Kim Hyun-Woo, Batista Luisa A, Hoppes Jodi L, Lee Kara J, Mykles Donald L
Department of Biology, Colorado State University, Fort Collins, CO 80523, USA.
J Exp Biol. 2004 Jul;207(Pt 16):2845-57. doi: 10.1242/jeb.01117.
NO signaling is involved in many physiological processes in invertebrates. In crustaceans, it plays a role in the regulation of the nervous system and muscle contraction. Nested reverse transcription-polymerase chain reaction (RT-PCR) and 5' and 3' rapid amplification of cDNA ends (RACE) PCR generated a full-length cDNA sequence (3982 bp) of land crab NO synthase (Gl-NOS) from molting gland (Y-organ) and thoracic ganglion mRNA. The open reading frame encoded a protein of 1199 amino acids with an estimated mass of 135 624 Da. Gl-NOS had the highest sequence identity with insect NOS. The amino acid sequences for binding heme and tetrahydrobiopterin in the oxygenase domain, binding calmodulin and binding FMN, FAD and NADPH in the reductase domain were highly conserved. Gl-NOS had single amino acid differences in all three highly conserved FAD-binding sequences, which distinguished it from other NOS sequences. RT-PCR showed that the Gl-NOS mRNA was present in testis, ovary, gill, eyestalk neural ganglia, thoracic ganglion and Y-organ. NOS mRNA varied between preparations of Y-organ, thoracic ganglion and gill, while NOS mRNA was at consistently high levels in the ovary, testis and eyestalk ganglia. Immunohistochemistry confirmed that the Gl-NOS protein was expressed in Y-organ, ovary and gill. These results suggest that NOS has functions in addition to neuromodulation in adults, such as regulating or modulating ecdysteroid synthesis in the Y-organ.
一氧化氮(NO)信号传导参与无脊椎动物的许多生理过程。在甲壳类动物中,它在神经系统调节和肌肉收缩中发挥作用。巢式逆转录聚合酶链反应(RT-PCR)以及5'和3' cDNA末端快速扩增(RACE)PCR从蜕壳腺(Y器官)和胸神经节mRNA中生成了陆地蟹一氧化氮合酶(Gl-NOS)的全长cDNA序列(3982 bp)。开放阅读框编码一个由1199个氨基酸组成的蛋白质,估计质量为135624 Da。Gl-NOS与昆虫一氧化氮合酶具有最高的序列同一性。加氧酶结构域中结合血红素和四氢生物蝶呤、结合钙调蛋白以及还原酶结构域中结合黄素单核苷酸(FMN)、黄素腺嘌呤二核苷酸(FAD)和烟酰胺腺嘌呤二核苷酸磷酸(NADPH)的氨基酸序列高度保守。Gl-NOS在所有三个高度保守的FAD结合序列中都有单个氨基酸差异,这使其与其他一氧化氮合酶序列区分开来。RT-PCR显示,Gl-NOS mRNA存在于睾丸、卵巢、鳃、眼柄神经节、胸神经节和Y器官中。Y器官、胸神经节和鳃的样本中一氧化氮合酶mRNA有所不同,而卵巢、睾丸和眼柄神经节中的一氧化氮合酶mRNA水平始终较高。免疫组织化学证实,Gl-NOS蛋白在Y器官、卵巢和鳃中表达。这些结果表明,一氧化氮合酶在成体中除了神经调节功能外,还具有其他功能,例如调节Y器官中蜕皮甾体的合成。