한국응용곤충학회지 (Korean journal of applied entomology)

  • 제61권1호
  • /
  • Pages.29-34
  • /
  • 2022
  • /
  • 1225-0171(pISSN)
  • /
  • 2287-545X(eISSN)
한국응용곤충학회 (Korean Society of Applied Entomology)
권호 표지
DOI QR코드

DOI QR Code

콩명나방의 성페로몬 생합성

Sex Pheromone Biosynthesis in the Legume Pod Borer, Maruca vitrata (Lepidoptera: Crambidae)

  • 차욱현 (경성대학교 생명보건대학 스마트바이오학과) ;
  • 박정준 (경상국립대학교 농업생명과학대학 식물의학과, 농업생명과학연구소) ;
  • 이대원 (경성대학교 생명보건대학 스마트바이오학과)
  • Cha, Wook Hyun (Department of SmartBio, Kyungsung University) ;
  • Park, Jung Jun (Department of Plant Medicine, Institute of Agriculture and Life Science, Gyeongsang National University) ;
  • Lee, Dae-Weon (Department of SmartBio, Kyungsung University)
  • 투고 : 2021.12.29
  • 심사 : 2022.02.08
  • 발행 : 2022.03.01
PDF 다운로드
⟨ 이전 논문 다음 논문 ⟩

초록

나방류의 페로몬 생합성은 식도아래 신경절에서 생산된 페로몬 생합성 촉진 신경펩타이드(pheromone biosynthesis activating neuropeptide, PBAN)의 분비로부터 시작된다. 분비된 PBAN은 페로몬샘의 상피세포막에 있는 PBAN 수용체와 결합하고, 신호전달과정을 거쳐 페로몬 생합성과정이 활성화되어, 페로몬이 외부로 방출된다. 본 종설은 콩명나방(Maruca vitrata)의 성페로몬, PBAN과 수용체, 성페로몬 생합성 경로를 소개한다.

Pheromone biosynthesis in the pheromone gland is triggered from release of pheromone biosynthesis-activating neuropeptide (PBAN) synthesized in the suboesophageal ganglion. PBAN binds to its receptor on the epithelial cell membrane and activates signal transduction pathways for the pheromone biosynthesis. This study reviews sex pheromone, PBAN and its receptor, and pheromone biosynthesis pathway of Maruca vitrata.

키워드

과제정보

본 연구는 2021년도 환경부 주관 「화학물질 안전관리 전문인력 양성사업」의 화학물질 특성화대학원 지원 사업을 통한 성과물임을 밝힙니다.

