Higuchi S, Murayama N, Saguchi K, Ohi H, Fujita Y, Camargo A C, Ogawa T, Deshimaru M, Ohno M
School of Pharmaceutical Sciences, Showa University, Tokyo, Japan.
Immunopharmacology. 1999 Oct 15;44(1-2):129-35. doi: 10.1016/s0162-3109(99)00119-8.
Cloning of cDNAs encoding bradykinin-potentiating peptides (BPPs)-C-type natriuretic peptide (CNP) precursor or its homologue was performed for cDNA libraries of Bothrops jararaca (South American snake), Trimeresurus flavoviridis, Trimeresurus gramineus and Agkistrodon halys blomhoffi (Asian snakes), all belonging to Crotalinae subfamily. Each cDNA library was constructed from the venom glands of a single snake to preclude ambiguity by intraspecies variation in venom components. Thirteen positive clones derived from B. jararaca were divided into two types depending on restriction sites. Differences in the nucleotide sequence arise at three locations and two of them accompanied amino acid conversions. Despite the differences, both types of cDNA clones encode the BPP-CNP precursor of 256 amino acid residues. Sequence analysis demonstrated that cDNA clones from three Asian snakes encode homologues of the BPP-CNP precursor from B. jararaca. In a precursor polypeptide, a signal sequence (approximately 25 aa) at the N-terminus is followed by sequences of BPP or the analogue (5-13 aa) with flanking spacer sequences (indefinite number of aa), an intervening linker sequence (approximately 144 aa) with unidentified function, and a CNP sequence (22 aa) with a preceding processing signal sequence (10 aa). cDNA clones from A. halys blomhoffi encode two distinct peptides in place of BPP, and T. flavoviridis and T. gramineus were shown to have considerably different sequences in the BPP domain from those known as BPP sequences. The present results provide evidence for a wide distribution of the orthologous gene expressing a series of bioactive peptides among Crotalinae subfamily.
对属于蝰蛇亚科的南美蛇类巴西矛头蝮、竹叶青、绿竹叶青和亚洲蝮蛇的cDNA文库进行了编码缓激肽增强肽(BPP)-C型利钠肽(CNP)前体或其同源物的cDNA克隆。每个cDNA文库由一条蛇的毒腺构建而成,以避免毒液成分的种内变异造成的模糊性。从巴西矛头蝮获得的13个阳性克隆根据限制性酶切位点分为两种类型。核苷酸序列在三个位置出现差异,其中两个差异伴随着氨基酸转换。尽管存在差异,但两种类型的cDNA克隆均编码256个氨基酸残基的BPP-CNP前体。序列分析表明,来自三种亚洲蛇的cDNA克隆编码巴西矛头蝮BPP-CNP前体的同源物。在前体多肽中,N端的信号序列(约25个氨基酸)之后是BPP或其类似物的序列(5-13个氨基酸)以及侧翼间隔序列(氨基酸数量不定)、具有未知功能的中间连接序列(约144个氨基酸)和具有前体加工信号序列(10个氨基酸)的CNP序列(22个氨基酸)。亚洲蝮蛇的cDNA克隆编码两种不同的肽来替代BPP,并且竹叶青和绿竹叶青在BPP结构域的序列与已知的BPP序列有很大不同。目前的结果为在蝰蛇亚科中广泛分布表达一系列生物活性肽的直系同源基因提供了证据。