Hyodo Susumu, Kawakoshi Akatsuki, Bartolo Ray C, Takei Yoshio, Toop Tes, Donald John A
Laboratory of Physiology, Ocean Research Institute, University of Tokyo, Nakano, Tokyo 164-8639, Japan.
Gen Comp Endocrinol. 2006 Sep 1;148(2):181-6. doi: 10.1016/j.ygcen.2006.02.014. Epub 2006 Apr 18.
C-type natriuretic peptide (CNP) is a crucial osmoregulatory hormone in elasmobranchs, participating in salt secretion and drinking. In contrast to teleosts and tetrapods in which the NP family is composed of a group of structurally related peptides, we have shown that CNP is the sole NP in sharks. In the present study, CNP cDNAs were cloned from four species of batoids, another group of elasmobranchs. The cloned batoid CNP precursors contained a plausible mature peptide of 22 amino acid residues that is identical to most shark CNP-22s, but five successive amino acids were consistently deleted in the prosegment compared with shark precursors, supporting the diphyletic classification of sharks and rays. In addition, molecular phylogenetic trees of CNP precursors were consistent with a diphyletic interpretation. Except for the deletion, the nucleotide and deduced amino acid sequences of the CNP cDNAs are extremely well-conserved among all elasmobranch species, even between sharks and rays. Surprisingly, high conservation is evident not only for the coding region, but also for the untranslated regions. It is most likely that the high conservation is due to the low nucleotide substitution rate in the elasmobranch genome, and high selection pressure. The 3'-untranslated region of the elasmobranch CNP cDNAs contained three to six repeats of the ATTTA motif that is associated with the regulation of mRNA stability and translation efficiency. Alternative polyadenylation sites were also found; the long 3'-untranslated region contains a core of ATTTA motifs while the short form has only one or no ATTTA motif, indicating that the post-transcriptional modification of mRNA is important for regulation of CNP synthesis. These characteristics in the 3'-untranslated region were conserved among all elasmobranch CNP cDNAs. Since CNP has been implicated as a fast-acting hormone to facilitate salt secretion from the rectal gland, the conserved 3'-untranslated region most likely contributes to rapid regulation of CNP synthesis in elasmobranchs in response to acute changes in internal and external environments.
C型利钠肽(CNP)是软骨鱼类中一种关键的渗透压调节激素,参与盐分分泌和饮水过程。与硬骨鱼类和四足动物不同,在硬骨鱼类和四足动物中,利钠肽家族由一组结构相关的肽组成,而我们已经证明,CNP是鲨鱼体内唯一的利钠肽。在本研究中,从另外一组软骨鱼类——四种鲼形目鱼类中克隆出了CNP cDNA。克隆出的鲼形目CNP前体包含一个由22个氨基酸残基组成的合理成熟肽,这与大多数鲨鱼的CNP-22相同,但与鲨鱼前体相比,前肽段中连续五个氨基酸一直缺失,这支持了鲨鱼和鲼形目鱼类的双系分类。此外,CNP前体的分子系统发育树与双系解释一致。除了缺失部分外,所有软骨鱼类物种中CNP cDNA的核苷酸和推导的氨基酸序列都极其保守,甚至在鲨鱼和鲼形目鱼类之间也是如此。令人惊讶的是,不仅编码区高度保守,非翻译区也高度保守。很可能这种高度保守是由于软骨鱼类基因组中核苷酸替换率低以及选择压力大。软骨鱼类CNP cDNA的3'非翻译区包含三到六个ATTTA基序重复,该基序与mRNA稳定性和翻译效率的调节有关。还发现了可变聚腺苷酸化位点;长的3'非翻译区包含ATTTA基序核心,而短形式只有一个或没有ATTTA基序,这表明mRNA的转录后修饰对CNP合成的调节很重要。3'非翻译区的这些特征在所有软骨鱼类CNP cDNA中都保守。由于CNP被认为是一种快速作用的激素,有助于直肠腺分泌盐分,保守的3'非翻译区很可能有助于软骨鱼类在内部和外部环境发生急性变化时快速调节CNP合成。