Chumak Nina, Mosiolek Magdalena, Schoft Vera Karolina
Gregor Mendel Institute, Austrian Academy of Sciences, Vienna, Austria.
Bio Protoc. 2015 Nov 20;5(22). doi: 10.21769/BioProtoc.1664.
One of the major topics in plant and animal biology is sexual reproduction. It is, therefore, of great interest to isolate and study germ cells and accessory cells. The male gametophyte of the flowering plant (), pollen, is the product of two post-meiotic mitotic divisions. Each mature pollen grain consists of two sperm cells contained within the vegetative cell, the non-reproductive companion cell. The tough pollen wall and its special nested structure make it difficult to study pollen cells separately. Here, we describe a simple and efficient method to fractionate sperm and vegetative cell nuclei by fluorescence activated cell sorting (FACS). Our protocol is based on differences in fluorescence intensity of sperm and vegetative cell nuclei stained with SYBR Green I. 100 plants yield about 1 x 10 sperm and 350,000 vegetative cell nuclei. This method can be used for purifying pollen nuclei of various wild-type accessions and mutant lines, and can, in principle, be adapted for pollen of other plant species.
动植物生物学的主要主题之一是有性繁殖。因此,分离和研究生殖细胞及辅助细胞极具意义。开花植物的雄配子体(),即花粉,是两次减数分裂后有丝分裂的产物。每个成熟花粉粒由营养细胞(非生殖伴随细胞)内的两个精细胞组成。坚硬的花粉壁及其特殊的嵌套结构使得单独研究花粉细胞变得困难。在此,我们描述了一种通过荧光激活细胞分选(FACS)分离精子和营养细胞核的简单高效方法。我们的方案基于用SYBR Green I染色的精子和营养细胞核荧光强度的差异。100株植物可产生约1×10个精子和350,000个营养细胞核。该方法可用于纯化各种野生型材料和突变系的花粉核,原则上也可适用于其他植物物种的花粉。