Abstract
The in vitro nucleoside incorporation and methylation of uterine RNA was examined
by incubating immature rat uteri with either 3H-uridine, 3H-uridine-3H-cytidine, and/or 14C-methyl-methionine. Radioactivity was determined in extracted RNA which was fractionated
by gel electrophoresis or by differential solubility in zine acetate or lithium chloride.
Estradiol (E2)-treated uteri respond by showing a maximum in vitro incorporation of nucleosides
into total RNA and high M.W. RNA within one hr of in vivo treatment. Nucleoside incorporation
into low M.W. RNA increased gradually throughout the first 3 hrs of a 4-hr hormone
treatment period. E2 in vivo also caused increased in vitro methylation of total, high, and low M.W. uterine
RNA fractions. Methylation of all fractions increased through the first 3 hrs of hormone
treatment, but greater methylation of low M.W. RNA was apparent. The data indicate
that in vivo E2 treatment stimulates an initial transitory stage of in vitro nucleoside incorporation
into uterine RNA followed by a more prolonged interval of RNA methylation.
Key words
Estradiol - Uterus (Rat) - RNA - Nucleosides - Methylation - Methyl-methionine
1 This investigation was supported in part by research grant GB 8386 from the National
Science Foundation. Paper No.
4474 of the Journal Series of the North Carolina State University Agricultural Experiment
Station.
2 Present address: Biology Department, University of North Carolina at Greensboro,
Greensboro, North Carolina 2.7412