Synthetic biology approaches to generate temperature-sensitive alleles for the Sterile Insect Technique

Chun Yin Leung , Ernst A. Wimmer , Hassan M. M. Ahmed

Insect Science ›› 2026, Vol. 33 ›› Issue (2) : 517 -532.

PDF (813KB)
Insect Science ›› 2026, Vol. 33 ›› Issue (2) :517 -532. DOI: 10.1111/1744-7917.70186
SPECIAL ISSUE ARTICLE
Synthetic biology approaches to generate temperature-sensitive alleles for the Sterile Insect Technique
Author information +
History +
PDF (813KB)

Abstract

The Sterile Insect Technique (SIT) is an environmentally friendly, sustainable pest control approach, which uses large-scale releases of sterile insects to suppress or eradicate target populations through infertile matings. The efficiency of SIT is enhanced by male-only releases requiring genetic sexing strains (GSSs) that are classically based on selectable recessive visible markers or temperature-sensitive lethal (tsl) mutations and a rescue by a wild-type allele translocated to the male-determining chromosome. The transfer of identified or designed temperature-sensitive alleles might allow the generation of neoclassical GSSs in additional SIT target species. By using precise genome-editing tools, such as CRISPR/Cas, the creation of specific mutations in target genes and the integration of a wild-type copy is feasible without the introduction of foreign DNA. This might ease regulation of neoclassical GSSs, since they are not considered transgenic. However, integration and expression of genes at male-determining loci or chromosomes is not reliably established. Therefore, additional strategies to link temperature-sensitive phenotypes to female development are required, which could be achieved by targeting genes involved in dosage compensation or sex determination. To create temperature-sensitive alleles, rational protein design using advanced modeling and prediction tools to evaluate and tailor the effect of mutations on protein stability and temperature sensitivity can be used. In addition, emerging synthetic biology strategies such as temperature-inducible N-degrons or temperature-sensitive inteins provide powerful tools to generate temperature sensitivity. Such approaches should enable conditional control over proteins causing female lethality or sex conversion and therefore promise straightforward generic approaches to generate GSSs for male-only production in SIT target species.

Keywords

CRISPR/Cas / genome editing / insect pest management / intein / N-degron / protein design

Cite this article

Download citation ▾
Chun Yin Leung, Ernst A. Wimmer, Hassan M. M. Ahmed. Synthetic biology approaches to generate temperature-sensitive alleles for the Sterile Insect Technique. Insect Science, 2026, 33 (2) : 517-532 DOI:10.1111/1744-7917.70186

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Allende, J.E. and Allende, C.C. (1995) Protein kinase CK2: an enzyme with multiple substrates and a puzzling regulation. The FASEB Journal, 9, 313–323.

[2]

Alphey, L., McKemey, A., Nimmo, D., Oviedo, M.N., Lacroix, R., Matzen, K. et al. (2016) Genetic control of Aedes mosquitoes. In: Global Health Impacts of Vector-Borne Diseases: Workshop Summary (ed. National Academies of Sciences, Engineering, and Medicine), pp. 1–10. National Academies Press, Washington, DC, USA.

[3]

Amrein, H., Maniatis, T. and Nöthiger, R. (1990) Alternatively spliced transcripts of the sex-determining gene tra-2 of Drosophila encode functional proteins of different size. The EMBO Journal, 9, 3619–3629.

[4]

Ant, T., Koukidou, M., Rempoulakis, P., Gong, H.-F., Economopoulos, A., Vontas, J. et al. (2012) Control of the olive fruit fly using genetics-enhanced sterile insect technique. BMC Biology, 10, 51.

[5]

Aumann, R.A., Gouvi, G., Gregoriou, M.-E., Rehling, T., Sollazzo, G., Bourtzis, K. et al. (2025) Decoding and engineering temperature-sensitive lethality in Ceratitis capitata for pest control. Proceedings of the National Academy of Sciences USA, 122, e2503604122.

[6]

Aumann, R.A., Häcker, I. and Schetelig, M.F. (2020) Female-to-male sex conversion in Ceratitis capitata by CRISPR/Cas9 HDR-induced point mutations in the sex determination gene transformer-2. Scientific Reports, 10, 18611.

[7]

Baker, B.S. (1989) Sex in flies: the splice of life. Nature, 340, 521–524.

[8]

Bell, L.R., Horabin, J.I., Schedl, P. and Cline, T.W. (1991) Positive autoregulation of Sex-lethal by alternative splicing maintains the female determined state in Drosophila. Cell, 65, 229–239.

