Proceedings of the National Academy of Sciences · 1993 · 166 citations · 16 references
Life SciencesEntomologyMolecular BiologyInsect GeneticsInsect NeurobiologyInsect PhysiologyProtein Sequence AnalysisProteolytic ProcessingCloningCockroach GeneticsCorpora Allata FunctionJuvenile Hormone BiosynthesisNeuropeptide AmidationNeuropeptide BiosynthesisNeuropeptide ProcessingSignal Peptides
Allatostatins (ASTs) are insect neuropeptides that inhibit juvenile hormone biosynthesis by the corpora allata. We have isolated a cDNA from the cockroach Diploptera punctata that encodes a 41.5-kDa precursor polypeptide containing the AST family of peptides. Translation of the cDNA revealed a 370-amino acid pre-pro-peptide consisting of 13 AST-type peptides and appropriate processing sites for endoproteolytic cleavage and amidation. The 13 potential AST sequences are characterized by the C-terminal AST corestructure Phe-Gly-Leu-NH2, with only one exception. Separating the clustered ASTs in the precursor, three acidic spacer regions are found. Contained within the largest of these are two potentially related peptides that may also be processed. Southern blot analysis revealed the presence of a single copy of the AST gene per haploid genome, as well as the probability that the gene may be present in at least two allelic forms. In situ hybridization indicated the AST-encoding gene is expressed in neurosecretory cells of D. punctata brain.
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Michael A. Frohman, Michael Dush, Gail R. Martin · Proceedings of the National Academy of Sciences · 1988 · 4.6K citations · Full text
Diethard Tautz, Christine Pfeifle · Chromosoma · 1989 · 2.6K citations
Mechanism of C-terminal amide formation by pituitary enzymes
A.F. Bradbury, M. D. A. FINNIE, D.G. Smyth · Nature · 1982 · 661 citations