The DOI matches its Crossref record; 79 of the 79 references it cites were found in a registry or an index.
Independent evolution of striated muscles in cnidarians and bilaterians
Open accessAbstract
Striated muscles are present in bilaterian animals (for example, vertebrates, insects and annelids) and some non-bilaterian eumetazoans (that is, cnidarians and ctenophores). The considerable ultrastructural similarity of striated muscles between these animal groups is thought to reflect a common evolutionary origin. Here we show that a muscle protein core set, including a type II myosin heavy chain (MyHC) motor protein characteristic of striated muscles in vertebrates, was already present in unicellular organisms before the origin of multicellular animals. Furthermore, 'striated muscle' and 'non-muscle' myhc orthologues are expressed differentially in two sponges, compatible with a functional diversification before the origin of true muscles and the subsequent use of striated muscle MyHC in fast-contracting smooth and striated muscle. Cnidarians and ctenophores possess striated muscle myhc orthologues but lack crucial components of bilaterian striated muscles, such as genes that code for titin and the troponin complex, suggesting the convergent evolution of striated muscles. Consistently, jellyfish orthologues of a shared set of bilaterian Z-disc proteins are not associated with striated muscles, but are instead expressed elsewhere or ubiquitously. The independent evolution of eumetazoan striated muscles through the addition of new proteins to a pre-existing, ancestral contractile apparatus may serve as a model for the evolution of complex animal cell types.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“This interpretation is compatible with a recent report that striated musculature evolved independently in bilaterians, cnidarians, and in the ctenophore Euplokamis dunlapae (49).”
From The Genome of the Ctenophore Mnemiopsis leidyi and Its Implications for Cell Type Evolution (2013) · cites this paper as [49]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Striated muscles have evolved at least three times: after the split of the Euplokamis dunlapae lineage from other ctenophores, in select Cnidaria 32 , and in bilaterians 32 (Supplementary Fig. S25).”
From Ctenophore relationships and their placement as the sister group to all other animals (2017) · cites this paper as [32]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“These data indicate that muscles 21 and, possibly, mesoderm evolved independently in Ctenophora to control the hydroskeleton, body shape and food capture.”
From The ctenophore genome and the evolutionary origins of neural systems (2014) · cites this paper as [21]
Experimental — accuracy not yet measuredIn the citing paper
“On the effector side, early metazoan cells already possessed a complex machinery for cellular contractions and shape changes based on a dynamic actomyosin cytoskeleton.”
From Gastric pouches and the mucociliary sole: setting the stage for nervous system evolution (2015) · cites this paper as [36]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
MUSCLE: multiple sequence alignment with high accuracy and high throughput
Edgar, R. C. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh340 · Cited by 44,662
Thompson, J. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.24.4876 · Cited by 38,685
MrBayes 3: Bayesian phylogenetic inference under mixed models
Ronquist, F., & Huelsenbeck, J. P. (2003) · Bioinformatics · doi:10.1093/bioinformatics/btg180 · Cited by 29,194
Guindon, S., Dufayard, J.-F., Lefort, V., Anisimova, M., Hordijk, W., & Gascuel, O. (2010) · Systematic Biology · doi:10.1093/sysbio/syq010 · Cited by 18,376
The Pfam Protein Families Database
Bateman, A. G. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.1.276 · Cited by 14,075
Selection of Conserved Blocks from Multiple Alignments for Their Use in Phylogenetic Analysis
Castresana, J. (2000) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a026334 · Cited by 10,681
Prediction of complete gene structures in human genomic DNA
Burge, C., & Karlin, S. (1997) · Journal of Molecular Biology · doi:10.1006/jmbi.1997.0951 · Cited by 4,211
Predicting coiled coils from protein sequences.
