Egan T M, Cox J A, Voigt M M
Department of Pharmacological and Physiological Sciences, Saint Louis University School of Medicine, 1402 S. Grand Blvd., 63104, St. Louis, MO 63104, USA.
FEBS Lett. 2000 Jun 23;475(3):287-90. doi: 10.1016/s0014-5793(00)01685-9.
We describe a P2X subunit cloned from the zebrafish (Danio rerio) that is an orthologue of the mammalian P2X(3) subunit. Like the mammalian P2X(3), this receptor desensitizes rapidly in the presence of agonist. However, it differs in that alphabeta-meATP is a much less potent agonist than ATP and the antagonist TNP-ATP is not active at low nanomolar concentrations. Similar to the rat P2X(3) subunit, the zebrafish subunit forms hetero-oligomeric assemblies with the rat P2X(2) that possesses a phenotype distinct from either parent. This novel clone will provide an important basis for future experiments investigating the structure/function relationships of P2X subunit domains.
我们描述了一种从斑马鱼(Danio rerio)中克隆出的P2X亚基,它是哺乳动物P2X(3)亚基的直系同源物。与哺乳动物P2X(3)一样,该受体在激动剂存在下会迅速脱敏。然而,它的不同之处在于,αβ-ATP是一种比ATP效力低得多的激动剂,并且拮抗剂TNP-ATP在低纳摩尔浓度下没有活性。与大鼠P2X(3)亚基类似,斑马鱼亚基与大鼠P2X(2)形成异源寡聚体,其表型与任一亲本都不同。这个新克隆将为未来研究P2X亚基结构/功能关系的实验提供重要基础。