Luan, J., Geng, J., Fang, S. et al. Developmental expression pattern of calmodulin gene in amphioxus Branchiostoma belcheri tsingtauense, ., Chin. J. Ocean. Limnol. 28, 1221–1226 (2010). https://doi.org/10.1007/s00343-010-9035-0
DOI:
Luan, J., Geng, J., Fang, S. et al. Developmental expression pattern of calmodulin gene in amphioxus Branchiostoma belcheri tsingtauense, ., Chin. J. Ocean. Limnol. 28, 1221–1226 (2010). https://doi.org/10.1007/s00343-010-9035-0DOI:
Developmental expression pattern of calmodulin gene in amphioxus Branchiostoma belcheri tsingtauense
摘要
Abstract
We investigated the developmental expression pattern of AmphiCaM in cephalochordate amphioxus (Branchiostoma belcheri tsingtauense). We cultured and sampled the animals at different developmental stages (eggs and larvae)
and used in-situ hybridization and northern blotting to document the spatial and temporal changes in AmphiCaM expression. The alimentary tract dominates the development from the late neurula stage to the adult stage. AmphiCaM expression increased significantly in the alimentary tract during the late neurula stage and remained elevated in the adults. Our results indicate that AmphiCaM is involved in the differentiation of the alimentary tract in amphioxus; and furthermore
provide an insight into the change in function of CaM genes during evolution.
关键词
Keywords
references
Bachs O, Agell N. 1995. Calmodulin and calmoudlin-binding proteins in the cell nucleus. In: Bachs O, Agell N eds. Calcium and Calmodulin Function in the Cell Nucleus. Springer-Verlag, New York. p. 217–240.
Bateson W. 1886. The ancestry of the chordata. Quart. J. Micro. Sci., 26: 535–571.
Chien Y H, Dawid I B. 1984. Isolation and characterization of calmodulingenes from Xenopus laevis. Mol. Cell. Biol., 4(3): 507–513.
Crivici A, Ikura M. 1996. Molecular and structural basis of target recognition by calmodulin. Annu. Rev. Biophys. Biomol. Struct., 24: 85–116.
Di G A, Villani M G, Locascio A, Ristoratore F, Aniello F, Branno M. 1998. Developmental regulation and tissue-specific localization of calmodulin mRNA in the protochordate Ciona intestinalis. Dev. Growth Differ., 40(4): 387–394.
Friedberg F, Taliaferro L. 2005. Calmodulin genes in zebrafish. Mol. Biol. Rep., 32(1): 55–60.
Garstang W. 1928. The morphology of the Tunicata, and its bearings on the phylogeny of the chordata. Quart. J. Micro. Sci., 72: 51–187.
Holland L Z, Holland P W H, Holland N D. 1996. Revealing homologies between body parts of distantly related animals by in situ hybridization to developmental genes: Amphioxus versus vertebrates. In: Ferraris J D ed. Molecular Zoology: Advances, Strategies, and Protocols. Wiley-Liss, New York. p. 267–282.
Hultschig C, Hecht H J, Frank R. 2004. Systematic delineation of a calmodulin peptide interaction. J. Mol. Biol., 343(3): 559–568.
Ikeshima H, Yuasa S, Matsuo K, Kawamura K, Hata J, Takano T. 1993. Expression of three non-allelic genes coding calmodulin exhibit similar localization on the central nervous system of adult rats. J. Neurosci. Res., 36(1): 111–119.
Kawasaki H, Kretsinger R H. 1995. Calcium binding proteins I: EFhands. Prot. Profile., 2(4): 297–490.
Kovalick G E, Beckingham K. 1992. Calmodulin transcription is limited to the nervous system during Drosophilia embryogenesis. Dev. Biol., 150(1): 33–46.
Lin Y, Zhang X, Liang K, Yang H, Zhang H. 2005. Phylogenetic analysis and developmental expression of brp-like genes in amphioxus and zebrafish. Comp. Biochem. Physiol. B Biochem. Mol. Biol., 141(1): 71–76.
Liu Z, Zhang S, Liu M, Wang Y, Chu J, Xu A. 2004. Evolution and expression of the amphioxus AmphiHMGB gene encoding an HMG-box protein. Comp. Biochem. Physiol. B. Biochem. Mol. Biol., 137(1): 131–138.
Luan J, Liu Z, Zhang S, Li H, Fan C, Li L. 2007. Characterization, evolution and expression of the calmodulin1 genes from the amphioxus Branchiostoma belcheri tsingtauense. Acta. Biochim. Biophys. Sin., 39(4): 255–264.
Smoake J A, Song S Y, Cheung W Y. 1974. Cyclic 3′, 5′-nucleotide phosphodiesterase distribution and developmental changes of the enzyme and its protein activator in mammalian tissues and cells. Biochim. Biophys. Acta, 341(2): 402–411.
Stokes M D, Holland N D. 1998. The lancelet: also known as “amphioxus”, this curious creature has returned to the limelight as a player in the phylogenetic history of the vertebrates. Amer. Sci., 86: 552–560.
Tung T C, Wu S C, Tung Y F. 1958. The development of isolated blastomeres of Amphioxus. Sci. Sin., 7(12): 1 280–1 320.
Van Eldik L J, Roberts D M. 1988. Calcium modulated proteins in pathophysiology. In: Thompson M P, ed. Calcium-binding Proteins. Volume II: Biological Functions. CRC Press, Florida, Washington DC. p. 401–403.
Van Eldik L J, Watterson D M. 1998. Calmodulin and Signal transduction. In: Van Eldik L J, Watterson D M, eds. Calmodulin and Signal Transduction. Academic Press, New York. p. 1–19.
Vogel H J. 1994. The Merck Frosst Award Lecture 1994. Calmodulin: a versatile calcium mediator protein. Biochem. Cell. Biol., 72(9–10): 357–376.
Zhang S C, Yuan J D, Li H Y. 2001. Amphioxus-model animal for insights into the origin and evolution of the vertebrates. Chin. Bull. Life Sci., 13(5): 214–218. (in Chinese)
Zhao B, Zhang S, Wang Y, Liu Z, Kong D. 2006. Characterization and expression of p23 gene in the amphioxus Branchiostoma belcheri. Comp. Biochem. Phys. B. Biochem. Mol. Biol., 145(1): 10–15.
The trial reading is over, you can activate your VIP account to continue reading.
Novel evolutionary insights into nemacheilid cavefish: evidence from comparative analysis of mitochondrial genomes
The role of Smad6 in immunity of the pearl oyster Pinctada fucata martensii
Cloning of catalase gene and antioxidant genes in Scophthalmus maximus response to metalloprotease of Vibrio anguillarum stress
Triterpenoid saponin biosynthesis genes and their expression patterns during the development of sea cucumber Apostichopus japonicus
TheUlva proliferagenome reveals the mechanism of green tides
Related Author
Lei ZHOU
Shihui HUANG
Qing WANG
Zhenhai LI
Zongyang LI
Anyou HE
Jiehu CHEN
Li LIU
Related Institution
Science Corporation of Gene
Guangxi Key Laboratory of Aquatic Genetic Breeding and Healthy Aquaculture, Guangxi Academy of Fishery Sciences
Joint Laboratory of Guangdong Province and Hong Kong Region on Marine Bioresource Conservation and Exploitation, College of Marine Sciences, South China Agricultural University
Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou)
CAS Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Provincial Key Laboratory of Applied Marine Biology, South China Sea Institute of Oceanology, Chinese Academy of Sciences