Lupas, A., Van Dyke, M., & Stock, J. (1991) · Science · doi:10.1126/science.252.5009.1162 · Cited by 3,953
ProtTest: selection of best-fit models of protein evolution
Abascal, F., Zardoya, R., & Posada, D. (2005) · Bioinformatics · doi:10.1093/bioinformatics/bti263 · Cited by 3,063
The Chlamydomonas Genome Reveals the Evolution of Key Animal and Plant Functions
Merchant, S., Prochnik, S. E., Vallon, O., Harris, E. H., Karpowicz, S. J., Witman, G. B., Terry, A., Salamov, A. A., Fritz‐Laylin, L. K., Maréchal‐Drouard, L., et al. (2007) · Science · doi:10.1126/science.1143609 · Cited by 2,703
Research works printed but not linked: 2
- Sarà, M., Sarà, A., Nickel, M. & Brümmer, F. Three new species of Tethya (Porifera: Demospongiae) from German aquaria Stuttg. Beitr. Naturkd. A. 631, 1–15 (2001)
- Weissenfels, N. Scanning electron microscope histology of spongy Ephydatia fluviatilis . Microsc. Acta 85, 345–350 (1982)
Cited by
Sorted by citations
The origin and evolution of cell types
Arendt, D., Musser, J. M., Baker, C. V. H., Bergman, A., Cepko, C., Erwin, D. H., Pavlicev, M., Schlosser, G., Widder, S., Laubichler, M. D., et al. (2016) · Nature Reviews Genetics · doi:10.1038/nrg.2016.127 · Cited by 764
The ctenophore genome and the evolutionary origins of neural systems
Moroz, L. L., Kocot, K. M., Citarella, M. R., Dosung, S., Norekian, T. P., Povolotskaya, I. S., Grigorenko, A. P., Dailey, C., Berezikov, E., Buckley, K. M., et al. (2014) · Nature · doi:10.1038/nature13400 · Cited by 716
The Genome of the Ctenophore Mnemiopsis leidyi and Its Implications for Cell Type Evolution
Ryan, J. F., Pang, K., Schnitzler, C. E., Nguyen, A.-D., Moreland, R. T., Simmons, D. K., Koch, B. J., Francis, W. R., Havlak, P., Program, N. C. S., et al. (2013) · Science · doi:10.1126/science.1242592 · Cited by 682
Forcing cells into shape: the mechanics of actomyosin contractility
Murrell, M. P., Oakes, P. W., Lenz, M., & Gardel, M. L. (2015) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm4012 · Cited by 675
Deep homology of arthropod central complex and vertebrate basal ganglia.
Strausfeld, N. J., & Hirth, F. (2013) · Science · doi:10.1126/science.1231828 · Cited by 354
Cnidarian Cell Type Diversity and Regulation Revealed by Whole-Organism Single-Cell RNA-Seq
Sebé-Pedrós, A., Saudemont, B., Chomsky, E., Plessier, F., Mailhé, M.-P., Renno, J., Loe-Mie, Y., Lifshitz, A., Mukamel, Z., Schmutz, S., et al. (2018) · Cell · doi:10.1016/j.cell.2018.05.019 · Cited by 330
Self-citationCtenophore relationships and their placement as the sister group to all other animals
Whelan, N. V., Kocot, K. M., Moroz, T. P., Mukherjee, K., Williams, P., Paulay, G., Moroz, L. L., & Halanych, K. M. (2017) · Nature Ecology & Evolution · doi:10.1038/s41559-017-0331-3 · Cited by 263
Early metazoan cell type diversity and the evolution of multicellular gene regulation
Sebé-Pedrós, A., Chomsky, E., Pang, K., Lara‐Astiaso, D., Gaiti, F., Mukamel, Z., Amit, I., Hejnol, A., Degnan, B. M., & Tanay, A. (2018) · Nature Ecology & Evolution · doi:10.1038/s41559-018-0575-6 · Cited by 301
Self-citationBudd, G. E., & Jensen, S. (2017) · Biological Reviews · doi:10.1111/brv.12239 · Cited by 242
Independent origins of neurons and synapses: insights from ctenophores
Moroz, L. L., & Kohn, A. B. (2016) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2015.0041 · Cited by 171
Spectrin- and Ankyrin-Based Membrane Domains and the Evolution of Vertebrates
Bennett, V., & Lorenzo, D. N. (2013) · Current topics in membranes · doi:10.1016/b978-0-12-417027-8.00001-5 · Cited by 159
Evolution and Classification of Myosins, a Paneukaryotic Whole-Genome Approach
Sebé-Pedrós, A., Grau‐Bové, X., Richards, T. A., & Ruiz‐Trillo, I. (2014) · Genome Biology and Evolution · doi:10.1093/gbe/evu013 · Cited by 162
Elements of a ‘nervous system’ in sponges
Leys, S. P. (2015) · Journal of Experimental Biology · doi:10.1242/jeb.110817 · Cited by 138
Medusozoan genomes inform the evolution of the jellyfish body plan
Khalturin, K., Shinzato, C., Khalturina, M., Hamada, M., Fujie, M., Koyanagi, R., Kanda, M., Goto, H., Anton‐Erxleben, F., Toyokawa, M., et al. (2019) · Nature Ecology & Evolution · doi:10.1038/s41559-019-0853-y · Cited by 135
Gut-like ectodermal tissue in a sea anemone challenges germ layer homology
