Takata Naoki, Taniguchi Toru
Forest Bio-Research Center, Forestry and Forest Products Research Institute, Hitachi, Ibaraki, 319-1301, Japan,
Planta. 2015 Jan;241(1):29-42. doi: 10.1007/s00425-014-2217-9. Epub 2014 Dec 9.
Secondary cell wall-associated CesA genes in Populus have undergone a functional differentiation in expression pattern that may be attributable to evolutionary alteration of regulatory modules. Gene duplication is an important mechanism for functional divergence of genes. Secondary cell wall-associated cellulose synthase genes (CesA4, CesA7 and CesA8) are duplicated in Populus plants due to a recent whole genome duplication event. Here, we demonstrate that duplicate CesA genes show tissue-dependent expression divergence in Populus plants. Real-time PCR analysis of Populus CesA genes suggested that Pt × tCesA8-B was more highly expressed than Pt × tCesA8-A in phloem and secondary xylem tissue of mature stem. Histochemical and histological analyses of transformants expressing a GFP-GUS fusion gene driven by Populus CesA promoters revealed that the duplicate CesA genes showed different expression patterns in phloem fibers, secondary xylem, root cap and leaf trichomes. We predicted putative cis-regulatory motifs that regulate expression of secondary cell wall-associated CesA genes, and identified 19 motifs that are highly conserved in the CesA gene family of eudicotyledonous plants. Furthermore, a transient transactivation assay identified candidate transcription factors that affect levels and patterns of expression of Populus CesA genes. The present study reveals that secondary cell wall-associated CesA genes in Populus have undergone a functional differentiation in expression pattern that may be attributable to evolutionary alteration of regulatory modules.
杨树中与次生细胞壁相关的纤维素合成酶基因(CesA)在表达模式上发生了功能分化,这可能归因于调控模块的进化改变。基因复制是基因功能分化的重要机制。由于近期的全基因组复制事件,杨树植物中与次生细胞壁相关的纤维素合成酶基因(CesA4、CesA7和CesA8)发生了复制。在此,我们证明了复制的CesA基因在杨树植物中表现出组织依赖性的表达差异。对杨树CesA基因的实时PCR分析表明,在成熟茎的韧皮部和次生木质部组织中,Pt×tCesA8-B的表达量高于Pt×tCesA8-A。对由杨树CesA启动子驱动的GFP-GUS融合基因表达的转化体进行组织化学和组织学分析,结果显示复制的CesA基因在韧皮部纤维、次生木质部、根冠和叶毛状体中表现出不同的表达模式。我们预测了调控与次生细胞壁相关的CesA基因表达的假定顺式调控基序,并鉴定出19个在双子叶植物的CesA基因家族中高度保守的基序。此外,瞬时反式激活分析确定了影响杨树CesA基因表达水平和模式的候选转录因子。本研究表明,杨树中与次生细胞壁相关的CesA基因在表达模式上发生了功能分化,这可能归因于调控模块的进化改变。