[9]

Belote, J.M. and Baker, B.S. (1982) Sex determination in Drosophila melanogaster: analysis of transformer-2, a sex-transforming locus. Proceedings of the National Academy of Sciences USA, 79, 1568–1572.

[10]

Betting, J. and Seufert, W. (1996) A yeast Ubc9 mutant protein with temperature-sensitive in vivo function is subject to conditional proteolysis by a ubiquitin- and proteasome-dependent pathway. Journal of Biological Chemistry, 271, 25790–25796.

[11]

Boggs, R.T., Gregor, P., Idriss, S., Belote, J.M. and McKeown, M. (1987) Regulation of sexual differentiation in D. melanogaster via alternative splicing of RNA from the transformer gene. Cell, 50, 739–747.

[12]

Buchman, A. and Akbari, O.S. (2019) Site-specific transgenesis of the Drosophila melanogaster Y-chromosome using CRISPR/Cas9. Insect Molecular Biology, 28, 65–73.

[13]

Burghardt, G., Hediger, M., Siegenthaler, C., Moser, M., Dübendorfer, A. and Bopp, D. (2005) The transformer2 gene in Musca domestica is required for selecting and maintaining the female pathway of development. Development Genes and Evolution, 215, 165–176.

[14]

Butterfield, G.L., Lajoie, M.J., Gustafson, H.H., Sellers, D.L., Nattermann, U., Ellis, D. et al. (2017) Evolution of a designed protein assembly encapsulating its own RNA genome. Nature, 552, 415–420.

[15]

Cao, L., Goreshnik, I., Coventry, B., Case, J.B., Miller, L., Kozodoy, L. et al. (2020) De novo design of picomolar SARS-CoV-2 miniprotein inhibitors. Science, 370, 426–431.

[16]

Capriotti, E., Fariselli, P. and Casadio, R. (2005) I-Mutant2.0: predicting stability changes upon mutation from the protein sequence or structure. Nucleic Acids Research, 33, W306–W310.

[17]

Chakshusmathi, G., Mondal, K., Lakshmi, G.S., Singh, G., Roy, A., Ch, R.B. et al. (2004) Design of temperature-sensitive mutants solely from amino acid sequence. Proceedings of the National Academy of Sciences USA, 101, 7925–7930.

[18]

Chen, S., Wei, H.M., Lv, W.W., Wang, D.L. and Sun, F.L. (2011) E2 ligase dRad6 regulates DMP53 turnover in Drosophila. Journal of Biological Chemistry, 286, 9020–9030.

[19]

Choo, A., Fung, E., Chen, I.Y., Saint, R., Crisp, P. and Baxter, S.W. (2020) Precise single base substitution in the shibire gene by CRISPR/Cas9-mediated homology directed repair in Bactrocera tryoni. BMC Genetics, 21, 127.

[20]

Ciechanover, A. (1994) The ubiquitin-proteasome proteolytic pathway. Cell, 79, 13–21.

[21]

Cline, T.W. (1978) Two closely linked mutations in Drosophila melanogaster that are lethal to opposite sexes and interact with daughterless. Genetics, 90, 683–697.

[22]

Cline, T.W. (1983) The interaction between daughterless and Sex-lethal in triploids: a lethal sex-transforming maternal effect linking sex determination and dosage compensation in Drosophila melanogaster. Developmental Biology, 95, 260–274.

[23]

Cline, T.W. (1984) Autoregulatory functioning of a Drosophila gene product that establishes and maintains the sexually determined state. Genetics, 107, 231–277.

[24]

Concha, C., Palavesam, A., Guerrero, F.D., Sagel, A., Li, F., Osborne, J.A. et al. (2016) A transgenic male-only strain of the New World screwworm for an improved control program using the sterile insect technique. BMC Biology, 14, 72.

[25]

Concha, C., Yan, Y., Arp, A., Quilarque, E., Sagel, A., de León, A.P. et al. (2020) An early female lethal system of the New World screwworm, Cochliomyia hominivorax, for biotechnology-enhanced SIT. BMC Genetics, 21, 143.

[26]

Dauwalder, B., Amaya-Manzanares, F. and Mattox, W. (1996) A human homologue of the Drosophila sex determination factor transformer-2 has conserved splicing regulatory functions. Proceedings of the National Academy of Sciences USA, 93, 9004–9009.

[27]

Dohmen, R.J., Wu, P. and Varshavsky, A. (1994) Heat-inducible degron: a method for constructing temperature-sensitive mutants. Science, 263, 1273–1276.