Steinmetz, P. R. H., Aman, A. J., Kraus, J. E. M., & Technau, U. (2017) · Nature Ecology & Evolution · doi:10.1038/s41559-017-0285-5 · Cited by 135
Self-citationConvergent evolution of neural systems in ctenophores
Moroz, L. L. (2015) · Journal of Experimental Biology · doi:10.1242/jeb.110692 · Cited by 134
Röttinger, E., Dahlin, P., & Martindale, M. Q. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1003164 · Cited by 140
Cilia and the life of ctenophores
Tamm, S. L. (2014) · Invertebrate Biology · doi:10.1111/ivb.12042 · Cited by 129
Brunet, T., & Arendt, D. (2015) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0043 · Cited by 130
Chari, T., Weissbourd, B., Gehring, J., Ferraioli, A., Leclère, L., Herl, M., Gao, F., Chevalier, S., Copley, R. R., Houliston, E., et al. (2021) · Science Advances · doi:10.1126/sciadv.abh1683 · Cited by 123
Self-citationGastric pouches and the mucociliary sole: setting the stage for nervous system evolution
Arendt, D., Benito-Gutierrez, E., Brunet, T., & Marlow, H. (2015) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2015.0286 · Cited by 112
Support for a clade of Placozoa and Cnidaria in genes with minimal compositional bias
Laumer, C. E., Gruber-Vodicka, H., Hadfield, M. G., Pearse, V. B., Riesgo, A., Marioni, J. C., & Giribet, G. (2018) · eLife · doi:10.7554/elife.36278 · Cited by 112
Lee, K. H., Sulbarán, G., Yang, S., Mun, J. Y., Álamo, L., Pinto, A., Satō, O., Ikebe, M., Liu, X., Korn, E. D., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1715247115 · Cited by 112
Diversity of Cnidarian Muscles: Function, Anatomy, Development and Regeneration
Leclère, L., & Röttinger, É. (2017) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2016.00157 · Cited by 108
The evolutionary origin of bilaterian smooth and striated myocytes
Brunet, T., Fischer, A., Steinmetz, P. R. H., Lauri, A., Bertucci, P., & Arendt, D. (2016) · eLife · doi:10.7554/elife.19607 · Cited by 103
Self-citationFunctions of crystallins in and out of lens: Roles in elongated and post-mitotic cells
Slingsby, C., & Wistow, G. J. (2014) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2014.02.006 · Cited by 98
Self-repairing symmetry in jellyfish through mechanically driven reorganization
Abrams, M. J., Basinger, T., Yuan, W., Guo, C., & Goentoro, L. A. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1502497112 · Cited by 94
Slime travelers: Early evidence of animal mobility and feeding in an organic mat world
Evans, S. D., Gehlîng, J. G., & Droser, M. L. (2019) · Geobiology · doi:10.1111/gbi.12351 · Cited by 89
The Musculature of Coleoid Cephalopod Arms and Tentacles
Kier, W. M. (2016) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2016.00010 · Cited by 84
Early animal evolution: a morphologist's view
Nielsen, C. (2019) · Royal Society Open Science · doi:10.1098/rsos.190638 · Cited by 77
Evolutionary cell type mapping with single-cell genomics
Tanay, A., & Sebé-Pedrós, A. (2021) · Trends in Genetics · doi:10.1016/j.tig.2021.04.008 · Cited by 76
The developmental biology of Charnia and the eumetazoan affinity of the Ediacaran rangeomorphs
Dunn, F. S., Liu, A., Grazhdankin, D. V., Vixseboxse, P. B., Flannery‐Sutherland, J. T., Green, E., Harris, S., Wilby, P. R., & Donoghue, P. C. J. (2021) · Science Advances · doi:10.1126/sciadv.abe0291 · Cited by 80
Convergence of ion channel genome content in early animal evolution
Liebeskind, B. J., Hillis, D. M., & Zakon, H. H. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1501195112 · Cited by 76
Senatore, A., Raiss, H., & Le, P. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00481 · Cited by 77
P05 imaging beamline at PETRA III: first results
Greving, I., Wilde, F., Ogurreck, M., Herzen, J., Hammel, J. U., Hipp, A. C., Friedrich, F., Lottermoser, L., Dose, T., Burmester, H., et al. (2014) · Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE · doi:10.1117/12.2061768 · Cited by 75
Self-citationMyogenesis in the sea urchin embryo: the molecular fingerprint of the myoblast precursors
Andrikou, C., Iovene, E., Rizzo, F. M., Oliveri, P., & Arnone, M. I. (2013) · EvoDevo · doi:10.1186/2041-9139-4-33 · Cited by 73
Novel scenarios of early animal evolution--is it time to rewrite textbooks?
