Holgate Stephen T, Davies Donna E, Powell Rob M, Holloway John W
Infection, Inflammation, and Repair Division, School of Medicine, University of Southampton, Southampton General Hospital, Tremona Road, Southampton, Hampshire, SO16 6YD, UK.
Immunol Allergy Clin North Am. 2005 Nov;25(4):655-68. doi: 10.1016/j.iac.2005.07.003.
There is much to find out about this fascinating and complex molecule in relation to the development and progression of asthma. Added to it are three further new asthma/allergy genes identified by positional cloning: PDH Finger Protein II (PHF11) on chromosome 13q14, which encodes NY-REN-34 a protein first described in patients with renal cell carcinoma [67]; Dipeptidyl diptidase 10 (DDP10) on chromosome 2q14 [68]; and G protein-coupled receptor for asthma susceptibility (GPRA) on chromosome 7p [69]. For each of these genes, as is the case for ADAM33, determining their normal function(s) and how these become disordered in asthma is the future challenge.
关于这种迷人而复杂的分子与哮喘的发生和发展,仍有许多有待发现的地方。此外,通过定位克隆又鉴定出另外三个新的哮喘/过敏相关基因:位于13q14染色体上的PDH指蛋白II(PHF11),它编码NY-REN-34,一种最初在肾细胞癌患者中发现的蛋白质[67];位于2q14染色体上的二肽基肽酶10(DDP10)[68];以及位于7p染色体上的哮喘易感性G蛋白偶联受体(GPRA)[69]。对于这些基因中的每一个,就像ADAM33的情况一样,确定它们的正常功能以及这些功能在哮喘中如何紊乱是未来的挑战。