Isolation and cell-free translation of immunoglobulin messenger RNA. |
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Authors: | M Green T Zehavi-Willner P N Graves J McInnes S Pestka |
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Affiliation: | Roche Institute of Molecular Biology, Nutley, New Jersey 07110 USA |
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Abstract: | The mRNA's for both the heavy chain (H315) and the light chain (L315) of the mineral oil-induced plasmacytoma-315 myeloma protein have been isolated and partially purified from both total cellular RNA and RNA derived from membrane-bound polysomes. The yields of both L315 mRNA and, in particular, of H315 mRNA were increased when total cellular RNA was used as starting material. Total poly(A)-containing mRNA and partially purified mRNA obtained by preparative sucrose gradient sedimentation stimulated protein synthesis in cell-free extracts derived from Ehrlich ascites tumor cells or wheat germ. Cell-free products antigenically and structurally related to both the authentic L315 and H315 secreted by intact cells were synthesized in the Ehrlich ascites cell-free system in response to the appropriate mRNA's. Only the L315 mRNA was efficiently translated in the cell-free system derived from wheat germ. |
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