scholarly journals STUDIES ON THE ORIGIN OF RIBOSOMES IN AMOEBA PROTEUS

1969 ◽  
Vol 40 (3) ◽  
pp. 622-632 ◽  
Author(s):  
Nessly Craig ◽  
Lester Goldstein
Keyword(s):  
Ribosomal Protein ◽  
Ribosomal Rna ◽  
Amoeba Proteus ◽  
Host Cell Cytoplasm ◽  
Cytoplasmic Rna ◽  
Nuclear Rna ◽  
Unlabeled Cell ◽  
Intact Molecule ◽  
Labeled Rna ◽  
Kinetics Of

The origin of cytoplasmic RNA and ribosomes was studied in Amoeba proteus by transplantation of a radioactive nucleus into an unlabeled cell followed by examination of the cytoplasm of the recipient for the presence of label. When a RNA-labeled nucleus was used, label appeared in the ribosomes, ribosomal RNA, and soluble RNA. Since the kinetics of appearance of labeled RNA indicates that the nucleus was not injured during the transfer, and since the transferred nuclear pool of labeled acid-soluble RNA precursors is inadequate to account for the amount of cytoplasmic RNA label, it is concluded that cytoplasmic ribosomal RNA is derived from acid-insoluble nuclear RNA and is probably transported as an intact molecule. Likewise, cytoplasmic soluble RNA probably originated in the nucleus, although labeling by terminal exchange in the cytoplasm is also possible. The results were completely different when a protein-labeled nucleus was grafted into an unlabeled host. In this case, label was found only in soluble proteins in the host cell cytoplasm, and there were no (or very few) radioactive ribosomes. This suggests that the nuclear pool of ribosomal protein and ribosomal protein precursors is relatively small and perhaps nonexistent (and, furthermore, shows that there was no cytoplasmic ribosomal contamination of the transferred nucleus).

RAPIDLY-LABELLED RNA IN THE MOUSE MAMMARY GLAND BEFORE AND DURING LACTATION

1973 ◽  
Vol 56 (1) ◽  
pp. 145-152 ◽  
Author(s):  
D. N. BANERJEE ◽  
M. R. BANERJEE
Keyword(s):  
Mammary Gland ◽  
Ribosomal Rna ◽  
Gradient Analysis ◽  
Sucrose Density Gradient ◽  
Mouse Mammary Gland ◽  
Nuclear Fraction ◽  
Cytoplasmic Rna ◽  
Nuclear Rna ◽  
Nuclear Synthesis

SUMMARY Linear sucrose density gradient analysis showed that the synthesis of rapidly-labelled high molecular weight RNA was virtually absent in the mammary glands of virgin mice. The rapidly-labelled RNA was first evident in the mammary gland in pregnancy and was also present during lactation. The bulk of this newly-made nuclear RNA sedimented as 45S and 32S fractions after a 15-min [3H]uridine pulse period in vivo. No labelled 18S RNA was detectable in the nuclear fraction after the 15-min pulse but it was present in the cytoplasm, suggesting that the 18S RNA migrates to the cytoplasm almost immediately after its formation. Thirty minutes after injection of [3H]uridine, the initial radioactivity of the 45S region migrated to the 32S fraction and a labelled 28S peak was also present in the cytoplasmic RNA at 60 min, suggesting that the processed 28S ribosomal RNA in the mammary gland began to migrate to the cytoplasm between 30 and 60 min after the nuclear synthesis of the precursor molecule.

