Institute of Botany, University of Kiel, Olshausenstrasse 40, 24098 Kiel, Germany.
Plant Mol Biol. 2010 Jul;73(4-5):379-90. doi: 10.1007/s11103-010-9618-3. Epub 2010 Mar 19.
The Arabidopsis thaliana AtS40-3 gene belongs to a group of genes sharing the conserved DUF548 sequence motif with up to now unknown function. One member of this group, the barley HvS40, was shown before to play a role in regulation of leaf senescence. Similar as the barley gene, AtS40-3 is induced during senescence and is also regulated in response to dark treatment, ABA, salicylic acid and pathogen attack. By localization of the GUS fusion protein, the AtS40-3 gene was shown to encode a nucleus targeted protein. The s40-3a mutant with a T-DNA insertion in the promoter region of the gene was observed to have a staygreen phenotype. By quantitative real-time PCR analyses expression of the AtS40-3 gene in this mutant was observed to be constitutive and not induced during senescence. This coincided with WRKY53 gene expression in nonsenescent leaves and lowered expression levels of WRKY53 and SAG12 at later stages of development. While in the wildtype expression of AtS40-3 was activated by darkness, in the s40-3a mutant the expression of AtS40-3 stayed at a low level. This coincided with lower expression of the SEN1 and SAG12 genes. In another promoter mutant with a T-DNA insertion further upstream of the coding sequence the levels of AtS40-3 and SAG12 transcripts increased in parallel both in a natural light-dark regime and in darkness. The data on gene expression in promoter T-DNA insertion mutants of the s40-3 gene indicate that AtS40 regulates senescence either by modulation of WRKY53 or by activation of SAG12 independent of WRKY53.
拟南芥 AtS40-3 基因属于一组具有保守 DUF548 序列基序的基因,其功能至今未知。该基因家族的一个成员,大麦 HvS40,先前被证明在叶片衰老的调控中发挥作用。与大麦基因相似,AtS40-3 在衰老过程中被诱导,并且对黑暗处理、ABA、水杨酸和病原体攻击也有响应的调节。通过 GUS 融合蛋白的定位,AtS40-3 基因被证明编码一种靶向细胞核的蛋白质。在该基因的启动子区域插入 T-DNA 的 s40-3a 突变体被观察到具有保持绿色表型。通过定量实时 PCR 分析,该突变体中 AtS40-3 基因的表达被观察到是组成型的,在衰老过程中没有被诱导。这与非衰老叶片中 WRKY53 基因的表达一致,并且在发育后期 WRKY53 和 SAG12 的表达水平降低。虽然在野生型中,AtS40-3 的表达被黑暗激活,但在 s40-3a 突变体中,AtS40-3 的表达保持在低水平。这与 SEN1 和 SAG12 基因的表达较低相一致。在另一个启动子突变体中,T-DNA 插入到编码序列的上游更远的位置,在自然光-暗周期和黑暗中,AtS40-3 和 SAG12 转录本的水平都平行增加。AtS40 基因启动子 T-DNA 插入突变体的基因表达数据表明,AtS40 通过调节 WRKY53 或通过激活 SAG12 而不依赖于 WRKY53 来调节衰老。