Wang Hong-Yu, Klatte Marco, Jakoby Marc, Bäumlein Helmut, Weisshaar Bernd, Bauer Petra
Department of Biosciences, Botany, Saarland University, PO Box 151150, 66041 Saarbrücken, Germany.
Planta. 2007 Sep;226(4):897-908. doi: 10.1007/s00425-007-0535-x. Epub 2007 May 22.
Networks of transcription factors control physiological, developmental and environmental responses. Root iron acquisition responses are controlled by the essential bHLH protein FIT. Recently, two group Ib BHLH genes were reported to be iron deficiency-regulated. Here, we studied expression patterns of these two group Ib BHLH genes and of their two closest homologs to analyze whether their regulation would support a function in iron deficiency responses. We found that BHLH038, BHLH039, BHLH100 and BHLH101 (comprising a subgroup of BHLH Ib genes) were up regulated by iron deficiency in roots and leaves. Single insertion mutants had no visible phenotype and were capable of inducing root iron acquisition responses, presumably due to functional redundancy. Specific metal treatments like nickel, high zinc or high copper resulted in induction of the four BHLH Ib genes whereas high iron, low copper and low zinc repressed gene expression. Induction of the four BHLH Ib genes was also found in multiple iron acquisition mutants including fit. Ectopic activation of FIT did not suppress the four BHLH Ib genes. Split-root analyses using promoter-GUS lines showed that FIT and BHLH100 promoters were controlled by different local and systemic signals involved in their regulation by iron. These results indicated that the four BHLH Ib genes were induced independently from FIT by conditions causing iron deficiency. Taken together, BHLH038, BHLH039, BHLH100 and BHLH101 function differently from FIT and may be involved in mediating a signal related to iron deficiency-induced stress and/or internal iron homeostasis.
转录因子网络控制着生理、发育和环境反应。根系铁吸收反应受必需的bHLH蛋白FIT调控。最近,有报道称两个Ib类BHLH基因受缺铁调控。在此,我们研究了这两个Ib类BHLH基因及其两个最接近的同源基因的表达模式,以分析它们的调控是否支持其在缺铁反应中的功能。我们发现,BHLH038、BHLH039、BHLH100和BHLH101(构成Ib类BHLH基因的一个亚组)在根和叶中受缺铁上调。单插入突变体没有可见表型,并且能够诱导根系铁吸收反应,这可能是由于功能冗余。镍、高锌或高铜等特定金属处理导致这四个Ib类BHLH基因的诱导,而高铁、低铜和低锌则抑制基因表达。在包括fit在内的多个铁吸收突变体中也发现了这四个Ib类BHLH基因的诱导。FIT的异位激活并没有抑制这四个Ib类BHLH基因。使用启动子-GUS系的分根分析表明,FIT和BHLH100启动子受参与其铁调控的不同局部和系统信号控制。这些结果表明,这四个Ib类BHLH基因在导致缺铁的条件下独立于FIT被诱导。综上所述,BHLH038、BHLH039、BHLH100和BHLH101的功能与FIT不同,可能参与介导与缺铁诱导的胁迫和/或内部铁稳态相关的信号。