2012
DOI: 10.1016/j.gene.2012.01.052
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Characterization, expression, and evolutionary aspects of Corazonin neuropeptide and its receptor from the House Fly, Musca domestica (Diptera: Muscidae)

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Cited by 17 publications
(24 citation statements)
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“…This corresponds to findings in D. melanogaster where Crz is expressed in neurons in the brain that send projections to the CC and CA [57]. The expression pattern is very similar in other dipterans, such as Musca domestica and P. terraenovae [58,59]. Crz was first identified as a cardioaccelerator in P. americana [60], but progressive research proved its pleiotropic nature, which also includes a role in ecdysis (reviewed in [61]).…”
Section: Crustacean Cardioactive Peptides -Corazoninecdysis Triggerinsupporting
confidence: 80%
“…This corresponds to findings in D. melanogaster where Crz is expressed in neurons in the brain that send projections to the CC and CA [57]. The expression pattern is very similar in other dipterans, such as Musca domestica and P. terraenovae [58,59]. Crz was first identified as a cardioaccelerator in P. americana [60], but progressive research proved its pleiotropic nature, which also includes a role in ecdysis (reviewed in [61]).…”
Section: Crustacean Cardioactive Peptides -Corazoninecdysis Triggerinsupporting
confidence: 80%
“…CrzR is a member of Class-A GPCR family [20], [29], [35]. A signaling pathway typical of these receptors involves PKA, which regulates activity of a transcription factor CREB via phosphorylation.…”
Section: Resultsmentioning
confidence: 99%
“…Although the sequence and structure of Crz is highly conserved among different insect species [20], it has been shown to affect diverse physiological functions in a species-specific manner; cardio-acceleration in the cockroach [19], induction of cuticular pigmentation in the migratory locust [21], reduction of the spinning rate and pupal development in the silkworm [22], and induction of ecdysis in a moth [23]. In Drosophila adult, Crz is produced by a major group of neurosecretory cells in the brain and abdominal ganglion [24], [25].…”
Section: Introductionmentioning
confidence: 99%
“…The reverse transcription reaction was purified by using Qiaquick kit (30 μL final elution). To this, the following reagents were added for poly-A tailing reaction (60 μL): dATP, Terminal deoxynucleotide transferase (Promega), and Qt primer, as described previously (Sha et al, 2012). The reaction was incubated at 37°C for 6 min, and then terminated at 65°C for 5 min.…”
Section: Methodsmentioning
confidence: 99%