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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1991 Mar 15;88(6):2412–2416. doi: 10.1073/pnas.88.6.2412

Identity of a second type of allatostatin from cockroach brains: an octadecapeptide amide with a tyrosine-rich address sequence.

G E Pratt 1, D E Farnsworth 1, K F Fok 1, N R Siegel 1, A L McCormack 1, J Shabanowitz 1, D F Hunt 1, R Feyereisen 1
PMCID: PMC51242  PMID: 2006179

Abstract

An octadecapeptide that inhibits juvenile hormone synthesis has been isolated by HPLC from brain-retrocerebral complexes of the cockroach Diploptera punctata. The primary structure of this allatostatin has been elucidated by tandem mass spectrometry: Ala-Tyr-Ser-Tyr-Val-Ser-Glu-Tyr-Lys-Arg-Leu-Pro-Val-Tyr-Asn-Phe-Gly-Leu- NH2 (ASB2). The amidated three-residue C terminus of this type B allatostatin is identical to that of four known type A allatostatins, and the preceding three residues show close structural homology. ASB2 has over twice the activity of the type A tridecapeptide Ala-Pro-Ser-Gly-Ala-Gln-Arg-Leu-Tyr-Gly-Phe-Gly-Leu-NH2 (ASA1) in inhibiting juvenile hormone biosynthesis in corpora allata from females in early vitellogenesis (day 2), and its efficacy persists during pregnancy, but it is equally effective as ASA1 on glands from day-10 females (IC50 = 0.31 nM). The octadecapeptide is characterized by a potential dibasic cleavage site, Lys9-Arg10, the integrity of which is needed for high potency. The ASB2-(11-18)-octapeptide amide gives a full response at high concentrations at day 10 (IC50 = 48 nM), but the C-truncated (1-9)-, (1-11)-, and (1-17)-amide fragments of ASB2 are inactive. Thus, the endocrine message is located at the C terminus. N alpha-acetylation of the N-truncated (9-18), (10-18), and (11-18) fragments of ASB2 increases activity relative to the nonacetylated peptides. The site of action of type A and type B allatostatins is located before mevalonate kinase in the biosynthetic pathway for juvenile hormone.

