The development of cotyledon and shoot apex in monocotyledons

1984 ◽  
Vol 62 (6) ◽  
pp. 1316-1318 ◽  
Author(s):  
J.-L. Guignard

Monocotyledonous embryos have a single cotyledon which is initiated very early. During development the differential growth in the cotyledon results in a lateral shoot apical meristem; its quiescent central zone, at first axial as in Palmae, becomes more lateral in the course of evolution owing to earlier development of the cotyledon. One can establish a phyletic sequence from a dicotyledonous embryo to an advanced monocotyledonous embryo through the Palmae.

1969 ◽  
Vol 20 (2) ◽  
pp. 279 ◽  
Author(s):  
JM Hopkinson ◽  
RV Hannam

Experiments were done with the objective of describing floral induction in tobacco. A short-day mutant, grown in controlled-environment cabinets, was used to define the stages of development, and the results were used to interpret the behaviour of both short-day and day-neutral plants grown in the field. The shoot apex passed through an apparent juvenile phase, characterized by a progressive increase in its size. Next, in the absence of floral induction it entered an equilibrium stage during which its size, staining properties, and activity remained constant. After 10 inductive cycles, apices of short-day plants became committed to flower. The rate of leaf inception increased, the apical meristem became domed, and the region of intense pyronin staining (indicative of RNA) spread to the central zone. Differentiation of the inflorescence followed, and the terminal flower was recognizable about 20 days after the start of induction. The apices of field plants remained juvenile for very much longer than did apices of cabinet-grown plants, and floral induction did not take effect until after recovery from transplanting. Apices of day-neutral plants then passed directly to the induced state, whilst those of the mutant remained indefinitely vegetative in the equilibrium stage, natural day lengths at the time being non-inductive. The protracted juvenility of field plants was attributed to the stresses of seed-bed conditions and transplanting damage.


Author(s):  
Filipa Lopes ◽  
Carlos Galvan-Ampudia ◽  
Benoit Landrein

Abstract The maintenance of the stem cell niche in the shoot apical meristem, the structure that generates all of the aerial organs of the plant, relies on a canonical feedback loop between WUSCHEL (WUS) and CLV3 (CLV3). WUS is a homeodomain transcription factor expressed in the organizing center that moves to the central zone to promote stem cell fate. CLAVATA3 is a peptide whose expression is induced by WUS in the central zone that can move back to the organizing center to inhibit WUS expression. Within the last 20 years since the initial formulation of the CLV/WUS feedback loop, the mechanisms of stem cell maintenance have been intensively studied and the function of WUS has been redefined. In this review, we will highlight the most recent advances in our comprehension of the molecular mechanisms of WUS function, of its interaction with other transcription factors and with hormonal signals and of its connection to environmental signals. Through this, we will show how WUS can integrate both internal and external cues to adapt meristem function to the plant environment.


1971 ◽  
Vol 49 (11) ◽  
pp. 1941-1945 ◽  
Author(s):  
Thomas H. Haight ◽  
Charles Carroll Kuehnert

Data from culture experiments presented strongly suggest that the development of leaf primordia at the shoot apex may be divided into three phases in Osmunda cinnamomea. Phase I lasts from inception (Im) to some point in time during P1. Phase II probably begins somewhere between Im and I1, and may be retained as long as P9. Phase III is evident as early as P1 and continues through the entire primordial sequence to include Pn. In nature, or under experimental conditions where physiological continuity between the primordium and shoot apical meristem complex is maintained, O. cinnamomea primordial expression is phase III expression (leaf only). However, if the primordia produced at the shoot apex are removed from certain external biological influences (specifically the shoot apical meristem and certain older primordia) terminal expression of the primordia may be either phase I, phase II, or phase III depending upon the developmental phase of the primordia at the time of their isolation.


