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Physical and functional heterogeneity in TYMV RNA : evidence for the existence of an independent messenger coding for coat protein
Author(s) -
Claudine Klein,
C. Fritsch,
JeanPaul Briand,
K. Richards,
G. Jonard,
L. Hirth
Publication year - 1976
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/3.11.3043
Subject(s) - rna , biology , turnip yellow mosaic virus , coat protein , messenger rna , translation (biology) , molecular mass , in vitro , coat , protein biosynthesis , transfer rna , biochemistry , microbiology and biotechnology , gene , enzyme , paleontology
Turnip yellow mosaic virus RNA can be separated into two distinct components of 2 times 10(6) and 300 000 daltons molecular weight after moderate heat treatment in the presence of SDS or EDTA. The two species cannot have arisen by accidental in vitro degradation of a larger RNA, as they both possess capped 5' ends. Analysis of the newly synthesized proteins resulting from translation of each RNA by a wheat germ extract shows that the 300 000 molecular weight RNA can be translated very efficiently into coat protein. When translated in vitro the longer RNA gave a series of high molecular weight polypeptides but only very small amounts of a polypeptide having about the same mass as the coat protein. Thus our results suggest that the small RNA is the functional messenger for coat protein synthesis in infected cells.

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