Abstract
The ability to estimate coral age using soft tissue would be useful for population biology or aging studies on corals. In this study, we investigated whether telomere length can be used to estimate coral age. We applied single telomere length analysis to a colonial coral, Galaxea fascicularis, and estimated telomere lengths of specific coral chromosomes at different developmental stages. If the telomere shortened at each cell division, the telomere length of the coral would be longest in sperm and shortest in adult colonies. However, the mean telomere length of sperm, planula larvae, and polyps was approximately 4 kb, with no significant differences among the developmental stages. The telomerase restriction fragment (TRF) analysis also showed no significant difference in the mean TRF length among the developmental stages. Our results suggested that telomere length is maintained during developmental stages and that estimating the age of colonial coral based on telomere length may not be possible. However, our findings can be used to examine avoidance of aging and rejuvenation during regeneration and asexual reproduction in colonial corals.
References
Azzalin CM, Nergadze SG, Giulotto E (2001) Human intrachromosomal telomeric-like repeats: sequence organization and mechanisms of origin. Chromosoma 110:75–82
Baird DM, Rowson J, Wynford-Thomas D, Kipling D (2003) Extensive allelic variation and ultrashort telomeres in senescent human cells. Nat Genet 33:203–207
Bendix L, Horn PB, Jensen UB, Rubelj I, Kolvraa S (2010) The load of short telomeres, estimated by a new method, Universal STELA, correlates with number of senescent cells. Aging Cell 9:383–397
Blackburn EH (1991) Structure and function of telomeres. Nature 350:569–573
Blackburn EH (2000) Telomere states and cell fates. Nature 408:53–56
Britt-Compton B, Rowson J, Locke M, Mackenzie I, Kipling D, Baird DM (2006) Structural stability and chromosome-specific telomere length is governed by cis-acting determinants in humans. Hum Mol Genet 15:725–733
Buddemeier RW, Kinzie RA (1976) Coral growth. Oceanogr Mar Biol Annu Rev 14:183–225
Cheung I, Schertzer M, Baross A, Rose AM, Lansdorp PM, Baird DM (2004) Strain-specific telomere length revealed by single telomere length analysis in Caenorhabditis elegans. Nucleic Acids Res 32:3383–3391
Coffroth MA, Lasker HR, Diamond ME, Bruenn JA, Bermingham E (1992) DNA fingerprints of a gorgonian coral: a method for detecting clonal structure in a vegetative species. Mar Biol 114:317–325
Dunshea G, Duffield D, Gales N, Hindell M, Wells RS, Jarman SN (2011) Telomeres as age markers in vertebrate molecular ecology. Mol Ecol Resour 11:225–235
Francis N, Gregg T, Owen R, Ebert T, Bodnar A (2006) Lack of age-associated telomere shortening in long- and short-lived species of sea urchins. FEBS Lett 580:4713–4717
Fukami H, Budd AF, Levitan DR, Jara J, Kersanach R, Knowlton N (2004) Geographic differences in species boundaries among members of the Montastraea annularis complex based on molecular and morphological markers. Evolution 58:324–337
Graakjaer J, Bischoff C, Korsholm L, Holsrtebroe S, Vach W, Bohr VA, Christensen K, Kolvraa S (2003) The pattern of chromosome-specific variations in telomere length in humans is determined by inherited, telomere-near factors and is maintained throughout life. Mech Ageing Dev 124:629–640
Greider CW, Blackburn EH (1985) Identification of a specific telomere terminal transferase activity in Tetrahymena extracts. Cell 43:405–413
Haussmann MF, Mauck RA (2008) New strategies for telomere-based age estimation. Mol Ecol Resour 8:264–274
Haussmann MF, Vleck CM (2002) Telomere length provides a new technique for aging animals. Oecologia 130:325–328
Hidaka M, Yamazato K (1982) Effect of light on budding of isolated polyps of the scleractinian coral Galaxea fascicularis. Galaxea 1:65–75
Highsmith RC (1982) Reproduction by fragmentation in corals. Mar Ecol Prog Ser 7:207–226
Hughes TP, Jackson JBC (1985) Population dynamics and life histories of foliaceous coral. Ecol Monogr 55:141–166
