Richard Odile, Paquet Nicolas, Haudecoeur Elise, Charrier Bénédicte
Institut de Biotechnologie des Plantes, Bât. 630, UMR CNRS 8618, Université Paris-Sud, 91405, Orsay Cedex, France.
J Mol Evol. 2005 Jul;61(1):99-113. doi: 10.1007/s00239-004-0302-6. Epub 2005 Jun 29.
GSK3/Shaggy kinases are involved in a wide range of fundamental processes in animal development and metabolism. In angiosperm plants, these kinases are encoded by moderate-sized gene families, which appear to have a complex set of functions. Here, we present the characterization of five members of the GSK3/Shaggy gene family in the bryophyte Physcomitrella patens. The P. patens GSK3/Shaggy kinases (PpSK) are organized in a group of closely related paralogues with respect to their gene sequence and structure. Indeed, a phylogenetic analysis of the GSK3/Shaggy kinase sequences from plants and animals showed that the five PpSK proteins are monophyletic, and closer to subgroups I and IV described in angiosperms. Expression analyses performed by quantitative real-time RT-PCR on a wide range of growing conditions showed that PpSK genes responded only to either desiccation, PEG or sorbitol. As demonstrated by both inductions of marker genes and protonemal cell plasmolyses, these treatments resulted in a hyperosmotic stress. Altogether, these data suggest that (1) GSK3/Shaggy kinase gene multiplication occurred early in plant evolution, before the separation between bryophytes and vascular plants, and (2) both gene loss and duplication occurred in the ancestor of P. patens along with functional gene diversification in angiosperms. However, conservation of the transcriptional responses between Physcomitrella and Arabidopsis suggests the identification of an ancestral response of the GSK3/Shaggy kinases genes to osmotic stress.
糖原合成酶激酶3/Shaggy激酶参与动物发育和新陈代谢中的一系列基本过程。在被子植物中,这些激酶由中等大小的基因家族编码,其功能似乎较为复杂。在此,我们对苔藓植物小立碗藓中糖原合成酶激酶3/Shaggy基因家族的五个成员进行了特性分析。小立碗藓的糖原合成酶激酶3/Shaggy激酶(PpSK)在基因序列和结构方面由一组密切相关的旁系同源物组成。实际上,对植物和动物的糖原合成酶激酶3/Shaggy激酶序列进行的系统发育分析表明,这五个PpSK蛋白是单系的,并且与被子植物中描述的亚组I和IV更为接近。在多种生长条件下通过定量实时逆转录PCR进行的表达分析表明,PpSK基因仅对脱水、聚乙二醇或山梨醇有反应。正如标记基因的诱导和原丝体细胞质壁分离所证明的那样,这些处理导致了高渗胁迫。总之,这些数据表明:(1)糖原合成酶激酶3/Shaggy激酶基因的倍增发生在植物进化的早期,即在苔藓植物和维管植物分离之前;(2)在小立碗藓的祖先中发生了基因丢失和复制,同时被子植物中也发生了功能基因多样化。然而,小立碗藓和拟南芥之间转录反应的保守性表明,糖原合成酶激酶3/Shaggy激酶基因对渗透胁迫存在一种祖先反应。