Dohrmann, M., & Worheide, G. (2013) · Integrative and Comparative Biology · doi:10.1093/icb/ict008 · Cited by 71
Self-citationAssmann, M., Kuhn, A., Dürrnagel, S., Holstein, T. W., & Gründer, S. (2014) · BMC Biology · doi:10.1186/s12915-014-0084-2 · Cited by 70
Multiple Origins of Neurons From Secretory Cells
Moroz, L. L. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.669087 · Cited by 67
Complex Homology and the Evolution of Nervous Systems
Liebeskind, B. J., Hillis, D. M., Zakon, H. H., & Hofmann, H. A. (2015) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2015.12.005 · Cited by 72
Telford, M. J., Moroz, L. L., & Halanych, K. M. (2016) · Nature · doi:10.1038/529286a · Cited by 65
The genome of the giant Nomura’s jellyfish sheds light on the early evolution of active predation
Kim, H., Weber, J. A., Lee, N., Park, S. G., Cho, Y. S., Bhak, Y., Lee, N., Jeon, Y., Jeon, S., Luria, V., et al. (2019) · BMC Biology · doi:10.1186/s12915-019-0643-7 · Cited by 66
Alp/Enigma Family Proteins Cooperate in Z-Disc Formation and Myofibril Assembly
Katzemich, A. R., Liao, K. A., Czerniecki, S., & Schöck, F. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003342 · Cited by 63
Dicyemida and Orthonectida: Two Stories of Body Plan Simplification
Zverkov, O. A., Mikhailov, K. V., Isaev, S. V., Rusin, L. Y., Popova, O. V., Logacheva, M. D., Penin, A. A., Moroz, L. L., Panchin, Y. V., Lyubetsky, V., et al. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.00443 · Cited by 65
Hilgers, L., Hartmann, S. A., Hofreiter, M., & von Rintelen, T. (2018) · Molecular Biology and Evolution · doi:10.1093/molbev/msy052 · Cited by 57
An invertebrate smooth muscle with striated muscle myosin filaments
Sulbarán, G., Álamo, L., Pinto, A., Márquez, G., Méndez, F. J., Padrón, R., & Craig, R. W. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1513439112 · Cited by 59
Poorly Understood Aspects of Striated Muscle Contraction
Månsson, A., Rassier, D. E., & Tsiavaliaris, G. (2015) · BioMed Research International · doi:10.1155/2015/245154 · Cited by 58
Pervasive Correlated Evolution in Gene Expression Shapes Cell and Tissue Type Transcriptomes
Liang, C., Musser, J. M., Cloutier, A., Prum, R. O., & Wagner, G. P. (2018) · Genome Biology and Evolution · doi:10.1093/gbe/evy016 · Cited by 54
Kwon, O. K., Kim, S. J., & Lee, S. (2018) · Scientific Reports · doi:10.1038/s41598-018-22069-3 · Cited by 59
Structural evolution of cell types by step-wise assembly of cellular modules
Achim, K., & Arendt, D. (2014) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2014.05.001 · Cited by 56
Peptide-gated ion channels and the simple nervous system of Hydra
Gründer, S., & Assmann, M. (2015) · Journal of Experimental Biology · doi:10.1242/jeb.111666 · Cited by 54
Expression of skeletogenic genes during arm regeneration in the brittle star Amphiura filiformis
Czarkwiani, A., Dylus, D. V., & Oliveri, P. (2013) · Gene Expression Patterns · doi:10.1016/j.gep.2013.09.002 · Cited by 55
Development and epithelial organisation of muscle cells in the sea anemone Nematostella vectensis
Jahnel, S. M., Walzl, M., & Technau, U. (2014) · Frontiers in Zoology · doi:10.1186/1742-9994-11-44 · Cited by 57
Self-citationThe ancient sarcomeric myosins found in specialized muscles