Kimura M, Barbieri M, Gardner JP, Skurnick J, Cao X, van Riel N, Rizzo MR, Paoliso G, Aviv A (2007) Leukocytes of exceptionally old persons display ultra-short telomeres. Am J Physiol Regul Integr Comp Physiol 293:R2210–R2217
Klein R, Loya Y (1991) Skeletal growth and density patterns of two Porites corals from the Gulf of Eilat, Red Sea. Mar Ecol Prog Ser 77:253–259
Laird DJ, Weissman IL (2004) Telomerase maintained in self-renewing tissues during serial regeneration of the urochordate Botryllus schlosseri. Dev Biol 273:185–194
Lian C, Hogetsu T (2002) Development of microsatellite markers in black locust (Robinia pseudoacacia) using a dual-suppression-PCR technique. Mol Ecol Notes 2:211–213
Lough JM, Barnes DJ (1997) Several centuries of variation in skeletal extension, density and calcification in massive Porites colonies from the Great Barrier Reef: a proxy for seawater temperature and a background of variability against which to identify unnatural change. J Exp Mar Biol Ecol 211:29–67
Nakagawa S, Gemmell NJ, Burke T (2004) Measuring vertebrate telomeres: applications and limitations. Mol Ecol 13:2523–2533
Nakamichi H, Ojimi MC, Isomura N, Hidaka M (2012) Somatic tissues of the coral Galaxea fascicularis possess telomerase activity. Galaxea, JCRS (in press)
Nilsson Sköld H, Obst M (2011) Potential for clonal animals in longevity and ageing studies. Biogerontology 12:387–396
Nilsson Sköld H, Asplund ME, Wood CA, Bishop JDD (2011a) Telomerase deficiency in a colonial ascidian after prolonged asexual propagation. J Exp Zool B Mol Dev Evol 316:276–283
Nilsson Sköld H, Stach T, Bishop JDD, Herbst E, Thorndyke MC (2011b) Pattern of cell proliferation during budding in the colonial ascidian Diplosoma listserianum. Biol Bull 221:126–136
Ojimi MC, Hidaka M (2010) Comparison of telomere length among different life cycle stages of the jellyfish Cassiopea andromeda. Mar Biol 157:2279–2287
Ojimi MC, Isomura N, Hidaka M (2009) Telomerase activity is not related to life history stage in the jellyfish Cassiopea sp. Comp Biochem Physiol A 152:240–244
Potts DC, Done TJ, Isdale PJ, Fisk DA (1985) Dominance of a coral community by the genus Porites (Scleractinia). Mar Ecol Prog Ser 23:79–84
Sinclair CS, Richmond RH, Ostrander GK (2007) Characterization of the telomere regions of scleractinian coral, Acropora surculosa. Genetica 129:227–233
Smith LD, Hughes TP (1999) An experimental assessment of survival, re-attachment and fecundity of coral fragments. J Exp Mar Biol Ecol 235:147–164
Tan TCJ, Rahman R, Jaber-Hijazi F, Felix DA, Chen C, Louis EJ, Aboobaker A (2012) Telomere maintenance and telomerase activity are differentially regulated in asexual and sexual worms. Proc Natl Acad Sci USA 101:8034–8038
Traut W, Szczepanowski M, Vítkova M, Opitz C, Marec F, Zrzavý J (2007) The telomere repeat motif of basal Metazoa. Chromosome Res 15:371–382
Urquidi V, Tarin D, Goodison S (2000) Role of telomerase in cell senescence and oncogenesis. Annu Rev Med 51:65–79
Villasante A, Abad JP, Méndez-Lago M (2007) Centromeres were derived from telomeres during the evolution of the eukaryotic chromosome. Proc Natl Acad Sci USA 104:10542–10547
Zielke S, Bodnar A (2010) Telomeres and telomerase activity in scleractinian corals and Symbiodinium spp. Biol Bull 218:113–121
Acknowledgments
This work was supported by the Grant-in-Aid for Scientific Research No. 20570093 and 23570080 from the Ministry of Education, Culture, Sports, Science and Technology, Japan. We would like to thank anonymous reviewers for constructive comments.
Author information
Authors and Affiliations
Corresponding author
Additional information
Communicated by Biology Eiditor Dr. Ruth Gates
Rights and permissions
About this article
Cite this article
Tsuta, H., Hidaka, M. Telomere length of the colonial coral Galaxea fascicularis at different developmental stages. Coral Reefs 32, 495–502 (2013). https://doi.org/10.1007/s00338-012-0997-6
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00338-012-0997-6