Abstract
The polychaete . Hydroides elegans (Serpulidae, Lophotrochozoa) is a problematic marine fouling organism in most tropical and subtropical coastal environment. Competent larvae of . H. elegans undergo the transition from the swimming larval stage to the sessile juvenile stage with substantial morphological, physiological, and behavior changes. This transition is often referred to as larval settlement and metamorphosis. In this study, we examined the possible involvement of calmodulin (CaM) - a multifunctional calcium metabolism regulator, in the larval settlement and metamorphosis of . H. elegans. A full-length . CaM cDNA was successfully cloned from . H. elegans (. He-CaM) and it contained an open reading frame of 450. bp, encoding 149 amino acid residues. It was highly expressed in 12. h post-metamorphic juveniles, and remained high in adults. . In situ hybridization conducted in competent larvae and juveniles revealed that . He-CaM gene was continuously expressed in the putative growth zones, branchial rudiments, and collar region, suggesting that . He-CaM might be involved in tissue differentiation and development. Our subsequent bioassay revealed that the CaM inhibitor W7 could effectively inhibit larval settlement and metamorphosis, and cause some morphological defects of unsettled larvae. In conclusion, our results revealed that CaM has important functions in the larval settlement and metamorphosis of . H. elegans. © 2012 Elsevier Inc..
Original language | English (US) |
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Pages (from-to) | 113-119 |
Number of pages | 7 |
Journal | Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology |
Volume | 162 |
Issue number | 4 |
DOIs | |
State | Published - Aug 2012 |
Externally published | Yes |
Bibliographical note
KAUST Repository Item: Exported on 2020-10-01Acknowledgements: We thank Dr. Yue Him Wong and Dr. Yu Zhang for their help with the sample collection; Dr. Kai He for technical assistance; Prof. Louis A Gosselin and Dr. Kiyokata Matsumura for assistance with revising the paper; and Fan Zhang, Dr. Shawn Arellano, and other lab members for their technical advice and constructive discussions. This study was supported by an award SA-C0040/UK-C0016 from the King Abdullah University of Science and Technology and grants (N_HKUST602/09 and AoE/P-04/04-2-II) from the Research Grants Council (RGC) of the Hong Kong SAR to PY Qian.
ASJC Scopus subject areas
- Biochemistry
- Molecular Biology
- Physiology