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A genomic view of 500 million years of cnidarian evolution
Open accessAbstract
Cnidarians (corals, anemones, jellyfish and hydras) are a diverse group of animals of interest to evolutionary biologists, ecologists and developmental biologists. With the publication of the genome sequences of Hydra and Nematostella, whose last common ancestor was the stem cnidarian, researchers are beginning to see the genomic underpinnings of cnidarian biology. Cnidarians are known for the remarkable plasticity of their morphology and life cycles. This plasticity is reflected in the Hydra and Nematostella genomes, which differ to an exceptional degree in size, base composition, transposable element content and gene conservation. It is now known what cnidarian genomes, given 500 million years, are capable of; as we discuss here, the next challenge is to understand how this genomic history has led to the striking diversity seen in this group.
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“Taking into account more than 500 million years of independent evolution of the bilaterian and cnidarian lineage [76], surprisingly, many elements of the developmental neuronal network and genes governing neuronal structure and function are conserved.”
From Evolution of eumetazoan nervous systems: insights from cnidarians (2015) · cites this paper as [76]
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Cites
Expansion of the eukaryotic proteome by alternative splicing
Nilsen, T. W., & Graveley, B. R. (2010) · Nature · doi:10.1038/nature08909 · Cited by 2,270
Genome-Wide Evolutionary Analysis of Eukaryotic DNA Methylation
Zemach, A., McDaniel, I. E., Silva, P., & Zilberman, D. (2010) · Science · doi:10.1126/science.1186366 · Cited by 1,829
Sea Anemone Genome Reveals Ancestral Eumetazoan Gene Repertoire and Genomic Organization
Putnam, N. H., Srivastava, M., Hellsten, U., Dirks, B., Chapman, J., Salamov, A., Terry, A., Shapiro, H., Lindquist, E., Kapitonov, V. V., et al. (2007) · Science · doi:10.1126/science.1139158 · Cited by 1,555
Self-citationThe Amphimedon queenslandica genome and the evolution of animal complexity
Srivastava, M., Simakov, O., Chapman, J., Fahey, B., Gauthier, M. E. A., Mitros, T., Richards, G. S., Conaco, C., Dacre, M., Hellsten, U., et al. (2010) · Nature · doi:10.1038/nature09201 · Cited by 1,049
Chapman, J. A., Kirkness, E. F., Simakov, O., Hampson, S. E., Mitros, T., Weinmaier, T., Rattei, T., Balasubramanian, P. G., Borman, J., Busam, D., et al. (2010) · Nature · doi:10.1038/nature08830 · Cited by 810
Self-citationEarly origins and evolution of microRNAs and Piwi-interacting RNAs in animals
Grimson, A., Srivastava, M., Fahey, B., Woodcroft, B. J., Chiang, H. R., King, N., Degnan, B. M., Rokhsar, D. S., & Bartel, D. P. (2008) · Nature · doi:10.1038/nature07415 · Cited by 756
Unexpected complexity of the Wnt gene family in a sea anemone
Kusserow, A., Pang, K., Sturm, C., Hrouda, M., Lentfer, J., Schmidt, H. A., Technau, U., von Haeseler, A., Hobmayer, B., Martindale, M. Q., et al. (2005) · Nature · doi:10.1038/nature03158 · Cited by 599
Self-citationThe genesis and evolution of homeobox gene clusters
García‐Fernàndez, J. (2005) · Nature Reviews Genetics · doi:10.1038/nrg1723 · Cited by 490
Lateral gene transfer in eukaryotes
Andersson, J. O. (2005) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-005-4539-z · Cited by 430
More than just orphans: are taxonomically-restricted genes important in evolution?
