2008
DOI: 10.1016/j.ygcen.2007.09.002
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Identification of A-type allatostatins possessing −YXFGI/Vamide carboxy-termini from the nervous system of the copepod crustacean Calanus finmarchicus

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Cited by 34 publications
(28 citation statements)
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“…With respects to nervous system development in copepodids, some relevant genes such as nicotinic acetylcholine receptor, flotillin, synaptotagmin, allotostatin, frequenin, and opsin were highly overexpressed. These results are congruent with previous studies of transcriptome profiles reported for copepodid stages [29], [45], [46]. Furthermore, a study by Wilson and Hartline [47] demonstrated high peripheral and central nervous system development in individuals transitioning from the nauplius to copepodid stage.…”
Section: Discussionsupporting
confidence: 92%
“…With respects to nervous system development in copepodids, some relevant genes such as nicotinic acetylcholine receptor, flotillin, synaptotagmin, allotostatin, frequenin, and opsin were highly overexpressed. These results are congruent with previous studies of transcriptome profiles reported for copepodid stages [29], [45], [46]. Furthermore, a study by Wilson and Hartline [47] demonstrated high peripheral and central nervous system development in individuals transitioning from the nauplius to copepodid stage.…”
Section: Discussionsupporting
confidence: 92%
“…16 sequences containing the signature of AST-A were present in the precursor, each with a size between 6–11 residues. This represents a greater number of copies than has been found previously in the insects (at 13–14 forms) [38], but fewer than in the majority of the crustaceans, where between 30 to more than 40 sequences have been characterised [39][41]. Each of the sequences appeared to be of a unique origin, which is in contrast to analyses in Macrobrachium rosenbergi [40] and Procambarus clarkii [39] where two AST-A sequences are present numerous times, indicating multiple duplication events.…”
Section: Resultsmentioning
confidence: 69%
“…The identification of native A-ASTs from Carcinus maenas, e.g., AGPYSFGLamide, followed shortly thereafter [16], with additional isoforms subsequently identified from a number of other decapod species [17,25,46,48,[50][51][52][77][78][79]. A-ASTs have also been identified by transcriptomics from several lower crustaceans, specifically the copepod Calanus finmarchicus [80] and the cladoceran Daphnia pulex [22]; in Calanus, the predicted isoforms exhibit variant -YXFGI/Vamide C-termini, e.g., APYGFGIamide and pQ/QPYNFGVamide [80].…”
Section: A-type Allatostatinsmentioning
confidence: 99%
“…A-ASTs are broadly distributed within the nervous systems of crustaceans, including regions of synaptic neuropil [22,76,80,81] and neuroendocrine organs [1,22,80,81], suggesting that they function as both locally released autocrines/paracrines and circulating hormones.…”
Section: A-type Allatostatinsmentioning
confidence: 99%