Initiation of Hemoglobin Synthesis: Comparison of Model Reactions That Use Artificial Templates with Those Using Natural Messenger RNA
- 1 March 1972
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 69 (3) , 706-711
- https://doi.org/10.1073/pnas.69.3.706
Abstract
PARTIAL REACTIONS DESIGNED TO STUDY THE INDIVIDUAL STEPS IN THE INITIATION OF PROTEIN SYNTHESIS MAY BE DIVIDED INTO TWO GROUPS: artificial models using artificial mRNA templates and natural models using naturally occurring mRNA. The requirements for each of the reticulocyte initiation factors, IF-M(1), IF-M(2), and IF-M(3), and for GTP are examined using these models in order to determine if either type of model is a valid representation of the events occurring in natural initiation. Binding of the initiator tRNA, Met-tRNA(F), to endogenous mRNA requires IF-M(1), IF-M(2), and GTP. A requirement for hydrolysis of GTP is not found when the artificial template ApUpG is used since GDPCP may be substituted for GTP. Met-tRNA(F) bound to the template ApUpG by IF-M(1) + IF-M(2) can form a peptide bond with the aminoacyl-tRNA analog, puromycin. Met-tRNA(F) bound by IF-M(1) + IF-M(2) to the initiator codon of natural globin mRNA, however, cannot form a peptide bond with either puromycin or valine-tRNA unless IF-M(3) is also present. The requirements for Met(F)-valine synthesis on exogenous globin mRNA are the same as the requirements on endogenous mRNA. Synthesis of the initial tripeptides of the alpha and beta chains of rabbit globin, Met(F)-Val-Leu and Met(F)-Val-His, requires, in addition, leucyl-tRNA and histidyl-tRNA. It appears, therefore, that model systems that use natural messenger RNA can duplicate the factor and energy requirements of natural initiation, but that the model systems thus far studied that use artificial messengers as templates do not.Keywords
This publication has 18 references indexed in Scilit:
- Requirement for GTP in the Initiation Process on Reticulocyte Ribosomes and Ribosomal SubunitsProceedings of the National Academy of Sciences, 1971
- Aurintricarboxylic Acid: Inhibitor of Initiation of Protein SynthesisProceedings of the National Academy of Sciences, 1971
- Isolation and Partial Characterization of Reticulocyte Factors M1 and M2Journal of Biological Chemistry, 1970
- Effect of aurintricarboxylic acid and of NaF on the binding of globin messenger RNA to reticulocyte 40S ribosomal subunitsBiochemical and Biophysical Research Communications, 1970
- Factor Dependent Binding of Methionyl-tRNAs to Reticulocyte RibosomesNature, 1970
- Cell-free hemoglobin synthesis. II. Characteristics of the transfer ribonucleic acid-dependent assay system.1970
- Factors for the Initiation of Haemoglobin Synthesis by Rabbit Reticulocyte RibosomesNature, 1970
- Inhibition by Fusidic Acid of Transferase II in Reticnlocyte Protein SynthesisThe Journal of Biochemistry, 1970
- EVIDENCE FOR A PROPOSED INITIATION COMPLEX FOR PROTEIN SYNTHESIS IN RETICULOCYTE POLYRIBOSOME PROFILESProceedings of the National Academy of Sciences, 1969
- Two additional reversed-phase chromatographic systems for the separation of transfer ribonucleic acids and their application to the preparation of two formylmethionine and a valine transfer ribonucleic acid from Escherichia coli BBiochemistry, 1968