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Transmission of genomic instability from a single irradiated human chromosome to the progeny of unirradiated cells.
- Source :
-
Radiation research [Radiat Res] 2007 Jun; Vol. 167 (6), pp. 675-81. - Publication Year :
- 2007
-
Abstract
- Ionizing radiation can induce chromosome instability that is transmitted over many generations after irradiation in the progeny of surviving cells, but it remains unclear why this instability can be transmitted to the progeny. To acquire knowledge about the transmissible nature of genomic instability, we transferred an irradiated human chromosome into unirradiated mouse recipient cells by microcell fusion and examined the stability of the transferred human chromosome in the microcell hybrids. The transferred chromosome was stable in all six microcell hybrids in which an unirradiated human chromosome had been introduced. In contrast, the transferred chromosome was unstable in four out of five microcell hybrids in which an irradiated human chromosome had been introduced. The aberrations included changes in the irradiated chromosome itself and rearrangements with recipient mouse chromosomes. Thus the present study demonstrates that genomic instability can be transmitted to the progeny of unirradiated cells by a chromosome exposed to ionizing radiation, implying that the instability is caused by the irradiated chromosome itself and also that the instability is induced by the nontargeted effect of radiation.
- Subjects :
- Animals
Cell Line
Dose-Response Relationship, Radiation
Genetic Variation genetics
Genetic Variation radiation effects
Humans
Mice
Radiation Dosage
Skin cytology
Chromosomes, Human genetics
Chromosomes, Human radiation effects
Genomic Instability genetics
Genomic Instability radiation effects
Skin radiation effects
Subjects
Details
- Language :
- English
- ISSN :
- 0033-7587
- Volume :
- 167
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Radiation research
- Publication Type :
- Academic Journal
- Accession number :
- 17523850
- Full Text :
- https://doi.org/10.1667/RR0835.1