참고문헌

  1. Adati, T., Tatsuki, S., 1999. Identification of female sex pheromone of the legume pod borer, Maruca vitrata and antagonistic effects of geometrical isomers. J. Chem. Ecol. 25, 105-115. https://doi.org/10.1023/A:1020841217376
  2. Albre, J., Lienard, M.A., Sirey, T.M., Schmidt, S., Tooman, L.K., Carraher, C., Greenwood, D.R., Lofstedt, C., Newcomb, R.D., 2012. Sex pheromone evolution is associated with differential regulation of the same desaturase gene in two genera of leafroller moths. PLoS Genet. 8, e1002489. https://doi.org/10.1371/journal.pgen.1002489
  3. Antony, B., Soffan, A., Jakse, J., Alfaifi, S., Sutanto, K.D., Aldosari, S.A., Aldawood, A.S., Pain, A., 2015. Genes involved in sex pheromone biosynthesis of Ephestia cautella, an important food storage pest, are determined by transcriptome sequencing. BMC Genom. 16, 532. https://doi.org/10.1186/s12864-015-1710-2
  4. Bober, R., Rafaeli, A., 2010. Gene-silencing reveals the functional significance of pheromone biosynthesis activating neuropeptide receptor (PBAN-R) in a male moth. Proc. Natl. Acad. Sci. 107, 16858-16862. https://doi.org/10.1073/pnas.1008812107
  5. Cha, W.H., Jung, J.K., Kim, Y., Lee, D.-.W., 2018. Identification and pheromonotropic activity of pheromone biosynthesis activating neuropeptide in Maruca vitrata. J. Asia-Pac. Entomol. 21, 156-160. https://doi.org/10.1016/j.aspen.2017.11.015
  6. Cha, W.H., Kim, W.J., Jung, J.K., Lee, D.-.W., 2017. Putative pheromone biosynthesis pathway in Maruca vitrata by transcriptomic analysis. J. Asia-Pac. Entomol. 20, 165-173. https://doi.org/10.1016/j.aspen.2016.12.008
  7. Chang, J.C., Ramasamy, S., 2014. Identification and expression analysis of diapause hormone and pheromone biosynthesis activating neuropeptide (DH-PBAN) in the legume pod borer, Maruca vitrata Fabricius. PLoS ONE 9, e84916. https://doi.org/10.1371/journal.pone.0084916
  8. Chen, D.S., Dai, J.Q., Han, S.C., 2017. Identification of the pheromone biosynthesis genes from the sex pheromone gland transcriptome of the diamondback moth, Plutella xylostella. Sci. Rep. 24, 7.
  9. Cheng, Y., Luo, L., Jiang, X., Zhang, L., Niu, C., 2010. Expression of pheromone biosynthesis activating neuropeptide and its receptor (PBANR) mRNA in adult female Spodoptera exigua (Lepidoptera: Noctuidae). Arch. Insect Biochem. Physiol. 75, 13-27. https://doi.org/10.1002/arch.20379
  10. Choi, M.Y., Fuerst, E.J., Rafaeli, A., Jurenka, R., 2003. Identification of a G protein coupled receptor for pheromone biosynthesis activating neuropeptide from pheromone glands of the moth Helicoverpa zea. Proc. Natl. Acad. Sci. 100, 9721-9726. https://doi.org/10.1073/pnas.1632485100
  11. Choi, M.Y., Tanaka, M., Kataoka, H., Boo, K.S., Tatsuki, S., 1998. Isolation and identification of the cDNA encoding the pheromone biosynthesis activating neuropeptide and additional neuropeptides in the oriental tobacco budworm, Helicoverpa assulta (Lepidoptera: Noctuidae). Insect Biochem. Mol. Biol. 28, 759-766. https://doi.org/10.1016/S0965-1748(98)00065-4
  12. Dhanyakumar, O., Srinivasan, R., Mohan, M., Venkatesan, T., Murali Mohan, K., Nagesha, N., Sotelo-Cardona, P., 2020. Effect of pheromone-mediated mating disruption on pest population density of Maruca vitrata (Fabricius) (Crambidae: Lepidoptera). Insects 11, 558. https://doi.org/10.3390/insects11090558
  13. Ding, B.J., Hofvander, P., Wang, H.L., Durrett, T.P., Stymne, S., Lofstedt, C., 2014. A plant factory for moth pheromone production. Nat. Commun. 5, 3353. https://doi.org/10.1038/ncomms4353
  14. Ding, B.J., Lofstedt, C., 2015. Analysis of the Agrotis segetum pheromone gland transcriptome in the light of sex pheromone biosynthesis. BMC Genom. 16, 711. https://doi.org/10.1186/s12864-015-1909-2
