水稻开花光周期调控相关基因研究进展

水稻开花调控是一个极其复杂的生命过程,由自身遗传因素和外界环境共同决定。光周期途径是调控水稻开花的关键途径,在这个途径中成花素基因Hd3a和RTF1处于核心地位,其上游调控途径主要包括Hd1依赖途径、Ehd1依赖途径及不依赖于Hd1和Ehd1的途径。这3条途径在汇集了光信号的各种信息后,将信号在Hd3a和RTF1处整合,并通过成花素形式将信息传递给下游开花基因,调控水稻开花。本文从成花素、光信号感受基因和昼夜节律基因、成花素上游调控基因、互作蛋白和下游调控基因等几方面阐述水稻开花光周期调控相关基因的研究现状,为水稻开花调控的深入研究提供参考。     

Identification of miRNA Targets by AtFT Overexpression in Tobacco

Plant Molecular Biology Reporter - The onset of flowering is regulated by complex gene networks that integrate multiple genetic cues to floral transition in plants. The highly conserved florigen...     

"Florigen ": an intriguing concept of plant biology.

"Florigen" is the name that Mikhail Chailakhyan coined in 1937 for the putative hormone regulating flowering. At this concept, plant physiologists arrived following early research concerning the effects of temperature and day length on the transition from vegetative to reproductive stages of plants. The existence of florigen was postulated on the experimental backgrounds involving i) the response of plants to inductive conditions; ii) transmission of a flowering stimulus by grafting; iii) extraction of this stimulus from induced plants. This experimental results showed the existence of florigen at least as concept because they always failed to offer the experimental evidence of its chemical existence. The myth of florigen persisted as long as the end of the Seventies, when physiologists began to consider flowering as a complex process in which various classes of hormones might variously interplay.     

Florigen goes molecular: Seventy years of the hormonal theory of flowering regulation

As early as in 1936, the comprehensive studies of flowering led M.Kh. Chailakhyan to the concept of florigen, a hormonal floral stimulus, and let him establish several characteristics of this stimulus. These studies set up for many years the main avenues for research into the processes that control plant flowering, and the notion of florigen became universally accepted by scientists worldwide. The present-day evidence of genetic control of plant flowering supports the idea that florigen participates in floral signal transduction. The recent study of arabidopsis plants led the authors to conclusion that the immediate products of the gene FLOWERING LOCUS I, its mRNA and/or protein, move from an induced leaf into the shoot apex and evoke flowering therein.     

ZCN8 encodes a potential orthologue of Arabidopsis FT florigen that integrates both endogenous and photoperiod flowering signals in maize

Higher plants use multiple perceptive measures to coordinate flowering time with environmental and endogenous cues. Physiological studies show that florigen is a mobile factor that transmits floral inductive signals from the leaf to the shoot apex. Arabidopsis FT protein is widely regarded as the archetype florigen found in diverse plant species, particularly in plants that use inductive photoperiods to flower. Recently, a large family of FT homologues in maize, the Zea CENTRORADIALIS (ZCN) genes, was described, suggesting that maize also contains FT-related proteins that act as a florigen. The product of one member of this large family, ZCN8, has several attributes that make it a good candidate as a maize florigen. Mechanisms underlying the floral transition in maize are less well understood than those of other species, partly because flowering in temperate maize is dependent largely on endogenous signals. The maize indeterminate1 (id1) gene is an important regulator of maize autonomous flowering that acts in leaves to mediate the transmission or production of florigenic signals. This study finds that id1 acts upstream of ZCN8 to control its expression, suggesting a possible new link to flowering in day-neutral maize. Moreover, in teosinte, a tropical progenitor of maize that requires short-day photoperiods to induce flowering, ZCN8 is highly up-regulated in leaves under inductive photoperiods. Finally, vascular-specific expression of ZCN8 in Arabidopsis complements the ft-1 mutation, demonstrating that leaf-specific expression of ZCN8 can induce flowering. These results suggest that ZCN8 may encode a florigen that integrates both endogenous and environmental signals in maize.     