Metabolism of high molecular weight, polydisperse, rapidly labeled nuclear RNA in rat liver

1968 ◽  
Vol 46 (12) ◽  
pp. 1497-1505 ◽  
Author(s):  
Maurice Brossard ◽  
Louis Nicole
Keyword(s):  
Molecular Weight ◽  
High Molecular Weight ◽  
Rat Liver ◽  
Ribosomal Rna ◽  
Base Composition ◽  
Orotic Acid ◽  
Chromosomal Origin ◽  
Base Analysis ◽  
Nuclear Rna ◽  
Kinetics Of

Studies of the metabolism of rat liver RNA showed the existence of two species of rapidly labeled nuclear RNA: a 45 S preribosomal type of nucleolar origin, and a 6–50 S polydisperse RNA of chromosomal origin. The kinetics of labeling with orotic acid-14C and the nature of the latter RNA have been investigated. The following findings are reported, (1) This RNA is composed of at least four main classes of RNA having sedimentation coefficients of approximately 45, 35, 24, and 18 S. (2) Except for the 18 S class which seems to be an end product, the three other classes have a rapid turnover and do not appear to leave the nucleus. (3) Base analysis after 32P incorporation indicates that these four classes of RNA have a similar base composition with a G+C/A + U ratio in the range of 0.98–1.07, which resembles DNA more closely than ribosomal RNA. (4) The 6–50 S polydisperse RNA has a different metabolism than that of the 45 S preribosomal type and there is no precursor-to-product relationship between these two species of RNA.

scholarly journals STABILITIES OF NUCLEAR AND MESSENGER RNA MOLECULES IN SEA URCHIN EMBRYOS

1972 ◽  
Vol 53 (2) ◽  
pp. 474-482 ◽  
Author(s):  
Bruce P. Brandhorst ◽  
Tom Humphreys
Keyword(s):  
Steady State ◽  
Sea Urchin ◽  
Half Life ◽  
Messenger Rna ◽  
Cell Fractionation ◽  
Rna Molecules ◽  
Sea Urchin Embryos ◽  
Cytoplasmic Rna ◽  
Nuclear Rna ◽  
Kinetics Of

The kinetics of accumulation of radioactive adenosine in adenosine triphosphate and in RNA of nuclear, cytoplasmic, and polysomal fractions of sea urchin embryos have been analyzed. 85% of the RNA synthesized decays in the nucleus with an apparently uniform half-life of about 7 min. The remaining 15% goes to the cytoplasm, mostly entering polysomes, and decays with a quite uniform half-life of about 75 min. The nuclear RNA accounts for one-third and the cytoplasmic RNA accounts for two-thirds of the total unstable RNA which accumulates at steady state in the embryo. The size distribution of short-labeled nuclear RNA is very similar to that of long-labeled messenger RNA, when both are extracted directly from the cells without a previous cell fractionation.

scholarly journals ELECTRON MICROSCOPIC EXAMINATION OF THE SITES OF NUCLEAR RNA SYNTHESIS DURING AMPHIBIAN EMBRYOGENESIS

1965 ◽  
Vol 26 (3) ◽  
pp. 937-958 ◽  
Author(s):  
Shuichi Karasaki
Keyword(s):  
Rna Synthesis ◽  
Developmental Stages ◽  
Early Embryo ◽  
Tail Bud ◽  
Electron Microscopic ◽  
Electron Microscopic Autoradiography ◽  
Nuclear Rna Synthesis ◽  
Nuclear Rna ◽  
Chromatin Material ◽  
Labeled Rna

The site of H3-uridine incorporation and the fate of labeled RNA during early embryo-genesis of the newt Triturus pyrrhogaster were studied with electron microscopic autoradiography. Isolated ectodermal and mesodermal tissues from the embryos were treated in H3-uridine for 3 hours and cultured in cold solution for various periods before fixation with OsO4 and embedding in Epon. At the blastula stage, the only structural component of the nucleus seen in electron micrographs is a mass of chromatin fibrils. At the early gastrula stage, the primary nucleoli originate as small dense fibrous bodies within the chromatin material. These dense fibrous nucleoli enlarge during successive developmental stages by the acquisition of granular components 150 A in diameter, which form a layer around them. Simultaneously larger granules (300 to 500 A) appear in the chromatin, and they fill the interchromatin spaces by the tail bud stage. Autoradiographic examination has demonstrated that nuclear RNA synthesis takes place in both the nucleolus and the chromatin, with the former consistently showing more label per unit area than the latter. When changes in the distribution pattern of radioactivity were studied 3 to 24 hours after immersion in isotope at each developmental stage, the following results were obtained. Labeled RNA is first localized in the fibrous region of the nucleolus and in the peripheral region of chromatin material. After longer culture in non-radioactive medium, labeled materials also appear in the granular region of the nucleolus and in the interchromatin areas. Further incubation gives labeling in cytoplasm.