Khalturin, K., Hemmrich, G., Fraune, S., Augustin, R., & Bosch, T. C. G. (2009) · Trends in Genetics · doi:10.1016/j.tig.2009.07.006 · Cited by 426
Mortality Patterns Suggest Lack of Senescence in Hydra
Martínez, D. E. (1998) · Experimental Gerontology · doi:10.1016/s0531-5565(97)00113-7 · Cited by 425
Apoptotic Cells Provide an Unexpected Source of Wnt3 Signaling to Drive Hydra Head Regeneration
Chera, S., Ghila, L., Dobretz, K., Wenger, Y., Bauer, C. R., Buzgariu, W., Martinou, J., & Galliot, B. (2009) · Developmental Cell · doi:10.1016/j.devcel.2009.07.014 · Cited by 424
Collins, A. G., Schuchert, P., Marques, A. C., Jankowski, T., Medina, M., & Schierwater, B. (2006) · Systematic Biology · doi:10.1080/10635150500433615 · Cited by 391
Telomeres: Cancer to Human Aging
Stewart, S. A., & Weinberg, R. A. (2006) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.22.010305.104518 · Cited by 349
Maintenance of ancestral complexity and non-metazoan genes in two basal cnidarians
Technau, U., Rudd, S., Maxwell, P., Gordon, P. M. K., Saina, M., Grasso, L. C., Hayward, D. C., Sensen, C. W., Saint, R., Holstein, T. W., et al. (2005) · Trends in Genetics · doi:10.1016/j.tig.2005.09.007 · Cited by 337
Self-citationLong-term maintenance of species-specific bacterial microbiota in the basal metazoan Hydra
Fraune, S., & Bosch, T. C. G. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703375104 · Cited by 331
Multiple Wnts are involved in Hydra organizer formation and regeneration
Lengfeld, T., Watanabe, H., Simakov, O., Lindgens, D., Gee, L., Law, L. Y., Schmidt, H. A., Özbek, S., Bode, H. R., & Holstein, T. W. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.02.004 · Cited by 300
Transgenic Hydra allow in vivo tracking of individual stem cells during morphogenesis
Wittlieb, J., Khalturin, K., Lohmann, J. U., Anton‐Erxleben, F., & Bosch, T. C. G. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510163103 · Cited by 298
Formation of the head organizer in hydra involves the canonical Wnt pathway.
Broun, M., Gee, L., Reinhardt, B., & Bode, H. R. (2005) · Development · doi:10.1242/dev.01848 · Cited by 287
Innexins: members of an evolutionarily conserved family of gap-junction proteins
Phelan, P. (2004) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2004.10.004 · Cited by 256
Anatomy and development of the nervous system of Nematostella vectensis , an anthozoan cnidarian
Marlow, H. Q., Srivastava, M., Matus, D. Q., Rokhsar, D., & Martindale, M. Q. (2009) · Developmental Neurobiology · doi:10.1002/dneu.20698 · Cited by 247
Naked corals: Skeleton loss in Scleractinia
Medina, M., Collins, A. G., Takaoka, T. L., Kuehl, J. V., & Boore, J. L. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602444103 · Cited by 241
Cell cycle kinetics and development of Hydra attenuata: III. nerve and nematocyte differentiation
David, C. N., & Gierer, A. (1974) · Journal of Cell Science · doi:10.1242/jcs.16.2.359 · Cited by 233
Self-citationCnidarians: An evolutionarily conserved model system for regeneration?
Holstein, T. W., Hobmayer, E., & Technau, U. (2003) · Developmental Dynamics · doi:10.1002/dvdy.10227 · Cited by 225
Self-citationThe interstitial cell lineage of hydra: a stem cell system that arose early in evolution
Bode, H. R. (1996) · Journal of Cell Science · doi:10.1242/jcs.109.6.1155 · Cited by 223
Rising starlet: the starlet sea anemone,Nematostella vectensis
Darling, J. A., Reitzel, A. M., Burton, P. M., Mazza, M. E., Ryan, J. F., Sullivan, J. C., & Finnerty, J. R. (2005) · BioEssays · doi:10.1002/bies.20181 · Cited by 214
Silencing of Developmental Genes in Hydra
Lohmann, J. U., Endl, I., & Bosch, T. C. G. (1999) · Developmental Biology · doi:10.1006/dbio.1999.9407 · Cited by 204
SL trans-splicing: easy come or easy go?
