scholarly journals Early ribonucleic acid synthesis during the germination of rye (Secale cereale) embryos and the relationship to early protein synthesis

1975 ◽  
Vol 148 (3) ◽  
pp. 381-387 ◽  
Author(s):  
S Sen ◽  
P I Payne ◽  
D J Osborne
Keyword(s):  
Protein Synthesis ◽  
Nucleic Acid ◽  
Secale Cereale ◽  
Ribonucleic Acid ◽  
Acid Synthesis ◽  
Fingerprint Analysis ◽  
5S Rna ◽  
Early Protein ◽  
Rrna Molecule ◽  
The Relationship

Incorporation studies with radioactive precursors showed that synthesis of protein and RNA is initiated in germinating embryos of rye within the first hour of imbibition of water. By polyacrylamide-gel fractionations of radioactive nucleic acid components, the appearance of products of transcription of the genome was shown to follow the sequence: heterogeneous (ribonuclease-sensitive) RNA, 4S and 5S RNA by 20min, 31S and 25S rRNA by 40min, and 18S RNA by 60min. “Fingerprint’ analysis of T1-ribonuclease digests show that all the large oligonucleotides present in 25S and 18S RNA are present in the 31S species, indicating that 31S RNA is the precursor rRNA molecule to both 25S and 18S RNA. The importance of these early RNA syntheses and in particular the possible template function of the heterogeneous RNA is discussed in relation to the concept of long-lived mRNA and the coding for protein synthesis in the first hours of germination.

Protein and Nucleic Acid Syntheses in Dark-dormant Common Purslane(Portulaca oleracea)Seed

Weed Science ◽  
1978 ◽  
Vol 26 (6) ◽  
pp. 669-672 ◽  
Author(s):  
Bonnie J. Reger ◽  
Ida E. Yates
Keyword(s):  
Protein Synthesis ◽  
Nucleic Acid ◽  
Rna Synthesis ◽  
Acid Synthesis ◽  
Portulaca Oleracea ◽  
Dark Incubation ◽  
Radicle Protrusion ◽  
Lag Period ◽  
Common Purslane ◽  
H Protein

Dark-incubated common purslane(Portulaca oleraceaL.) seed synthesize very little protein and essentially no nucleic acids. Dark-incubated seed incorporate only 14 × 10−3nmoles14C-leucine/mg protein/12-h dark. In contrast, seed exposed to 12-h light following 24-h dark incubation incorporate 365 × 10−3-nmoles14C-leucine/mg protein/12-h light. Once dormancy is broken by exposure of seed to light, initiation of radicle protrusion occurs at 12 h. Protein synthesis gradually increases with time in the light and precedes nucleic acid synthesis which is associated with radicle protrusion. During the 12-h lag period preceding radicle protrusion protein synthesis increases significantly by 3 to 9 h in light, RNA synthesis by 9 h in light, and DNA synthesis by 12 h in light. After 12 h in light,32P can be detected in all nucleic acid fractions, DNA and RNAs.

scholarly journals Antimicrobial Drug Interactions: Systematic Evaluation of Protein and Nucleic Acid Synthesis Inhibitors

Antibiotics ◽  
2019 ◽  
Vol 8 (3) ◽  
pp. 114 ◽  
Author(s):  
Yilancioglu
Keyword(s):  
Protein Synthesis ◽  
Multidrug Resistance ◽  
Nucleic Acid ◽  
Drug Interactions ◽  
Treatment Options ◽  
Acid Synthesis ◽  
Mechanisms Of Action ◽  
Nucleic Acid Synthesis ◽  
Protein Synthesis Inhibitors ◽  
Nucleic Acid Synthesis Inhibitors

Antimicrobial multidrug resistance and its transmission among strains are serious problems. Success rate is decreased and treatment options are narrowed due to increasing bacterial multidrug resistance. On the other hand, the need for long-term efforts to discover new antibiotics and difficulties finding new treatment protocols make this problem more complex. Combination therapy, especially with synergistic use of antimicrobials is a rational treatment option with huge benefits. Thus, screening antibiotic interactions is crucial for finding better treatment options. Clinicians currently use combinatorial antibiotic treatment as an effective treatment option. However, antibiotics can show synergistic or antagonistic interactions when used together. In our study, we aimed to investigate interactions of antibiotics with different mechanisms of action. Antibiotics, which act as protein synthesis inhibitors (P) and nucleic acid synthesis inhibitors (N) were used in our study. We tested 66 (PN), 15 (NN), and 55 (PP) drug pairs on the Escherichia coli strain. The Loewe additivity model was used and alpha scores were calculated for analysis of interactions of drug combinations. Drug interactions were categorized as synergistic or antagonistic. Accordingly, pairwise combinations of protein synthesis inhibitors (PP) showed stronger synergistic interactions than those of nucleic acid synthesis inhibitors (NN) and nucleic acid synthesis–protein synthesis inhibitors (PN). As a result, the importance of mechanisms of action of drugs is emphasized in the selection of synergistic drug combinations.

