Structure of Drosophila polytene chromosomes. Evidence for a toroidal organization of the bands

1982 ◽  
Vol 57 (1) ◽  
pp. 73-113
Author(s):  
L.I. Mortin ◽  
J.W. Sedat
Keyword(s):  
Electron Microscopy ◽  
Fluorescent Microscopy ◽  
Polytene Chromosomes ◽  
Three Dimensional ◽  
Structural Features ◽  
Serial Sections ◽  
High Voltage Electron Microscopy ◽  
Voltage Electron ◽  
Chromosome Bands ◽  
Whole Mounts

Avoiding acid fixation or squashing, the structure of Drosophila salivary gland polytene chromosomes has been examined in detail in nuclei, with special emphasis on the organization of the DNA in the chromosome bands. Cut serial sections, optical serial sections, scanning electron microscopy (SEM) on whole mounts, high-voltage electron microscopy (HVEM) on whole mounts, and pancreatic DNase I digestion monitored by fluorescent microscopy have been used to complement one another in this analysis. With all five of these techniques, stereo pairs were used to aid in the three-dimensional reconstruction of chromosomal structures. Evidence is presented that most, if not all, of the polytene chromosome bands are torus-shaped. The DNA of these bands is largely confined to the rim, with the interior essentially DNA-free. The chromatin in each polytene band is also seen to have an extremely regular and highly ordered substructure. This substructural organization is largely radially symmetric in the bands and generally parallel to the chromosome axis. In addition, each band appears to be a distinct architectural entity with regard to its exact structural features and dimensions. A model is presented that follows these organizational boundary conditions.

Staining Serial Thick Sections For High-Voltage Electron Microscopy

1985 ◽  
Vol 43 ◽  
pp. 708-709
Author(s):  
John C. Kinnamon ◽  
Terri A. Sherman
Keyword(s):  
Electron Microscopy ◽  
High Voltage ◽  
Carbon Coating ◽  
Three Dimensional ◽  
Taste Bud ◽  
Serial Sections ◽  
High Voltage Electron Microscopy ◽  
Ultrastructural Studies ◽  
Voltage Electron ◽  
High Voltage Electron

Ultrastructural studies often require three-dimensional reconstructions from serial electron micrographs. The use of thick sections and high voltage electron microscopy can reduce the numbers of serial sections needed, but we have found that over 300 serial sections (0.5 μm thick) are still needed for our studies of taste bud ultrastructure. Serial reconstructions are almost always done with sections mounted onto formvar-coated slot grids, because they provide an unobscured view of the specimen. Staining and carbon coating several hundred formvar-coated slot grids often results in the loss of serial sections because the formvar films break due to handling during the staining and carbon-coating procedures. In addition, the staining process itself can be tedious and time-consuming when staining thick sections because staining times of hours are often required. Such lengthy staining times may result in staining artifacts due to exposure of the stain to the atmosphere, especially with lead stains.

Three-Dimensional Visualization of the T-System of Frog Muscle Using High Voltage Electron Microscopy and a Lanthanum Stain

1977 ◽  
Vol 35 ◽  
pp. 570-571 ◽  
Author(s):  
Lee D. Peachey ◽  
Clara Franzini-Armstrong
Keyword(s):  
Electron Microscopy ◽  
High Voltage ◽  
Three Dimensional ◽  
Biological Tissues ◽  
High Voltage Electron Microscopy ◽  
Transverse Tubular System ◽  
Peroxidase Reaction ◽  
Voltage Electron ◽  
High Voltage Electron ◽  
T System

The effective study of biological tissues in thick slices of embedded material by high voltage electron microscopy (HVEM) requires highly selective staining of those structures to be visualized so that they are not hidden or obscured by other structures in the image. A tilt pair of micrographs with subsequent stereoscopic viewing can be an important aid in three-dimensional visualization of these images, once an appropriate stain has been found. The peroxidase reaction has been used for this purpose in visualizing the T-system (transverse tubular system) of frog skeletal muscle by HVEM (1). We have found infiltration with lanthanum hydroxide to be particularly useful for three-dimensional visualization of certain aspects of the structure of the T- system in skeletal muscles of the frog. Specifically, lanthanum more completely fills the lumen of the tubules and is denser than the peroxidase reaction product.