Hastings, K. E. M. (2005) · Trends in Genetics · doi:10.1016/j.tig.2005.02.005 · Cited by 198
Minimal ProtoHox cluster inferred from bilaterian and cnidarian Hox complements
Chourrout, D., Delsuc, F., Chourrout, P., Edvardsen, R. B., Rentzsch, F., Renfer, E., Jensen, M. F., Zhu, B., de Jong, P., Steele, R. E., et al. (2006) · Nature · doi:10.1038/nature04863 · Cited by 197
Self-citationCELL CYCLE KINETICS AND DEVELOPMENT OF HYDRA ATTENUATA
David, C. N., & Campbell, R. D. (1974) · Open access LMU (Ludwid Maxmilian's Universitat Munchen) · Cited by 189
Self-citationBosch, T. C. G. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.12.012 · Cited by 186
Takahashi, T., Muneoka, Y., Lohmann, J. U., de Haro, M. S. L., Solleder, G., Bosch, T. C. G., David, C. N., Bode, H. R., Koizumi, O., Shimizu, H., et al. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.4.1241 · Cited by 186
Self-citationCharacterization of interstitial stem cells in hydra by cloning
David, C. N., & Murphy, S. (1977) · Developmental Biology · doi:10.1016/0012-1606(77)90098-7 · Cited by 170
Self-citationExpression and evolutionary conservation of nanos-related genes in Hydra
Mochizuki, K., Sano, H., Kobayashi, S., Nishimiya‐Fujisawa, C., & Fujisawa, T. (2000) · Development Genes and Evolution · doi:10.1007/s004270000105 · Cited by 165
Lenhoff, H. M. (1983) · Springer eBooks · doi:10.1007/978-1-4757-0596-6 · Cited by 164
A muscle-specific transgenic reporter line of the sea anemone, Nematostella vectensis
Renfer, E., Amon-Hassenzahl, A., Steinmetz, P. R. H., & Technau, U. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909148107 · Cited by 164
Self-citationStem cells of Hydra magnipapillata can differentiate into somatic cells and germ line cells
Bosch, T. C. G., & David, C. N. (1987) · Developmental Biology · doi:10.1016/0012-1606(87)90151-5 · Cited by 163
Self-citationBlumenthal, T. (2004) · Briefings in Functional Genomics and Proteomics · doi:10.1093/bfgp/3.3.199 · Cited by 163
Genomic inventory and expression of Sox and Fox genes in the cnidarian Nematostella vectensis
Magie, C. R., Pang, K., & Martindale, M. Q. (2005) · Development Genes and Evolution · doi:10.1007/s00427-005-0022-y · Cited by 158
Evolution of complex structures: minicollagens shape the cnidarian nematocyst
David, C. N., Özbek, S., Adamczyk, P., Meier, S., Pauly, B. S., Chapman, J., Hwang, J. S., Gojobori, T., & Holstein, T. W. (2008) · Trends in Genetics · doi:10.1016/j.tig.2008.07.001 · Cited by 152
Self-citationBode, H. R. (2003) · Developmental Dynamics · doi:10.1002/dvdy.10225 · Cited by 146
Hydra and the evolution of stem cells
Bosch, T. C. G. (2009) · BioEssays · doi:10.1002/bies.200800183 · Cited by 140
Mini-collagens in hydra nematocytes.
Kurz, E. M., Holstein, T. W., Petri, B., Engel, J., & David, C. N. (1991) · The Journal of Cell Biology · doi:10.1083/jcb.115.4.1159 · Cited by 135
Self-citationDenker, E., Manuel, M., Leclère, L., Guyader, H. L., & Rabet, N. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.12.023 · Cited by 130
Clytia hemisphaerica: a jellyfish cousin joins the laboratory
Houliston, E., Momose, T., & Manuel, M. (2010) · Trends in Genetics · doi:10.1016/j.tig.2010.01.008 · Cited by 128
Martínez, D. E., Iñiguez, A. R., Percell, K. M., Willner, J. B., Signorovitch, J., & Campbell, R. D. (2010) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2010.06.016 · Cited by 120
Trans-spliced leader addition to mRNAs in a cnidarian
Stover, N. A., & Steele, R. E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.101049998 · Cited by 120
Self-citationTotipotent migratory stem cells in a hydroid
Müller, W. A., Teo, R., & Frank, U. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.08.006 · Cited by 116
A Novel Gene Family Controls Species-Specific Morphological Traits in Hydra