[28]

Dyck, V.A., Hendrichs, J. and Robinson, A.S. (2021) Sterile Insect Technique: Principles and Practice in Area-Wide Integrated Pest Management. CRC Press, Boca Raton, USA.

[29]

EFSA Panel on Genetically Modified Organisms (EFSA GMO Panel), Naegeli, H., Bresson, J.-L., Dalmay, T., Dewhurst, I.C., Epstein, M.M. et al. (2020) Applicability of the EFSA opinion on site-directed nucleases type 3 for the safety assessment of plants developed using site-directed nucleases type 1 and 2 and oligonucleotide-directed mutagenesis. EFSA Journal, 18, e06299.

[30]

Ellison, K.S., Gwozd, T., Prendergast, J.A., Paterson, M.C. and Ellison, M.J. (1991) A site-directed approach for constructing temperature-sensitive ubiquitin-conjugating enzymes reveals a cell cycle function and growth function for RAD6. Journal of Biological Chemistry, 266, 24116–24120.

[31]

Epps, J.L. and Tanda, S. (1998) The Drosophila semushi mutation blocks nuclear import of Bicoid during embryogenesis. Current Biology, 8, S1–S2.

[32]

Erickson, J.W. and Quintero, J.J. (2007) Indirect effects of ploidy suggest X chromosome dose, not the X: a ratio, signals sex in Drosophila. PLoS Biology, 5, e332.

[33]

Faden, F., Ramezani, T., Mielke, S., Almudi, I., Nairz, K., Froehlich, M.S. et al. (2016) Phenotypes on demand via switchable target protein degradation in multicellular organisms. Nature Communications, 7, 12202.

[34]

Fletcher, S. and Hamilton, A.D. (2006) Targeting protein–protein interactions by rational design: mimicry of protein surfaces. Journal of the Royal Society Interface, 3, 215–233.

[35]

Franz, G., Bourtzis, K. and Cáceres, C. (2021) Practical and operational genetic sexing systems based on classical genetic approaches in fruit flies, an example for other species amenable to large-scale rearing for the sterile insect technique. In: Sterile Insect Technique: Principles and Practice in Area-Wide Integrated Pest Management (eds. V.A. Dyck, J. Hendrichs & A.S. Robinson), pp. 575–604. CRC Press, Boca Raton, USA.

[36]

Freist, W. and Gauss, D.H. (1995) Lysyl-tRNA synthetase. Biological Chemistry Hoppe Seyler, 376, 451–451.

[37]

Fried, M. (1965) Cell-transforming ability of a temperature-sensitive mutant of polyoma virus. Proceedings of the National Academy of Sciences USA, 53, 486–491.

[38]

Fu, G., Lees, R. S., Nimmo, D., Aw, D., Jin, L., Gray, P. et al. (2010) Female-specific flightless phenotype for mosquito control. Proceedings of the National Academy of Sciences USA, 107, 4550–4554.

[39]

Gailite, I., Egger-Adam, D. and Wodarz, A. (2012) The phosphoinositide-associated protein Rush hour regulates endosomal trafficking in Drosophila. Molecular Biology of the Cell, 23, 433–447.

[40]

Gebauer, F., Merendino, L., Hentze, M.W. and Valcárcel, J. (1998) The Drosophila splicing regulator sex-lethal directly inhibits translation of male-specific-lethal 2 mRNA. RNA, 4, 142–150.

[41]

Gergen, J.P. (1987) Dosage compensation in Drosophila: evidence that daughterless and Sex-lethal control X chromosome activity at the blastoderm stage of embryogenesis. Genetics, 117, 477–485.

[42]

Handler, A.M. (2016) Enhancing the stability and ecological safety of mass-reared transgenic strains for field release by redundant conditional lethality systems. Insect Science, 23, 225–234.

[43]

Hanna, D.E., Rethinaswamy, A. and Glover, C.V.C. (1995) Casein kinase II is required for cell cycle progression during G1 and G2/M in Saccharomyces cerevisiae. Journal of Biological Chemistry, 270, 25905–25914.

[44]

Hediger, M., Henggeler, C., Meier, N., Perez, R., Saccone, G. and Bopp, D. (2010) Molecular characterization of the key switch F provides a basis for understanding the rapid divergence of the sex-determining pathway in the housefly. Genetics, 184, 155–170.

