The fine structure of the nuclear membrane in the larval salivary gland and midgut of Chironomus

1954 ◽  
Vol 6 (2) ◽  
pp. 519-522 ◽  
Author(s):  
G.F. Bahr ◽  
W. Beermann
Genetics ◽  
2000 ◽  
Vol 156 (1) ◽  
pp. 229-244
Author(s):  
Martina Vaskova ◽  
A M Bentley ◽  
Samantha Marshall ◽  
Pamela Reid ◽  
Carl S Thummel ◽  
...  

Abstract The 63F early puff in the larval salivary gland polytene chromosomes contains the divergently transcribed E63-1 and E63-2 ecdysone-inducible genes. E63-1 encodes a member of the EF-hand family of Ca2+-binding proteins, while E63-2 has no apparent open reading frame. To understand the functions of the E63 genes, we have determined the temporal and spatial patterns of E63-1 protein expression, as well as undertaken a genetic analysis of the 63F puff. We show that E63-1 is expressed in many embryonic and larval tissues, but the third-instar larval salivary gland is the only tissue where increases in protein levels correlate with increases in ecdysone titer. Furthermore, the subcellular distribution of E63-1 protein changes dynamically in the salivary glands at the onset of metamorphosis. E63-1 and E63-2 null mutations, however, have no effect on development or fertility. We have characterized 40 kb of the 63F region, defined as the interval between Ubi-p and E63-2, and have identified three lethal complementation groups that correspond to the dSc-2, ida, and mge genes. We show that mge mutations lead to first-instar larval lethality and that Mge protein is similar to the Tom22 mitochondrial import proteins of fungi, suggesting that it has a role in mitochondrial function.


1959 ◽  
Vol s3-100 (49) ◽  
pp. 13-15
Author(s):  
K. DEUTSCH ◽  
M. M. SWANN

The fine structure of a species of small free-living amoeba, Hartmanella astronyxis, has been investigated. The mitochondria resemble those of other species of amoeba. Structureless bodies of about the same size as mitochondria are sometimes found in association with them. Double membranes are common in the cytoplasm, and may show granules along their outer borders. The nuclear membrane is a double-layered structure, with a honeycomb structure evident in tangential sections. The cell membrane is also double-layered, or occasionally multi-layered.


1971 ◽  
Vol 49 (1) ◽  
pp. 132-133 ◽  
Author(s):  
Albert E. Moorman

Acetic-acid-fixed smears of Drosophila larval salivary gland chromosomes and of neuroblast cells from the larval ganglion undergoing mitosis are prepared by a modification of Heidenhain's iron-haematoxylin technique, in which absolute methyl alcohol is the solvent of all reagents used in the staining process.


1965 ◽  
Vol s3-106 (73) ◽  
pp. 15-21
Author(s):  
JOHN R. BAKER

The exocrine cells of the mouse pancreas were fixed in potassium dichromate solution, embedded in araldite or other suitable medium, and examined by electron microscopy. Almost every part of these cells is seriously distorted or destroyed by this fixative. The ergastoplasm is generally unrecognizable, the mitochondria and zymogen granules are seldom visible, and no sign of the plasma membrane, microvilli, or Golgi apparatus is seen. The contents of the nucleus are profoundly rearranged. It is seen to contain a large, dark, irregularly shaped, finely granular object; the evidence suggests that this consists of coagulated histone. The sole constituent of the cell that is well fixed is the inner nuclear membrane. The destructive properties of potassium dichromate are much mitigated when it is mixed in suitable proportions with osmium tetroxide or formaldehyde.


1988 ◽  
Vol 8 (5) ◽  
pp. 1877-1886
Author(s):  
B M Benton ◽  
S Berrios ◽  
P A Fisher

A 75-kilodalton polypeptide has been identified which copurifies with karyoskeletal protein-enriched fractions prepared from Drosophila melanogaster embryos. Results of indirect immunofluorescence experiments suggest that this protein, here designated p75, is primarily associated with puffed regions of larval salivary gland polytene chromosomes. In nonpolytenized Schneider 2 tissue culture cells, p75 appeared to be localized throughout the nuclear interior during interphase. In mitotic cells, p75 was redistributed diffusely. A possible role for karyoskeletal elements in transcriptional regulation is discussed.


1984 ◽  
Vol 179 (3) ◽  
pp. 289-314 ◽  
Author(s):  
Gregory M. Guild ◽  
Eileen Malko Shore

1964 ◽  
Vol 42 (6) ◽  
pp. 1147-1155 ◽  
Author(s):  
V. I. Kalnins ◽  
H. F. Stich ◽  
S. A. Bencosme

Electron microscope studies of salivary gland nuclei of four chironomid species have shown that the RNA-containing chromosome regions and associated structures, which by light microscopy exhibit a great variety of structures such as bands, granules, micronucleoli, nucleoli, puffs, and Balbiani rings, consist of only few basic units: pars amorpha, nucleolonema, and Balbiani ring granules. The fine structure of the nucleoli and spherical micronucleoli located at various chromosome regions appears to be identical, consisting of pars amorpha, which contains fibers of varying diameters, and strands of nucleolonema composed of fibers and ribosome-like granules. The arrangement of pars amorpha and nucleolonema of nucleoli and spherical micronucleoli follows a consistent pattern. Chromosome fibers are closely associated with pars amorpha, whereas strands of nucleolonema border only the surfaces of pars amorpha. Balbiani ring granules, which have a diameter of 300 Å to 500 Å and are characterized by a particular structure, accumulate in Balbiani rings, in many chromosome regions, and in nuclear sap. In the Balbiani ring these granules seem to be attached to 100 Å chromosome fibers. They are absent in nucleoli and micronucleoli. The possible correlation between our electron microscopic observations and the present-day concept of ribosomal and messenger RNA production is discussed.


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