Pan Junmin, Misamore Michael J, Wang Qian, Snell William J
Department of Cell Biology, University of Texas South-western Medical Center, Dallas, Texas 75390-9039, USA.
Traffic. 2003 Jul;4(7):452-9. doi: 10.1034/j.1600-0854.2003.00105.x.
Fertilization in Chlamydomonas begins with flagellar adhesion between mating type plus and mating type minus gametes and is consummated within minutes by zygote formation. Once fusion occurs, the newly merged gametes cease existence as distinct entities, and the diploid zygote immediately initiates transcription of zygote-specific genes. Accomplishing fertilization within such a short time requires the rapid and signaled movement of pre-existing membrane and cytoplasmic proteins between and within several cellular compartments. Generation within the adhering flagella of the initial signals for protein movement, as well as movement itself of at least one cytoplasmic protein from the cell body to the flagella, depend on the microtubule motor, kinesin-II and presumably on intraflagellar transport (IFT). Adhesion and fusion of the two gametes depend on a second translocation event, the movement of an adhesion/fusion protein onto the surface of a rapidly elongating, microvillous-like fusion organelle. Finally, the merging of the two separate gametes, each containing sex-specific proteins, into a single cell allows the formerly separate proteins to form new interactions that regulate zygote development. Two proteins - a nuclease and a homeodomain protein - which were present only in the plus gamete, are 'delivered' to the cytoplasm of the zygote during gamete fusion. The nuclease is selectively imported into the minus chloroplast, where it degrades the chloroplast DNA, thereby ensuring uniparental inheritance of plus chloroplast traits. The homeodomain protein binds with an as yet unidentified protein delivered by the minus gamete, and the new complex activates transcription of zygote-specific genes.
衣藻的受精过程始于正交配型和负交配型配子之间的鞭毛黏附,并在数分钟内通过合子形成完成。一旦发生融合,新融合的配子就不再作为独立的实体存在,二倍体合子立即启动合子特异性基因的转录。在如此短的时间内完成受精需要预先存在的膜蛋白和细胞质蛋白在几个细胞区室之间以及区室内快速且有信号引导的移动。在黏附的鞭毛中产生蛋白质移动的初始信号,以及至少一种细胞质蛋白从细胞体向鞭毛的移动本身,都依赖于微管马达驱动蛋白——驱动蛋白-II,可能还依赖于鞭毛内运输(IFT)。两个配子的黏附和融合依赖于另一个转运事件,即一种黏附/融合蛋白移动到快速伸长的微绒毛样融合细胞器表面。最后,两个分别含有性别特异性蛋白的独立配子融合成一个细胞,使得先前分离的蛋白形成新的相互作用来调节合子发育。两种蛋白——一种核酸酶和一种同源结构域蛋白——仅存在于正配子中,在配子融合过程中被“传递”到合子的细胞质中。核酸酶被选择性地导入负叶绿体,在那里它降解叶绿体DNA,从而确保正叶绿体性状的单亲遗传。同源结构域蛋白与负配子传递的一种尚未鉴定的蛋白结合,新的复合物激活合子特异性基因的转录。