[45]

Heinrichs, V., Ryner, L.C. and Baker, B.S. (1998) Regulation of sex-specific selection of fruitless 5′ splice sites by transformer and transformer-2. Molecular and Cellular Biology, 18, 450–458.

[46]

Horowitz, N.H. (1950) Biochemical genetics of Neurospora. Advances in Genetics, 3, 33–71.

[47]

Inui, M., Miyado, M., Igarashi, M., Tamano, M., Kubo, A., Yamashita, S. et al. (2014) Rapid generation of mouse models with defined point mutations by the CRISPR/Cas9 system. Scientific Reports, 4, 5396.

[48]

Jin, L., Walker, A.S., Fu, G., Harvey-Samuel, T., Dafa'alla, T., Miles, A. et al. (2013) Engineered female-specific lethality for control of pest Lepidoptera. ACS Synthetic Biology, 2, 160–166.

[49]

Joanisse, D.R., Inaguma, Y. and Tanguay, R.M. (1998) Cloning and developmental expression of a nuclear ubiquitin-conjugating enzyme (DmUbc9) that interacts with small heat shock proteins in Drosophila melanogaster. Biochemical and Biophysical Research Communications, 244, 102–109.

[50]

Joosten, R.P., Te Beek, T.A., Krieger, E., Hekkelman, M.L., Hooft, R.W., Schneider, R. et al. (2010) A series of PDB related databases for everyday needs. Nucleic Acids Research, 39, D411–D419.

[51]

Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O. et al. (2021) Highly accurate protein structure prediction with AlphaFold. Nature, 596, 583–589.

[52]

Kabsch, W. and Sander, C. (1983) Dictionary of protein secondary structure: pattern recognition of hydrogen-bonded and geometrical features. Biopolymers: Original Research on Biomolecules, 22, 2577–2637.

[53]

Kaiser, P.E., Seawright, J.A., Dame, D.A. and Joslyn, D.J. (1978) Development of a genetic sexing system for Anopheles albimanus. Journal of Economic Entomology, 71, 766–771.

[54]

Kane, P.M., Yamashiro, C.T., Wolczyk, D.F., Neff, N., Goebl, M. and Stevens, T.H. (1990) Protein splicing converts the yeast TFP1 gene product to the 69-kd subunit of the vacuolar H+-adenosine triphosphatase. Science, 250, 651–657.

[55]

Klassen, W. and Vreysen, M.J.B. (2021) Area-wide integrated pest management and the sterile insect technique. In: Sterile Insect Technique: Principles and Practice in Area-Wide Integrated Pest Management (eds. V.A. Dyck, J. Hendrichs & A.S. Robinson), pp. 75–112. CRC Press, Boca Raton, USA.

[56]

Knipling, E.F. (1955) Possibilities of insect control or eradication through the use of sexually sterile males. Journal of Economic Entomology, 48, 459–462.

[57]

Koskinioti, P., Augustinos, A.A., Carvalho, D.O., Misbah-ul-Haq, M., Pillwax, G., de la Fuente, L.D. et al. (2020) Genetic sexing strains for the population suppression of the mosquito vector Aedes aegypti. Philosophical Transactions of the Royal Society B: Biological Sciences, 376, 20190808.

[58]

Krafsur, E.S. (1998) Sterile insect technique for suppressing and eradicating insect population: 55 years and counting. Journal of Agricultural Entomology, 15, 303–317.

[59]

Krafsur, E.S. and Lindquist, D.A. (1996) Did the sterile insect technique or weather eradicate screwworms (Diptera: Calliphoridae) from Libya? Journal of Medical Entomology, 33, 877–887.

[60]

Krzywinska, E., Ferretti, L., Li, J., Li, J.-C., Chen, C.-H. and Krzywinski, J. (2021) femaleless controls sex determination and dosage compensation pathways in females of Anopheles mosquitoes. Current Biology, 31, 1084–1091.e4.

[61]

Kuntamalla, P.P., Kunttas-Tatli, E., Karandikar, U., Bishop, C.P. and Bidwai, A.P. (2009) Drosophila protein kinase CK2 is rendered temperature-sensitive by mutations of highly conserved residues flanking the activation segment. Molecular and Cellular Biochemistry, 323, 49–60.

[62]

Laohakieat, K., Aketarawong, N., Isasawin, S., Thitamadee, S. and Thanaphum, S. (2016) The study of the transformer gene from Bactrocera dorsalis and B. correcta with putative core promoter regions. BMC Genetics, 17, 34.