  15. Downham, M.C., Hall, D.R., Chamberlain, D.J., Cork, A., Farman, D.I., Tamo, M., Dahounto, D., Datinon, B., Adetonah, S., 2003. Minor components in the sex pheromone of legume podborer: Maruca vitrata development of an attractive blend. J. Chem. Ecol. 29, 989-1011. https://doi.org/10.1023/A:1022996103147
  16. Eurekha, S., Sreekumar, K.M., Subaharan, K., Ramesha, B., Santhoshkumar, T., 2019. Study on adult emergence, female calling and mating behaviour in Maruca vitrata F. (Lepidoptera: Crambidae) in Kerala, India. Entomon. 44, 73-78. https://doi.org/10.33307/entomon.v44i1.428
  17. Fujii, T., Yasukochi, Y., Rong, Y., Matsuo, T., Ishikawa, Y., 2015. Multiple Δ11-desaturase genes selectively used for sex pheromone biosynthesis are conserved in Ostrinia moth genomes. Insect Biochem. Mol. Biol. 61, 62-68. https://doi.org/10.1016/j.ibmb.2015.04.007
  18. Hariton-Shalev, A., Shalev, M., Adir, N., Belausov, E., Altstein, M., 2013. Structural and functional differences between pheromonotropic and melanotropic PK/PBAN receptors. Biochim. Biophys. Acta. 1830, 5036-5048. https://doi.org/10.1016/j.bbagen.2013.06.041
  19. He, P., Zhang, Y.F., Hong, D.Y., Wang, J., Wang, X.L., Zuo, L.H., Tang, X.F., Xu, W.M., He, M., 2017. A reference gene set for sex pheromone biosynthesis and degradation genes from the diamondback moth, Plutella xylostella, based on genome and transcriptome digital gene expression analyses. BMC Genom. 18, 219. https://doi.org/10.1186/s12864-017-3592-y
  20. Hull, J.J., Ohnishi, A., Moto, K., Kawasaki, Y., Kurata, R., Suzuki, M.G., Matsumoto, S., 2004. Cloning and characterization of the pheromone biosynthesis activating neuropeptide receptor from the silk moth, Bombyx mori. J. Biol. Chem. 279, 51500-51507. https://doi.org/10.1074/jbc.M408142200
  21. Jurenka, R., 2004. Insect pheromone biosynthesis. Top Curr. Chem. 239, 97-132. https://doi.org/10.1007/b95450
  22. Jurenka, R., 2017. Regulation of pheromone biosynthesis in moths. Curr. Opin. Insect Sci. 24, 29-35. https://doi.org/10.1016/j.cois.2017.09.002
  23. Jurenka, R., Rafaeli, A., 2011. Regulatory role of PBAN in sex pheromone biosynthesis of Heliothine moths. Front. Endocrinol. 2, 46. https://doi.org/10.3389/fendo.2011.00046
  24. Kim, Y.-J., Nachman, R.J., Aimanova, K., Gill, S., Adams, M.E., 2008. The pheromone biosynthesis activating neuropeptide (PBAN) receptor of Heliothis virescens: identification, functional expression, and structure-activity relationships of ligand analogs. Peptides 29, 268-275. https://doi.org/10.1016/j.peptides.2007.12.001
  25. Lee, D-.W., Boo, K.S., 2005. Molecular characterization of pheromone biosynthesis activating neuropeptide from the diamondback moth, Plutella xylostella (L.). Peptides 26, 2404-2411. https://doi.org/10.1016/j.peptides.2005.04.016
  26. Lee, D-.W., Kim, Y., Koh, Y.H., 2011a. RNA interference of PBAN receptor suppresses expression of two fatty acid desaturases in female Plutella xylostella. J. Asia-Pac. Entomol. 14, 405-410. https://doi.org/10.1016/j.aspen.2011.05.004
  27. Lee, D-.W., Shrestha, S., Kim, A.Y., Park, S.J., Yang, C.Y., Kim, Y., Koh, Y.H., 2011b. RNA interference of pheromone biosynthesis-activating neuropeptide receptor suppresses mating behavior by inhibiting sex pheromone production in Plutella xylostella (L.). Insect Biochem. Mol. Biol. 41, 236-243. https://doi.org/10.1016/j.ibmb.2011.01.001
  28. Lin, X., Wang, B., Du, Y., 2018. Key genes of the sex pheromone biosynthesis pathway in female moths are required for pheromone quality and possibly mediate olfactory plasticity in conspecific male moths in Spodoptera litura. Insect Mol. Biol. 27, 8-21. https://doi.org/10.1111/imb.12335
  29. Lu, P.F., Qiao, H.L., Luo, Y.Q., 2013. Female sex pheromone blends and male response of the legume pod borer, Maruca vitrata (Lepidoptera: Crambidae), in two populations of mainland China. Z. Naturforsch. C. 68, 416-427. https://doi.org/10.1515/znc-2013-9-1009
