Organisation and expression of a cluster of yolk protein genes in the Australian sheep blowfly, Lucilia cuprina

被引:11
|
作者
Scott, Maxwell J. [1 ]
Atapattu, Asela [1 ]
Schiemann, Anja H. [1 ]
Concha, Carolina [1 ]
Henry, Rebecca [1 ]
Carey, Brandi-lee [1 ]
Belikoff, Esther J. [1 ]
Heinrich, Joerg C. [1 ]
Sarkar, Abhimanyu [1 ]
机构
[1] Massey Univ, Inst Mol Biol, Ctr Funct Genom, Palmerston North, New Zealand
关键词
Yolk protein; Sterile insect technique; Lucilia cuprina; DROSOPHILA DOUBLESEX PROTEINS; STERILE INSECT TECHNIQUE; FEMALE KILLING SYSTEMS; CERATITIS-CAPITATA; TRANSFORMER GENE; DNA-BINDING; MELANOGASTER; STRAINS; DIPTERA; DIFFERENTIATION;
D O I
10.1007/s10709-010-9492-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The Australian sheep blowfly Lucilia cuprina is a major pest for the Australian and New Zealand sheep industries. With the long-term aim of making a strain of L. cuprina suitable for a genetic control program, we previously developed a tetracycline-repressible female lethal genetic system in Drosophila. A key part of this system is a female-specific promoter from a yolk protein (yp) gene controlling expression of the tetracycline-dependent transactivator (tTA). Here we report the sequence of a 14.2 kb genomic clone from L. cuprina that contains a cluster of three complete yp genes and one partial yp gene. The Lcyp genes are specifically expressed in females that have received a protein meal. A bioinformatic analysis of the promoter of one of the yp genes (LcypA) identified several putative binding sites for DSX, a known regulator of yp gene expression in other Diptera. A transgenic strain of L. cuprina was made that contained the LcypA promoter driving the expression of the Escherichia coli lacZ reporter gene. Transgenic females express high levels of beta-galactosidase after a protein meal. Thus the LcypA promoter could be used to obtain female-specific expression of tTA in transgenic L. cuprina.
引用
收藏
页码:63 / 70
页数:8
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