@article{edman_linger_belikoff_li_sze_tarone_scott_2014, title={Functional characterization of calliphorid cell death genes and cellularization gene promoters for controlling gene expression and cell viability in early embryos}, volume={24}, ISSN={0962-1075 1365-2583}, url={http://dx.doi.org/10.1111/imb.12135}, DOI={10.1111/imb.12135}, abstractNote={AbstractThe New World screwworm fly, Cochliomyia hominivorax, and the Australian sheep blow fly, Lucilia cuprina, are major pests of livestock. The sterile insect technique was used to eradicate C. hominivorax from North and Central America. This involved area‐wide releases of male and female flies that had been sterilized by radiation. Genetic systems have been developed for making ‘male‐only’ strains that would improve the efficiency of genetic control of insect pests. One system involves induction of female lethality in embryos through activation of a pro‐apoptotic gene by the tetracycline‐dependent transactivator. Sex‐specific expression is achieved using an intron from the transformer gene, which we previously isolated from several calliphorids. In the present study, we report the isolation of the promoters from the C. hominivorax slam and Lucilia sericata bnk cellularization genes and show that these promoters can drive expression of a GFP reporter gene in early embryos of transgenic L. cuprina. Additionally, we report the isolation of the L. sericata pro‐apoptotic hid and rpr genes, identify conserved motifs in the encoded proteins and determine the relative expression of these genes at different stages of development. We show that widespread expression of the L. sericata pro‐apoptotic genes was lethal in Drosophila melanogaster. The isolated gene promoters and pro‐apoptotic genes could potentially be used to build transgenic embryonic sexing strains of calliphorid livestock pests.}, number={1}, journal={Insect Molecular Biology}, publisher={Wiley}, author={Edman, R. M. and Linger, R. J. and Belikoff, E. J. and Li, F. and Sze, S.‐H. and Tarone, A. M. and Scott, M. J.}, year={2014}, month={Sep}, pages={58–70} }
 @article{sze_dunham_carey_chang_li_edman_fjeldsted_scott_nuzhdin_tarone_2012, title={A <i>de novo</i> transcriptome assembly of <i>Lucilia sericata</i> (Diptera: Calliphoridae) with predicted alternative splices, single nucleotide polymorphisms and transcript expression estimates}, volume={21}, ISSN={0962-1075 1365-2583}, url={http://dx.doi.org/10.1111/j.1365-2583.2011.01127.x}, DOI={10.1111/j.1365-2583.2011.01127.x}, abstractNote={AbstractThe blow flyLucilia sericata(Diptera: Calliphoridae) (Meigen) is a nonmodel organism with no reference genome that is associated with numerous areas of research spanning the ecological, evolutionary, medical, veterinary and forensic sciences. To facilitate scientific discovery in this species, the transcriptome was assembled from more than six billion bases of Illumina and twenty‐one million bases of 454 sequence derived from embryonic, larval, pupal, adult and larval salivary gland libraries. The assembly was carried out in a manner that enabled identification of putative single nucleotide polymorphisms (SNPs) and alternative splices, and that provided expression estimates for various life history stages and for salivary tissue. The assembled transcriptome was also used to identify transcribed transposable elements inL. sericata. The results of this study will enable blow fly biologists, dipterists and comparative genomicists to more rapidly develop and test molecular and genetic hypotheses, especially those regarding blow fly development and salivary gland biology.}, number={2}, journal={Insect Molecular Biology}, publisher={Wiley}, author={Sze, S‐H. and Dunham, J. P. and Carey, B. and Chang, P. L. and Li, F. and Edman, R. M. and Fjeldsted, C. and Scott, M. J. and Nuzhdin, S. V. and Tarone, A. M.}, year={2012}, month={Jan}, pages={205–221} }
 @article{concha_edman_belikoff_schiemann_carey_scott_2012, title={Organization and expression of the Australian sheep blowfly (<i>Lucilia cuprina</i>) <i>hsp23</i>, <i>hsp24, hsp70</i> and <i>hsp83</i> genes}, volume={21}, ISSN={0962-1075 1365-2583}, url={http://dx.doi.org/10.1111/j.1365-2583.2011.01123.x}, DOI={10.1111/j.1365-2583.2011.01123.x}, abstractNote={AbstractIn this study we report the isolation and characterization of a heat shock protein 70 (hsp70) gene, the hsp83 gene and two genes that encode small Hsps (Lchsp23 and Lchsp24) from the Australian sheep blowfly, Lucilia cuprina, a major agricultural pest. Phylogenetic analyses indicate that the LcHsp23 protein is the orthologue of Drosophila melanogaster Hsp23 and LcHsp24 is the orthologue of Sarcophaga crassipalpis Hsp23. Quantitative reverse‐transcriptase PCR analysis showed that the basal level of Lchsp83 RNA is relatively high at all developmental stages and only moderately induced by heat shock. In contrast, Lchsp70 transcripts are present at low levels and strongly induced by heat shock at all stages. The basal levels of expression and degrees of heat induction of the Lchsp23 and Lchsp24 transcripts were more variable across the different developmental stages. Putative heat shock factor binding sites were identified in the Lchsp24, Lchsp70 and Lchsp83 gene promoters. The isolation of these hsp gene promoters will facilitate constitutive or conditional expression of a gene of interest in transgenic Lucilia.}, number={2}, journal={Insect Molecular Biology}, publisher={Wiley}, author={Concha, C. and Edman, R. M. and Belikoff, E. J. and Schiemann, A. H. and Carey, B. and Scott, M. J.}, year={2012}, month={Jan}, pages={169–180} }