  30. Lu, P.F., Qiao, H.L., Wang, X.P., Wang, X.Q., 2007. The emergence and mating rhythms of the legume pod borer, Maruca vitrata (Fabricius, 1787) (Lepidoptera: Pyralidae). Pan-Pac. Entomol. 83, 226-234. https://doi.org/10.3956/0031-0603-83.3.226
  31. Ma, P.W.K., Knipple, D.C., Roelofs, W.L., 1998. Expression of a gene that encodes pheromone biosynthesis activating neuropeptide in the central nervous system of corn earworm, Helicoverpa zea. Insect Biochem. Mol. Biol. 28, 373-385. https://doi.org/10.1016/S0965-1748(98)00009-5
  32. Matouskova, P., Pichova, I., Svatos, A., 2007. Functional characterization of a desaturase from the tobacco hornworm moth (Manduca sexta) with bifunctional Z11- and 10,12-desaturase activity. Insect Biochem. Mol. Biol. 37, 601-610. https://doi.org/10.1016/j.ibmb.2007.03.004
  33. Moto, K., Suzuki, M.G., Hull, J.J., Kurata, R., Takahashi, S., Yamamoto, M., Okano, K., Imai, K., Ando, T., Matsumoto, S., 2004. Involvement of a bifunctional fatty-acyl desaturase in the biosynthesis of the silkmoth, Bombyx mori, sex pheromone. Proc. Natl. Acad. Sci. 101, 8631-8636. https://doi.org/10.1073/pnas.0402056101
  34. Nusawardani, T., Kroemer, J.A., Choi, M.Y., Jurenka, R.A., 2013. Identification and characterization of the pyrokinin/pheromone biosynthesis activating neuropeptide family of G protein-coupled receptors from Ostrinia nubilalis. Insect Mol. Biol. 22, 331-340. https://doi.org/10.1111/imb.12025
  35. Petkevicius, K., Lofstedt, C., Borodina, I., 2020. Insect sex pheromone production in yeasts and plants. Curr. Opin. Biotechnol. 65, 259-267. https://doi.org/10.1016/j.copbio.2020.07.011
  36. Roelofs, W.L., Liu, W., Hao, G., Jiao, H., Rooney, A.P., Linn, C.E. Jr. 2002. Evolution of moth sex pheromones via ancestral genes. Proc. Natl. Acad. Sci. 99, 13621-13626. https://doi.org/10.1073/pnas.152445399
  37. Roelofs, W.L., Rooney, A.P., 2003. Molecular genetics and evolution of pheromone biosynthesis in Lepidoptera. Proc. Natl. Acad. Sci. 100, 14599. https://doi.org/10.1073/pnas.1233767100
  38. Schlager, S., Beran, F., Groot, A.T., Ulrichs, C., Veit, D., Paetz, C., Karumuru, B.R., Srinivasan, R., Schreiner, M., Mewis, I., 2015. Pheromone blend analysis and cross-attraction among populations of Maruca vitrata from Asia and West - 185 - Africa. J. Chem. Ecol. 41, 1155-1162. https://doi.org/10.1007/s10886-015-0653-z
  39. Shalev, A.H., Altstein, M., 2015. Pheromonotropic and melanotropic PK/PBAN receptors: differential ligand-receptor interactions. Peptides 63, 81-89. https://doi.org/10.1016/j.peptides.2014.10.014
  40. Sharma, H.C., 1998. Bionomics, host plant resistance, and management of the legume pod borer, Maruca vitrata. Crop. Prot. 17, 373-386. https://doi.org/10.1016/S0261-2194(98)00045-3
  41. Stokl, J., Steiger, S., 2017. Evolutionary origin of insect pheromones. Curr. Opin. Insect Sci. 24, 36-42. https://doi.org/10.1016/j.cois.2017.09.004
  42. Vogel, H., Heidel, A.J., Heckel, D.G., Groot, A.T., 2010. Transcriptome analysis of the sex pheromone gland of the noctuid moth Heliothis virescens. BMC Genom. 11, 29. https://doi.org/10.1186/1471-2164-11-29
  43. Yoshiga, T., Okano, K., Mita, K., Shimada, T., Matsumoto, S., 2000. cDNA cloning of acyl-CoA desaturase homologs in the silkworm, Bombyx mori. Gene 246, 339-345. https://doi.org/10.1016/S0378-1119(00)00047-0
  44. Zheng, L., Lytle, C., Njauw, C. N., Altstein, M., Martins-Green, M., 2007. Cloning and characterization of the pheromone biosynthesis activating neuropeptide receptor gene in Spodoptera littoralis larvae. Gene 393, 20-30. https://doi.org/10.1016/j.gene.2006.12.025
  45. Zhou, J., Zhang, N., Wang, P., Zhang, S., Li, D., Liu, K., Wang, G., Wang, X., Ai, H., 2015. Identification of host-plant volatiles and characterization of two novel general odorant-binding proteins from the legume pod borer, Maruca vitrata Fabricius (Lepidoptera: Crambidae). PLoS ONE 10, e0141208. https://doi.org/10.1371/journal.pone.0141208