Florigen is involved in axillary bud development at multiple stages in Arabidopsis

The wide variety of plant architectures is largely based on diverse and flexible modes of axillary shoot development. In Arabidopsis, floral transition (flowering) stimulates axillary bud development. The mechanism that links flowering and axillary bud development is, however, largely unknown. We recently showed that FLOWERING LOCUS T (FT) protein, which acts as florigen, promotes the phase transition of axillary meristems, whereas BRANCHED1 (BRC1) antagonizes the florigen action in axillary buds. Here, we present evidences for another possible role of florigen in axillary bud development. Ectopic overexpression of FT or another florigen gene TWIN SISTER OF FT (TSF) with LEAFY (LFY) induces ectopic buds at cotyledonary axils, confirming the previous proposal that these genes are involved in formation of axillary buds. Taken together with our previous report that florigen promotes axillary shoot elongation, we propose that florigen regulates axillary bud development at multiple stages to coordinate it with flowering in Arabidopsis.     

FTIP1 is an essential regulator required for florigen transport

The capacity to respond to day length, photoperiodism, is crucial for flowering plants to adapt to seasonal change. The photoperiodic control of flowering in plants is mediated by a long-distance mobile floral stimulus called florigen that moves from leaves to the shoot apex. Although the proteins encoded by FLOWERING LOCUS T (FT) in Arabidopsis and its orthologs in other plants are identified as the long-sought florigen, whether their transport is a simple diffusion process or under regulation remains elusive. Here we show that an endoplasmic reticulum (ER) membrane protein, FT-INTERACTING PROTEIN 1 (FTIP1), is an essential regulator required for FT protein transport in Arabidopsis. Loss of function of FTIP1 exhibits late flowering under long days, which is partly due to the compromised FT movement to the shoot apex. FTIP1 and FT share similar mRNA expression patterns and subcellular localization, and they interact specifically in phloem companion cells. FTIP1 is required for FT export from companion cells to sieve elements, thus affecting FT transport through the phloem to the SAM. Our results provide a mechanistic understanding of florigen transport, demonstrating that FT moves in a regulated manner and that FTIP1 mediates FT transport to induce flowering.     

植物成花素的研究进展

许多植物由营养生长向生殖生长的转换都是由日照长度控制的,而植物叶片可感知日长信号并诱导成花素的合成。成花素从韧皮部运输到茎顶端,使顶端分生组织基因表达发生变化进而成花。其中,FT作为成花素的主要组分,在该转换过程中处于核心地位。本文综合近年的研究,介绍成花素及其作用机理。     

Florigen （Ⅱ）： It is a Mobile Protein

The true identity of florigen - the molecule（s） that migrates from leaves to apical meristem to initiate flowering - was notoriously elusive, having made it almost the ＂Bigfoot＂ of plant biology. There was never a lack of drama in the field of florigen study, and florigen researchers have once again experienced such a swing in the last two years. We wrote a minireview last year in this journal （Yu et al. 2006） to excitedly salute, among other discoveries, the notion that the flowering locus T （FT） mRNA might be the molecular form of a florigen. However, this hypothesis was challenged in a little less than two years after its initial proposition, and the original paper proposed that the FT mRNA hypothesis was retracted （Huang et al. 2005; Bohlenius et al. 2007）. Interestingly enough, the FT gene previously proposed to encode a florigen was never challenged. Rather, the FT protein, instead of the FT mRNA, is now believed to migrate from leaves to the apical meristem to promote floral initiation. In this update, we will share with our readers some entertaining stories concerning the recent studies of florigen in five different plant species. In addition to the published reports referenced inthis update, readers may also refer to our previous minireview and references therein for additional background information （Yu et al. 2006）.     

