ANALYSIS OF RIBOSOMES AND POLYSOMES DERIVED FROM RABBIT MAMMARY GLANDS DURING PREGNANCY AND LACTATION

1971 ◽  
Vol 49 (4) ◽  
pp. 667-NP ◽  
Author(s):  
I. D. HERRIMAN ◽  
G. D. BAIRD ◽  
JUDY M. BRUCE
Keyword(s):  
Electron Microscopy ◽  
Density Gradient ◽  
Gradient Analysis ◽  
Late Pregnancy ◽  
Sucrose Density Gradient ◽  
Mammary Glands ◽  
Pregnancy And Lactation

SUMMARY Whole-ribosome and polysome-enriched fractions were prepared from the mammary glands of rabbits during late pregnancy and lactation. The composition of the fractions was determined by sucrose density gradient analysis and electron microscopy. The range of size of polysomal aggregates was similar in the late-pregnant and lactating gland, with aggregates containing five to nine ribosomal units predominating. However, the amount of polysomes relative to monosomes was invariably found to increase after parturition. The greater portion of this increase was accounted for by the increased abundance of aggregates containing five to nine units.

scholarly journals Ribonucleic Acid Biosynthesis in Human Leukocytes

Blood ◽  
1966 ◽  
Vol 28 (2) ◽  
pp. 188-200 ◽  
Author(s):  
MARTIN J. CLINE
Keyword(s):  
Density Gradient ◽  
Ribonucleic Acid ◽  
Turnover Rate ◽  
Rna Synthesis ◽  
Gradient Analysis ◽  
Sucrose Density Gradient ◽  
Acid Biosynthesis ◽  
Total Load ◽  
Human Leukocytes ◽  
Particle Ingestion

Abstract Phagocytosis has profound effects on several aspects of the RNA metabolism of human leukocytes. The major changes induced by particle ingestion appear to be (1) an increased uptake of pyrimidine precursors from the suspending medium, (2) a contraction in the size of the nucleotide pool, (3) an accelerated rate of destruction of preexisting RNA, and (4) an increased rate of RNA synthesis. Sucrose density gradient analysis of the newly synthesized RNA suggests that several classes of RNA are involved in this process. The increased turnover rate of the nucleotide pool and of the cellular RNA of the leukocyte is proportional, within limits, to the total load of ingested particles.

scholarly journals The miR-200 family in normal mammary gland development

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Majesta J. Roth ◽  
Roger A. Moorehead
Keyword(s):  
Mammary Tumor ◽  
Mammalian Species ◽  
Late Pregnancy ◽  
Mammary Glands ◽  
Mammary Development ◽  
Normal Mammary Gland ◽  
Ductal Morphogenesis ◽  
Mammary Tumor Growth ◽  
Pregnancy And Lactation ◽  
The Impact

AbstractThe miR-200 family of microRNAs plays a significant role in inhibiting mammary tumor growth and progression, and its members are being investigated as therapeutic targets. Additionally, if future studies can prove that miR-200s prevent mammary tumor initiation, the microRNA family could also offer a preventative strategy. Before utilizing miR-200s in a therapeutic setting, understanding how they regulate normal mammary development is necessary. No studies investigating the role of miR-200s in embryonic ductal development could be found, and only two studies examined the impact of miR-200s on pubertal ductal morphogenesis. These studies showed that miR-200s are expressed at low levels in virgin mammary glands, and elevated expression of miR-200s have the potential to impair ductal morphogenesis. In contrast to virgin mammary glands, miR-200s are expressed at high levels in mammary glands during late pregnancy and lactation. miR-200s are also found in the milk of several mammalian species, including humans. However, the relevance of miR-200s in milk remains unclear. The increase in miR-200 expression in late pregnancy and lactation suggests a role for miR-200s in the development of alveoli and/or regulating milk production. Therefore, studies investigating the consequence of miR-200 overexpression or knockdown are needed to identify the function of miR-200s in alveolar development and lactation.

scholarly journals Bacteriophage-like particles associated with the gene transfer agent of Methanococcus voltae PS

1999 ◽  
Vol 80 (12) ◽  
pp. 3305-3308 ◽  
Author(s):  
F. Eiserling ◽  
A. Pushkin ◽  
M. Gingery ◽  
G. Bertani
Keyword(s):  
Electron Microscopy ◽  
Gene Transfer ◽  
Density Gradient ◽  
Sucrose Density Gradient ◽  
Bacterial Dna ◽  
Methanococcus Voltae ◽  
Long Tails ◽  
Gene Transfer Agent ◽  
Bacterial Genes ◽  
Derivatives Of

The methanogenic archaeobacterium Methanococcus voltae (strain PS) is known to produce a filterable, DNase-resistant agent (called VTA, for voltae transfer agent), which carries very small fragments (4400 bp) of bacterial DNA and is able to transduce bacterial genes between derivatives of the strain. Examination by electron microscopy of two preparations of VTA that were concentrated and partially purified by different methods showed virus-like particles with isometric heads, about 40 nm in diameter, and with 61 nm long tails. These particles co-sedimented with the minute bacteriophage ϕX174 in a sucrose density gradient.

scholarly journals Preparation of ribosome-free membranes from rat liver microsomes by means of lithium chloride

1969 ◽  
Vol 115 (5) ◽  
pp. 1063-1069 ◽  
Author(s):  
T. Scott-Burden ◽  
A. O. Hawtrey
Keyword(s):  
Density Gradient ◽  
Rat Liver ◽  
Lithium Chloride ◽  
Ribosomal Rna ◽  
Gradient Analysis ◽  
Extraction Procedure ◽  
Liver Microsomes ◽  
Sucrose Density Gradient ◽  
Rat Liver Microsomes ◽  
Phenol Extraction

