## Abstract We previously identified an anchorage independence‐suppressor gene, __SAII__, on rat chromosome (RNO) 5. RNO5 is homologous to human chromosomes (HSA) I and 9. In order to find the human homolog of the __SAII__ gene, we transferred HSAI and HSA9 to an anchorage‐independent and tumorigen
Growth and transformation suppressor genes for BHK syrian hamster cells on human chromosomes 1 and 11
✍ Scribed by Lois A. Annab; Jin-Tang Dong; P. Andrew Futreal; Hitoshi Satoh; Mitsuo Oshimura; J. Carl Barrett
- Book ID
- 102946508
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 820 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0899-1987
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
To map putative tumor suppressor genes for the near‐diploid baby hamster kidney fibrosarcoma cell line BHK, we transferred five different normal human chromosomes (1, 3, 7, 11, and 12) into these tumor cells by microcell‐mediated chromosome transfer. Transfer of human chromosome 1 into BHK cells resulted in suppression of cell growth both on plastic and in soft agar, indicating that chromosome 1 has a generalized effect on cell growth and thereby suppresses anchorage‐independent growth. Selection against cells with an intact chromosome 1 was observed. In contrast, the introduction of chromosome 11 into BHK cells resulted in suppression of anchorage independence but not growth on plastic. Most chromosome‐11 growth‐suppressed BHK hybrids retained intact copies of human chromosome 11. Tumorigenic derivatives of chromosome 11 hybrids had lost this chromosome. Transfer of human chromosome 3, 7, or 12 into BHK cells did not correlate with growth suppression of BHK cells on plastic or in soft agar. Thus, we conclude that genes that suppress BHK‐cell growth in general or in agar reside on human chromosomes 1 and 11, respectively. © 1992 Wiley‐Liss. Inc.
📜 SIMILAR VOLUMES
During the development of skin cancer, normal kera-nign tumors. With later-passage HaCaT cells, which had accumulated a high number of chromosomal aber-tinocytes accumulate a number of genetic aberrations that finally allow a cell to clonally expand and form a rations, the same oncogene caused malig
We have previously reported that losses of genomic material from the long arm of chromosome 18 are frequent in atypical and anaplastic meningiomas but rare in benign meningiomas. In the present study, we have investigated a series of 37 meningiomas for mutation and expression of 4 tumor suppressor g
Murine B lymphocytes, adipocytes, and olfactory neurons contain a DNA-binding protein that participates in the regulation of genes encoding tissue-specific components of signal transduction. Purification and cloning of this protein, termed early B-cell factor (EBF), from murine B lymphocytes and ind