Plant Biology Laboratory, Howard Hughes Medical Institute, The Salk Institute for Biological Sciences, La Jolla, California 92037, USA.
Genetics. 2009 Oct;183(2):723-32, 1SI-7SI. doi: 10.1534/genetics.109.104984. Epub 2009 Aug 3.
Flowering time, a critical adaptive trait, is modulated by several environmental cues. These external signals converge on a small set of genes that in turn mediate the flowering response. Mutant analysis and subsequent molecular studies have revealed that one of these integrator genes, FLOWERING LOCUS T (FT), responds to photoperiod and temperature cues, two environmental parameters that greatly influence flowering time. As the central player in the transition to flowering, the protein coding sequence of FT and its function are highly conserved across species. Using QTL mapping with a new advanced intercross-recombinant inbred line (AI-RIL) population, we show that a QTL tightly linked to FT contributes to natural variation in the flowering response to the combined effects of photoperiod and ambient temperature. Using heterogeneous inbred families (HIF) and introgression lines, we fine map the QTL to a 6.7 kb fragment in the FT promoter. We confirm by quantitative complementation that FT has differential activity in the two parental strains. Further support for FT underlying the QTL comes from a new approach, quantitative knockdown with artificial microRNAs (amiRNAs). Consistent with the causal sequence polymorphism being in the promoter, we find that the QTL affects FT expression. Taken together, these results indicate that allelic variation at pathway integrator genes such as FT can underlie phenotypic variability and that this may be achieved through cis-regulatory changes.
开花时间是一个关键的适应性特征,受多种环境线索的调节。这些外部信号汇聚到一小部分基因上,这些基因反过来介导开花反应。突变分析和随后的分子研究表明,这些整合基因之一,FT(FLOWERING LOCUS T),对光周期和温度线索做出反应,这两个环境参数极大地影响开花时间。作为向开花过渡的核心参与者,FT 的蛋白质编码序列及其功能在物种间高度保守。我们使用具有新的先进互交重组近交系 (AI-RIL) 群体的 QTL 作图,表明与 FT 紧密连锁的 QTL 对光周期和环境温度综合作用下的开花反应的自然变异有贡献。使用异质近交系 (HIF) 和导入系,我们将 QTL 精细映射到 FT 启动子中的 6.7 kb 片段。我们通过定量互补验证证实 FT 在两个亲本品系中具有不同的活性。FT 是 QTL 基础的进一步证据来自一种新方法,即使用人工 microRNAs(amiRNAs)进行定量敲低。与因果序列多态性位于启动子中的情况一致,我们发现 QTL 影响 FT 的表达。总之,这些结果表明,途径整合基因(如 FT)的等位基因变异可以为表型变异性提供基础,并且这可能是通过顺式调控变化实现的。