[63]

Li, J. and Handler, A.M. (2017) Temperature-dependent sex-reversal by a transformer-2 gene-edited mutation in the spotted wing drosophila, Drosophila suzukii. Scientific Reports, 7, 12363.

[64]

Liang, R., Liu, X., Liu, J., Ren, Q., Liang, P., Lin, Z. et al. (2007) A T7-expression system under temperature control could create temperature-sensitive phenotype of target gene in Escherichia coli. Journal of Microbiological Methods, 68, 497–506.

[65]

Lin, J.-M., Kilman, V.L., Keegan, K., Paddock, B., Emery-Le, M., Rosbash, M. et al. (2002) A role for casein kinase 2α in the Drosophila circadian clock. Nature, 420, 816–820.

[66]

Liu, G., Wu, Q., Li, J., Zhang, G. and Wan, F. (2015) RNAi-mediated knock-down of transformer and transformer 2 to generate male-only progeny in the oriental fruit fly, Bactrocera dorsalis (Hendel). PLoS ONE, 10, e0128892.

[67]

Lőrincz, P., Kenéz, L.A., Tóth, S., Kiss, V., Varga, Á., Csizmadia, T. et al. (2019) Vps8 overexpression inhibits HOPS-dependent trafficking routes by outcompeting Vps41/Lt. eLife, 8, e45631.

[68]

Lucchesi, J.C. and Skripsky, T. (1981) The link between dosage compensation and sex differentiation in Drosophila melanogaster. Chromosoma, 82, 217–227.

[69]

McCombs, S.D. and Saul, S.H. (1995) Translocation-based genetic sexing system for the oriental fruit fly (Diptera: Tephritidae) based on pupal color dimorphism. Annals of the Entomological Society of America USA, 88, 695–698.

[70]

McInnis, D.O., Tam, S., Lim, R., Komatsu, J., Kurashima, R. and Albrecht, C. (2004) Development of a pupal color-based genetic sexing strain of the melon fly, Bactrocera cucurbitae (Coquillett) (Diptera: Tephritidae). Annals of the Entomological Society of America, 97, 1026–1033.

[71]

McKeown, M., Belote, J.M. and Baker, B.S. (1987) A molecular analysis of transformer, a gene in Drosophila melanogaster that controls female sexual differentiation. Cell, 48, 489–499.

[72]

Meise, M., Hilfiker-Kleiner, D., Dübendorfer, A., Brunner, C., Nöthiger, R. and Bopp, D. (1998) Sex-lethal, the master sex-determining gene in Drosophila, is not sex-specifically regulated in Musca domestica. Development (Cambridge, England), 125, 1487–1494.

[73]

Meccariello, A., Salvemini, M., Primo, P., Hall, B., Koskinioti, P., Dalíková, M. et al. (2019) Maleness-on-the-Y (MoY) orchestrates male sex determination in major agricultural fruit fly pests. Science, 365, 1457–1460.

[74]

Meza, J.S., ul Hag, I., Vreysen, M.J.B., Bourtzis, K., Kyritsis, G.A. and Cáceres, C. (2018) Comparison of classical and transgenic genetic sexing strains of Mediterranean fruit fly (Diptera: Tephritidae) for application of the sterile insect technique. PLoS ONE, 13, e0208880.

[75]

Meza, J.S., Bourtzis, K., Zacharopoulou, A., Gariou-Papalexiou, A. and Cáceres, C. (2020) Development and characterization of a pupal-colour based genetic sexing strain of Anastrepha fraterculus sp. 1 (Diptera: Tephritidae). BMC Genetics, 21, 134.

[76]

Modarres, H.P., Mofrad, M.R. and Sanati-Nezhad, A. (2016) Protein thermostability engineering. RSC Advances, 6, 115252–115270.

[77]

Mondal, K., VijayRaghavan, K. and Varadarajan, R. (2007) Design and utility of temperature-sensitive Gal4 mutants for conditional gene expression in Drosophila. Fly, 1, 282–286.

[78]

Motzik, A., Nechushtan, H., Foo, S.Y. and Razin, E. (2013) Non-canonical roles of lysyl-tRNA synthetase in health and disease. Trends in Molecular Medicine, 19, 726–731.

[79]

Ndo, C., Poumachu, Y., Metitsi, D., Awono-Ambene, H.P., Tchuinkam, T., Gilles, J.L.R. et al. (2018) Isolation and characterization of a temperature-sensitive lethal strain of Anopheles arabiensis for SIT-based application. Parasites & Vectors, 11, 659.