2016 ◽  
Author(s):  
Margaret E. Wilson ◽  
Matthew Mixdorf ◽  
R. Howard Berg ◽  
Elizabeth S. Haswell

ABSTRACTThe balance between proliferation and differentiation in the plant shoot apical meristem is controlled by regulatory loops involving the phytohormone cytokinin and stem cell identity genes. Concurrently, cellular differentiation in the developing shoot is coordinated with the environmental and developmental status of plastids within those cells. Here we employ an Arabidopsis thaliana mutant exhibiting constitutive plastid osmotic stress to investigate the molecular and genetic pathways connecting plastid osmotic stress with cell differentiation at the shoot apex. msl2 msl3 mutants exhibit dramatically enlarged and deformed plastids in the shoot apical meristem, and develop a mass of callus tissue at the shoot apex. Callus production in this mutant requires the cytokinin receptor AHK2 and is characterized by increased cytokinin levels, down-regulation of cytokinin signaling inhibitors ARR7 and ARR15, and induction of the stem cell identity gene WUSCHEL. Furthermore, plastid stress-induced apical callus production requires elevated plastidic ROS, ABA biosynthesis, the retrograde signaling protein GUN1, and ABI4. These results are consistent with a model wherein the cytokinin/WUS pathway and retrograde signaling control cell differentiation at the shoot apex.SUMMARY STATEMENTPlastid osmotic stress influences differentiation at the plant shoot apex. Two established mechanisms that control proliferation, the cytokinin/WUSCHEL stem cell identity loop and a plastid-to-nucleus signaling pathway, are implicated.


2018 ◽  
Author(s):  
Carlos S. Galvan-Ampudia ◽  
Guillaume Cerutti ◽  
Jonathan Legrand ◽  
Romain Azais ◽  
Géraldine Brunoud ◽  
...  

AbstractRhythmic patterning is central to the development of eukaryotes, particularly in plant shoot post-embryonic development. The plant hormone auxin drives rhythmic patterning at the shoot apical meristem, but the spatio-temporal dynamics of the auxin gradients is unknown. We used quantitative imaging to demonstrate that auxin provides high-definition graded information not only in space but also in time. We provide evidence that developing organs are auxin-emitting centers that could self-organize spatio-temporal auxin gradients through a transport network converging on the meristem center. We further show that a memory of the exposition of cells to auxin allows to differentiate temporally sites of organ initiation, providing a remarkable example of how the dynamic redistribution of a morphogenetic regulator can be used to create rhythmicity.


2012 ◽  
Vol 3 (1) ◽  
pp. 3 ◽  
Author(s):  
Chui E. Wong ◽  
Mohan B. Singh ◽  
Prem L. Bhalla

The shoot apical meristem houses stem cells responsible for the continuous formation of aerial plant organs including leaves and stems throughout the life of plants. Laser-microdissection in combination with high-throughput technology such as next generation sequencing permits an in-depth analysis of molecular events associated with specific cell type of interest. Sample preparation is the most critical step in ensuring good quality RNA to be extracted from samples following laser-microdissection. Here, we optimized the sample preparation for a major legume crop, soybean. We used Farmer’s solution as a fixative and paraffin as the embedding medium for soybean shoot apical meristem tissue without the use of any specialized equipment. Shorter time for tissue fixation (two days) was found to be critical for the preservation of RNA in soybean shoot apical meristem. We further demonstrated the utility of this method for different tissues derived from soybean and rice. The method outlined here shall facilitate studies on crop plants involving laser-microdissection.


Planta ◽  
2002 ◽  
Vol 214 (6) ◽  
pp. 829-836 ◽  
Author(s):  
Andreas Mordhorst ◽  
Marijke Hartog ◽  
Mazen El Tamer ◽  
Thomas Laux ◽  
Sacco de Vries

Cell ◽  
2011 ◽  
Vol 145 (2) ◽  
pp. 242-256 ◽  
Author(s):  
Hongliang Zhu ◽  
Fuqu Hu ◽  
Ronghui Wang ◽  
Xin Zhou ◽  
Sing-Hoi Sze ◽  
...  

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