scholarly journals The Distribution of Nucleic Acids in Rat Eggs in Fertilization and Early Segmentation II. Histochemical Studies

1953 ◽  
Vol 6 (4) ◽  
pp. 665 ◽  
Author(s):  
AWH Braden ◽  
CR Austin

Sections of rat eggs in various stages of fertilization and early cleavage were stained with buffered solutions of methylene blue or light green to show the distribution of basophilia and acidophilia respectively, or were treated by the Feulgen technique to show the distribution of desoxyribonucleic acid (DNA).

1953 ◽  
Vol 6 (2) ◽  
pp. 324 ◽  
Author(s):  
CR Austin ◽  
AWH Braden

Observations have been made on the absorption of ultraviolet radiation at 260� mft by living rat eggs, as full-grown oocytes and during fertilization and early' cleavage. Precautions have been taken to permit the results to be interpreted in terms of nucleic acid concentrations.


1938 ◽  
Vol s2-80 (318) ◽  
pp. 293-319
Author(s):  
MARGARET I. DANIELS

A. Three gregarine species are found to inhabit the mid-gut of the mealworm larvae used: Gregarina cuneata Stein, Gregarina polymorpha Hamm, and Gregarina steini Berndt. The often described Steinina ovalis is probably seldom or never found. They live only in the mid-gut of larvae. They are never found in pupal or adult forms. Gregarines have been seen moving when in a stratified condition. B. The gregarine cytoplasm has five important inclusions, each having a characteristic position in a centrifuged animal (Text-fig. 2). 1. Paraglycogen.--This gives a dark brown colour with iodine, a pinkish general colour with the acid fuchsin of the Feulgen technique, and often a red colour with Bauer's reaction. It occupies the centrifugal pole of the centrifuged cell and is in the form of disc-like granules of varying size. 2. In young centrifuged Gregarina steini chromidial granules are seen in the paraglycogen area, and have, therefore, approximately the same specific gravity. They arise by karyosomic budding with the subsequent extrusion of these buds into the cytoplasm. They stain with iron alum haematoxylin, like the karyosome, and both give a negative result with the Feulgen test for thymonucleic acid. They probably correspond to Joyet-Lavergne's ‘albuminoid reserves’, but do not have the mitochondrial‘cap’ he describes. 3. Mitochondria.--These are usually granular, but sometimes rod-like. They are seen between the ‘alveoli’ formed by the paraglycogen granules. They lie distally to the paraglycogen in a centrifuged parasite; they stain by the iron alum haematoxylin long method, after Benoit, Champy, or Altmann fixation, also with Altmann's fuchsin picric acid stain and the Bensley Cowdry modification of it. 4. The Nucleus is karyosomic, and the karyosome is moved to the centrifugal pole by pressure as is the nucleolus of metazoan cells. The nucleus shows budding of the karyosome. There is plasmatic as well as chromatic material in the karyosome, as shown by centrifuging. The nucleus gives a negative result with Feulgen's nuclear reaction, but chromatin may exist in a very dispersed condition. 5. Golgi Material.--This lies at the centripetal end of the nucleus. It is best shown by Weigl fixation. The large and regular Golgi elements are slightly heavier than the granular Golgi material, which may be compared with that of young oocytes. 6. Fatty Material lies at the extreme centripetal pole of the cell, in globules of varying size. It becomes brown or black after treatment with osmium tetroxide, and vivid cherry red with Sudan IV. It gives a negative result with the Schultz reaction for cholestrol. C. Large globules are seen in the protomerite of Gregarina steini , eosinophile, sometimes fuchsinophile, and also staining with methylene blue. These move towards the centrifugal pole. Methylene blue preparations show blue granules among the paraglycogen granules in the centrifuged animal. They are remarkably resistant to dilute sulphuric acid. They are possibly allied to volutin or chromidia. Tests for the presence of Vitamin C yielded negative results. Only the inclusions of the gregarines in the gut lumen were studied, and the complete life-cycles of the species were not followed out.


Blood ◽  
1953 ◽  
Vol 8 (3) ◽  
pp. 249-261 ◽  
Author(s):  
LEON PAUL WEISS

Abstract In acid solution, tissues tend to acquire a net positive charge and bind acid dye; binding of basic dye is enhanced in basic solution where tissues tend to possess a net negative charge. A measure of the acid or basic strength of a given tissue structure is afforded by its ability to bind basic or acid dye over a range of pH. The capacity of blood cell components to bind light green and methylene blue in the pH range 0.05 to 12.3, and their affinity for eosin after acetylation and treatment with nitrous acid, procedures used to block or destroy primary and secondary amines and guanidino groups, was studied. Observations were also made of blood smears stained with the Serra test for arginine. Erythrocytes bound light green through pH 12.3 and methylene blue to pH 6.0. The ground substance of white blood cells and immature blood cells stained with light green through about pH 9 consistently, and often to pH 11: methylene blue was bound through approximately pH 4.0. Eosinophilic granules bound light green through pH 12.0, and did not bind methylene blue. Basophilic granules bound methylene blue in the pH range 8.0 to 1.0 but were dissolved in more acid and basic solutions: they bound no acid dye. Neutrophilic granules were stained with methylene blue through pH 5.3. Nuclei of immature blood cells and monocytes bound methylene blue to about pH 4.0: polymorphous nuclei and nuclei of lymphocytes and normoblasts were stained very faintly to pH 0.05. Many nuclei bound light green to about pH 12.0. Nuclear and cytoplasmic acidophilia was reduced or destroyed by acetylation or treatment of smears with nitrous acid. Nuclei and cytoplasm of blood cells were stained with the Serra test. Eosinophilic granules were stained strongly. The cytochemical significance of certain experimental findings have been discussed.


1987 ◽  
Vol 45 (2) ◽  
pp. 167-175 ◽  
Author(s):  
John M. Kelly ◽  
Wilhelm J. M. Putten ◽  
David J. Mcconnell

1955 ◽  
Vol 1 (1) ◽  
pp. 17-28 ◽  
Author(s):  
David P. Bloch ◽  
Gabriel C. Godman

1. The fast green stain of Alfert and Geschwind for nuclear basic protein is shown to obey the Beer-Lambert laws when used on purified histone. Interference from acid substances other than nucleic acids as a possible source of error is indicated. 2. Use of this technique after a modified Feulgen stain enables determination of relative amounts of desoxyribonucleic acid and histone in the same individual cells. 3. DNA and histone are shown to have the same distribution in formalin-fixed nuclei. 4. The syntheses of DNA and histone proceed simultaneously resulting in the doubling of both these substances prior to cell division. 5. The standard error for histone values is greater than that for DNA; however, the source of this variability is not known.


1948 ◽  
Vol 31 (5) ◽  
pp. 457-457
Author(s):  
Gerhard Schmidt ◽  
Liselotte Hecht ◽  
S. J. Thannhauser

The authors wish to correct an error in the paper "The behavior of the nucleic acids during the early development of the sea urchin egg (Arbacia)" (J. Gen. Physiol., 1947–48, 31, 203). Owing to an oversight, the figures for the amounts of various P fractions in a single Arbacia egg have been erroneously expressed in γ x 10–3 units (Tables I and II, page 205; the last two lines of page 206). The figures should have been expressed in γ x 10–5 units. Thus, the fertilized Arbacia egg contains an average of 20 γ x 10–5 ribonucleic acid P and 0.7 to 1 γ x 10–5 desoxyribonucleic acid P.


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