Khalturin, K., Anton‐Erxleben, F., Sassmann, S., Wittlieb, J., Hemmrich, G., & Bosch, T. C. G. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060278 · Cited by 109
The telomere repeat motif of basal Metazoa
Traut, W., Szczepanowski, M., Zrzavá, M., Opitz, C., Marec, F., & Zrzavý, J. (2007) · Chromosome Research · doi:10.1007/s10577-007-1132-3 · Cited by 107
β-catenin plays a central role in setting up the head organizer in hydra
Gee, L., Hartig, J. V., Law, L. Y., Wittlieb, J., Khalturin, K., Bosch, T. C. G., & Bode, H. R. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2009.12.036 · Cited by 105
Hartl, M., Mitterstiller, A., Valovka, T., Breuker, K., Hobmayer, B., & Bister, K. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911060107 · Cited by 105
No backbone but lots of Sox: Invertebrate Sox genes
Phochanukul, N., & Russell, S. R. H. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.06.013 · Cited by 104
Pacemaker Hierarchies Controlling the Behaviour of Hydras
Passano, L. M., & MCCULLOUGH, C. B. (1963) · Nature · doi:10.1038/1991174a0 · Cited by 101
A Hypervariable Invertebrate Allodeterminant
Nicotra, M. L., Powell, A. E., Rosengarten, R. D., Moreno, M. A., Grimwood, J., Lakkis, F. G., Dellaporta, S. L., & Buss, L. W. (2009) · Current Biology · doi:10.1016/j.cub.2009.02.040 · Cited by 100
HyAlx, an aristaless-related gene, is involved in tentacle formation in hydra
Smith, K. M., Gee, L., & Bode, H. R. (2000) · Development · doi:10.1242/dev.127.22.4743 · Cited by 95
Evidence for Multiple Independent Origins of trans-Splicing in Metazoa
Douris, V., Telford, M. J., & Averof, M. (2009) · Molecular Biology and Evolution · doi:10.1093/molbev/msp286 · Cited by 95
Hwang, J. S., Ohyanagi, H., Hayakawa, S., Osato, N., Nishimiya‐Fujisawa, C., Ikeo, K., David, C. N., Fujisawa, T., & Gojobori, T. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703331104 · Cited by 91
Self-citationChera, S., de Rosa, R., Miljkovic‐Licina, M., Dobretz, K., Ghila, L., Kaloulis, K., & Galliot, B. (2006) · Journal of Cell Science · doi:10.1242/jcs.02807 · Cited by 90
Head regeneration in wild-type hydra requires de novo neurogenesis
Miljkovic‐Licina, M., Chera, S., Ghila, L., & Galliot, B. (2007) · Development · doi:10.1242/dev.02804 · Cited by 90
Evolution of gap junctions: the missing link?
Alexopoulos, H., Böttger, A., Fischer, S., Levin, A., Wolf, A., Fujisawa, T., Hayakawa, S., Gojobori, T., Davies, J. A., David, C. N., et al. (2004) · Current Biology · doi:10.1016/j.cub.2004.09.067 · Cited by 80
Self-citationPankow, S., & Bamberger, C. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000782 · Cited by 79
Hwang, J. S., Takaku, Y., Momose, T., Adamczyk, P., Özbek, S., Ikeo, K., Khalturin, K., Hemmrich, G., Bosch, T. C. G., Holstein, T. W., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1003256107 · Cited by 79
Self-citationThe cell junctions of hydra as viewed by freeze-fracture replication
Wood, R. L. (1977) · Journal of Ultrastructure Research · doi:10.1016/s0022-5320(77)90021-1 · Cited by 78
Molecular phylogenetics in Hydra, a classical model in evolutionary developmental biology
Hemmrich, G., Anokhin, B. A., Zacharias, H., & Bosch, T. C. G. (2006) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2006.10.031 · Cited by 78
Rebscher, N., Volk, C., Teo, R., & Plickert, G. (2008) · Developmental Dynamics · doi:10.1002/dvdy.21562 · Cited by 77
Expansion of the SOX gene family predated the emergence of the Bilateria
Jager, M., Quéinnec, É., Houliston, E., & Manuel, M. (2006) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2005.12.005 · Cited by 73
Nanog Regulates Proliferation During Early Fish Development
Camp, E., Sánchez-Sánchez, A. V., García‐España, A., DeSalle, R., Odqvist, L., O’Connor, J., & Mullor, J. L. (2009) · Stem Cells · doi:10.1002/stem.133 · Cited by 72
