Cutler Christopher P, Maciver Bryce, Cramb Gordon, Zeidel Mark
Department of Biology, Georgia Southern University Statesboro, GA, USA.
Front Physiol. 2012 Jan 10;2:107. doi: 10.3389/fphys.2011.00107. eCollection 2011.
The dogfish ortholog of aquaporin 4 (AQP4) was amplified from cDNA using degenerate PCR followed by cloning and sequencing. The complete coding region was then obtained using 5' and 3' RACE techniques. Alignment of the sequence with AQP4 amino acid sequences from other species showed that dogfish AQP4 has high levels (up to 65.3%) of homology with higher vertebrate sequences but lower levels of homology to Agnathan (38.2%) or teleost (57.5%) fish sequences. Northern blotting indicated that the dogfish mRNA was approximately 3.2 kb and was highly expressed in the rectal gland (a shark fluid secretory organ). Semi-quantitative PCR further indicates that AQP4 is ubiquitous, being expressed in all tissues measured but at low levels in certain tissues, where the level in liver > gill > intestine. Manipulation of the external environmental salinity of groups of dogfish showed that when fish were acclimated in stages to 120% seawater (SW) or 75% SW, there was no change in AQP4 mRNA expression in either rectal gland, kidney, or esophagus/cardiac stomach. Whereas quantitative PCR experiments using the RNA samples from the same experiment, showed a significant 63.1% lower abundance of gill AQP4 mRNA expression in 120% SW-acclimated dogfish. The function of dogfish AQP4 was also determined by measuring the effect of the AQP4 expression in Xenopus laevis oocytes. Dogfish AQP4 expressing-oocytes, exhibited significantly increased osmotic water permeability (P(f)) compared to controls, and this was invariant with pH. Permeability was not significantly reduced by treatment of oocytes with mercury chloride, as is also the case with AQP4 in other species. Similarly AQP4 expressing-oocytes did not exhibit enhanced urea or glycerol permeability, which is also consistent with the water-selective property of AQP4 in other species.
使用简并PCR从cDNA中扩增出星鲨水通道蛋白4(AQP4)的直系同源基因,随后进行克隆和测序。然后利用5'和3' RACE技术获得完整的编码区。将该序列与其他物种的AQP4氨基酸序列进行比对,结果显示星鲨AQP4与高等脊椎动物序列具有较高的同源性(高达65.3%),但与无颌类(38.2%)或硬骨鱼(57.5%)鱼类序列的同源性较低。Northern印迹分析表明,星鲨mRNA约为3.2 kb,在直肠腺(鲨鱼的一种液体分泌器官)中高度表达。半定量PCR进一步表明,AQP4在所有检测组织中均有表达,但在某些组织中表达水平较低,其中肝脏中的表达水平>鳃>肠道。对星鲨群体的外部环境盐度进行调控,结果显示,当鱼逐步适应120%海水(SW)或75% SW时,直肠腺、肾脏或食管/贲门胃中的AQP4 mRNA表达均无变化。而使用同一实验的RNA样本进行定量PCR实验,结果显示,适应120% SW的星鲨鳃中AQP4 mRNA表达丰度显著降低63.1%。还通过测量AQP4在非洲爪蟾卵母细胞中的表达效果来确定星鲨AQP4的功能。与对照组相比,表达星鲨AQP4的卵母细胞表现出显著增强的渗透水通透性(Pf),且这种通透性不受pH影响。用氯化汞处理卵母细胞后,通透性并未显著降低,其他物种的AQP4也是如此。同样,表达AQP4的卵母细胞并未表现出增强的尿素或甘油通透性,这也与其他物种中AQP4的水选择性特性一致。