4.6 Article

Diverse cadherin mutations conferring resistance to Bacillus thuringiensis toxin Cry1Ac in Helicoverpa armigera

期刊

INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY
卷 40, 期 2, 页码 113-118

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ibmb.2010.01.001

关键词

Helicoverpa armigera; Bacillus thuringiensis; Cadherin; Resistance; Bt cotton

资金

  1. Ministry of Science and Technology of China [2007CB1092G4, 2007AA10Z420, 2008ZX08012-04]
  2. National Natural Science Foundation of China [30870343]

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Transgenic cotton expressing Bacillus thuringiensis (Bt) toxins has been widely adopted to control some key lepidopteran pests including the bollworm Helicoverpa armigera. Evolution of resistance to Bt cotton by target pests is a major threat to the continued success of Bt cotton. Previous results revealed 3 null alleles (r1-r3) of a cadherin gene (Ha-BtR) conferring Cry1Ac resistance in H. armigera. An F, screen of 123 single-pair families was conducted between a Cry1Ac-resistant strain (the SCD-r1 strain, homozygous for the r1 allele of Ha-BtR) and field-derived insects from Jiangpu population (Jiangsu province, China) in 2008. Five new null alleles of Ha_BtR (r4-r8) were identified in six candidate single-pair families. These null alleles were created through either an insertion or a point mutation. Interestingly, intact alleles of Ha-BtR were found in two field-derived insects from another two candidate single-pair families. It suggests that these two field-derived insects may carry novel resistance alleles of Ha-BtR, with missense mutations resulting in a non-functional cadherin protein, or a major dominant mutation at a locus other than cadherin. The resistance allele frequency of Ha_BtR was detected at an appreciable level (0.024) in the Jiangpu population of H. armigera in 2008. Together with previous findings, a total of eight different resistance alleles of Ha_BtR were identified from three Chinese strains of H. armigera. Mutational diversity of Ha_BtR could impair DNA screening for Bt resistance allele frequency in the field, and an F-1 screen should be used routinely for monitoring cadherin-based resistance allele frequencies in H. armigera. (C) 2010 Elsevier Ltd. All rights reserved.

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