[80]

Noren, C.J., Wang, J. and Perler, F.B. (2000) Dissecting the chemistry of protein splicing and its applications. Angewandte Chemie International Edition, 39, 450–466.

[81]

Ogaugwu, C.E., Schetelig, M.F. and Wimmer, E.A. (2013) Transgenic sexing system for Ceratitis capitata (Diptera: Tephritidae) based on female-specific embryonic lethality. Insect Biochemistry and Molecular Biology, 43, 1–8.

[82]

Pane, A., Salvemini, M., Bovi, P.D., Polito, C. and Saccone, G. (2002) The transformer gene in Ceratitis capitata provides a genetic basis for selecting and remembering the sexual fate. Development (Cambridge, England), 129, 3715–3725.

[83]

Parker, A.G., Mamai, W. and Maiga, H. (2021) Mass-rearing for the sterile insect technique. In: Sterile Insect Technique: Principles and Practice in Area-Wide Integrated Pest Management (eds. V.A. Dyck, J. Hendrichs & A.S. Robinson). CRC Press, Boca Raton, USA.

[84]

Penalva, L.O. and Sánchez, L. (2003) RNA binding protein sex-lethal (Sxl) and control of Drosophila sex determination and dosage compensation. Microbiology and Molecular Biology Reviews, 67, 343–359.

[85]

Petrucci, G., Gregoriou, M.-E., Papathanos, P.A., Schetelig, M.F., Tu, Z.J. and Bourtzis, K. (2025) Neoclassical development of genetic sexing strains for insect pest and disease vector control. Insect Science

[86]

Poultney, C.S., Butterfoss, G.L., Gutwein, M.R., Drew, K., Gresham, D., Gunsalus, K.C. et al. (2011) Rational design of temperature-sensitive alleles using computational structure prediction. PLoS ONE, 6, e23947.

[87]

Quintero-Fong, L., Luis, J.H., Montoya, P. and Orozco-Dávila, D. (2018) In situ sexual competition between sterile males of the genetic sexing Tapachula-7 strain and wild Anastrepha ludens flies. Crop Protection, 106, 1–5.

[88]

Raymann, K., Shaffer, Z. and Moran, N.A. (2017) Antibiotic exposure perturbs the gut microbiota and elevates mortality in honeybees. PLoS Biology, 15, e2001861.

[89]

Rempoulakis, P., Taret, G., ul Haq, I., Wornayporn, V., Ahmad, S., Tomas, U.S. et al. (2016) Evaluation of quality production parameters and mating behavior of novel genetic sexing strains of the Mediterranean fruit fly Ceratitis capitata (Wiedemann) (Diptera: Tephritidae). PLoS ONE, 11, e0157679.

[90]

Rendón, P., McInnis, D., Lance, D. and Stewart, J. (2004) Medfly (Diptera: Tephritidae) genetic sexing: large-scale field comparison of males-only and bisexual sterile fly releases in Guatemala. Journal of Economic Entomology, 97, 1547–1553.

[91]

Rohl, C.A., Strauss, C.E., Misura, K.M. and Baker, D. (2004) Protein structure prediction using Rosetta. In: Methods in Enzymology (eds. L. Brand & M.L. Johnson), 383: pp. 66–93. Elsevier. PMID: 15063647.

[92]

Romero, M.L., Garcia Seisdedos, H. and Ibarra-Molero, B. (2022) Active site center redesign increases protein stability preserving catalysis in thioredoxin. Protein Science, 31, e4417.

[93]

Salvemini, M., Robertson, M., Aronson, B., Atkinson, P., Polito, L.C. and Saccone, G. (2009) Ceratitis capitata transformer-2 gene is required to establish and maintain the autoregulation of Cctra, the master gene for female sex determination. International Journal of Developmental Biology, 53, 109.

[94]

Salz, H.K. (2011) Sex determination in insects: a binary decision based on alternative splicing. Current Opinion in Genetics & Development, 21, 395–400.

[95]

Salz, H.K. and Erickson, J.W. (2010) Sex determination in Drosophila: the view from the top. Fly, 4, 60–70.

[96]

Schetelig, M.F. and Handler, A.M. (2012) A transgenic embryonic sexing system for Anastrepha suspensa (Diptera: Tephritidae). Insect Biochemistry and Molecular Biology, 42, 790–795.

[97]

Schetelig, M.F., Targovska, A., Meza, J.S., Bourtzis, K. and Handler, A.M. (2016) Tetracycline-suppressible female lethality and sterility in the Mexican fruit fly, Anastrepha ludens. Insect Molecular Biology, 25, 500–508.

