Abstract
SISTER chromatid exchange (SCE), that is, the reciprocal interchange of DNA between chromatids, is easily visualised in metaphase chromosomes1,2 and has been applied to study chromosome structure3,4, chromosome damage5, and instability and DNA repair deficiency syndromes 6-9. Since SCEs can be induced by subtoxic doses of carcinogens and mutagens5,10-13, their analysis offers the possibility of a rapid, sensitive and quantitative assay for genetic damage. We have begun to examine the relation between SCEs and mutations in Chinese hamster ovary (CHO) cells by quantifying the induction of SCEs in parallel with the induction of mutations producing 8-azaguanine resistance, that is, mutations predominately at the hypoxanthine phosphoribosyltransferase, hprt, locus. Since the conversion of a chemically induced DNA lesion to a SCE or mutation may depend on the nature of that lesion, we tested four chemicals that differ in their interaction with DNA - ethyl methanesulphonate (EMS; O6: N7 guanyl alkylation ratio14 of 0.03), N-ethyl-N-nitrosourea (ENU; O6: N 7 guanyl alkylation ratio15 of about 0.35), the crosslinking agent mitomycin C (MMC)16 and the intercalator proflavine sulphate (PRO)17. Our results indicate a linear relation between induced SCEs and mutations. The relative efficiency, however, is different for each chemical.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 551-553 |
| Number of pages | 3 |
| Journal | Nature |
| Volume | 271 |
| Issue number | 5645 |
| DOIs | |
| State | Published - 1978 |
| Externally published | Yes |
Fingerprint
ASJC Scopus subject areas
- General
Cite this
Sister chromatid exchange as an indicator of mutagenesis. / Carrano, A. V.; Thompson, L. H.; Lindl, P. A.; Minkler, J. L.
In: Nature, Vol. 271, No. 5645, 1978, p. 551-553.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Sister chromatid exchange as an indicator of mutagenesis
AU - Carrano, A. V.
AU - Thompson, L. H.
AU - Lindl, P. A.
AU - Minkler, J. L.
PY - 1978
Y1 - 1978
N2 - SISTER chromatid exchange (SCE), that is, the reciprocal interchange of DNA between chromatids, is easily visualised in metaphase chromosomes1,2 and has been applied to study chromosome structure3,4, chromosome damage5, and instability and DNA repair deficiency syndromes 6-9. Since SCEs can be induced by subtoxic doses of carcinogens and mutagens5,10-13, their analysis offers the possibility of a rapid, sensitive and quantitative assay for genetic damage. We have begun to examine the relation between SCEs and mutations in Chinese hamster ovary (CHO) cells by quantifying the induction of SCEs in parallel with the induction of mutations producing 8-azaguanine resistance, that is, mutations predominately at the hypoxanthine phosphoribosyltransferase, hprt, locus. Since the conversion of a chemically induced DNA lesion to a SCE or mutation may depend on the nature of that lesion, we tested four chemicals that differ in their interaction with DNA - ethyl methanesulphonate (EMS; O6: N7 guanyl alkylation ratio14 of 0.03), N-ethyl-N-nitrosourea (ENU; O6: N 7 guanyl alkylation ratio15 of about 0.35), the crosslinking agent mitomycin C (MMC)16 and the intercalator proflavine sulphate (PRO)17. Our results indicate a linear relation between induced SCEs and mutations. The relative efficiency, however, is different for each chemical.
AB - SISTER chromatid exchange (SCE), that is, the reciprocal interchange of DNA between chromatids, is easily visualised in metaphase chromosomes1,2 and has been applied to study chromosome structure3,4, chromosome damage5, and instability and DNA repair deficiency syndromes 6-9. Since SCEs can be induced by subtoxic doses of carcinogens and mutagens5,10-13, their analysis offers the possibility of a rapid, sensitive and quantitative assay for genetic damage. We have begun to examine the relation between SCEs and mutations in Chinese hamster ovary (CHO) cells by quantifying the induction of SCEs in parallel with the induction of mutations producing 8-azaguanine resistance, that is, mutations predominately at the hypoxanthine phosphoribosyltransferase, hprt, locus. Since the conversion of a chemically induced DNA lesion to a SCE or mutation may depend on the nature of that lesion, we tested four chemicals that differ in their interaction with DNA - ethyl methanesulphonate (EMS; O6: N7 guanyl alkylation ratio14 of 0.03), N-ethyl-N-nitrosourea (ENU; O6: N 7 guanyl alkylation ratio15 of about 0.35), the crosslinking agent mitomycin C (MMC)16 and the intercalator proflavine sulphate (PRO)17. Our results indicate a linear relation between induced SCEs and mutations. The relative efficiency, however, is different for each chemical.
UR - http://www.scopus.com/inward/record.url?scp=0017801610&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0017801610&partnerID=8YFLogxK
U2 - 10.1038/271551a0
DO - 10.1038/271551a0
M3 - Article
C2 - 622190
AN - SCOPUS:0017801610
VL - 271
SP - 551
EP - 553
JO - Nature
JF - Nature
SN - 0028-0836
IS - 5645
ER -