Few W Preston, Zakon Harold H
Section of Neurobiology and Institute for Neuroscience, University of Texas, Austin, Texas 78712, USA.
Dev Neurobiol. 2007 Apr;67(5):535-49. doi: 10.1002/dneu.20305.
Electric fish communicate with electric organ (EO) discharges (EODs) that are sexually dimorphic, hormone-sensitive, and often individually distinct. The cells of the EO (electrocytes) of the weakly electric fish Sternopygus possess delayed rectifying K+ currents that systematically vary in their activation and deactivation kinetics, and this precise variation in K+ current kinetics helps shape sex and individual differences in the EOD. Because members of the Kv1 subfamily produce delayed rectifier currents, we cloned a number of genes in the Kv1 subfamily from the EO of Sternopygus. Using our sequences and those from genome databases, we found that in teleost fish Kv1.1 and Kv1.2 exist as duplicate pairs (Kv1.1a&b, Kv1.2a&b) whereas Kv1.3 does not. Using real-time quantitative RT-PCR, we found that Kv1.1a and Kv1.2a, but not Kv1.2b, expression in the EO is higher in high EOD frequency females (which have fast EO K+ currents) than in low EOD frequency males (which have slow EO K+ currents). Systemic treatment with dihydrotestosterone decreased Kv1.1a and Kv1.2a, but not Kv1.2b, expression in the EO, whereas treatment with human chorionic gonadotropin (hCG) increased Kv1.2a but not Kv1.1a or Kv1.2b expression in the EO. Thus, systematic variation in the ratios of Kv1 channels expressed in the EO is correlated with individual differences in and sexual dimorphism of a communication signal.
电鱼通过电器官(EO)放电(EODs)进行交流,这些放电具有性别二态性、对激素敏感,且通常个体独特。弱电鱼裸背电鳗属的电器官(电细胞)的细胞具有延迟整流钾离子电流,其激活和失活动力学系统地变化,而钾离子电流动力学的这种精确变化有助于塑造电鱼放电的性别和个体差异。由于Kv1亚家族的成员产生延迟整流电流,我们从裸背电鳗属的电器官中克隆了Kv1亚家族的一些基因。利用我们的序列和来自基因组数据库的序列,我们发现硬骨鱼中的Kv1.1和Kv1.2以重复对的形式存在(Kv1.1a和b、Kv1.2a和b),而Kv1.3则不存在。使用实时定量逆转录聚合酶链反应,我们发现,与低放电频率雄性(其电器官钾离子电流较慢)相比,高放电频率雌性(其电器官钾离子电流较快)的电器官中Kv1.1a和Kv1.2a的表达更高,但Kv1.2b并非如此。用二氢睾酮进行全身治疗会降低电器官中Kv1.1a和Kv1.2a的表达,但不会降低Kv1.2b的表达,而用人绒毛膜促性腺激素(hCG)治疗会增加电器官中Kv1.2a的表达,但不会增加Kv1.1a或Kv1.2b的表达。因此,电器官中表达的Kv1通道比例的系统变化与一种通讯信号的个体差异和性别二态性相关。