How repeated epiphylly correlates with gene expression of resident knox1 in the leaves of tobacco epiphyllous shoots

2006 ◽  
Vol 1 (2) ◽  
pp. 263-274 ◽  
Author(s):  
Kai Müller ◽  
Jinxing Lin ◽  
Rainer Fischer ◽  
Dirk Prüfer

AbstractThe tobacco knox1 genes tokn1 and tokn2 were isolated and their neomorphic capacities were tested while expressed in tobacco and potato. In addition, their neomorphic capacities were compared to barley bkn3 transgenic plant material. While tokn2 and bkn3 induced epiphylly in tobacco and supercompound leaves in potato, tokn1 failed to produce such prominent knox1 specific phenotypes. In wild type tobacco, alleles of the tokn genes were found to be expressed within distinct zones of the shoot apical meristem (SAM), leaving out regions that correlated with leaf founder cells [1]. In contrast, the expression of the tokn genes was detected throughout the meristem and in leaf primordia of epiphyllous shoots that developed in tobacco over-expressing the barley hooded gene bkn3. It was determined that such extended expression domains of resident tobacco knox1 genes were mediated through an enhanced expression domain of bkn3 within the tissue confined to the epiphylls, and this contributed to “repeated epiphylly”, i.e. an iterated development of epiphyllous shoots on leaves of progenitor epiphylls.

Botany ◽  
2010 ◽  
Vol 88 (5) ◽  
pp. 528-536 ◽  
Author(s):  
Denis Barabé ◽  
Laura Bourque ◽  
Xiaofeng Yin ◽  
Christian Lacroix

Previous studies on palm phyllotaxis deal mainly with the mature trunk. The goals of this study are (i) to determine the relationship between the number of parastichies, the divergence angle, and the plastochrone ratio at the level of the shoot apical meristem; (ii) to examine whether there are fluctuations in the divergence angle; (iii) to interpret the significance of phyllotactic parameters with respect to the mode of growth of the apex. The tubular base of the leaf primordium is more or less asymmetrical, and completely surrounds the shoot apical meristem. The phyllotactic system corresponds to a (2, 3) conspicuous parastichy pair. The mean divergence angle per apex varies between 126.9° ± 9.3° (mean ± SD) and 135. 8° ± 8.0°. Divergence angles for all apices fluctuate within a range of 115.89° to 157.33°. The mean plastochrone ratios between apices varies from 1.35 ± 0.18 to 1.58 ± 0.12. The plastochrone ratio at each plastochrone for all apices ranges from 1.09 to 2.00. There is no correlation between the angle of divergence and the plastochrone ratio. There is a fluctuation in the value of the divergence angle that falls within the range predicted by the fundamental theorem of phyllotaxis. The high value of the ratio of the diameter of leaf primordia over the diameter of the apex, and the long plastochrone might explain the lack of correlation between certain phyllotactic parameters.


2005 ◽  
Vol 21 (Suppl 1) ◽  
pp. i232-i240 ◽  
Author(s):  
H. Jonsson ◽  
M. Heisler ◽  
G. V. Reddy ◽  
V. Agrawal ◽  
V. Gor ◽  
...  

Development ◽  
1992 ◽  
Vol 115 (3) ◽  
pp. 745-753 ◽  
Author(s):  
V. F. Irish ◽  
I. M. Sussex

We have mapped the fate of cells in the Arabidopsis embryonic shoot apical meristem by irradiating seed and scoring the resulting clonally derived sectors. 176 white, yellow, pale green or variegated sectors were identified and scored for their position and extent in the resulting plants. Most sectors were confined to a fraction of a leaf, and only occasionally extended into the inflorescence. Sectors that extended into the inflorescence were larger, and usually encompassed about a third to a half of the inflorescence circumference. We also find that axillary buds in Arabidopsis are clonally related to the subtending leaf. Sections through the dry seed embryo indicate that the embryonic shoot apical meristem contains approximately 110 cells in the three meristematic layers prior to the formation of the first two leaf primordia. The histological analysis of cell number in the shoot apical meristem, in combination with the sector analysis have been used to construct a map of the probable fate of cells in the embryonic shoot apical meristem.


PLoS Genetics ◽  
2007 ◽  
Vol 3 (6) ◽  
pp. e101 ◽  
Author(s):  
Xiaolan Zhang ◽  
Shahinez Madi ◽  
Lisa Borsuk ◽  
Dan Nettleton ◽  
Robert J Elshire ◽  
...  

Development ◽  
1992 ◽  
Vol 116 (2) ◽  
pp. 397-403 ◽  
Author(s):  
H. M. Ottoline Leyser ◽  
I. J. Furner

The shoot apical meristem of dicotyledonous plants is highly regulated both structurally and functionally, but little is known about the mechanisms involved in this regulation. Here we describe the genetic and phenotypic characterisation of recessive mutations at three loci of Arabidopsis thaliana in which meristem structure and function are disrupted. The loci are Clavata1 (Clv1), Fasciata1 (Fas1) and Fasciata2 (Fas2). Plants mutant at these loci are fasciated having broad, flat stems and disrupted phyllotaxy. In all cases, the fasciations are associated with shoot apical meristem enlargement and altered floral development. While all the mutants share some phenotypic features they can be divided into two classes. The pleiotropic fas1 and fas2 mutants are unable to initiate wild- type organs, show major alterations in meristem structure and have reduced root growth. In contrast, clv1 mutant plants show near wild-type organ phenotypes, more subtle changes in shoot apical meristem structure and wild-type root growth.


2019 ◽  
Vol 20 (1) ◽  
pp. 180 ◽  
Author(s):  
Alicja Banasiak ◽  
Magdalena Biedroń ◽  
Alicja Dolzblasz ◽  
Mateusz Adam Berezowski

In the shoot apical meristem (SAM) of Arabidopsis, PIN1-dependent polar auxin transport (PAT) regulates two crucial developmental processes: organogenesis and vascular system formation. However, the knockout mutation in the PIN1 gene does not fully inhibit these two processes. Therefore, we investigated a potential source of auxin for organogenesis and vascularization during inflorescence stem development. We analyzed auxin distribution in wild-type (WT) and pin1 mutant plants using a refined protocol of auxin immunolocalization; auxin activity, with the response reporter pDR5:GFP; and expression of auxin biosynthesis genes YUC1 and YUC4. Our results revealed that regardless of the functionality of PIN1-mediated PAT, auxin is present in the SAM and vascular strands. In WT plants, auxin always accumulates in all cells of the SAM, whereas in pin1 mutants, its localization within the SAM changes ontogenetically and is related to changes in the structure of the vascular system, organogenic activity of SAM, and expression levels of YUC1 and YUC4 genes. Our findings indicate that the presence of auxin in the meristem of pin1 mutants is an outcome of at least two PIN1-independent mechanisms: acropetal auxin transport from differentiated tissues with the use of vascular strands and auxin biosynthesis within the SAM.


2015 ◽  
Vol 62 (5) ◽  
pp. 684-694 ◽  
Author(s):  
M. Wu ◽  
J. Li ◽  
S. L. Fan ◽  
M. Z. Song ◽  
C. Y. Pang ◽  
...  

1993 ◽  
Vol 5 (3) ◽  
pp. 297-309 ◽  
Author(s):  
A J Fleming ◽  
T Mandel ◽  
I Roth ◽  
C Kuhlemeier

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