Intranuclear Accumulation of Rna Resembling the Smaller Ribosomal Rna Component

1970 ◽  
Vol 6 (1) ◽  
pp. 53-72
Author(s):  
M. E. BRAMWELL
Keyword(s):  
Ribosomal Rna ◽  
Base Composition ◽  
Actinomycin D ◽  
Total Radioactivity ◽  
16S Ribosomal Rna ◽  
Low Concentrations ◽  
Rapid Accumulation ◽  
Nuclear Rna ◽  
Step Down ◽  
Nucleolar Rna

A study was made of the nuclear RNA in HeLa cells with particular reference to the rapidly labelled fractions. It was found that if cells were incubated at a high density, that is, under ‘step-down’ conditions, there was a rapid accumulation of RNA in the nucleus. The fraction of the nuclear RNA which includes rapidly labelled RNA and which binds tightly to columns of methylated albumin on kieselguhr increased in amount and reached levels which permitted enough of the material to be isolated for direct measurement of its base composition. This was found to be very similar to that of 16s ribosomal RNA. When cells growing logarithmically were treated with low concentrations of actinomycin D and then incubated in the presence of [3H]uridine it was found that an RNA fraction which bound tightly to methylated albumin on kieselguhr again accumulated in the nucleus. This fraction resembled that which accumulated under ‘step-down’ conditions. It contained over 85% of the total radioactivity in the nuclear RNA and again had a base composition very similar to 16s ribosomal RNA. Since nucleolar RNA synthesis was inhibited by the concentrations of actinomycin D used, it appeared that an RNA closely resembling 16s ribosomal RNA was synthesized outside the nucleolus. Sedimentation patterns on sucrose density gradients and thermal denaturation profiles lent support to the view that the RNA which binds tightly to columns of methylated albumin on kieselguhr probably represents ‘nascent’ 16s ribosomal RNA.

The appearance and quantitation of cytoplasmic ribonucleic acid in the early chick embryo

Development ◽  
1972 ◽  
Vol 28 (2) ◽  
pp. 367-384
Author(s):  
C. C. Wylie
Keyword(s):  
Chick Embryo ◽  
Ribosomal Rna ◽  
Rna Synthesis ◽  
Specific Activity ◽  
Cell Number ◽  
Present Knowledge ◽  
Precursor Pool ◽  
Cytoplasmic Rna ◽  
Labelling Experiment ◽  
Neurula Stage

This paper seeks to extend our knowledge about RNA synthesis in early embryogenesis to the domestic fowl, Gallus domesticus. Using this species for research, apart from increasing our knowledge of higher vertebrate embryology, has certain advantages such as rapid uptake of isotopic precursors and ease of microdissection in culture. The following results are presented: (1) The cell number in the whole chick embryos is shown to be increasing logarithmically between the time of laying and the early neurula stage; with a doubling time of 7·4 h. (2) The onset of ribosomal RNA synthesis has been shown to be during mid-cleavage of the chick embryo, while development is taking place in the oviduct and uterus of the mother. (3) In a cumulative labelling experiment, embryos were labelled at the unincubated-egg stage, allowed to develop to various morphological stages up to neurulation, and their cytoplasmic RNA prepared and analysed by gel electrophoresis. (4) The specific activity of the precursor pool for RNA synthesis was measured at several stages, using the same labelling conditions, and the results were used to quantitate the RNA synthesis from the incorporated radioactivity. (5) Using these techniques, it was found that newly synthesized cytoplasmic RNA accumulates steadily in the whole chick embryo, reaching a level of 104 μg by the early neurula stage. On a per cell basis, however, the amount of newly synthesized cytoplasmic RNA seems to decrease slightly. These findings are discussed in the light of present knowledge about embryos of other vertebrates and certain invertebrates.

Sign in / Sign up

Export Citation Format

Share Document