[98]

Schymkowitz, J., Borg, J., Stricher, F., Nys, R., Rousseau, F. and Serrano, L. (2005) The FoldX web server: an online force field. Nucleic Acids Research, 33, W382–W388.

[99]

Scolari, F., Schetelig, M.F., Bertin, S., Malacrida, A.R., Gasperi, G. and Wimmer, E.A. (2008) Fluorescent sperm marking to improve the fight against the pest insect Ceratitis capitata (Wiedemann; Diptera: Tephritidae). New Biotechnology, 25, 76–84.

[100]

Scott, M.J., Kriticou, D. and Robinson, A.S. (1993) Isolation of cDNAs encoding 6-phosphogluconate dehydrogenase and glucose-6-phosphate dehydrogenase from the mediterranean fruit fly Ceratitis capitata: correlating genetic and physical maps of chromosome 5. Insect Molecular Biology, 1, 213–222.

[101]

Shah, N.H. and Muir, T.W. (2014) Inteins: nature's gift to protein chemists. Chemical Science, 5, 446–461.

[102]

Sharma, A., Heinze, S.D., Wu, Y., Kohlbrenner, T., Morilla, I., Brunner, C. et al. (2017) Male sex in houseflies is determined by Mdmd, a paralog of the generic splice factor gene CWC22. Science, 356, 642–645.

[103]

Shestopal, S.A., Makunin, I.V., Belyaeva, E.S., Ashburner, M. and Zhimulev, I.F. (1997) Molecular characterisation of the deep orange (dor) gene of Drosophila melanogaster. Molecular and General Genetics (MGG), 253, 642–648.

[104]

Skripsky, T. and Lucchesi, J.C. (1982) Intersexuality resulting from the interaction of sex-specific lethal mutations in Drosophila melanogaster. Developmental Biology, 94, 153–162.

[105]

Sollazzo, G., Gouvi, G., Nikolouli, K., Aumann, R.A., Djambazian, H., Whitehead, M.A. et al. (2023) Genomic and cytogenetic analysis of the Ceratitis capitata temperature-sensitive lethal region. G3 Genes|Genomes|Genetics, 13, jkad074.

[106]

Sollazzo, G., Nikolouli, K., Gouvi, G., Aumann, R.A., Schetelig, M.F. and Bourtzis, K. (2024) Deep orange gene editing triggers temperature-sensitive lethal phenotypes in Ceratitis capitata. BMC Biotechnology, 24, 7.

[107]

Sprink, T. and Wilhelm, R. (2024) Genome editing in biotech regulations worldwide. In: A Roadmap for Plant Genome Editing (eds. A. Ricroch, D. Eriksson, D. Miladinović, J. Sweet, K. Van Laere & E. Woźniak-Gientka), pp. 425–435. Springer, Cham.

[108]

Tasaka, S.E. and Suzuki, D.T. (1973) Temperature-sensitive mutations in Drosophila melanogaster. XVII. Heat- and cold-sensitive lethals on chromosome 3. Genetics, 74, 509–520.

[109]

Tunyasuvunakool, K., Adler, J., Wu, Z., Green, T., Zielinski, M., Žídek, A. et al. (2021) Highly accurate protein structure prediction for the human proteome. Nature, 596, 590–596.

[110]

Varadarajan, R., Nagarajaram, H.A. and Ramakrishnan, C. (1996) A procedure for the prediction of temperature-sensitive mutants of a globular protein based solely on the amino acid sequence. Proceedings of the National Academy of Sciences USA, 93, 13908–13913.

[111]

Varshavsky, A. (1995) The N-end rule. Cold Spring Harbor Symposia on Quantitative Biology, 60, 461–478.

[112]

Varshavsky, A. (2024) N-degron pathways. Proceedings of the National Academy of Sciences USA, 121, e2408697121.

[113]

Velayudhan, S.S. and Ellis, R.E. (2022) Functional divergence of orthologous temperature-sensitive mutations in C. elegans and C. briggsae. Micropublication Biology, 2022, 10.17912/micropub.biology.000705.

[114]

Venables, J.P., Tazi, J. and Juge, F. (2012) Regulated functional alternative splicing in Drosophila. Nucleic Acids Research, 40, 1–10.

[115]

Verhulst, E.C., van de Zande, L. and Beukeboom, L.W. (2010) Insect sex determination: it all evolves around transformer. Current Opinion in Genetics & Development, 20, 376–383.

