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酿酒酵母有丝分裂和减数分裂染色体增加的检测:甲基苯并咪唑-2-基氨基甲酸酯、甲磺酸甲酯、乙磺酸乙酯、二甲基亚砜、丙腈和一水合环磷酰胺的影响。

The detection of mitotic and meiotic chromosome gain in the yeast Saccharomyces cerevisiae: effects of methyl benzimidazol-2-yl carbamate, methyl methanesulfonate, ethyl methanesulfonate, dimethyl sulfoxide, propionitrile and cyclophosphamide monohydrate.

作者信息

Whittaker S G, Moser S F, Maloney D H, Piegorsch W W, Resnick M A, Fogel S

机构信息

University of California, Department of Plant Biology, Berkley 94720.

出版信息

Mutat Res. 1990 Nov;242(3):231-58. doi: 10.1016/0165-1218(90)90089-k.

Abstract

The diploid yeast strain BR1669 was used to study induction of mitotic and meiotic chromosome gain by selected chemical agents. The test relies on a gene dosage selection system in which hyperploidy is detected by the simultaneous increase in copy number of two alleles residing on the right arm of chromosome VIII: arg4-8 and cup1S (Rockmill and Fogel. 1988; Whittaker et al., 1988). Methyl methanesulfonate (MMS) induced mitotic, but not meiotic, chromosome gain. Methyl benzimidazol-2-yl carbamate (MBC) and ethyl methanesulfonate (EMS) induced both mitotic and meiotic chromosome gain. Propionitrile, a polar aprotic solvent, induced only mitotic chromosome gain; a reliable response was only achieved by overnight incubation of treated cultures at 0 degrees C. MBC is postulated to act by binding directly to tubulin. The requirement for low-temperature incubation suggests that propionitrile also induces aneuploidy by perturbation of microtubular dynamics. The alkylating agents MMS and EMS probably induce recombination which might in turn perturb chromosome segregation. Cyclophosphamide monohydrate and dimethyl sulfoxide (DMSO) failed to induce mitotic or meiotic chromosome gain.

摘要

二倍体酵母菌株BR1669被用于研究特定化学试剂诱导有丝分裂和减数分裂染色体增加的情况。该测试依赖于一种基因剂量选择系统,其中通过位于第八条染色体右臂上的两个等位基因(arg4 - 8和cup1S)拷贝数的同时增加来检测超倍体(Rockmill和Fogel,1988年;Whittaker等人,1988年)。甲磺酸甲酯(MMS)诱导有丝分裂染色体增加,但不诱导减数分裂染色体增加。甲基苯并咪唑 - 2 - 基氨基甲酸酯(MBC)和甲磺酸乙酯(EMS)诱导有丝分裂和减数分裂染色体均增加。丙腈,一种极性非质子溶剂,仅诱导有丝分裂染色体增加;只有将处理后的培养物在0℃过夜孵育才能获得可靠的反应。据推测,MBC通过直接与微管蛋白结合起作用。低温孵育的要求表明丙腈也通过干扰微管动力学诱导非整倍体。烷基化剂MMS和EMS可能诱导重组,这反过来可能干扰染色体分离。一水合环磷酰胺和二甲基亚砜(DMSO)未能诱导有丝分裂或减数分裂染色体增加。

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