Cancer Research Audrey Hepburn  EMT and Cancer Progression and Treatment
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

[Cancer Research 33, 323-331, February 1, 1973]
© 1973 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Liau, M. C.
Right arrow Articles by Hurlbert, R. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Liau, M. C.
Right arrow Articles by Hurlbert, R. B.

Inhibition of Transfer and Ribosomal RNA Methylases by Polyinosinate1

Ming C. Liau, John B. Hunt, Don W. Smith and Robert B. Hurlbert

The Department of Biochemistry, Texas Medical Center, The University of Texas M. D. Anderson Hospital and Tumor Institute at Houston, Houston, Texas 77025

Polyinosinate [poly(1)] inhibited transfer RNA methylases prepared from the cell-soluble fraction and the nucleolar fraction of Novikoff rat hepatoma cells. Polyinosinate-cytidylate duplex, polyinosinate-cytidylate copolymer, and other homopolymers such as polycytidylate and polyadenylate showed very little effect. The mechanism of inhibition has been attributed to specific interactions between the single-stranded poly(I) and the methylating enzymes. Methylases of individual bases were differentially inhibited by poly(I), adenine methylase to the greatest extent and guanine methylases to the least.

The methylation of bases of endogenous ribosomal precursor RNA in isolated nucleoli was also inhibited by poly(I), resulting in preferential inhibition of the methylation of adenine.

The methylation of ribose moieties of ribosomal precursor RNA in isolated nucleoli has been detected in all 16 of the possible alkali-stable dinucleotide monophosphates by an improved method for resolution of these O2'-methyl dinucleoside monophosphate compounds. Poly(I) caused nonuniform inhibition of methylation of ribose moieties, although the pattern differed from the inhibition of base methylation.

A potentially pervasive effect of poly(I) on cell metabolism and a potential rationale for use in cancer chemotherapy are hereby demonstrated.

1 An abstract of this work has appeared (26). This work was supported by USPHS Grant CA-10244 and by American Cancer Society Grant E-609.

Received 8/ 3/72. Accepted 10/25/72.




This article has been cited by other articles:


Home page
Cold Spring Harb Symp Quant BiolHome page
H. Busch, N. R. Ballal, R. K. Busch, Y. C. Choi, F. Davis, I. L. Goldknopf, S.-I. Matsui, M. S. Rao, and L. I. Rothblum
The Nucleolus, a Model for Analysis of Chromatin Controls
Cold Spring Harb Symp Quant Biol, January 1, 1978; 42(0): 665 - 683.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1973 by the American Association for Cancer Research.