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1.
Sex Dev ; 8(1-3): 127-36, 2014.
Article in English | MEDLINE | ID: mdl-24401199

ABSTRACT

Elucidation of the sex differentiation pathway in insects offers an opportunity to understand key aspects of evolutionary developmental biology. In addition, it provides the understanding necessary to manipulate insects in order to develop new synthetic genetics-based tools for the control of pest insects. Considerable progress has been made in this, especially in improvements to the sterile insect technique (SIT). Large scale sex separation is considered highly desirable or essential for most SIT targets. This separation can be provided by genetic methods based on sex-specific gene expression. Investigation of sex determination by many groups has provided molecular components and methods for this. Though the primary sex determination signal varies considerably, key regulatory genes and mechanisms remain surprisingly similar. In most cases studied so far, a primary signal is transmitted to a basal gene at the bottom of the hierarchy (dsx) through an alternative splicing cascade; dsx is itself differentially spliced in males and females. A sex-specific alternative splicing system therefore offers an attractive route to achieve female-specific expression. Experience has shown that alternative splicing modules can be developed with cross-species function; modularity and standardisation and re-use of parts are key principles of synthetic biology. Both female-killing and sex reversal (XX females to phenotypic males) can in principle also be used as efficient alternatives to sterilisation in SIT-like methods. Sexual maturity is yet another area where understanding of sexual development may be applied to insect control programmes. Further detailed understanding of this crucial aspect of insect biology will undoubtedly continue to underpin innovative practical applications.


Subject(s)
Insecta/physiology , Pest Control , Sexual Development/physiology , Alternative Splicing/genetics , Animals , Sex Determination Processes , Sexual Maturation/physiology
2.
Insect Mol Biol ; 16(2): 221-30, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17298554

ABSTRACT

Transformer (tra) is the second gene of a regulatory cascade based on RNA splicing that determines sex in Drosophila melanogaster. Splicing of tra transcripts is regulated by the master gene Sex lethal and tra itself regulates splicing of the transcriptional regulator doublesex (dsx). We present the isolation and characterization of Botra, the olive fruit fly Bactrocera oleae orthologue to the Drosophila gene transformer. As in Drosophila, Botra transcripts are spliced in a sex-specific manner so that only females encode a functional polypeptide of 422 amino acids, whereas males encode presumably nonfunctional peptide(s). The identification of multiple TRA/TRA-2 binding sites within the Botra male-specific exons, suggests an autoregulation mechanism of tra, through TRA/TRA2 activities. The fundamental role of the TRA protein in sex determination of Bactrocera was investigated by RNA interference, where the introduction of Botra dsRNA into embryos resulted in complete transformation of XX flies into fertile males.


Subject(s)
Insect Proteins/genetics , Sex Determination Processes , Tephritidae/genetics , Amino Acid Sequence , Animals , Drosophila Proteins , Female , Fertility , Genome, Insect , Homeostasis/genetics , Karyotyping , Male , Molecular Sequence Data , Nuclear Proteins/genetics , RNA Interference , RNA, Double-Stranded , Reverse Transcriptase Polymerase Chain Reaction , Sequence Analysis, DNA
3.
Insect Mol Biol ; 15(1): 95-103, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16469073

ABSTRACT

The olive fruit fly (olive fly) Bactrocera oleae (Dacus), recently introduced in North America, is the most destructive pest of olives worldwide. The lack of an efficient gene transfer technology for olive fly has hampered molecular analysis, as well as development of genetic techniques for its control. We have developed a Minos-based transposon vector carrying a self-activating cassette which overexpresses the enhanced green fluorescent protein (EGFP). Efficient transposase-mediated integration of one to multiple copies of this vector was achieved in the germ line of B. oleae by coinjecting the vector along with in vitro synthesized Minos transposase mRNA into preblastoderm embryos. The self-activating gene construct combined with transposase mRNA present a system with potential for transgenesis of very diverse species.


Subject(s)
Green Fluorescent Proteins/genetics , Tephritidae/genetics , Transformation, Genetic , Animals , Animals, Genetically Modified , Base Sequence , Biolistics/methods , Blotting, Southern , DNA, Recombinant , Female , Genetic Markers , HeLa Cells , Humans , Male , Molecular Sequence Data , Tephritidae/embryology , Transposases/genetics
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