Newcomb R D, East P D, Russell R J, Oakeshott J G
CSIRO, Division of Entomology, Canberra, Australia.
Insect Mol Biol. 1996 Aug;5(3):211-6. doi: 10.1111/j.1365-2583.1996.tb00056.x.
PCR primers designed from the alpha-esterase gene cluster of Drosophila melanogaster have been used to isolate fragments from eight esterase genes in the Australian sheep blowfly, Lucilia cuprina. Phylogenetic analysis suggests that three are homologues of the alpha E7, alpha E8 and alpha E9 genes of the alpha-esterase cluster of D. melanogaster. A further three are also probably alpha-esterases, whereas the remaining two more closely resemble beta-esterases. Transcripts for five of the alpha-esterase genes were detected by PCR in adult midgut, consistent with a role for these enzymes in digestion and/or detoxification. Based on the tissue distribution of these transcripts, Lc alpha E7 may possibly encode the esterase, E3, which is involved in organophosphate resistance.
从黑腹果蝇的α - 酯酶基因簇设计的PCR引物,已被用于从澳大利亚羊蝇(绿蝇属铜绿蝇)的八个酯酶基因中分离片段。系统发育分析表明,其中三个是黑腹果蝇α - 酯酶簇的αE7、αE8和αE9基因的同源物。另外三个可能也是α - 酯酶,而其余两个更类似于β - 酯酶。通过PCR在成年中肠中检测到五个α - 酯酶基因的转录本,这与这些酶在消化和/或解毒中的作用一致。基于这些转录本的组织分布,LcαE7可能编码参与有机磷抗性的酯酶E3。