Excitability of nerve-free hydra
Campbell, R. D., Josephson, R. K., Schwab, W., & Rushforth, N. B. (1976) · Nature · doi:10.1038/262388a0 · Cited by 72
Nakanishi, N., Yuan, D., Jacobs, D. K., & Hartenstein, V. (2008) · Development Genes and Evolution · doi:10.1007/s00427-008-0239-7 · Cited by 71
A fragmented metazoan organellar genome: the two mitochondrial chromosomes of Hydra magnipapillata
Voigt, O., Erpenbeck, D., & Wörheide, G. (2008) · BMC Genomics · doi:10.1186/1471-2164-9-350 · Cited by 71
Hydractinia Allodeterminant alr1 Resides in an Immunoglobulin Superfamily-like Gene Complex
Rosa, S., Powell, A. E., Rosengarten, R. D., Nicotra, M. L., Moreno, M. A., Grimwood, J., Lakkis, F. G., Dellaporta, S. L., & Buss, L. W. (2010) · Current Biology · doi:10.1016/j.cub.2010.04.050 · Cited by 70
Formation of junctions in regeneratin hydra: Gap junctions
Wood, R. L., & Kuda, A. M. (1980) · Journal of Ultrastructure Research · doi:10.1016/s0022-5320(80)90094-5 · Cited by 69
Axial Patterning in HydraPreprint
Bode, H. R. (2009) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a000463 · Cited by 66
Characterization of taxonomically restricted genes in a phylum-restricted cell type
Milde, S., Hemmrich, G., Anton‐Erxleben, F., Khalturin, K., Wittlieb, J., & Bosch, T. C. G. (2009) · Genome biology · doi:10.1186/gb-2009-10-1-r8 · Cited by 64
The novel peptide HEADY specifies apical fate in a simple radially symmetric metazoanPreprint
Lohmann, J. U., & Bosch, T. C. G. (2000) · Genes & Development · doi:10.1101/gad.830100 · Cited by 58
Dixon, J. E., Allegrucci, C., Redwood, C., Kump, K., Bian, Y., Chatfield, J., Chen, Y., Sottile, V., Voss, S. R., Alberio, R., et al. (2010) · Development · doi:10.1242/dev.049262 · Cited by 55
APPARENT ABSENCE OF GAP JUNCTIONS IN TWO CLASSES OF CNIDARIA
Mackie, G. O., Anderson, P. A. V., & Singla, C. L. (1984) · Biological Bulletin · doi:10.2307/1541341 · Cited by 55
Genikhovich, G., & Technau, U. (2009) · Cold Spring Harbor Protocols · doi:10.1101/pdb.emo129 · Cited by 51
Self-citationNew tricks with old genes: the genetic bases of novel cnidarian traits
Forêt, S., Knack, B., Houliston, E., Momose, T., Manuel, M., Quéinnec, É., Hayward, D. C., Ball, E. E., & Miller, D. J. (2010) · Trends in Genetics · doi:10.1016/j.tig.2010.01.003 · Cited by 51
Peduncle of Hydra and the heart of higher organisms share a common ancestral origin
Shimizu, H., & Fujisawa, T. (2003) · genesis · doi:10.1002/gene.10213 · Cited by 47
Fisher, D. A., & Bode, H. R. (1989) · Gene · doi:10.1016/0378-1119(89)90139-x · Cited by 47
Neuro-epitheliomuscular cell and neuro-neuronal gap junctions inHydra
Westfall, J. A., Kinnamon, J. C., & Sims, D. (1980) · Journal of Neurocytology · doi:10.1007/bf01205015 · Cited by 46
Germ cell restricted expression of chick Nanog
Cañón, S., Herranz, C., & Manzanares, M. (2006) · Developmental Dynamics · doi:10.1002/dvdy.20927 · Cited by 46
Terminology for Morphology and Cell Types
Campbell, R. D., & Bode, H. R. (1983) · Springer eBooks · doi:10.1007/978-1-4757-0596-6_2 · Cited by 44
Minicollagen-15, a Novel Minicollagen Isolated from Hydra, Forms Tubule Structures in Nematocysts
Adamczyk, P., Meier, S., Gross, T., Hobmayer, B., Grzesiek, S., Bächinger, H. P., Holstein, T. W., & Özbek, S. (2007) · Journal of Molecular Biology · doi:10.1016/j.jmb.2007.10.090 · Cited by 43
Hym-301, a novel peptide, regulates the number of tentacles formed in hydra
Takahashi, T., Hatta, M., Yum, S., Gee, L., Ohtani, M., Fujisawa, T., & Bode, H. R. (2005) · Development · doi:10.1242/dev.01792 · Cited by 42
Genome sizes and chromosomes in the basal metazoan Hydra
Zacharias, H., Anokhin, B. A., Khalturin, K., & Bosch, T. C. G. (2004) · Zoology · doi:10.1016/j.zool.2004.04.005 · Cited by 41
