Department of Plant Developmental Biology, Max-Planck-Institute for Plant Breeding, Cologne, Germany.
Fundación Instituto Leloir, IIBBA-CONICET, Buenos Aires, Argentina.
PLoS Genet. 2019 Apr 4;15(4):e1008065. doi: 10.1371/journal.pgen.1008065. eCollection 2019 Apr.
Integration of environmental and endogenous cues at plant shoot meristems determines the timing of flowering and reproductive development. The MADS box transcription factor FLOWERING LOCUS C (FLC) of Arabidopsis thaliana is an important repressor of floral transition, which blocks flowering until plants are exposed to winter cold. However, the target genes of FLC have not been thoroughly described, and our understanding of the mechanisms by which FLC represses transcription of these targets and how this repression is overcome during floral transition is still fragmentary. Here, we identify and characterize TARGET OF FLC AND SVP1 (TFS1), a novel target gene of FLC and its interacting protein SHORT VEGETATIVE PHASE (SVP). TFS1 encodes a B3-type transcription factor, and we show that tfs1 mutants are later flowering than wild-type, particularly under short days. FLC and SVP repress TFS1 transcription leading to deposition of trimethylation of Iysine 27 of histone 3 (H3K27me3) by the Polycomb Repressive Complex 2 at the TFS1 locus. During floral transition, after downregulation of FLC by cold, TFS1 transcription is promoted by SUPPRESSOR OF OVEREXPRESSION OF CONSTANS1 (SOC1), a MADS box protein encoded by another target of FLC/SVP. SOC1 opposes PRC function at TFS1 through recruitment of the histone demethylase RELATIVE OF EARLY FLOWERING 6 (REF6) and the SWI/SNF chromatin remodeler ATPase BRAHMA (BRM). This recruitment of BRM is also strictly required for SQUAMOSA PROMOTER BINDING PROTEIN-LIKE 9 (SPL9) binding at TFS1 to coordinate RNAPII recruitment through the Mediator complex. Thus, we show that antagonistic chromatin modifications mediated by different MADS box transcription factor complexes play a crucial role in defining the temporal and spatial patterns of transcription of genes within a network of interactions downstream of FLC/SVP during floral transition.
植物茎尖分生组织中环境和内源性信号的整合决定了开花和生殖发育的时间。拟南芥的 MADS 盒转录因子 FLOWERING LOCUS C(FLC)是花转变的重要抑制剂,它阻止植物开花,直到植物暴露在冬季寒冷中。然而,FLC 的靶基因尚未被彻底描述,我们对 FLC 抑制这些靶基因转录的机制以及在花转变过程中如何克服这种抑制的理解仍然是零碎的。在这里,我们鉴定并描述了 FLC 和其互作蛋白 SHORT VEGETATIVE PHASE(SVP)的一个新的靶基因 TARGET OF FLC AND SVP1(TFS1)。TFS1 编码 B3 型转录因子,我们表明 tfs1 突变体比野生型开花晚,特别是在短日照条件下。FLC 和 SVP 抑制 TFS1 转录,导致多梳抑制复合物 2(PRC2)在 TFS1 基因座上沉积组蛋白 H3 赖氨酸 27 的三甲基化(H3K27me3)。在花转变过程中,FLC 被低温下调后,TFS1 的转录由另一个 FLC/SVP 靶基因 SUPPRESSOR OF OVEREXPRESSION OF CONSTANS1(SOC1)编码的 MADS 盒蛋白促进。SOC1 通过招募组蛋白去甲基酶 RELATIVE OF EARLY FLOWERING 6(REF6)和 SWI/SNF 染色质重塑酶 ATPase BRAHMA(BRM)来对抗 TFS1 上的 PRC 功能。BRM 的这种募集也严格需要 SQUAMOSA PROMOTER BINDING PROTEIN-LIKE 9(SPL9)在 TFS1 上的结合,以通过中介复合物协调 RNAPII 的募集。因此,我们表明,不同的 MADS 盒转录因子复合物介导的拮抗染色质修饰在花转变过程中 FLC/SVP 下游相互作用网络中基因的转录的时空模式的定义中起着至关重要的作用。