Lee, L. A., Karabina, A., Broadwell, L. J., & Leinwand, L. A. (2019) · Skeletal Muscle · doi:10.1186/s13395-019-0192-3 · Cited by 62
Adoption of conserved developmental genes in development and origin of the medusa body plan
Kraus, J. E. M., Fredman, D., Wang, W., Khalturin, K., & Technau, U. (2015) · EvoDevo · doi:10.1186/s13227-015-0017-3 · Cited by 54
Self-citationHydrozoan insights in animal development and evolution
Leclère, L., Copley, R. R., Momose, T., & Houliston, E. (2016) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2016.07.006 · Cited by 52
Self-citationFrom single neurons to behavior in the jellyfish Aurelia aurita
Pallasdies, F., Goedeke, S., Braun, W., & Memmesheimer, R.-M. (2019) · eLife · doi:10.7554/elife.50084 · Cited by 54
Neuromuscular organization of the Ctenophore Pleurobrachia bachei
Norekian, T. P., & Moroz, L. L. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24546 · Cited by 52
Andrikou, C., Pai, C.-Y., Su, Y., & Arnone, M. I. (2015) · eLife · doi:10.7554/elife.07343 · Cited by 51
Acoel regeneration mechanisms indicate an ancient role for muscle in regenerative patterning
Raz, A. A., Srivastava, M., Salvamoser, R., & Reddien, P. W. (2017) · Nature Communications · doi:10.1038/s41467-017-01148-5 · Cited by 47
Woodhead, J. L., Zhao, F.-Q., & Craig, R. W. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1218462110 · Cited by 50
Moran, Y., & Zakon, H. H. (2014) · Genome Biology and Evolution · doi:10.1093/gbe/evu177 · Cited by 52
The Genome of Intoshia linei Affirms Orthonectids as Highly Simplified Spiralians
Mikhailov, K. V., Slyusarev, G. S., Nikitin, M. A., Logacheva, M. D., Penin, A. A., Aleoshin, V. V., & Panchin, Y. V. (2016) · Current Biology · doi:10.1016/j.cub.2016.05.007 · Cited by 50
Evolution of Animal Neural Systems
Liebeskind, B. J., Hofmann, H. A., Hillis, D. M., & Zakon, H. H. (2017) · Annual Review of Ecology Evolution and Systematics · doi:10.1146/annurev-ecolsys-110316-023048 · Cited by 55
At the origin of animals: the revolutionary Cambrian fossil record
Budd, G. (2013) · Current Genomics · doi:10.2174/13892029113149990011 · Cited by 44
MRTF specifies a muscle-like contractile module in Porifera
Colgren, J. J., & Nichols, S. (2022) · Nature Communications · doi:10.1038/s41467-022-31756-9 · Cited by 45
The nebulin repeat protein Lasp regulates I-band architecture and filament spacing in myofibrils
Fernandes, I., & Schöck, F. (2014) · The Journal of Cell Biology · doi:10.1083/jcb.201401094 · Cited by 47
Think like a sponge: The genetic signal of sensory cells in sponges
Mah, J. L., & Leys, S. P. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2017.06.012 · Cited by 44
Servetnick, M. D., Steinworth, B. M., Babonis, L. S., Simmons, D., Salinas‐Saavedra, M., & Martindale, M. Q. (2017) · Development · doi:10.1242/dev.145839 · Cited by 45
Nödl, M., Fossati, S. M., Domíngues, P., Sánchez, F. J., & Zullo, L. (2015) · EvoDevo · doi:10.1186/s13227-015-0012-8 · Cited by 46
Huxleys’ Missing Filament: Form and Function of Titin in Vertebrate Striated Muscle
Lindstedt, S. L., & Nishikawa, K. C. (2016) · Annual Review of Physiology · doi:10.1146/annurev-physiol-022516-034152 · Cited by 43
Myofibril diameter is set by a finely tuned mechanism of protein oligomerization in Drosophila
González‐Morales, N., Xiao, Y. S., Schilling, M. A., Marescal, O., Liao, K. A., & Schöck, F. (2019) · eLife · doi:10.7554/elife.50496 · Cited by 45