Sweet Tooth, a Novel Receptor Protein-tyrosine Kinase with C-type Lectin-like Extracellular Domains
Reidling, J. C., Miller, M. A., & Steele, R. E. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.14.10323 · Cited by 41
Self-citationBridge, D. M., Stover, N. A., & Steele, R. E. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9653 · Cited by 40
Self-citationThree digestive movements in Hydra regulated by the diffuse nerve net in the body column
Shimizu, H., Koizumi, O., & Fujisawa, T. (2004) · Journal of Comparative Physiology A · doi:10.1007/s00359-004-0518-3 · Cited by 39
Derelle, R., Momose, T., Manuel, M., Silva, C. D., Wincker, P., & Houliston, E. (2010) · RNA · doi:10.1261/rna.1975210 · Cited by 39
What transgenic mice tell us about neurodegenerative disease
Gurney, M. E. (2000) · BioEssays · doi:10.1002/(sici)1521-1878(200003)22:3 · Cited by 38
STAGING AND INDUCTION OF MEDUSA METAMORPHOSIS IN CARYBDEA MARSUPIALIS (CNIDARIA, CUBOZOA)
Stangl, K., Salvini-Plawen, L. V., & Holstein, T. W. (2002) · HAL (Le Centre pour la Communication Scientifique Directe) · Cited by 36
Hwang, J. S., Takaku, Y., Chapman, J., Ikeo, K., David, C. N., & Gojobori, T. (2008) · Molecular Biology and Evolution · doi:10.1093/molbev/msn154 · Cited by 31
Self-citationMigration of interstitial cells and their derivatives in a hydrozoan planula
Martin, V. J., & Archer, W. E. (1986) · Developmental Biology · doi:10.1016/0012-1606(86)90149-1 · Cited by 29
Cardenas, M. M., & Salgado, L. M. (2003) · Developmental Biology · doi:10.1016/j.ydbio.2003.08.022 · Cited by 28
Important roles for epithelial cell peptides in hydra development
Takahashi, T., & Fujisawa, T. (2009) · BioEssays · doi:10.1002/bies.200800163 · Cited by 19
Total nucleotide analysis of Hydra DNA and RNA by MEKC with LIF detection and 32P‐postlabeling
Hassel, M., Cornelius, M. G., Brocke, J. V., & Schmeiser, H. H. (2010) · Electrophoresis · doi:10.1002/elps.200900458 · Cited by 17
Cadavid, L. F. (2004) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2004.01.007 · Cited by 13
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Fidler, A. L., Vanacore, R., Chetyrkin, S. V., Pedchenko, V. K., Bhave, G. B., Yin, V. P., Stothers, C. L., Rose, K. L., McDonald, W. H., Clark, T. A., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1318499111 · Cited by 170
Self-citation
Metadata
- Authors
- Steele, R. E., David, C. N., & Technau, U.
- Affiliations
- University of California, Irvine (US)
- Ludwig-Maximilians-Universität München (DE)
- University of Vienna (AT)
- Venue
- Trends in Genetics
- Publisher
- Elsevier BV
- Published
- 2011-01
- Volume
- 27
- Issue
- 1
- Pages
- 7-13
- ISSN
- 0168-9525 (ISSN-L)
- PMC
- PMC3058326
- OpenAlex
- W1993001731
- Cited by
- 111
- References
- 100
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 3 · 2023: 11 · 2022: 6 · 2021: 5 · 2020: 4 · 2019: 9 · 2018: 5 · 2017: 7 · 2016: 8 · 2015: 12 · 2014: 9 · 2013: 10 · 2012: 8
- FWCI
- 1.03
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Trends in Genetics (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of General Medical Sciences (R24GM080537)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Marine Invertebrate Physiology and Ecology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Chromosomal and Genetic Variations
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Keywords
- cnidarian evolution, genome evolution, Hydra, Nematostella, genome size variation, transposable elements, genetic conservation, morphological plasticity
- MeSH terms
- Animals, Cnidaria, Biological Evolution, Gene Expression Regulation, Phylogeny, Genome, Evolution, Molecular, Gene Transfer, Horizontal
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