1. Treatment of washed rat liver microsomes in a medium containing 0·12m-sucrose, 12·5mm-potassium chloride, 2·5mm-magnesium chloride and 25mm-tris–hydrochloric acid buffer, pH7·6, with 2m-lithium chloride at 5° for 16hr. leads to the formation of membranes free of ribosomes and ribosomal subunits. 2. Confirmation of the absence of ribosomes from lithium chloride-prepared membranes was obtained by treatment of the membranes with sodium deoxycholate, followed by sucrose-density-gradient centrifugation, which showed the complete absence of ribosomes. 3. Treatment of membranes with phenol, followed by sucrose-density-gradient analysis of the isolated RNA, showed the presence of a small amount of 4s material. Repetition of the phenol extraction procedure in the presence of liver cell sap as a ribonuclease inhibitor again showed the presence of only 4s material. The 4s RNA was shown to be transfer RNA by the fact that it had the same capacity for accepting 14C-labelled amino acids as isolated transfer RNA from rat liver pH5 enzyme. 4. Analysis showed that microsomes and membranes possessed similar glucose 6-phosphatase, NADH–2,6-dichlorophenol-indophenol reductase, NADH–neo-tetrazolium reductase, NADH–cytochrome c reductase and ribonuclease activities. 5. 3H-labelled ribosomal RNA binds to membranes. However, isolation of the bound RNA by the phenol extraction procedure, followed by sucrose-density-gradient analysis, shows the RNA to be degraded to 7s material. Very little breakdown of 3H-labelled ribosomal RNA bound to membranes occurs if the binding and isolation are carried out in the presence of liver cell sap.

ENZYMES OF LACTOSE BIOSYNTHESIS IN NORMAL AND HORMONALLY STIMULATED RABBIT MAMMARY GLANDS

1968 ◽  
Vol 40 (1) ◽  
pp. 81-84 ◽  
Author(s):  
R. J. HEITZMAN
Keyword(s):  
Enzyme Activities ◽  
Deoxyribonucleic Acid ◽  
Late Pregnancy ◽  
Mammary Glands ◽  
Uridine Diphosphate ◽  
Early Lactation ◽  
Uridine Diphosphate Glucose ◽  
Pregnancy And Lactation ◽  
Diphosphate Glucose ◽  
The Difference

SUMMARY The activities of uridine diphosphate glucose (UDPG) pyrophosphorylase and UDPG-4′-epimerase in mammary glands of rabbits were determined in late pregnancy and lactation. The activities in animals during the last 4 days of pregnancy and during days 0–4, 5–9 and 11–21 of lactation increased but the difference in the activities was significant between the days 5–9 and 11–21 only and for the pyrophosphorylase activity between days for 0–4 and 5–9. Prolactin and cortisol acetate given daily for 3 or 5 days to rabbits pseudopregnant for 15 days caused increases in enzyme activities that were several times greater than those found in controls. The enzyme activities in the stimulated glands were similar to those observed in early lactation. The levels of deoxyribonucleic acid/g. wet tissue were the same in the stimulated and lactating glands.

Purine ribonucleoside and deoxyribonucleoside kinase activities in thymocytes. Specificity and optimal assay conditions for phosphorylation

1980 ◽  
Vol 58 (9) ◽  
pp. 677-682 ◽  
Author(s):  
Trevor Lukey ◽  
Floyd F. Snyder
Keyword(s):  
Density Gradient ◽  
Gradient Analysis ◽  
Sucrose Density Gradient ◽  
Adenosine Kinase ◽  
The Other ◽  
Deoxycytidine Kinase ◽  
Deoxyguanosine Kinase ◽  
Assay Conditions ◽  
Kinase A ◽  
Broad Specificity

The optimal assay conditions and specificity for the principal reactions of purine nucleoside phosphorylation were studied in mouse thymocytes. The following relative activities were obtained for the nucleoside substrates: adenosine, 100; deoxyguanosine, 24; and deoxyadenosine, 14. The phosphorylation of adenosine, 45 μM, was optimal between pH 5.8 and 6.0 with a millimolar Mg:ATP ratio of 1:5. This activity was insensitive to inhibition by other nucleosides and dCTP. Optimal phosphorylation of deoxyguanosine, 350 μM, occurred at pH 8.4 with a millimolar Mg:ATP ratio of 10:3.5. Phosphorylation of 80 μM deoxyguanosine was inhibited approximately 90% by 10 μM deoxycytidine or dCTP and was inhibited 70% by 200 μM deoxyadenosine but unaffected by adenosine. Deoxyadenosine, 450 μM, phorphorylation was optimal between pH 6.5 and 8.5 with a millimolar Mg:ATP ratio of 5:1. Phosphorylation of deoxyadenosine, 100 μM, was partially inhibited by 200 μM adenosine, 34%; 200 μM deoxyguanosine, 10%; and 100 μM deoxycytidine or dCTP, 33%. Only deoxyadenosine phosphorylation was inhibited by 200 μM deoxyinosine, 10%. These results and those obtained from isokinetic sucrose density gradient analysis are consistent with there being a specific adenosine kinase, a faster sedimenting deoxycytidine kinase of broad specificity which also catalyzes the phosphorylation of deoxyguanosine and deoxyadenosine, and a specific deoxyguanosine kinase sedimenting more rapidly than either of the other activities.

Sign in / Sign up

Export Citation Format

Share Document