Chijiwa Takahito, Yamaguchi Yoko, Ogawa Tomohisa, Deshimaru Masanobu, Nobuhisa Ikuo, Nakashima Kinichi, Oda-Ueda Naoko, Fukumaki Yasuyuki, Hattori Shosaku, Ohno Motonori
Department of Applied Life Science, Faculty of Engineering, Sojo University, 4-22-1 Ikeda, Kumamoto 860-0082, Japan.
J Mol Evol. 2003 Mar;56(3):286-93. doi: 10.1007/s00239-002-2400-7.
Trimeresurus flavoviridis snakes inhabit the southwestern islands of Japan. A phospholipase A(2) (PLA(2)), named PL-Y, was isolated from Okinawa T. flavoviridis venom and its amino acid sequence was determined from both protein and cDNA. PL-Y was unable to induce edema. In contrast, PLA-B, a PLA(2) from Tokunoshima T. flavoviridis venom, which is different at only three positions from PL-Y, is known to induce edema. A new PLA(2), named PLA-B', which is similar to PLA-B, was cloned from Amami-Oshima T. flavoviridis venom gland. Three T. flavoviridis venom basic [Asp(49)]PLA(2) isozymes, PL-Y (Okinawa), PLA-B (Tokunoshima), and PLA-B' (Amami-Oshima), are identical in the N-terminal half but have one to four amino acid substitutions in the beta1-sheet and its vicinity. Such interisland sequence diversities among them are due to isolation in the different environments over 1 to 2 million years and appear to have been brought about by natural selection for point mutation in their genes. Otherwise, a major PLA(2), named PLA2, ubiquitously exists in the venoms of T. flavoviridis snakes from the three islands with one to three synonymous substitutions in their cDNAs. It is assumed that the PLA2 gene is a prototype among T. flavoviridis venom PLA(2) isozyme genes and has hardly undergone nonsynonymous mutation as a principal toxic component. Phylogenetic analysis based on the amino acid sequences revealed that T. flavoviridis PLA(2) isozymes are clearly separated into three groups, PLA2 type, basic [Asp(49)]PLA(2) type, and [Lys(49)]PLA(2) type. Basic [Asp(49)]PLA(2)-type isozymes may manifest their own particular toxic functions different from those of the isozymes of the PLA2 type and [Lys(49)]PLA(2) type.
绿蝮蛇栖息于日本西南诸岛。从冲绳绿蝮蛇毒液中分离出一种磷脂酶A(2)(PLA(2)),命名为PL - Y,并通过蛋白质和cDNA确定了其氨基酸序列。PL - Y不能诱导水肿。相比之下,来自德之岛绿蝮蛇毒液的PLA(2),即PLA - B,与PL - Y仅在三个位置不同,已知其能诱导水肿。从奄美大岛绿蝮蛇毒腺中克隆出一种与PLA - B相似的新PLA(2),命名为PLA - B'。三种绿蝮蛇毒液碱性[天冬氨酸(49)]PLA(2)同工酶,即PL - Y(冲绳)、PLA - B(德之岛)和PLA - B'(奄美大岛),在N端的一半相同,但在β1折叠及其附近有一到四个氨基酸取代。它们之间这种岛屿间的序列差异是由于在100万到200万年的不同环境中隔离造成的,似乎是由其基因点突变的自然选择导致的。否则,一种主要的PLA(2),命名为PLA2,普遍存在于来自这三个岛屿的绿蝮蛇毒液中,其cDNA中有一到三个同义替换。据推测,PLA2基因是绿蝮蛇毒液PLA(2)同工酶基因中的原型,作为主要毒性成分几乎没有经历非同义突变。基于氨基酸序列的系统发育分析表明,绿蝮蛇PLA(2)同工酶明显分为三组,即PLA2型、碱性[天冬氨酸(49)]PLA(2)型和[赖氨酸(49)]PLA(2)型。碱性[天冬氨酸(49)]PLA(2)型同工酶可能表现出与PLA2型和[赖氨酸(49)]PLA(2)型同工酶不同的特殊毒性功能。