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Aplysia capsulin is localized to egg capsules and egg cordon sheaths and shares sequence homology with Drosophila dec-1 gene products

  • Scott F. Cummins
    ,
  • Gregg T. Nagle(corresponding author)
*Corresponding author for this work
  • University of Texas Medical Branch at Galveston
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Differential library screening of an albumen gland cDNA library, Western blot analysis, protein expression, immunolocalization studies, comparative genomics, and secretion assays identified a major Aplysia californica albumen gland protein ('capsulin') that is localized to egg capsules and to the sheaths of the egg cordon. Capsulin shared sequence homology with eggshell proteins encoded by the Drosophila dec-1 gene. The 1790-amino acid A. californica precursor contains 17 repeat sequences that are flanked by basic residue processing sites. The numerous proteolytic processing sites may facilitate the breakdown of capsulin prior to when veliger larvae break out of egg capsules as free-swimming larvae. An Aplysia brasiliana capsulin repeat sequence was 97% identical to its A. californica homolog. Capsulin fragments were not detected in the eluates of egg cordons, suggesting that capsulin is not a candidate water-borne pheromone precursor.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 589-596 (8 pages)

Journal (Volume, Issue Number)

Peptides (Volume 26, Issue 4)

Publication milestones

  • Published - 04/2005

Publication status

Published - 04/2005

ISSN

0196-9781

Publication IDs

  • Scopus: 14744279740
  • PubMed: 15752572

Publication metrics

Metrics

SciVal
FWCI
0.18
SciVal
Author count
2
SciVal
citations
6
SciVal
Paper percentile
53
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
1
Scopus
citations

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Captures
14
Citation count
6

Funding Details

Supported by the National Science Foundation (IBN-0314377) and the John Sealy Memorial Endowment Fund Grant (2579-02R). We acknowledge the assistance of the UTMB Protein Chemistry Lab, and we thank S.D. Painter for critical review of the manuscript. The GenBank accession numbers reported in this paper are AY162292 and AY761092 .
FundersFunding numbers
John Sealy Memorial Endowment Fund for Biomedical Research
2579-02R
NSF
IBN-0314377