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Selected References

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  1. Aclé D., Brookes V. J., Pratt G. E., Feyereisen R. Activity of the corpora allata of adult female Leucophaea maderae: effects of mating and feeding. Arch Insect Biochem Physiol. 1990;14(3):121–129. doi: 10.1002/arch.940140302. [DOI] [PubMed] [Google Scholar]
  2. Bek E., Berry R. Prohormonal cleavage sites are associated with omega loops. Biochemistry. 1990 Jan 9;29(1):178–183. doi: 10.1021/bi00453a024. [DOI] [PubMed] [Google Scholar]
  3. Bhaskaran G., Dahm K. H., Barrera P., Pacheco J. L., Peck K. E., Muszynska-Pytel M. Allatinhibin, a neurohormonal inhibitor of juvenile hormone biosynthesis in Manduca sexta. Gen Comp Endocrinol. 1990 Apr;78(1):123–136. doi: 10.1016/0016-6480(90)90053-o. [DOI] [PubMed] [Google Scholar]
  4. Feyereisen R., Farnsworth D. E. Precursor supply for insect juvenile hormone III biosynthesis in a cockroach. J Biol Chem. 1987 Feb 25;262(6):2676–2681. [PubMed] [Google Scholar]
  5. Granger N. A., Janzen W. P. Inhibition of Manduca sexta corpora allata in vitro by a cerebral allatostatic neuropeptide. Mol Cell Endocrinol. 1987 Feb;49(2-3):237–248. doi: 10.1016/0303-7207(87)90218-8. [DOI] [PubMed] [Google Scholar]
  6. Hunt D. F., Yates J. R., 3rd, Shabanowitz J., Winston S., Hauer C. R. Protein sequencing by tandem mass spectrometry. Proc Natl Acad Sci U S A. 1986 Sep;83(17):6233–6237. doi: 10.1073/pnas.83.17.6233. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Kataoka H., Toschi A., Li J. P., Carney R. L., Schooley D. A., Kramer S. J. Identification of an allatotropin from adult manduca sexta. Science. 1989 Mar 17;243(4897):1481–1483. doi: 10.1126/science.243.4897.1481. [DOI] [PubMed] [Google Scholar]
  8. Landymore-Lim A. E., Bradbury A. F., Smyth D. G. The amidating enzyme in pituitary will accept a peptide with C-terminal D-alanine as substrate. Biochem Biophys Res Commun. 1983 Nov 30;117(1):289–293. doi: 10.1016/0006-291x(83)91573-5. [DOI] [PubMed] [Google Scholar]
  9. Leszczynski J. F., Rose G. D. Loops in globular proteins: a novel category of secondary structure. Science. 1986 Nov 14;234(4778):849–855. doi: 10.1126/science.3775366. [DOI] [PubMed] [Google Scholar]
  10. Loftfield R. B., Eigner E. A. Molecular order of participation of inhibitors (or activators) in biological systems. Science. 1969 Apr 18;164(3877):305–308. doi: 10.1126/science.164.3877.305. [DOI] [PubMed] [Google Scholar]
  11. Mentlein R. Proline residues in the maturation and degradation of peptide hormones and neuropeptides. FEBS Lett. 1988 Jul 18;234(2):251–256. doi: 10.1016/0014-5793(88)80092-9. [DOI] [PubMed] [Google Scholar]
  12. Pratt G. E., Farnsworth D. E., Feyereisen R. Changes in the sensitivity of adult cockroach corpora allata to a brain allatostatin. Mol Cell Endocrinol. 1990 Apr 17;70(2):185–195. doi: 10.1016/0303-7207(90)90158-5. [DOI] [PubMed] [Google Scholar]
  13. Pratt G. E., Farnsworth D. E., Siegel N. R., Fok K. F., Feyereisen R. Identification of an allatostatin from adult Diploptera punctata. Biochem Biophys Res Commun. 1989 Sep 29;163(3):1243–1247. doi: 10.1016/0006-291x(89)91111-x. [DOI] [PubMed] [Google Scholar]
  14. Rankin S. M., Stay B. Ovarian inhibition of juvenile hormone synthesis in the viviparous cockroach, Diploptera punctata. Gen Comp Endocrinol. 1985 Aug;59(2):230–237. doi: 10.1016/0016-6480(85)90374-0. [DOI] [PubMed] [Google Scholar]
  15. Robinson E. A., Yoshimura T., Leonard E. J., Tanaka S., Griffin P. R., Shabanowitz J., Hunt D. F., Appella E. Complete amino acid sequence of a human monocyte chemoattractant, a putative mediator of cellular immune reactions. Proc Natl Acad Sci U S A. 1989 Mar;86(6):1850–1854. doi: 10.1073/pnas.86.6.1850. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Thompson C. S., Lococo D. J., Tobe S. S. Anatomy and electrophysiology of neurons terminating in the corpora allata of the cockroach Diploptera punctata. J Comp Neurol. 1987 Jul 1;261(1):120–129. doi: 10.1002/cne.902610110. [DOI] [PubMed] [Google Scholar]
  17. Van Eldik L. J., Watterson D. M., Fok K. F., Erickson B. W. Elucidation of a minimal immunoreactive site of vertebrate calmodulin. Arch Biochem Biophys. 1983 Dec;227(2):522–533. doi: 10.1016/0003-9861(83)90481-2. [DOI] [PubMed] [Google Scholar]
  18. Woodhead A. P., Stay B., Seidel S. L., Khan M. A., Tobe S. S. Primary structure of four allatostatins: neuropeptide inhibitors of juvenile hormone synthesis. Proc Natl Acad Sci U S A. 1989 Aug;86(15):5997–6001. doi: 10.1073/pnas.86.15.5997. [DOI] [PMC free article] [PubMed] [Google Scholar]

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