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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1972 Jun;69(6):1606–1609. doi: 10.1073/pnas.69.6.1606

Calf Crystallin Synthesis in Frog Cells: The Translation of Lens-Cell 14S RNA in Oocytes

A J M Berns *, M Van Kraaikamp *, H Bloemendal *,, C D Lane
PMCID: PMC426758  PMID: 4504377

Abstract

14S RNA isolated from calf-lens polyribosomes was injected into oocytes of the frog Xenopus laevis. Oocytes injected with 14S RNA and buffer contained a protein resembling the A2 chain of calf α-crystallin; oocytes injected with buffer alone contained no crystallin-like material. αA2 crystallin polypeptides were identified by various criteria: urea-gel electrophoresis under acidic and basic conditions, gel electrophoresis in sodium dodecyl sulfate, N-terminal analysis, and paper chromatography of methionine-containing tryptic peptides.

It is concluded that when it is injected into a living frog oocyte, the 14S RNA from lens tissue is reasonably stable and has the properties of an αA2 crystallin messenger. The messenger requires no lens cell-specific components for translation within the oocyte, and the translational machinery of the frog cell will accept messenger RNA from a totally different cell type from another species.

The A2 chains of α-crystallin extracted from lens tissue possess an acetylated N-terminal methionine residue; the N-terminal methionine of αA2 chains derived from frog oocytes injected with 14S RNA was also acetylated.

Keywords: messenger RNA, initiation factors, protein synthesis, acetyl methionine

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Selected References

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