首页> 外文期刊>Insect Biochemistry and Molecular Biology >Three mutations identified in the voltage-sensitive sodium channel l-subunit gene of permethrin-resistant human head lice reduce the permethrin sensitivity of house fly Vssc1 sodium channels expressed in Xenopus oocytes
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Three mutations identified in the voltage-sensitive sodium channel l-subunit gene of permethrin-resistant human head lice reduce the permethrin sensitivity of house fly Vssc1 sodium channels expressed in Xenopus oocytes

机译:耐氯菊酯的人头虱的电压敏感钠通道l亚​​基基因中鉴定的三个突变降低了非洲爪蟾卵母细胞中表达的家蝇Vssc1钠通道对氯菊酯的敏感性

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摘要

Point mutations in the para-orthologous sodium channel l-subunit of the head louse (M815I, T917I, and L920F) are associated with permethrin resistance and DDT resistance. These mutations were inserted in all combinations using site-directed mutagenesis at the corresponding amino acid sequence positions (M827I, T929I, and L932F) of the house fly para-orthologous voltage-sensitive sodium channel l-subunit (Vssc1WT) gene and heterologously co-expressed with the sodium channel auxiliary subunit of house fly (Vsscss) in Xenopus oocytes. The double mutant possessing M827I and T929I (Vssc1MITI/Vsscss) caused a 4.0 mV hyperpolarizing shift and the triple mutant, Vssc1MITILF/Vsscss, caused a 3.2 mV depolarizing shift in the voltage dependence of activation curves. ssc1MITI/Vsscss, Vssc1TILF/Vsscss, and Vssc1MITILF/Vsscss caused depolarizing shifts (6.6, 7.6, and 8.8 mV, respectively) in the voltage dependence of steady-state inactivation curves. The M827I and L932F mutations reduced permethrin sensitivity when expressed alone but the T929I mutation, either alone or in combination, virtually abolished permethrin sensitivity. Thus, the T929I mutation is the principal cause of permethrin resistance in head lice. Comparison of the expression rates of channels containing single, double and triple mutations with that of Vssc1WT/Vsscss channels indicates that the M827I mutation may play a role in rescuing the decreased expression of channels containing T929I.
机译:头虱旁直系钠通道L亚基的点突变(M815I,T917I和L920F)与氯菊酯抗性和DDT抗性有关。使用定点诱变将这些突变插入到所有组合中的家蝇对直向同源的电压敏感钠通道L亚基(Vssc1WT)基因的相应氨基酸序列位置(M827I,T929I和L932F),并异源共诱变。在爪蟾卵母细胞中用家蝇的钠通道辅助亚基(Vsscss)表达。拥有M827I和T929I的双突变体(Vssc1MITI / Vsscss)引起4.0 mV的超极化移位,而具有三重突变体Vssc1MITILF / Vsscss的活化曲线电压依赖性引起3.2 mV的去极化移位。 ssc1MITI / Vsscss,Vssc1TILF / Vsscss和Vssc1MITILF / Vsscss导致稳态失活曲线的电压依赖性发生去极化偏移(分别为6.6、7.6和8.8 mV)。当单独表达时,M827I和L932F突变降低了苄氯菊酯的敏感性,但单独或组合使用的T929I突变实际上消除了苄氯菊酯的敏感性。因此,T929I突变是头虱对氯菊酯耐药的主要原因。含有单,双和三突变的通道的表达率与Vssc1WT / Vsscss通道的表达率比较表明,M827I突变可能在挽救含有T929I的通道表达下降中起作用。

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