Sommer Aniela, Geist Birgit, Da Ines Olivier, Gehwolf Renate, Schäffner Anton R, Obermeyer Gerhard
Molecular Plant Biophysics and Biotechnology, Department of Molecular Biology, University of Salzburg, Billrothstr. 11, 5020 Salzburg, Austria.
New Phytol. 2008;180(4):787-97. doi: 10.1111/j.1469-8137.2008.02607.x. Epub 2008 Aug 25.
To investigate the role of aquaporin-mediated water transport during pollen grain germination and tube growth, Arabidopsis thaliana plasma membrane intrinsic proteins (PIPs) were expressed in pollen of Lilium longiflorum (lily). Successful expression of AtPIPs in particle-bombarded lily pollen grains was monitored by co-expression with fluorescent proteins and single-cell RT-PCR, and by measuring the water permeability coefficient (P(os)) in swelling assays using protoplasts prepared from transformed pollen grains and tubes. Expression of AtPIP1;1 and AtPIP1;2 in pollen grains resulted in P(os) values similar to those measured in nontransformed pollen grain protoplasts (6.65 +/- 2.41 microm s(-1)), whereas expression of AtPIP2 significantly increased P(os) (AtPIP2;1, 13.79 +/- 6.38; AtPIP2;2, 10.16 +/- 3.30 microm s(-1)). Transformation with combinations of AtPIP1 and AtPIP2 did not further enhance P(os). Native pollen tube protoplasts showed higher P(os) values (13.23 +/- 4.14 microm s(-1)) than pollen grain protoplasts but expression of AtPIP2;1 (18.85 +/- 7.60 microm s(-1)) did not significantly increase their P(os) values. Expression of none of the tested PIPs had any effect on pollen tube growth rates. The ectopic expression of AtPIP2s in lily pollen increased the water permeability of the plasma membrane in pollen grains, but not in pollen tubes. The measured endogenous water permeability does not limit water uptake during tube growth, but has to be regulated to prevent tube bursting.
为了研究水通道蛋白介导的水运输在花粉粒萌发和花粉管生长过程中的作用,拟南芥质膜内在蛋白(PIPs)在麝香百合(百合)花粉中进行了表达。通过与荧光蛋白共表达和单细胞逆转录聚合酶链反应(RT-PCR),以及使用从转化的花粉粒和花粉管制备的原生质体在肿胀试验中测量水渗透系数(P(os)),监测了AtPIPs在粒子轰击的百合花粉粒中的成功表达。花粉粒中AtPIP1;1和AtPIP1;2的表达导致P(os)值与未转化花粉粒原生质体中测量的值相似(6.65±2.41μm s(-1)),而AtPIP2的表达显著增加了P(os)(AtPIP2;1,13.79±6.38;AtPIP2;2,10.16±3.30μm s(-1))。用AtPIP1和AtPIP2组合进行转化并没有进一步提高P(os)。天然花粉管原生质体显示出比花粉粒原生质体更高的P(os)值(13.23±4.14μm s(-1)),但AtPIP2;1的表达(18.85±7.60μm s(-1))并没有显著增加其P(os)值。所测试的PIPs中没有一种对花粉管生长速率有任何影响。AtPIP2s在百合花粉中的异位表达增加了花粉粒中质膜的水渗透性,但在花粉管中没有增加。测量的内源性水渗透性并不限制花粉管生长过程中的水分吸收,但必须进行调节以防止花粉管破裂。