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Fraenkel's pupariation factor identified at last
Authors:Verleyen Peter  Clynen Elke  Huybrechts Jurgen  Van Lommel Alfons  Vanden Bosch Luc  De Loof Arnold  Zdarek Jan  Schoofs Liliane
Institution:Laboratory of Developmental Physiology, Genomics and Proteomics, KU Leuven, B-3000 Louvain, Belgium. peter.verleyen@bio.kuleuven.ac.be
Abstract:Thirty-five years ago, Zdarek and Fraenkel demonstrated that nervous tissue extracts influenced development by accelerating pupariation in the grey flesh fly, Neobellieria bullata. We have now identified this pupariation factor as SVQFKPRLamide, designated Neb-pyrokinin-2 (Neb-PK-2). To achieve this, the central nervous system of N. bullata wandering stage larvae, that is, preceding pupariation, were dissected and extracted before HPLC separation. Chromatographic fractions were screened with a bioassay for pupariation accelerating activity. Only one fraction showed huge pupariation activity. Mass spectrometry revealed the presence of a pyrokinin, whose primary sequence could not be unequivocally determined by tandem mass spectrometry. However, this Neb-pyrokinin appeared to be very prominent in the ring gland from which it was subsequently purified and identified. Synthetic Neb-PK-2 accelerates pupariation with a threshold dose of only 0.2 pmol and therefore, Neb-pyrokinin is considered to be the genuine pupariation factor. The immunohistochemical distribution pattern of Neb-PK-2 is very similar to that of Drosophila pyrokinin-2, from which it differs by only one amino acid residue. Hence, the recently identified G-protein coupled receptors (CG8784, CG8795) for Drosophila pyrokinin-2 might play an important role in puparium formation.
Keywords:Neobellieria bullata  Pupariation factor  Pyrokinin  Drm-PK-2  immunohistochemistry
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