High-voltage electron microscopy of maxillary gland of spirochete-infected brine shrimp: lesion of efferent tubule

1988 ◽  
Vol 46 ◽  
pp. 362-363
Author(s):  
G. E. Tyson ◽  
M. J. Song
Keyword(s):  
Electron Microscopy ◽  
High Voltage ◽  
Brine Shrimp ◽  
Natural Populations ◽  
Three Dimensional ◽  
Dimensional Structure ◽  
High Voltage Electron Microscopy ◽  
Voltage Electron ◽  
High Voltage Electron ◽  
Infected Adult

Natural populations of the brine shrimp, Artemia, may possess spirochete- infected animals in low numbers. The ultrastructure of Artemia's spirochete has been described by conventional transmission electron microscopy. In infected shrimp, spirochetal cells were abundant in the blood and also occurred intra- and extracellularly in the three organs examined, i.e. the maxillary gland (segmental excretory organ), the integument, and certain muscles The efferent-tubule region of the maxillary gland possessed a distinctive lesion comprised of a group of spirochetes, together with numerous small vesicles, situated in a cave-like indentation of the base of the tubule epithelium. in some instances the basal lamina at a lesion site was clearly discontinuous. High-voltage electron microscopy has now been used to study lesions of the efferent tubule, with the aim of understanding better their three-dimensional structure.Tissue from one maxillary gland of an infected, adult, female brine shrimp was used for HVEM study.

scholarly journals Three-dimensional ultrastructure of a unicellular cyanobacterium.

1983 ◽  
Vol 97 (3) ◽  
pp. 713-722 ◽  
Author(s):  
S A Nierzwicki-Bauer ◽  
D L Balkwill ◽  
S E Stevens
Keyword(s):  
Inclusion Bodies ◽  
Cytoplasmic Membrane ◽  
Three Dimensional ◽  
Thylakoid Membranes ◽  
Serial Sections ◽  
Unicellular Cyanobacterium ◽  
High Voltage Electron Microscopy ◽  
Voltage Electron ◽  
Inner Surface ◽  
Computer Aided

The first complete three-dimensional ultrastructural reconstruction of a cyanobacterium was accomplished with high-voltage electron microscopy and computer-aided assembly of serial sections. The precise arrangement of subcellular features within the cell body was very consistent from one cell to another. Specialized inclusion bodies always occupied specific intracellular locations. The photosynthetic thylakoid membranes entirely surrounded the central portion of the cytoplasm, thereby compartmentalizing it from the rest of the cell. The thylakoid membranes formed an interconnecting network of concentric shells, merging only at the inner surface of the cytoplasmic membrane. The thylakoids were in contact with the cytoplasmic membrane at several locations, apparently to maintain the overall configuration of the thylakoid system. These results clarified several unresolved issues regarding structure-function relationships in cyanobacteria.

scholarly journals Three-Dimensional Imaging of a Long-Period Stacking Ordered Phase in Mg97Zn1Gd2 Using High-Voltage Electron Microscopy

2016 ◽  
Vol 57 (6) ◽  
pp. 918-921 ◽  
Author(s):  
Kazuhisa Sato ◽  
Shunya Tashiro ◽  
Yohei Yamaguchi ◽  
Takanori Kiguchi ◽  
Toyohiko J. Konno ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
High Voltage ◽  
Three Dimensional ◽  
Three Dimensional Imaging ◽  
High Voltage Electron Microscopy ◽  
Long Period ◽  
Voltage Electron ◽  
High Voltage Electron

Correlated 3D Light and Electron Microscopy of Large, Complex Structures: Analysis of Transverse Tubules in Heart Failure

1998 ◽  
Vol 4 (S2) ◽  
pp. 440-441
Author(s):  
Maryann E. Martone ◽  
Andrea Thor ◽  
Stephen J. Young ◽  
Mark H. Ellisman.
Keyword(s):  
Electron Microscopy ◽  
Electron Tomography ◽  
Light And Electron Microscopy ◽  
Structural Features ◽  
Electron Microscopic Level ◽  
Specimen Preparation ◽  
Large Sample Size ◽  
Electron Microscopic ◽  
High Voltage Electron Microscopy ◽  
Voltage Electron

Light microscopic imaging has experienced a renaissance in the past decade or so, as new techniques for high resolution 3D light microscopy have become readily available. Light microscopic (LM) analysis of cellular details is desirable in many cases because of the flexibility of staining protocols, the ease of specimen preparation and the relatively large sample size that can be obtained compared to electron microscopic (EM) analysis. Despite these advantages, many light microscopic investigations require additional analysis at the electron microscopic level to resolve fine structural features.High voltage electron microscopy allows the use of relatively thick sections compared to conventional EM and provides the basis for excellent new methods to bridge the gap between microanatomical details revealed by LM and EM methods. When combined with electron tomography, investigators can derive accurate 3D data from these thicker specimens. Through the use of correlated light and electron microscopy, 3D reconstructions of large cellular or subcellular structures can be obtained with the confocal microscope,

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