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2-乙酰氨基芴在鼠伤寒沙门氏菌四种DNA修复背景下的移码和碱基取代等位基因处的致突变性及突变谱

Mutagenicity and mutation spectra of 2-acetylaminofluorene at frameshift and base-substitution alleles in four DNA repair backgrounds of Salmonella.

作者信息

Shelton M L, DeMarini D M

机构信息

Genetic Toxicology Division, U.S. Environmental Protection Agency, Research Triangle Park, NC 27711.

出版信息

Mutat Res. 1995 Mar;327(1-2):75-86. doi: 10.1016/0027-5107(94)00186-9.

Abstract

We used colony probe hybridization procedures to determine the mutations in approximately 600 revertants of the -1 frameshift allele hisD3052 and approximately 200 revertants of the base-substitution allele hisG46 of Salmonella typhimurium induced by 2-acetylaminofluorene (2-AAF) in the presence of Aroclor-induced rat liver S9. 2-AAF was primarily a frameshift mutagen, exhibiting 5 times more frameshift than base-substitution activity. The only frameshift mutation 2-AAF induced at the hisD3052 allele was a hotspot (-2) deletion within the sequence CGCGCGCG. The addition of the pKM101 plasmid had a small effect on the mutagenic potency of 2-AAF at this allele in a uvr+ background and no effect on the mutation spectra in either a uvr+ or uvr- background. The small amount of base-substitution activity exhibited by 2-AAF at the hisG46 allele required the presence of both the pKM101 plasmid and the uvrB mutation. The base substitutions were G.C-->T.A transversions (86%) and G.C-->A.T transitions (14%), and 85% of the substitutions were at the second position of the CCC target of the hisG46 allele; the remainder were at the first position. We propose that the hotspot frameshift may be initiated by N-acetyl-2-aminofluorene adducts located at the C(8) position of any of the guanines except the first one in the CGCGCGCG hotspot sequence. The mutation might then result from correct incorporation of cytosine opposite the adducted guanine, followed by a 2-base slippage according to our recently proposed correct-incorporation/slippage model. The hotspot mutation may also result from a 2-AAF-induced B- to Z-DNA transition at the repeating GpC site as well as by the action of enzymes involved in DNA metabolism, such as DNA resolvases or topoisomerases, on DNA structures that have been distorted by 2-AAF adducts. The small amount of 2-AAF-induced base-substitution activity may be due to mispairing of adenine opposite the minor aminofluorene adduct at the C(8) position of guanine.

摘要

我们采用菌落探针杂交程序,来确定在艾氏剂诱导的大鼠肝脏S9存在的情况下,2-乙酰氨基芴(2-AAF)诱导的鼠伤寒沙门氏菌-1移码等位基因hisD3052的约600个回复突变体以及碱基替换等位基因hisG46的约200个回复突变体中的突变情况。2-AAF主要是一种移码诱变剂,其移码活性比碱基替换活性高5倍。2-AAF在hisD3052等位基因上诱导的唯一移码突变是CGCGCGCG序列内的热点(-2)缺失。在uvr+背景下,添加pKM101质粒对2-AAF在该等位基因上的诱变效力有微小影响,而在uvr+或uvr-背景下对突变谱均无影响。2-AAF在hisG46等位基因上表现出的少量碱基替换活性需要同时存在pKM101质粒和uvrB突变。碱基替换为G.C→T.A颠换(86%)和G.C→A.T转换(14%),85%的替换发生在hisG46等位基因CCC靶标的第二位;其余的发生在第一位。我们提出,热点移码可能由位于CGCGCGCG热点序列中除第一个鸟嘌呤外任何一个鸟嘌呤C(8)位置的N-乙酰-2-氨基芴加合物引发。然后,根据我们最近提出的正确掺入/滑动模型,突变可能是由于与加合鸟嘌呤相对的胞嘧啶的正确掺入,随后发生2个碱基的滑动导致的。热点突变也可能是由于2-AAF诱导的在重复GpC位点的B型到Z型DNA转变,以及DNA代谢相关酶(如DNA分解酶或拓扑异构酶)对被2-AAF加合物扭曲的DNA结构的作用。2-AAF诱导的少量碱基替换活性可能是由于腺嘌呤与鸟嘌呤C(8)位置的次要氨基芴加合物错配所致。

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