Sex steroid dynamics and mRNA transcript profiles of growth- and development-related genes during embryogenesis following induced follicular maturation in European eel

In life, genetic and epigenetic networks precisely coordinate the expression of genes—but in death, it is not known if gene expression diminishes gradually or abruptly stops or if specific genes and pathways are involved. We studied this by identifying mRNA transcripts that apparently increase in relative abundance after death, assessing their functions, and comparing their abundance profiles through postmortem time in two species, mouse and zebrafish. We found mRNA transcript profiles of 1063 genes became significantly more abundant after death of healthy adult animals in a time series spanning up to 96 h postmortem. Ordination plots revealed non-random patterns in the profiles by time. While most of these transcript levels increased within 0.5 h postmortem, some increased only at 24 and 48 h postmortem. Functional characterization of the most abundant transcripts revealed the following categories: stress, immunity, inflammation, apoptosis, transport, development, epigenetic regulation and cancer. The data suggest a step-wise shutdown occurs in organismal death that is manifested by the apparent increase of certain transcripts with various abundance maxima and durations.

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An ultrastructural study of vegetative incompatibility in plants

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100083047 ◽

1978 ◽

Vol 36 (2) ◽

pp. 436-437

Author(s):

Randy Moore

Keyword(s):

Ultrastructural Study ◽

Cell Walls ◽

Growth And Development ◽

Solanum Pennellii ◽

Initial Product ◽

Basic Aspect ◽

Tissue Interactions ◽

Graft Interface ◽

Antigen Antibody ◽

Standard Fixation

Cell and tissue interactions are a basic aspect of eukaryotic growth and development. While cell-to-cell interactions involving recognition and incompatibility have been studied extensively in animals, there is no known antigen-antibody reaction in plants and the recognition mechanisms operating in plant grafts have been virtually neglected.An ultrastructural study of the Sedum telephoides/Solanum pennellii graft was undertaken to define possible mechanisms of plant graft incompatibility. Grafts were surgically dissected from greenhouse grown plants at various times over 1-4 weeks and prepared for EM employing variations in the standard fixation and embedding procedure. Stock and scion adhere within 6 days after grafting. Following progressive cell senescence in both Sedum and Solanum, the graft interface appears as a band of 8-11 crushed cells after 2 weeks (Fig. 1, I). Trapped between the buckled cell walls are densely staining cytoplasmic remnants and residual starch grains, an initial product of wound reactions in plants.

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Identification of calcium oxalate crystals in dried or fixed tobacco leaf

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100111550 ◽

1984 ◽

Vol 42 ◽

pp. 288-289

Author(s):

Vicki L. Baliga ◽

Mary Ellen Counts

Keyword(s):

Electron Microscopy ◽

Scanning Electron Microscopy ◽

Calcium Oxalate ◽

Growth And Development ◽

Polarized Light ◽

Calcium Oxalate Crystals ◽

X Ray Diffraction ◽

X Ray ◽

Transmission Electron ◽

Scanning Electron

Calcium is an important element in the growth and development of plants and one form of calcium is calcium oxalate. Calcium oxalate has been found in leaf seed, stem material plant tissue culture, fungi and lichen using one or more of the following methods—polarized light microscopy (PLM), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and x-ray diffraction.Two methods are presented here for qualitatively estimating calcium oxalate in dried or fixed tobacco (Nicotiana) leaf from different stalk positions using PLM. SEM, coupled with energy dispersive x-ray spectrometry (EDS), and powder x-ray diffraction were used to verify that the crystals observed in the dried leaf with PLM were calcium oxalate.

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SEM study of the morphological effects of kinetin and zeatin on the growth and development of the apical meristem in wheat

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100141263 ◽

1995 ◽

Vol 53 ◽

pp. 978-979

Author(s):

G. M. Hutchins ◽

J. S. Gardner

Keyword(s):

Growth And Development ◽

Furfuryl Alcohol ◽

Apical Meristem ◽

Plant Cells ◽

Triticum Aestivum L ◽

Morphological Development ◽

Naturally Occurring ◽

Chinese Spring Wheat ◽

Sem Study ◽

Moist Environment

Cytokinins are plant hormones that play a large and incompletely understood role in the life-cycle of plants. The goal of this study was to determine what roles cytokinins play in the morphological development of wheat. To achieve any real success in altering the development and growth of wheat, the cytokinins must be applied directly to the apical meristem, or spike of the plant. It is in this region that the plant cells are actively undergoing mitosis. Kinetin and Zeatin were the two cytokinins chosen for this experiment. Kinetin is an artificial hormone that was originally extracted from old or heated DNA. Kinetin is easily made from the reaction of adenine and furfuryl alcohol. Zeatin is a naturally occurring hormone found in corn, wheat, and many other plants.Chinese Spring Wheat (Triticum aestivum L.) was used for this experiment. Prior to planting, the seeds were germinated in a moist environment for 72 hours.

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