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Hormonal regulation of sex pheromone biosynthesis in the turnip moth, Agrotis segetum

Zhu, Junwei ; Millar, Jocelyn and Löfstedt, Christer LU (1995) In Archives of Insect Biochemistry and Physiology 30(1). p.41-59
Abstract

Pheromone production in the female turnip moth, Agrotis segetum, is under the control of a brain factor. This factor was demonstrated to be a proteinaceous substance termed pheromone biosynthesis activating neuropeptide‐like substance (PBAN‐like substance). The sex pheromone of Swedish A. segetum includes (Z)‐5‐decenyl acetate, (Z)‐7‐dodecenyl acetate, and (Z)‐9‐tetradecenyl acetate as major components. Decapitation of a female decreased pheromone production significantly. Pheromone production was restored by injection of homogenates of either male or female brain‐suboesophageal ganglion or the corpora cardiaca alone. Pheromonotropic activity was also found in homogenates of the female thoracic ganglion and abdominal ganglion that were... (More)

Pheromone production in the female turnip moth, Agrotis segetum, is under the control of a brain factor. This factor was demonstrated to be a proteinaceous substance termed pheromone biosynthesis activating neuropeptide‐like substance (PBAN‐like substance). The sex pheromone of Swedish A. segetum includes (Z)‐5‐decenyl acetate, (Z)‐7‐dodecenyl acetate, and (Z)‐9‐tetradecenyl acetate as major components. Decapitation of a female decreased pheromone production significantly. Pheromone production was restored by injection of homogenates of either male or female brain‐suboesophageal ganglion or the corpora cardiaca alone. Pheromonotropic activity was also found in homogenates of the female thoracic ganglion and abdominal ganglion that were obtained during scotophase. Injection of female brain and thoracic ganglion homogenates made from insects during the scotophase induced two and four times as much Z7‐12:OAc, respectively, as injection with similar homogenates from photophase. As little as one‐eighth female equivalent (FE) brain homogenate was sufficient to increase the amount of Z7‐12:OAc. The effect of brain homogenate on pheromone titer reached its maximum after 30 min. The activity of the PBAN‐like substance present in female brain extracts was not correlated to the age of the donor. Injection of hemolymph collected during either photophase or scotophase into decapitated females did not increase the pheromone titer. The target site of the PBAN‐like substance was not the pheromone gland, and the ventral nerve cord was not involved in the transportation of the PBAN‐like substance, which implies a mode of action different from what has been reported in other moths. Brain homogenates obtained during photophase from females of African A. segetum, Spodoptera littoralis, or Ostrinia nubilalis as well as synthetic Bombyx‐PBAN also induced pheromone production in decapitated Swedish female A. segetum. © 1995 Wiley‐Liss, Inc.

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type
Contribution to journal
publication status
published
subject
keywords
Incorporation, Labeled precursors, Lepidoptera, Noctuidae, PBAN‐like substance, Pheromone production
in
Archives of Insect Biochemistry and Physiology
volume
30
issue
1
pages
19 pages
publisher
John Wiley & Sons Inc.
external identifiers
  • scopus:84985653058
ISSN
0739-4462
DOI
10.1002/arch.940300104
project
Evolutionary mechanisms of pheromone divergence in Lepidoptera
language
English
LU publication?
yes
id
d6caa0b2-df94-47d7-a13e-5bcd4e95f4f1
date added to LUP
2020-05-26 16:26:54
date last changed
2024-05-16 11:34:45
@article{d6caa0b2-df94-47d7-a13e-5bcd4e95f4f1,
  abstract     = {{<p>Pheromone production in the female turnip moth, Agrotis segetum, is under the control of a brain factor. This factor was demonstrated to be a proteinaceous substance termed pheromone biosynthesis activating neuropeptide‐like substance (PBAN‐like substance). The sex pheromone of Swedish A. segetum includes (Z)‐5‐decenyl acetate, (Z)‐7‐dodecenyl acetate, and (Z)‐9‐tetradecenyl acetate as major components. Decapitation of a female decreased pheromone production significantly. Pheromone production was restored by injection of homogenates of either male or female brain‐suboesophageal ganglion or the corpora cardiaca alone. Pheromonotropic activity was also found in homogenates of the female thoracic ganglion and abdominal ganglion that were obtained during scotophase. Injection of female brain and thoracic ganglion homogenates made from insects during the scotophase induced two and four times as much Z7‐12:OAc, respectively, as injection with similar homogenates from photophase. As little as one‐eighth female equivalent (FE) brain homogenate was sufficient to increase the amount of Z7‐12:OAc. The effect of brain homogenate on pheromone titer reached its maximum after 30 min. The activity of the PBAN‐like substance present in female brain extracts was not correlated to the age of the donor. Injection of hemolymph collected during either photophase or scotophase into decapitated females did not increase the pheromone titer. The target site of the PBAN‐like substance was not the pheromone gland, and the ventral nerve cord was not involved in the transportation of the PBAN‐like substance, which implies a mode of action different from what has been reported in other moths. Brain homogenates obtained during photophase from females of African A. segetum, Spodoptera littoralis, or Ostrinia nubilalis as well as synthetic Bombyx‐PBAN also induced pheromone production in decapitated Swedish female A. segetum. © 1995 Wiley‐Liss, Inc.</p>}},
  author       = {{Zhu, Junwei and Millar, Jocelyn and Löfstedt, Christer}},
  issn         = {{0739-4462}},
  keywords     = {{Incorporation; Labeled precursors; Lepidoptera; Noctuidae; PBAN‐like substance; Pheromone production}},
  language     = {{eng}},
  month        = {{01}},
  number       = {{1}},
  pages        = {{41--59}},
  publisher    = {{John Wiley & Sons Inc.}},
  series       = {{Archives of Insect Biochemistry and Physiology}},
  title        = {{Hormonal regulation of sex pheromone biosynthesis in the turnip moth, Agrotis segetum}},
  url          = {{http://dx.doi.org/10.1002/arch.940300104}},
  doi          = {{10.1002/arch.940300104}},
  volume       = {{30}},
  year         = {{1995}},
}