drosulfakinin-1 and neomyosuppressin

drosulfakinin-1 has been researched along with neomyosuppressin* in 2 studies

Other Studies

2 other study(ies) available for drosulfakinin-1 and neomyosuppressin

ArticleYear
Dromyosuppressin and drosulfakinin, two structurally related Drosophila neuropeptides, are uniquely expressed in the adult central nervous system.
    Annals of the New York Academy of Sciences, 1997, Apr-24, Volume: 814

    Drosophila myosuppressin (TDVDHVFLRFamide; DMS) and sulfakinin (FDDYGHMRFamide; DSK) have similar C-terminal structures. To determine the neuronal expression patterns of these structurally related peptides, we have generated DMS- and DSK-specific antisera to multiple antigenic peptides and performed double-label immunochemistry with antisera raised on different animals of the same species host animal. Our data indicate that DMS and DSK staining patterns in the adult central nervous system are unique and nonoverlapping.

    Topics: Amino Acid Sequence; Animals; Central Nervous System; Drosophila; Immunohistochemistry; Insect Hormones; Insect Proteins; Neuropeptides; Oligopeptides

1997
Immunocytochemistry of sequence-related neuropeptides in Drosophila.
    Neuropeptides, 1993, Volume: 24, Issue:6

    Based on structure, activity, and expression, the Drosophila drosulfakinin I peptide (DSK I; FDDY(OSO3H)GHMRFamide) is similar to the vertebrate peptide, cholecystokinin. Dromyosuppressin (DMS; TDVDHVFLRFamide) is an abundant peptide isolated from adult Drosophila which shares a high degree of sequence homology with peptides isolated from chicken, cockroach, fleshfly, and locust. DSK I and DMS, encoded by different precursors, have similar expression patterns in larval brain tissue; each localizes to cells in the anterior and medial protocerebrum. Because of the precedence for coexistence of neural messengers, it was of interest to determine the cellular expression patterns relative to one another. The question of whether the two peptides were expressed in the same cells was resolved using an immunofluorescent double-labeling technique developed for sequence-specific antisera raised in separate animals of the same species. Double labeling was done using a combination of indirect and direct immunofluorescence. DSK I and DMS were shown to localize to different cells in close proximity to one another in the larval brain. The non-overlapping expression patterns of these peptides illustrate the complete lack of cross-staining with this technique.

    Topics: Amino Acid Sequence; Animals; Brain Chemistry; Cholecystokinin; Drosophila melanogaster; Fluorescent Antibody Technique; Gene Expression; Immune Sera; Immunohistochemistry; Insect Hormones; Molecular Sequence Data; Neuropeptides; Oligopeptides; Sequence Homology

1993