Constructional and functional anatomy of Ediacaran rangeomorphs
Butterfield, N. J. F. (2020) · Geological Magazine · doi:10.1017/s0016756820000734 · Cited by 47
Homology versus Convergence in Resolving Transphyletic Correspondences of Brain Organization
Strausfeld, N. J., & Hirth, F. (2013) · Brain Behavior and Evolution · doi:10.1159/000356102 · Cited by 45
Padrón, R., Ma, W., Duno-Miranda, S., Koubassova, N. A., Lee, K. H., Pinto, A., Álamo, L., Bolaños, P., Tsaturyan, A. K., Irving, T. C., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1921312117 · Cited by 44
Álamo, L., Pinto, A., Sulbarán, G., Mavárez, J., & Padrón, R. (2017) · Biophysical Reviews · doi:10.1007/s12551-017-0292-4 · Cited by 41
Neural system and receptor diversity in the ctenophore Beroe abyssicola
Norekian, T. P., & Moroz, L. L. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24633 · Cited by 41
Investigation of structural proteins in sea cucumber (Apostichopus japonicus) body wall
Wang, Y., Tian, M., Chang, Y., Xue, C., & Li, Z. (2020) · Scientific Reports · doi:10.1038/s41598-020-75580-x · Cited by 44
Norekian, T. P., & Moroz, L. L. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24770 · Cited by 40
The evo‐devo of molluscs: Insights from a genomic perspective
Yang, Z., Zhang, L., Hu, J., Wang, J., Bao, Z., & Wang, S. (2020) · Evolution & Development · doi:10.1111/ede.12336 · Cited by 40
The evolution of the dystroglycan complex, a major mediator of muscle integrity
Adams, J. C., & Brancaccio, A. (2015) · Biology Open · doi:10.1242/bio.012468 · Cited by 35
Yan, Z., Yan, Z., Liu, S., Yin, Y., Yang, T. L., & Chen, Q. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.714567 · Cited by 37
Smith, C. L., Abdallah, S., Wong, Y. Y., Le, P., Harracksingh, A. N., Artinian, L. R., Tamvacakis, A. N., Rehder, V., Reese, T. S., & Senatore, A. (2017) · The Journal of General Physiology · doi:10.1085/jgp.201611683 · Cited by 39
Degnan, B. M., Adamska, M., Richards, G. S., Larroux, C., Leininger, S., Bergum, B., Calcino, A., Taylor, K., Nakanishi, N., & Degnan, B. M. (2015) · Springer eBooks · doi:10.1007/978-3-7091-1862-7_4 · Cited by 38
Self-citationThe emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development
Nogueira, J. M., Hawrot, K., Sharpe, C. R., Noble, A. M., Wood, W. M., Jorge, É. C., Goldhamer, D. J., Kardon, G., & Dietrich, S. (2015) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2015.00062 · Cited by 36
The Cosmic Zoo: The (Near) Inevitability of the Evolution of Complex, Macroscopic Life
Bains, W., & Schulze‐Makuch, D. (2016) · Life · doi:10.3390/life6030025 · Cited by 37
Evo-devo of non-bilaterian animals
Lanna, E. (2015) · Genetics and Molecular Biology · doi:10.1590/s1415-475738320150005 · Cited by 34
Did the notochord evolve from an ancient axial muscle? The axochord hypothesis
Brunet, T., Lauri, A., & Arendt, D. (2015) · BioEssays · doi:10.1002/bies.201500027 · Cited by 34
Molecular Motor Transport through Hollow Nanowires
Lard, M., ten Siethoff, L., Generosi, J., Månsson, A., & Linke, H. (2014) · Nano Letters · doi:10.1021/nl404714b · Cited by 34
Hammel, J. U., & Nickel, M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0113153 · Cited by 35
Self-citationDo Actomyosin Single-Molecule Mechanics Data Predict Mechanics of Contracting Muscle?