EFFECT OF OESTRADIOL-17β ON CLEAVAGE, NUCLEIC ACID METABOLISM AND PROTEIN SYNTHESIS IN SEA URCHIN, STRONGYLOCENTROTUS PURPURATUS, EMBRYOS

1962 ◽  
Vol 25 (2) ◽  
pp. 183-NP ◽  
Author(s):  
W. B. JOLLEY ◽  
W. E. MARTIN ◽  
J. W. BAMBERGER ◽  
L. W. STEARNS
Keyword(s):  
Protein Synthesis ◽  
Nucleic Acid ◽  
Sea Urchin ◽  
Ribonucleic Acid ◽  
Deoxyribonucleic Acid ◽  
Acid Metabolism ◽  
Strongylocentrotus Purpuratus ◽  
Nucleic Acid Metabolism ◽  
Dna And Rna ◽  
Moderate Effect

SUMMARY Oestradiol-17β at a concentration of 3 × 10−3 m inhibits cleavage in sea urchin (Strongylocentrotus purpuratus) embryos. This inhibition is accompanied by a reduction in deoxyribonucleic acid (DNA) synthesis and little change in ribonucleic acid (RNA). The effects of oestradiol-17β upon the incorporation of glycine-1-14C and glycine-2-14C into the purines of DNA and RNA and the incorporation of glycine-2-14C into serine were studied. The incorporation of glycine-1-14C and glycine-2-14C into RNA was reduced, but the incorporation of glycine-2-14C into DNA was increased considerably over that of the controls. The incorporation of glycine-2-14C into serine was also accelerated by oestradiol. A possible explanation of the action of oestradiol-17β is offered. The moderate effect upon RNA is not surprising because there is little or no synthesis of this compound from the time of fertilization to blastulation under normal conditions.

scholarly journals Anabolism versus catabolism of [5-3H]uridine and its relationship to ribonucleic acid labelling in mouse liver after partial hepatectomy

1979 ◽  
Vol 178 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Torsten Yngner ◽  
Claes Engelbrecht ◽  
Lillemor Lewan ◽  
Jan-Erik Annerfeldt
Keyword(s):  
Nucleic Acid ◽  
Partial Hepatectomy ◽  
Ribonucleic Acid ◽  
Mouse Liver ◽  
Rna Synthesis ◽  
Specific Radioactivity ◽  
Acid Synthesis ◽  
Liver Cells ◽  
Control Value

The balance between anabolism and catabolism of [5-3H]uridine was studied in the mouse after partial hepatectomy. Labelling of RNA and UDP-glucose was determined and evaluated in relation to changes in the specific radioactivity of UTP. The amounts of labelled catabolic products of uridine were increased several-fold in liver and blood after partial hepatectomy. The specific radioactivity of RNA decreased to about 60% of the control value at 6h and was in the same range as that of control liver at 24h after operation. Decreased labelling of RNA and UDP-glucose was attributable to decreased specific radioactivity of UTP. No changes in the size of the UTP pool or in the balance between uridine anabolism and catabolism were found that could explain the decreased specific radioactivity of UTP. Rather, the alterations in the labelling of this metabolite induced by the partial hepatectomy may be related to decreased phosphorylating capacity in the liver cells and/or dilution of the labelled precursor in an expanded uridine pool. The enhanced amounts of uridine catabolic products in liver and blood were probably a consequence of accumulation and altered incorporation of the metabolites from the blood into the liver cells. Despite the increased amounts of labelled catabolic products and the decreased labelling of RNA, the results reported here actually suggest decreased uridine catabolism and slightly increased RNA synthesis in mouse liver after partial hepatectomy. The results stress the importance of proper controls in determination of nucleic acid synthesis and in metabolic studies by use of labelled precursors.

scholarly journals Decline in ribonucleic acid and protein synthesis with loss of viability during the early hours of imbibition of rye (Secale cereale L.) embryos

1977 ◽  
Vol 166 (1) ◽  
pp. 33-38 ◽  
Author(s):  
S Sen ◽  
D J Osborne
Keyword(s):  
Molecular Weight ◽  
Protein Synthesis ◽  
Secale Cereale ◽  
Ribonucleic Acid ◽  
Major Part ◽  
Low Molecular Weight ◽  
Nucleolar Material ◽  
Early Germination ◽  
Secale Cereale L

A decline in protein synthesis and slow germination accompanies loss of viability in embryos of rye (Secale cereale L.) grains. Associated with this, incorporation of precursors into all the major classes of RNA is decreased and the processing of precursor rRNA to 25S and 18S RNA is retarded. Embryos that just reach 0% viability still synthesize some low-molecular-weight non-nucleolar material, although they do not synthesize protein. It is suggested that early-synthesized RNA could play a major part in determining the extent of protein synthesis at early germination, and thereby regulate the rate at which germination can proceed.

RELATIONSHIP BETWEEN NUCLEIC ACIDS, HISTONE AND NON-HISTONE PROTEIN SYNTHESIS IN HUMAN LYMPHOCYTES STIMULATED WITH PHYTOHEMAGGLUTININ

1970 ◽  
Vol 12 (1) ◽  
pp. 151-159 ◽  
Author(s):  
Anil B. Mukherjee
Keyword(s):  
Protein Synthesis ◽  
Nucleic Acid ◽  
Nucleic Acids ◽  
Temporal Relationship ◽  
Human Lymphocytes ◽  
Acid Synthesis ◽  
Nucleic Acid Synthesis ◽  
Culture Period ◽  
Histone Protein ◽  
Pha Stimulation

The temporal relationship between the synthesis of histone and non-histone proteins and nucleic acids has been investigated by autoradiography in PHA stimulated human lymphocytes throughout the 72-hour culture period. It was found that a significant amount of 3H-arginine and 3H-lysine incorporation took place at a time when the cells were actively synthesizing DNA. Non-histone protein synthesis, as evidenced by 3H-tryptophan incorporation, was found to be dependent on PHA stimulation in human lymphocytes. Inhibition of histone and/or non-histone protein synthesis leads to the inhibition of nucleic acid synthesis.

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