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Frameshift mutagenesis

LaVelle JM. 1986b. Potassium chromate potentiates frameshift mutagenesis in E. coli and S. typhimurium. MutatRes 171 1-10. [Pg.437]

Efficient error-free nucleotide insertion opposite an AAF-dG adduct can be catalyzed by Polr in vitro. The human Polr is more efficient in subsequent extension synthesis as compared to the yeast Polq. If the error-free translesion synthesis activity of Polr is utilized in cells in response to AAF-dG adducts, this polymerase would function to suppress AAF-induced mutagenesis. In one study with yeast cells, both an error-free bypass role and a frameshift mutagenesis role of Polq were reported. Hence, it is still unknown about the contribution of Polq to AAF-induced mutagenesis. Opposite a template AAF-dG adduct, human Poll is able to insert predominantly a C in vitro. Subsequent extension synthesis, however, was not observed. [Pg.488]

Rodriguez, H., and Loechler, E. L. (1995). Are base substitution and frameshift mutagenesis pafliways interrelated An analysis based upon studies of flie frequencies and specificities of mutations induced by the (+)-anti diol epoxide of benzo[a]pyrene. Mutat Res 326, 29-37. [Pg.189]

Milhe, C., Fuchs, R.P., and Lefevre, J.F. (1996) NMR data show that the carcinogen N-2-acetylaminofluorene stabilises an intermediate of -2 frameshift mutagenesis in a region of high mutation frequency. Bur. J. Biochem., 235,120-127. [Pg.236]

Broschard, T.H., Koffel-Schwartz, N., and Fuchs, R.P.P. (1999) Sequence-dependent modulation of frameshift mutagenesis at the Narl-derived mutation hot spots. [Pg.238]

Gill, J.P. and Romano, L.J. (2005) Mechanism for N-acetyl-2-aminoflu-orene-induced frameshift mutagenesis by Escherichia coli DNA polymerase I (Klenow fragment). Biochemistry, 44, 15387-15395. [Pg.238]

The compound bergapten was found to induce lethal and mutagenic photosensitization of bacteria, "dark"-induced frameshift mutagenesis in bacteria, and lethal and clastogenic effects on mammalian cells in tissue cultures (Ashwood-Smith et al. 1980). [Pg.235]

Mutagenesis studies showed that this type of mutation induced a -1 frameshift. A further report describes the incorporation of an (adjacent) cis-syn cyclobutane dimer site specifically into a nucleosome The templating properties of the thymine photoproducts, including the Dewar photoproduct (176), have been examined using the pyrene C-nucleoside triphosphate. The pyrene nucleotide was inserted in preference to dATP opposite the 3 -T of the photoproducts in all cases except for a trans,syn photoproduct, whereas dATP was preferentially incorporated opposite the 5 -T in all cases. This suggests that the incorporation opposite the 3 -end of the photoproduct takes place via a transient abasic site-like intermediate. [Pg.236]

Reuven, N. B., Tomer, G., and Livneh, Z. (1998). The mutagenesis proteins UmuD and UmuG prevent lethal frameshifts while increasing base substitution mutations. Mol. Cell 2, 191-199. [Pg.262]

T. Kada, M. Moriya, and Y. Shirasu, Screening of pesticides for DNA interactions by rec-assay and mutagenesis testing, and frameshift mutagens detected, Mutat. Res. 26, 243... [Pg.172]


See other pages where Frameshift mutagenesis is mentioned: [Pg.36]    [Pg.37]    [Pg.236]    [Pg.238]    [Pg.110]    [Pg.74]    [Pg.237]    [Pg.36]    [Pg.37]    [Pg.236]    [Pg.238]    [Pg.110]    [Pg.74]    [Pg.237]    [Pg.163]    [Pg.106]    [Pg.636]    [Pg.488]    [Pg.133]    [Pg.828]    [Pg.1238]    [Pg.117]    [Pg.354]    [Pg.482]    [Pg.170]    [Pg.184]    [Pg.238]    [Pg.587]    [Pg.239]    [Pg.188]    [Pg.565]    [Pg.239]    [Pg.379]    [Pg.378]   


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