Månsson, A., Ušaj, M., Moretto, L., & Rassier, D. E. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19071863 · Cited by 34
Regulation and evolution of muscle development in tunicates
Razy‐Krajka, F., & Stolfi, A. (2019) · EvoDevo · doi:10.1186/s13227-019-0125-6 · Cited by 33
A myxozoan genome reveals mosaic evolution in a parasitic cnidarian
Guo, Q., Atkinson, S. D., Xiao, B., Zhai, Y., Bartholomew, J. L., & Gu, Z. (2022) · BMC Biology · doi:10.1186/s12915-022-01249-8 · Cited by 31
Cole, A. G., Jahnel, S. M., Kaul, S., Steger, J., Hagauer, J., Denner, A., Murguia, P. F., Taudes, E., Zimmermann, B., Reischl, R., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-37220-6 · Cited by 28
Self-citationCellular Processes in Myxozoans
Feist, S. W., Morris, D. J., Alama-Bermejo, G., & Holzer, A. S. (2015) · Springer eBooks · doi:10.1007/978-3-319-14753-6_8 · Cited by 34
Chiodin, M., Børve, A., Berezikov, E., Ladurner, P., Martı́nez, P., & Hejnol, A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055499 · Cited by 32
The enigmatic Placozoa part 1: Exploring evolutionary controversies and poor ecological knowledge
Schierwater, B., Osigus, H., Bergmann, T., Blackstone, N. W., Hadrys, H., Hauslage, J., Humbert, P. O., Kamm, K., Kvansakul, M., Wysocki, K., et al. (2021) · BioEssays · doi:10.1002/bies.202100080 · Cited by 32
Hartigan, A., Estensoro, I., Vancová, M., Bílý, T., Patra, S., Eszterbauer, E., & Holzer, A. S. (2016) · Scientific Reports · doi:10.1038/srep39093 · Cited by 32
All for One and One for All: Regenerating Skeletal MusclePreprint
Hindi, S. M., & Millay, D. P. (2021) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a040824 · Cited by 29
Metadata
- Authors
- Steinmetz, P. R. H., Kraus, J. E. M., Larroux, C., Hammel, J. U., Amon-Hassenzahl, A., Houliston, E., Wörheide, G., Nickel, M., Degnan, B. M., & Technau, U.
- Affiliations
- University of Vienna (AT)
- The University of Queensland (AU)
- Friedrich Schiller University Jena (DE)
- Technische Universität Darmstadt (DE)
- Centre National de la Recherche Scientifique (FR)
- Bayerische Staatssammlung für Paläontologie und Geologie (DE)
- Corresponding author
- Technau, Ulrich
- ORCID
- Venue
- Nature
- Published
- 2012-06-27
- Volume
- 487
- Issue
- 7406
- Pages
- 231-234
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3398149
- OpenAlex
- W2005570641
- Cited by
- 252
- References
- 78
- Citations by year
- 2026: 11 · 2025: 15 · 2024: 5 · 2023: 13 · 2022: 19 · 2021: 19 · 2020: 15 · 2019: 24 · 2018: 20 · 2017: 17 · 2016: 23 · 2015: 33 · 2014: 16 · 2013: 19 · 2012: 3
- FWCI
- 16.89
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- HAL (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Marine Invertebrate Physiology and Ecology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Keywords
- convergent evolution, Cnidaria, bilaterians, muscle proteins, sponges, ctenophores, jellyfish, Z-disc proteins, contractile apparatus, muscle ultrastructure, titin, troponin, functional diversification
- MeSH terms
- Animals, Cnidaria, Biological Evolution, Gene Expression Regulation, Phylogeny, Myosin Heavy Chains, Gene Duplication, Muscle, Striated
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review