Distinctive chromosomal structures are formed very early in the amplification of CAD genes in Syrian hamster cells
- PMID: 1979757
- DOI: 10.1016/0092-8674(90)90417-d
Distinctive chromosomal structures are formed very early in the amplification of CAD genes in Syrian hamster cells
Abstract
As visualized by in situ hybridization with fluorescence detection, newly amplified CAD genes in 10(5) cell colonies are contained in multiple copies of very large regions of DNA, each tens of megabases long. The extra DNA is usually linked to the short arm of chromosome B9, which retains CAD at its normal site. The widely spaced genes are often interspersed with new G-negative regions. Individual cells within a clone have highly variable numbers of CAD genes (range 2-15). When resistant clones are examined later, at the 10(15) cell stage, the amplified genes are usually found in much more condensed structures. We propose that, in the initial event of CAD gene amplification, much of the short arm is transferred from one B9 chromosome to another. In subsequent cell cycles this initial duplication expands rapidly through unequal but homologous sister chromatid exchanges. Relatively rare secondary events lead to more condensed structures.
Similar articles
-
Fusions near telomeres occur very early in the amplification of CAD genes in Syrian hamster cells.Proc Natl Acad Sci U S A. 1992 Jun 15;89(12):5427-31. doi: 10.1073/pnas.89.12.5427. Proc Natl Acad Sci U S A. 1992. PMID: 1351682 Free PMC article.
-
Identification of an origin of bidirectional DNA replication in the ubiquitously expressed mammalian CAD gene.Mol Cell Biol. 1995 Aug;15(8):4136-48. doi: 10.1128/MCB.15.8.4136. Mol Cell Biol. 1995. PMID: 7623808 Free PMC article.
-
Co-amplification of rRNA genes with CAD genes in N-(phosphonacetyl)-L-aspartate-resistant Syrian hamster cells.Mol Cell Biol. 1983 Nov;3(11):2066-75. doi: 10.1128/mcb.3.11.2066-2075.1983. Mol Cell Biol. 1983. PMID: 6318080 Free PMC article.
-
CAD gene sequence and the domain structure of the mammalian multifunctional protein CAD.Biochem Soc Trans. 1993 Feb;21(1):186-91. doi: 10.1042/bst0210186. Biochem Soc Trans. 1993. PMID: 8095469 Review. No abstract available.
-
[Gene amplification].Tanpakushitsu Kakusan Koso. 1984 Mar;29(3):152-63. Tanpakushitsu Kakusan Koso. 1984. PMID: 6425988 Review. Japanese. No abstract available.
Cited by
-
Oncogenes result in genomic alterations that activate a transcriptionally silent, dominantly selectable reporter gene (neo).Mol Cell Biol. 1992 Jan;12(1):198-206. doi: 10.1128/mcb.12.1.198-206.1992. Mol Cell Biol. 1992. PMID: 1309588 Free PMC article.
-
Relationship of eukaryotic DNA replication to committed gene expression: general theory for gene control.Microbiol Rev. 1991 Sep;55(3):512-42. doi: 10.1128/mr.55.3.512-542.1991. Microbiol Rev. 1991. PMID: 1943999 Free PMC article. Review.
-
Co-amplified markers alternate in megabase long chromosomal inverted repeats and cluster independently in interphase nuclei at early steps of mammalian gene amplification.EMBO J. 1992 Jul;11(7):2665-73. doi: 10.1002/j.1460-2075.1992.tb05332.x. EMBO J. 1992. PMID: 1628626 Free PMC article.
-
Homology-mediated end-capping as a primary step of sister chromatid fusion in the breakage-fusion-bridge cycles.Nucleic Acids Res. 2013 Nov;41(21):9732-40. doi: 10.1093/nar/gkt762. Epub 2013 Aug 23. Nucleic Acids Res. 2013. PMID: 23975201 Free PMC article.
-
Satellite DNA sequences flank amplified DHFR domains in marker chromosomes of mouse fibrosarcoma cells.Genetica. 1994;94(1):9-16. doi: 10.1007/BF01429215. Genetica. 1994. PMID: 7729700
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous