Using a purified cDNA probe of human antithrombin III (AT3) gene and a series of human/Chinese hamster cell hybrids, we established the chromosomal location of the structural gene for AT3 in human chromosome 1 by Southern blot analysis.
Mapping G1 phase by the structural morphology of the prematurely condensed chromosomes
β Scribed by Walter N. Hittelman; Potu N. Rao
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- English
- Weight
- 909 KB
- Volume
- 95
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
The object of this study was to develop a map of G1 phase on the basis of the progressive changes taking place in the morphology of the prematurely condensed chromosomes as the cells traverse through G1 and then use this technique to determine the cell cycle location of normal and transformed cell populations in plateau phase. The morphology of the prematurely condensed chromosomes (PCC) of G1 cells in random populations was found to be highly variable. For a better understanding of the relationship between the morphology of the G1βPCC and their position within G1 phase, synchronized populations of Chinese hamster ovary (CHO) cells in early, midβ, and late G1 phase were fused with mitotic cells. Early G1 cells resulted in highly condensed G1βPCC, while late G1 cells gave very extended G1βPCC. MidβG1 cells resulted in PCC of intermediate condensation. To test the validity of these criteria for mapping the position of a cell in the cell cycle, synchronous G1 cell populations were treated with a variety of metabolic inhibitors. Cycloheximide and actinomycin D were shown to block cell in early G1 phase, while excess thymidine and hydroxyurea blocked cells in early S phase. The results presented here indicate that, upon reaching plateau phase, normal cell populations (BALBβC mouse 3T3, human PAβ2, and WI 38) stop in early G1, while most cells in transformed cell lines (CHO, HeLa, and mouse SVβ3T3) accumulate in late G1.
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