词条 | TMEM18 |
释义 |
FunctionTMEM18 seems to affect energy levels through insulin and glucagon signaling, and in flies, its downregulation induces a metabolic state resembling type-II diabetes[2] Overexpression of the TMEM18 protein increases the migration capacity of neural stem cells while inactivation of TMEM18 results in almost complete loss of migration activity.[3] The TMEM18 gene is ubiquitously expressed in both mammalian and fly tissues,[2] which suggests a basic cellular function. In the mouse brain, it is found in the majority of all cells, but is more abundant in neurons than other cell types.[5] Clinical significanceGenetic variants in the proximity of the TMEM18 gene are associated with obesity,[4][5][6][7][8] insulin levels, and blood sugar levels [2] Evolutionary historyThe TMEM18 gene has a long evolutionary history as it is present in both plants and animals.[2][4] The TMEM18 protein's amino acid sequence is well conserved, which suggests that it has retained its function since the divergence of human and plants. The gene seems to have been lost in two separate lineages, but is not found duplicated in any analyzed genomes. Hence, it is not essential for eukaryotic organisms, but there appears to be selection against multiple copies of the TMEM18 gene.[2] References1. ^{{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 |date=December 2002 | pmid = 12477932 | pmc = 139241 | doi = 10.1073/pnas.242603899 | url = }} 2. ^1 2 3 4 {{cite journal | vauthors = Wiemerslage L, Gohel PA, Maestri G, Hilmarsson TG, Mickael M, Fredriksson R, Williams MJ, Schioth HB | title = The Drosophila ortholog of TMEM18 regulates insulin and glucagon-like signaling. | journal = J Endocrinol | year = 2016 | pmid = 27029472 | doi = 10.1530/JOE-16-0040 | volume=229 | pages=233–43}} 3. ^{{cite journal | vauthors = Jurvansuu J, Zhao Y, Leung DS, Boulaire J, Yu YH, Ahmed S, Wang S | title = Transmembrane protein 18 enhances the tropism of neural stem cells for glioma cells | journal = Cancer Res. | volume = 68 | issue = 12 | pages = 4614–22 |date=June 2008 | pmid = 18559506 | doi = 10.1158/0008-5472.CAN-07-5291 | url = }} 4. ^1 2 {{cite journal | vauthors = Almén MS, Jacobsson JA, Shaik JH, Olszewski PK, Cedernaes J, Alsiö J,Sreedharan S, Levine AS, Fredriksson R, Marcus C, Schiöth HB| title = The obesity gene, TMEM18, is of ancient origin, found in majority of neuronal cells in all major brain regions and associated with obesity in severely obese children| journal = BMC Med. Genet. | volume = 11 | pages = 58 |date=April 2010 | pmid = 20380707 | pmc = 2858727| doi = 10.1186/1471-2350-11-58 | url =http://www.biomedcentral.com/1471-2350/11/58/abstract }} 5. ^{{cite journal |vauthors=Thorleifsson G, Walters GB, Gudbjartsson DF, etal |title=Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity |journal= Nat. Genet. |volume= 41 |issue= 1 |pages= 18–24 |date=January 2009 |pmid=19079260 |doi= 10.1038/ng.274|url= }} 6. ^{{cite journal |vauthors=Willer CJ, Speliotes EK, Loos RJ, etal |title=Six new loci associated with body mass index highlight a neuronal influence on body weight regulation |journal= Nat. Genet. |volume= 41 |issue= 1 |pages= 24–34 |date=January 2009 |pmid=19079261 |doi= 10.1038/ng.287|url= |pmc= 2695662 }} 7. ^{{cite journal |vauthors=Zhao J, Bradfield JP, Li M, etal |title=The role of obesity-associated loci identified in genome wide association studies in the determination of pediatric BMI |journal=Obesity (Silver Spring) |volume= 17|issue= 12|pages= 2254–7|date=May 2009 |pmid=19478790 |doi=10.1038/oby.2009.159 |pmc=2860782}} 8. ^{{cite journal | vauthors = Renström F, Payne F, Nordström A, Brito EC, Rolandsson O, Hallmans G, Barroso I, Nordström P, Franks PW | title = Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden | journal = Hum. Mol. Genet. | volume = 18 | issue = 8 | pages = 1489–96 |date=April 2009 | pmid = 19164386 | pmc = 2664142 | doi = 10.1093/hmg/ddp041 | url = }} Further reading{{refbegin | 2}}
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