Understanding the genetic and epigenetic architecture in complex network of rice flowering pathways

Although the molecular basis of flowering time control is well dissected in the long day (LD) plant Arabidopsis, it is still largely unknown in the short day (SD) plant rice. Rice flowering time (heading date) is an important agronomic trait for season adaption and grain yield, which is affected by both genetic and environmental factors. During the last decade, as the nature of florigen was identified, notable progress has been made on exploration how florigen gene expression is genetically controlled. In Arabidopsis expression of certain key flowering integrators such as FLOWERING LOCUS C (FLC) and FLOWERING LOCUS T (FT) are also epigenetically regulated by various chromatin modifications, however, very little is known in rice on this aspect until very recently. This review summarized the advances of both genetic networks and chromatin modifications in rice flowering time control, attempting to give a complete view of the genetic and epigenetic architecture in complex network of rice flowering pathways.     

Developing a method for customized induction of flowering

Background  

The ability to induce flowering on demand is of significant biotechnological interest. FT protein has been recently identified as an important component of the mobile flowering hormone, florigen, whose function is conserved across the plant kingdom. We therefore focused on manipulation of both endogenous and heterologous FT genes to develop a floral induction system where flowering would be inhibited until it was induced on demand. The concept was tested in the model plant Arabidopsis thaliana (Arabidopsis).     

Mikhail Khristoforovich Chailakhyan: The fate of the scientist under the sign of florigen

The more significant is a discovery made by the scientist, the greater influence it exerts on the fate of its author. The theory of florigen, a hormone of flowering, put forward by M.Kh. Chailakhyan in 1936 initially was inconvenient for Soviet authorities and brought severe trials to the scientist. However, as distinct from many others, Chailakhyan did not deny his scientific beliefs but continued to defend them in spite of harassment and threats. Later, on the contrary, this theory promoted the worldwide fame of its creator, although during Chailakhyan lifetime florigen has not been definitely identified chemically. Chailakhyan was close to the establishing of florigen protein nature, but even his long life was not enough to identify this elusive substance.     

Mobile signals in day length-regulated flowering: Gibberellins, flowering locus T, and sucrose

Despite low activity for stem growth, the gibberellins GA₅ and GA₆ act as long-day (LD) florigens in Lolium temulentum L. This claim is based on extensive evidence covering GA synthesis in LD in the induced leaf and their transport to the shoot apex where they act in a dose-dependent manner. GAs also act as a LD florigen in association with cold vernalization of L. perenne. In contrast, highly bioactive GA₄ and, possibly, GA₁ are important florigens in Arabidopsis thaliana (L.) Heynh. This species contrast reflects differences in GA deactivation, which is unimportant for Arabidopsis but dominant in L. temulentum. It is unclear if GAs participate in flowering responses of short-day (SD) species since it is LD, which up-regulate enzymes for GA biosynthesis. Sugars (sucrose) may also act directly as a florigen and, specifically, with increase in photosynthesis as in LD or when light intensity is increased in SD. In addition, in LD sucrose can indirectly cause flowering by up-regulating FT expression, the FT protein acting as a further leaf-to-apex transported florigen. Thus, there are not only multiple florigens but there can be complex interactions between the signaling pathways controlling production of these various florigens.     

14-3-3-Regulated Ca2+-dependent protein kinase CPK3 is required for sphingolipid-induced cell death in Arabidopsis

In eukaryotic cells, sphingoid long chain bases (LCBs) such as sphingosine or phytosphingosine (PHS) behave as second messengers involved in various processes including programmed cell death (PCD). In plants, induction of PCD by LCBs has now been described, but the signalling pathway is still enigmatic. Using Arabidopsis, we identify new key steps in this pathway. We demonstrate that PHS induces activation of the calcium-dependent kinase CPK3, which phosphorylates its binding partners, the 14-3-3 proteins. This phosphorylation leads to the disruption of the complex and to CPK3 degradation. Using cpk3 knockout lines, we demonstrate that CPK3 is a positive regulator of LCB-mediated PCD. These findings establish 14-3-3-regulated CPK3 as a key component of the LCB pathway leading to PCD in plants.