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Title: Eukaryotic transcription and processing: regulation of gene expression. Progress report, November 1, 1977--October 31, 1978

Technical Report ·
OSTI ID:6687013

We are attempting to prepare a cell-free protein synthesizing system from corn embryos that will translate mRNA's isolated from corn grain or transcribed from corn DNA by corn RNA polymerase II. The experience of others utilizing heterologous translation systems and isolated plant mRNA fractions suggests that the extent as well as the nature of the RNA sequences translated into peptide sequences may be influenced by components in the heterologous system. We wish to prepare a homologous system to compare with a heterologous system for detection and identification of potentially regulatory components required for in vitro polypeptide synthesis. The notion is that subtle differences in mRNA recognition by homologous versus heterologous components in the in vitro translation systems may be identified by comparison of the products accumulated by each system translating the same mRNA. Potentially the approach provides both an assay and a source of the putative ''regulatory components.'' To this end we have undertaken: establishment of an active wheat germ translating system, reestablishment of the maize seedling amino acid incorporating system and its conversion to an S23 translator of endogeneous mRNAs, propagation of Barley Stripe Mosaic Virus in barley, isolation of its genome and resolution of the RNAs on a preparative scale, isolation of the poly A bearing RNA fraction from seedling and developing kernel systems, and isolation of the zein mRNAs from maize protein bodies.

Research Organization:
Florida Univ., Gainesville (USA). Dept. of Biochemistry and Molecular Biology
DOE Contract Number:
EY-76-S-05-3982
OSTI ID:
6687013
Report Number(s):
ORO-3982-48
Country of Publication:
United States
Language:
English