RNA Synthesis during Synchronous Cell Division in Cultured Explants of Jerusalem Artichoke Tuber
Explants of Jerusalem artichoke tuber tissue were cultured in nutrient medium with the hormone, 2,4-dichlorophenoxyacetic acid. After a lag period, 90 per cent of the cells divided synchronously. During the first two cell cycles, the rate of ribosomal RNA synthesis increased sharply in two steps; be...
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Published in: | Journal of experimental botany Vol. 25; no. 5; pp. 847 - 859 |
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Main Authors: | , |
Format: | Journal Article |
Language: | English |
Published: |
Oxford University Press
01-10-1974
OXFORD AT THE CLARENDON PRESS |
Subjects: | |
Online Access: | Get full text |
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Summary: | Explants of Jerusalem artichoke tuber tissue were cultured in nutrient medium with the hormone, 2,4-dichlorophenoxyacetic acid. After a lag period, 90 per cent of the cells divided synchronously. During the first two cell cycles, the rate of ribosomal RNA synthesis increased sharply in two steps; before the onset of DNA synthesis for the first division, and early in interphase before the second division. Rates of RNA and protein accumulation, and phosphate uptake also increased sharply at these times. From experiments with explants in which DNA synthesis and cell division had been inhibited, it was concluded that the stepwise pattern of ribosomal RNA synthesis was not caused by the replication of ribosomal RNA genes, as can happen in mammalian cells. Instead, the periodicity of metabolism was found to be independent of the DNA synthesis-cell division cycle. A cause of the stepwise nature of ribosomal RNA synthesis is suggested. It is considered that despite the high synchrony of division, the system is not completely suited for the study of events associated with the cell cycle in higher plants. However, the synchrony of much of early metabolism suits it to the study of induction of cell division in previously non-dividing cells, and the consequent process of de-differentiation. |
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Bibliography: | 1Present address: Department of Zoology, Univesity of Edinburgh, West Mains Road, Edinburgh EH9 3JT. ark:/67375/HXZ-9WK13896-2 ArticleID:25.5.847 istex:B7AD971952933DB22029CF392BDE62E0584224E3 |
ISSN: | 0022-0957 1460-2431 |
DOI: | 10.1093/jxb/25.5.847 |