10.1038/sj.onc.1207680. PMC 4143251. PMID 15064722.
• Bennett CL, Shirk AJ, Huynh HM, et al. (2004). "SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve". Ann. Neurol. 55 (5): 713–20. doi:10.1002/ana.20094. PMID 15122712.
• Matsumura Y, Matsumura Y, Nishigori C, et al. (2004). "PIG7/LITAF gene mutation and overexpression of its gene product in extramammary Paget's disease". Int. J. Cancer. 111 (2): 218–23. doi:10.1002/ijc.20251. PMID 15197774.
• 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.
• Saifi GM, Szigeti K, Wiszniewski W, et al. (2006). "SIMPLE mutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation". Hum. Mutat. 25 (4): 372–83. doi:10.1002/humu.20153. PMID 15776429.
• Meggouh F, de Visser M, Arts WF, et al. (2005). "Early onset neuropathy in a compound form of Charcot-Marie-Tooth disease". Ann. Neurol. 57 (4): 589–91. doi:10.1002/ana.20434. PMID 15786462.
• Tang X, Marciano DL, Leeman SE, Amar S (2005). "LPS induces the interaction of a transcription factor, LPS-induced TNF-alpha factor, and STAT6(B) with effects on multiple cytokines". Proc. Natl. Acad. Sci. U.S.A. 102 (14): 5132–7. doi:10.1073/pnas.0501159102. PMC 555602. PMID 15793005.
• Beauvais K, Furby A, Latour P (2006). "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". Neuromuscul. Disord. 16 (1): 14–8. doi:10.1016/j.nmd.2005.09.008. PMID 16373087.
• Latour P, Gonnaud PM, Ollagnon E, et al. (2006). "SIMPLE mutation analysis in dominant demyelinating Charcot-Marie-Tooth disease: three novel mutations". J. Peripher. Nerv. Syst. 11 (2): 148–55. doi:10.1111/j.1085-9489.2006.00080.x. PMID 16787513.
• Stucchi A, Reed K, O'Brien M, et al. (2007). "A new transcription factor that regulates TNF-alpha gene expression, LITAF, is increased in intestinal tissues from patients with CD and UC". Inflamm. Bowel Dis. 12 (7): 581–7. doi:10.1097/01.MIB.0000225338.14356.d5. PMID 16804395.