Abstract

BackgroundThe Arabidopsis FILAMENTOUS FLOWER (FIL) gene encodes a YABBY (YAB) family putative transcription factor that has been implicated in specifying abaxial cell identities and thus regulating organ polarity of lateral organs. In contrast to double mutants of fil and other YAB genes, fil single mutants display mainly floral and inflorescence morphological defects that do not reflect merely a loss of abaxial identity. Recently, FIL and other YABs have been shown to regulate meristem organization in a non-cell-autonomous manner. In a screen for new mutations affecting floral organ morphology and development, we have identified a novel allele of FIL, fil-9 and characterized its floral and meristem phenotypes.ResultsThe fil-9 mutation results in highly variable disruptions in floral organ numbers and size, partial homeotic transformations, and in defective inflorescence organization. Examination of meristems indicates that both fil-9 inflorescence and floral meristems are enlarged as a result of an increase in cell number, and deformed. Furthermore, primordia emergence from these meristems is disrupted such that several primordia arise simultaneously instead of sequentially. Many of the organs produced by the inflorescence meristems are filamentous, yet they are not considered by the plant as flowers. The severity of both floral organs and meristem phenotypes is increased acropetally and in higher growth temperature.ConclusionsDetailed analysis following the development of fil-9 inflorescence and flowers throughout flower development enabled the drawing of a causal link between multiple traits of fil-9 phenotypes. The study reinforces the suggested role of FIL in meristem organization. The loss of spatial and temporal organization of fil-9 inflorescence and floral meristems presumably leads to disrupted cell allocation to developing floral organs and to a blurring of organ whorl boundaries. This disruption is reflected in morphological and organ identity aberrations of fil-9 floral organs and in the production of filamentous organs that are not perceived as flowers. Here, we show the role of FIL in reproductive meristem development and emphasize the potential of using fil mutants to study mersitem organization and the related effects on flower morphogenesis.

Highlights

  • The Arabidopsis FILAMENTOUS FLOWER (FIL) gene encodes a YABBY (YAB) family putative transcription factor that has been implicated in specifying abaxial cell identities and regulating organ polarity of lateral organs

  • The indeterminate state of cells within the meristem is dependent on members of the KNOX gene family that are expressed in the shoot apical meristem (SAM) but excluded from incipient organ primordia [7]

  • Mutations in boundary genes, such as BOP1 and BOP2, as well as mutations in auxin influx carriers produce inflorescence and floral defects similar to those we observe in fil-9 mutants [45,46,47,48]. Based on these similarities in phenotype, in conjunction with the defects observed in inflorescence meristem (IM) and floral meristems (FMs) organization, we suggest that FIL is required for the appropriate delineation of central zone (CZ) and peripheral zone (PZ) boundaries within these meristems

Read more

Summary

Introduction

The Arabidopsis FILAMENTOUS FLOWER (FIL) gene encodes a YABBY (YAB) family putative transcription factor that has been implicated in specifying abaxial cell identities and regulating organ polarity of lateral organs. The SAM is organized into three zones, namely a central zone (CZ) at the SAM summit in which cells divide slowly to replenish the SAM population, a These meristematic domains are maintained in part by a negative feedback loop between WUSCHEL (WUS) and CLAVATA3 (CLV3) (for recent reviews, see [2,3,4]). The indeterminate state of cells within the meristem is dependent on members of the KNOX gene family that are expressed in the SAM but excluded from incipient organ primordia [7]. Lateral organ polarity is determined by the converse activities of abaxially-expressed KANADI and members of the YABBY (YAB) gene family and of the adaxially-expressed PHABULOSA and PHAVOLUTA genes [10]. In Petunia, the HAIRY MERISTEM gene that is expressed in organ primordia is required for SAM maintenance [14]

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call