[116]

Wappner, P., Hopkins, T.L., Kramer, K.J., Cladera, J.L., Manso, F. and Quesada-Allué, L.A. (1996) Role of catecholamines and β-alanine in puparial color of wild-type and melanic mutants of the Mediterranean fruit fly (Ceratitis capitata). Journal of Insect Physiology, 42, 455–461.

[117]

Ward, C.M., Aumann, R.A., Whitehead, M.A., Nikolouli, K., Leveque, G., Gouvi, G. et al. (2021) White pupae phenotype of tephritids is caused by parallel mutations of a MFS transporter. Nature Communications, 12, 491.

[118]

Weber, W., Marty, R.R., Link, N., Ehrbar, M., Keller, B., Weber, C.C. et al. (2003) Conditional human VEGF-mediated vascularization in chicken embryos using a novel temperature-inducible gene regulation (TIGR) system. Nucleic Acids Research, 31, e69.

[119]

Whitten, M.J. (1969) Automated sexing of pupae and its usefulness in control by sterile insects. Journal of Economic Entomology, 62, 271–273.

[120]

Wimmer, E.A. (2005) Eco-friendly insect management. Nature Biotechnology, 23, 432–433.

[121]

Wray-Cahen, D., Hallerman, E. and Tizard, M. (2024) Global regulatory policies for animal biotechnology: overview, opportunities and challenges. Frontiers in Genome Editing, 6, 1467080.

[122]

Wu, K., Chen, A., Tan, P. and Pan, Z.-Q. (2002) The Nedd8-conjugated ROC1-CUL1 core ubiquitin ligase utilizes Nedd8 charged surface residues for efficient polyubiquitin chain assembly catalyzed by Cdc34. Journal of Biological Chemistry, 277, 516–527.

[123]

Yamada, H., Vreysen, M.J.B., Bourtzis, K., Tschirk, W., Chadee, D.D. and Gilles, J.R.L. (2015) The Anopheles arabiensis genetic sexing strain ANO IPCL1 and its application potential for the sterile insect technique in integrated vector management programmes. Acta Tropica, 142, 138–144.

[124]

Yan, Y., Ahmed, H.M.M., Wimmer, E.A. and Schetelig, M.F. (2025) Biotechnology-enhanced genetic controls of the global pest Drosophila suzukii. Trends in Biotechnology, 43, 826–837.

[125]

Yan, Y. and Scott, M.J. (2015) A transgenic embryonic sexing system for the Australian sheep blow fly Lucilia cuprina. Scientific Reports, 5, 16090.

[126]

Yan, Y. and Scott, M.J. (2020) Building a transgenic sexing strain for genetic control of the Australian sheep blow fly Lucilia cuprina using two lethal effectors. BMC Genetics, 21, 141.

[127]

Zeidler, M.P., Tan, C., Bellaiche, Y., Cherry, S., Häder, S., Gayko, U. et al. (2004) Temperature-sensitive control of protein activity by conditionally splicing inteins. Nature Biotechnology, 22, 871–876.

[128]

Zepeda-Cisneros, C.S., Meza Hernández, J.S., García-Martínez, V., Ibañez-Palacios, J., Zacharopoulou, A. and Franz, G. (2014) Development, genetic and cytogenetic analyses of genetic sexing strains of the Mexican fruit fly, Anastrepha ludens Loew (Diptera: Tephritidae). BMC Genomic Data, 15, S1.

[129]

Zhang, X., Wang, X., Guo, Z., Liu, X., Wang, P., Yuan, X. et al. (2022) Antibiotic treatment reduced the gut microbiota diversity, prolonged the larval development period and lessened adult fecundity of Grapholita molesta (Lepidoptera: Tortricidae). Insects, 13, 838.

[130]

Zhao, Y., Schetelig, M.F. and Handler, A.M. (2020) Genetic breakdown of a Tet-off conditional lethality system for insect population control. Nature Communications, 11, 3095.

[131]

Zhimulev, Z.F., Belyaera, E.S., Pokholkova, G.V., Kotchneva, G.V., Fomina, O.V., Bgatov, A.V. et al. (1981) Report on new mutants. Drosophila Information Service, 56, 192.

RIGHTS & PERMISSIONS

2025 The Author(s). Insect Science published by John Wiley & Sons Australia, Ltd on behalf of Institute of Zoology, Chinese Academy of Sciences.

PDF (813KB)

0

Accesses

0

Citation

Detail

Sections
Recommended

/