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.2011 Jun;107(9):1557-66.
doi: 10.1093/aob/mcr045. Epub 2011 Mar 7.

Alternate transcripts of a floral developmental regulator have both distinct and redundant functions in opium poppy

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Alternate transcripts of a floral developmental regulator have both distinct and redundant functions in opium poppy

Philip Hands et al. Ann Bot.2011 Jun.

Abstract

Background and aims: The MADS-box transcription factor AGAMOUS (AG) is an important regulator of stamen and fruit identity as well as floral meristem determinacy in a number of core eudicots and monocots. However, its role outside of these groups has not been assessed explicitly. Examining its role in opium poppy, a basal eudicot, could uncover much about the evolution and development of flower and fruit development in the angiosperms.

Methods: AG orthologues were isolated by degenerate RT-PCR and the gene sequence and structure examined; gene expression was characterized using in situ hybridization and the function assessed using virus-induced gene silencing.

Key results: In opium poppy, a basal eudicot, the AGAMOUS orthologue is alternatively spliced to produce encoded products that vary at the C-terminus, termed PapsAG-1 and PapsAG-2. Both transcripts are expressed at high levels in stamens and carpels. The functional implications of this alternative transcription were examined using virus-induced gene silencing and the results show that PapsAG-1 has roles in stamen and carpel identity, reflecting those found for Arabidopsis AG. In contrast, PapsAG-2, while displaying redundancy in these functions, has a distinctive role in aspects of carpel development reflected in septae, ovule and stigma defects seen in the loss-of-function line generated.

Conclusions: These results describe the first explicit functional analysis of an AG-clade gene in a basal eudicot; illustrate one of the few examples of the functional consequences of alternative splicing in transcription factors and reveal the importance of alternative transcription, as well as gene duplication, as a driving force in evolution.

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Figures

Fig. 1.
Fig. 1.
Gene structure of thePapaver somniferum AG gene. (A) Schematic showing how alternative splicing at the 3′ end of the coding sequence generates two transcripts,PapsAG-1 andPapsAG-2 (not drawn to scale). Regions underlined in red are gene-specific fragments used for gene-silencing with VIGS and forin situ mRNA hybridization probes. The region overlined with a red bar indicates the presence of a forward primer outside of the region used in vigs lines for expression analysis. Black arrows indicate the splicing donor site. AG MI, AG Motif I; AG MII, AG Motif II. (B) Alignment of the C-terminal regions of translated PapsAG-1 and PapsAG-2 sequences with AG orthologues from tomato (TAG; Q40168),Antirrhinum majus (AmFAR; CAB42988),Arabidopsis thaliana (AtAG; P17839) andEschscholzia californica (EScaAG1 and EScaAG2; AAZ53205 and AAZ53206). PapsAG-2 has a 24-amino-acid extension. The conserved AG motifs are indicated.
Fig. 2.
Fig. 2.
Expression analyses ofPapsAG-1 andPapsAG-2. (A)In situ hybridization ofPapsAG-1 andPapsAG-2 transcript-specific probes on youngP. somniferum flowers showing similar expression patterns. P1 stage, Young meristem in longitudinal section before visible organ primordia appear; P3 stage, longitudinal section of developing flower bud; P5 stage, cross-section of older flower bud; P7 stage, cross-section through developing anthers with adjacent filament sections. The stages are as in Dreaet al. (2007). Scale bar = 200 µm. (B) RT-PCR withPapsAG-1 andPapsAG-2 transcript-specific primers using cDNA from dissected floral organs (sepal, se; petal, pe; stamen, st; carpel, ca) of older bud stages (P6, 3-mm buds; P7, 7-mm buds). Amplification of theP. somniferum ACTIN gene,PapsACT1, was used as a control.
Fig. 3.
Fig. 3.
Phenotypes of vigsAG1,vigsAG2 and vigAG-D plants at pendant flower stage: (A) wild-type poppy flower; (B) vigsAG1 flower showing extended gynophore (black arrow), partially transformed anthers (red arrow) and open stigma (blue arrow); (C) vigsAG1 capsule cut in transverse showing sepals developing inside (arrow); (D) vigsAG2 curved capsule (inset shows normal stamens from a wild-type flower); (E, F) vigsAG2 flower showing defective stigma (red arrow); (G, I) vigsAG-D flowers showing petaloid stamens and sepaloid carpel with petals inside (G), petaloid carpel with another flower inside with extra pedicel indicated (red arrow, H) and elongated sepaloid carpel which was completely empty inside (inset, I). Scale bars = 2 mm.
Fig. 4.
Fig. 4.
Distinct effects ofPapsAG-1 andPapsAG-2 gene silencing in capsule development: (A) wild-type stigma; (B) wild-type capsule cut open in transverse orientation showing ovules and septae; (C, E) vigsAG1 deformed stigmas; (D) vigsAG1 capsule cut in longitudinal orientation showing defective ovule development particularly at the distal end; (F) vigsAG1 open flower showing extended gynophores and modified anthers; (G, H) vigsAG2 stigma and open capsule cut in transverse orientation showing the deformed stigma and corresponding ovule defects within the capsule; (I, J) scanning electron micrographs of vigsAG2 stigmas, showing a retracted stigmatic ray (blue arrow) and a stigmatic pore in reverse orientation, i.e. it is directed towards the centre of the stigma (red arrow, I); disorganized stigma with ectopic papillae (blue arrow) and ovule (red arrow, J). Scale bars: (A–E, G, H) = 2 mm; (F) = 5 mm; (I) = 200 µm; (J) = 100 µm.
Fig. 5.
Fig. 5.
Phenotypes of vigsAG-D plants: (A) strongly transformed vigsAG-D flower with no distinguishable stamens and rudimentary gynoecium (boxed); (B–D) scanning electron micrographs of adaxial transformed carpels (boxed in A) showing the lack of any ovule initiation (B), in some lines there are rudimentary ovules without developing integuments (red arrow, C) and some stigmatic papillae at the distal end (D). (E–H) Phenotypes of weaker vigsAG-D lines showing partially petaloid (E, F) or generally normal stamens (G, H) and recognizable carpels that show a reduced stigmatic ray area (E, F) or resemble fused carpels (G, H). Scale bars: (B–D) = 50 µm; (A, E–H) = 2 mm.
Fig. 6.
Fig. 6.
RT-PCR of vigs lines. RT-PCR on RNA/cDNA extracted from the two innermost whorls (stamen and carpels) of pendant flowers from vigs lines for five representative plants transformed with each construct to test for the presence of the TRV construct and for reduced expression of thePapsAG transcripts. Three individual wild-type plants with tissue from the same stage (pendant) were included for comparison.
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References

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