Cis-regulatory Changes at FLOWERING LOCUS T Mediate Natural Variation in Flowering Responses of Arabidopsis thaliana

被引:102
作者
Schwartz, Christopher [2 ,5 ]
Balasubramanian, Sureshkumar [1 ,7 ]
Warthmann, Norman [1 ,2 ]
Michael, Todd P. [2 ,6 ]
Lempe, Janne [1 ]
Sureshkumar, Sridevi [1 ]
Kobayashi, Yasushi [1 ]
Maloof, Julin N. [2 ,4 ]
Borevitz, Justin O. [2 ,3 ]
Chory, Joanne [2 ,8 ]
Weigel, Detlef [1 ,2 ]
机构
[1] MPI Dev Biol, Dept Mol Biol, D-72076 Tubingen, Germany
[2] Salk Inst Biol Studies, Plant Biol Lab, La Jolla, CA 92037 USA
[3] Univ Chicago, Dept Ecol & Evolut, Chicago, IL 60637 USA
[4] Univ Calif Davis, Plant Biol Sect, Davis, CA 95616 USA
[5] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
[6] Rutgers State Univ, Waksman Inst, Piscataway, NJ 08855 USA
[7] Univ Queensland, Sch Biol Sci, St Lucia, Qld 4072, Australia
[8] Salk Inst Biol Sci, Howard Hughes Med Inst, La Jolla, CA 92037 USA
基金
日本学术振兴会; 美国国家卫生研究院;
关键词
QUANTITATIVE TRAIT LOCI; HETEROGENEOUS INBRED FAMILY; FT PROTEIN; FLORAL INDUCTION; LONG-DISTANCE; MOLECULAR ANALYSIS; LINE POPULATIONS; TIME-VARIATION; GENE; VERNALIZATION;
D O I
10.1534/genetics.109.104984
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Flowering time, a critical adaptive trait, is modulated by several environmental cues. These external signals converge oil 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 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 1,7 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 ill 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.
引用
收藏
页码:723 / 732
页数:10
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