Simultaneous demonstration of deoxyribonucleic acid, ribonucleic acid and lipids.
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Growth of organs relative to body weight and cellular protein, RNA, DNA, and cell unit size of breast muscle, liver, and small intestinal tissue were measured in females from four lines of chickens. Two lines had undergone 32 generations of divergent selection for 56-day body weight, and the other two lines were derived by sampling the first two lines at Generation 28 and relaxing selection for the next five generations. The diet used in the present experiment was the same diet under which selection was practiced (20% crude protein and 2,685 kcal of ME/kg). Comparisons at common chronological ages and a common body weight revealed that supply organ weights, especially that of the small intestine, were associated with subsequent growth of demand organs. Although the upper gastrointestinal tract was also important in this respect, it was more susceptible to influences such as feed intake. Selection for juvenile body weight resulted in correlated changes in cell size of breast muscle but not liver and small intestine. Muscle increased posthatch as cells underwent hypertrophy but liver and small intestine grew chiefly by hyperplasia.
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The concentrations of messenger ribonucleic acids (mRNAs) in three stages in cotton cotyledon ontogeny were examined by total poly(A)+ mRNA hybridization with unfractionated complementary DNA. This study and others show that these RNAs are representative of the total mRNA population. A novel analysis of all reciprocal hybridization reactions detected at least 17 groups of mRNAs, the sequences of which change together in concentration during this developmental period. We have defined an mRNA subset as a group or groups of mRNAs that change together in concentration in a similar fashion, regardless of the abundance of its members. About 11 such subsets are detected, several of which contain at least two groups which change in concentration in parallel. These experiments have identified the same mRNA subsets detected in a companion study of the abundant proteins synthesized in vivo and in vitro during this developmental period and indicate that similar changes occur for less abundant mRNAs as well.
Highly purified trachoma elementary bodies (T'ang strain), incubated in the presence of the four nucleoside triphosphates [Mg(2+), Mn(2+), 2-mercaptoethanol, tris(hydroxymethyl)aminomethane buffer (pH 7.5)] were found to incorporate (3)H-uridine triphosphate (UTP) into ribonucleic acid (RNA) molecules. Eighty-seven per cent of the labeled molecules were sensitive to ribonuclease treatment. In vitro RNA synthesis was almost completely inhibited by actinomycin D. Rifampin was also inhibitory, but allowed some initial RNA synthesis before complete inhibition occurred. When the reaction mixture lacked Mn(2+), trachoma elementary bodies synthesized, for a limited period, high-molecular-weight RNA species (23 to 24S, 16 to 17S, and 10 to 11S). Addition of 0.2 m NaCl to the same reaction mixture stimulated and prolonged (3)H-UTP incorporation into the same radioactive RNA species. Addition of 0.001 m Mn(2+) instead of NaCl also stimulated (3)H-UTP incorporation but prevented the synthesis of the high-molecular-weight RNA species.
The synthesis of cell-specific ribonucleic acid (RNA) appeared to be stimulated in human embryonic kidney (HEK) cultures infected with adenovirus 2 or 12. Deoxyribonucleic acid (DNA)-RNA hybridization experiments revealed that by 44 to 70 hr after infection with either virus, the relative amount of pulse-labeled RNA capable of hybridizing with HEK cell DNA increased considerably; such RNA was detected in both nuclear and cytoplasmic fractions. The main increase in apparent host RNA synthesis was preceded by (i) a relatively early transient stimulation of the DNA-dependent RNA polymerase activity in isolated nuclei, and (ii) a small but consistently observed increase in the rate of acetylation of lysine-rich and arginine-rich histone fractions. The Mn(2+)-(NH(4))(2)SO(4) and Mg(2+)-activated RNA polymerase reactions measured in nuclei isolated from cells infected with adenovirus 2 or 12 were stimulated at about the same time; a rapid loss of polymerase activity followed. The augmentation of the two RNA polymerase reactions found in adenovirus 12-infected cells was independent of protein synthesis. After the initial increase, the acetylation rate of histones of cells infected with adenovirus 2 or 12 declined, until late in infection it was approximately 40 to 70% of the control cell rate.
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