To determine the influence of some bacterial DNA repair pathways on the mutagenic and the lethal effects of N-(2-chloroethyl)-N´-cyclohexyl-N-nitrosourea (CCNU), pZ189 plasmids treated in vitro with 2 mM CCNU were transfected into Escherichia coli strains with different repair capacities (uvr + ada
Mutation spectra of N-ethyl-N′-nitro-N-nitrosoguanidine and 1-(2-hydroxyethyl)-1-nitrosourea in Escherichia coli
✍ Scribed by Richardson, Katherine K. ;Crosby, Renae M. ;Skopek, Thomas R.
- Publisher
- Springer
- Year
- 1988
- Tongue
- English
- Weight
- 710 KB
- Volume
- 214
- Category
- Article
- ISSN
- 0026-8925
No coin nor oath required. For personal study only.
✦ Synopsis
DNA sequencing was used to determine the specific types of DNA base changes induced following in vivo exposure of Escherichia coli to the ethylating agent N-ethyl-N'-nitro-N-nitrosoguanidine (ENNG) and the hydroxyethylating agent 1-(2-hydroxyethyl)-1-nitrosourea (HENU) using the xanthine guanine phosphoribosyltransferase (gpt) gene as the genetic target. We observed that 22/30 of the ENNG-induced mutations were GC----AT transitions, 4/30 were AT----GC transitions, 3/30 were AT----TA transversions, and 1/30 was an AT----CG transversion. We observed that 37/40 HENU-induced mutations were GC----AT transitions and that the remaining 3/40 were AT----GC transitions. A majority of the GC----AT transitions induced by ENNG and HENU (68% and 73%, respectively) occurred at the second guanine of the sequence 5'-GG(A or T)-3'; this sequence specificity was similar to that previously seen with the alkylating agents N-methyl- and N-ethyl-N-nitrosourea (MNU and ENU) and N-methyl-N'-nitro-N-nitrosoguanidine (MNNG). A DNA strand preference for the G----A changes (antisense strand), previously noted for MNU, ENU, and MNNG, was observed following exposure to HENU and ENNG. The AT----GC transitions induced by ENNG, HENU, and ENU also exhibit a sequence specificity with 13/13 mutations occurring at the T of the sequence 5'-NTC-3'. A strand preference was not apparent for these mutations.
📜 SIMILAR VOLUMES
DNA base sequence changes induced by N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) mutagenesis have been determined for the Escherichia coli gpt gene stably incorporated in a chromosome of Chinese hamster ovary cells and in the chromosome of both growing and starving E. coli cells, instead of on a pla
In the absence of nucleotide excision repair, the spectra were dominated by G:CrA:T transitions, additional deficiency of the DNA alkyltransferase consistent with the major role of the O 6 -alkylguanine (ATase) encoded by the constitutive ogt gene of miscoding lesion in mutagenesis by alkylating Esc
We have prepared the 14C-labeled analogs of NSC 261036, 1-(2,3-dIhydroxypropy1)-2-ni t r0-1H-imIda~ole-2-~~C, and NSC 301467, N-(2-hydroxyethyl)-2-(2-nitro-lH-imldazol-l-yl-2-14C) acetamide, for pharmacological, drug distribution, and mechanisms of action studies. The latter is an analog designed fo
## Abstract Forward mutations induced by 1‐(2‐chloroethyl)‐3‐cyclohexyl‐1‐nitrosourea (a) in the __lacl__ gene of __Escherichia coli__ were recovered from bacteria proficient (Ogt^+^ Ada^+^) and deficient (Ogt^−^ Ada^−^) in __O__^6^‐alkylguanine‐DNA alkyltransferase activity. A CCNU dose of 1 mM wa