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
The Pfam protein families database
Finn, R. D., Mistry, J., Tate, J., Coggill, P., Heger, A., Pollington, J. E., Gavin, O. L., Gunasekaran, P., Ceric, G., Forslund, K., et al. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkp985 · Cited by 2,694
Non-muscle myosin II takes centre stage in cell adhesion and migration
Vicente‐Manzanares, M., Ma, X., Adelstein, R. S., & Horwitz, A. R. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2786 · Cited by 2,137
InterPro: the integrative protein signature database
Hunter, S., Apweiler, R., Attwood, T. K., Bairoch, A., Bateman, A., Binns, D., Bork, P., Das, U., Daugherty, L., Duquenne, L., et al. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkn785 · Cited by 2,107
Somlyo, A. P., & Somlyo, A. V. (2003) · Physiological Reviews · doi:10.1152/physrev.00023.2003 · Cited by 2,012
The genome sequence of Schizosaccharomyces pombe
Wood, V., Gwilliam, R., Rajandream, M.-A., Lyne, M. H., Lyne, R., Stewart, A., SGOUROS, J. G., Peat, N., Hayles, J., Baker, S. G., et al. (2002) · Nature · doi:10.1038/nature724 · Cited by 1,671
The amphioxus genome and the evolution of the chordate karyotype
Putnam, N. H., Butts, T., Ferrier, D. E. K., Furlong, R. F., Hellsten, U., Kawashima, T., Robinson‐Rechavi, M., Shoguchi, E., Terry, A., Yu, J., et al. (2008) · Nature · doi:10.1038/nature06967 · Cited by 1,595
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 genome of the social amoeba Dictyostelium discoideum
Eichinger, L., Pachebat, J. A., Glöckner, G., Rajandream, M.-A., Sucgang, R., Berriman, M., Song, J., Olsen, R., Szafranski, K., Xu, Q., et al. (2005) · Nature · doi:10.1038/nature03481 · Cited by 1,351
Parallel Metropolis coupled Markov chain Monte Carlo for Bayesian phylogenetic inference
Altekar, G., Dwarkadas, S., Huelsenbeck, J. P., & Ronquist, F. (2004) · Bioinformatics · doi:10.1093/bioinformatics/btg427 · Cited by 1,149
The genome of the choanoflagellate Monosiga brevicollis and the origin of metazoans
King, N., Westbrook, M. J., Young, S. L., Kuo, A., Abedin, M., Chapman, J., Fairclough, S., Hellsten, U., Isogai, Y., Letunic, I., et al. (2008) · Nature · doi:10.1038/nature06617 · Cited by 1,139
TRIM family proteins and their emerging roles in innate immunity
Ozato, K., Shin, D., Chang, T.-H., & Morse, H. C. (2008) · Nature reviews. Immunology · doi:10.1038/nri2413 · Cited by 1,131
The 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
Self-citationThe Trichoplax genome and the nature of placozoans
Srivastava, M., Begovic, E., Chapman, J., Putnam, N. H., Hellsten, U., Kawashima, T., Kuo, A., Mitros, T., Salamov, A., Carpenter, M. L., et al. (2008) · Nature · doi:10.1038/nature07191 · Cited by 889
The Selaginella Genome Identifies Genetic Changes Associated with the Evolution of Vascular Plants
Banks, J. A., Nishiyama, T., Hasebe, M., Bowman, J. L., Gribskov, M., dePamphilis, C. W., Albert, V. A., Aono, N., Aoyama, T., Ambrose, B. A., et al. (2011) · Science · doi:10.1126/science.1203810 · Cited by 867
Using the Acropora digitifera genome to understand coral responses to environmental change
Shinzato, C., Shoguchi, E., Kawashima, T., Hamada, M., Hisata, K., Tanaka, M., Fujie, M., Fujiwara, M., Koyanagi, R., Ikuta, T., et al. (2011) · Nature · doi:10.1038/nature10249 · Cited by 855
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-citationStriated Muscle Cytoarchitecture: An Intricate Web of Form and Function
Clark, K. A., McElhinny, A., Beckerle, M. C., & Gregorio, C. C. (2002) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.18.012502.105840 · Cited by 705
Phylogenomics Revives Traditional Views on Deep Animal Relationships
Philippe, H., Derelle, R., Lopez, P., Pick, K., Borchiellini, C., Boury-Esnault, N., Vacelet, J., Renard, E., Houliston, E., Quéinnec, E., et al. (2009) · Current Biology · doi:10.1016/j.cub.2009.02.052 · Cited by 695
Self-citationDedicated Myosin Light Chain Kinases with Diverse Cellular Functions
Kamm, K. E., & Stull, J. T. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.r000028200 · Cited by 574
The troponin complex and regulation of muscle contraction
Farah, C. S., & Reinach, F. C. (1995) · The FASEB Journal · doi:10.1096/fasebj.9.9.7601340 · Cited by 572
The Genome of Naegleria gruberi Illuminates Early Eukaryotic Versatility
Fritz‐Laylin, L. K., Prochnik, S. E., Ginger, M. L., Dacks, J. B., Carpenter, M. L., Field, M. C., Kuo, A., Paredez, A. R., Chapman, J., Pham, J. K., et al. (2010) · Cell · doi:10.1016/j.cell.2010.01.032 · Cited by 472
Martindale, M. Q., Pang, K., & Finnerty, J. R. (2004) · Development · doi:10.1242/dev.01119 · Cited by 396
Fernández‐Fueyo, E., Ruiz-Dueñas, F. J., Ferreira, P., Floudas, D., Hibbett, D. S., Canessa, P., Larrondo, L. F., James, T. Y., Daniela Seelenfreund, H., Sergio Lobos, A., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1119912109 · Cited by 298
Muscle Giants: Molecular Scaffolds in Sarcomerogenesis
Kontrogianni‐Konstantopoulos, A., Ackermann, M. A., Bowman, A. L., Yap, S. V., & Bloch, R. J. (2009) · Physiological Reviews · doi:10.1152/physrev.00017.2009 · Cited by 268
The Evolution of Organ Systems
Schmidt‐Rhaesa, A. (2007) · doi:10.1093/acprof:oso/9780198566687.001.0001 · Cited by 264
The sarcomeric Z-disc: a nodal point in signalling and disease
Frank, D., Kuhn, C., Katus, H. A., & Frey, N. (2006) · Journal of Molecular Medicine · doi:10.1007/s00109-005-0033-1 · Cited by 235
Structure and function of myosin filaments
Craig, R., & Woodhead, J. L. (2006) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2006.03.006 · Cited by 232
Induction of gametogenesis in the basal cnidarian Nematostella vectensis (Anthozoa)
Fritzenwanker, J. H., & Technau, U. (2002) · Development Genes and Evolution · doi:10.1007/s00427-002-0214-7 · Cited by 218
Self-citationCytological Basis of Photoresponsive Behavior in a Sponge Larva
Leys, S. P., & Degnan, B. M. (2001) · The Biological Bulletin · doi:10.2307/1543611 · Cited by 212
Self-citationThe origins of multicellularity: a multi-taxon genome initiative
Ruiz‐Trillo, I., Burger, G., Holland, P. W. H., King, N., Lang, B. F., Roger, A. J., & Gray, M. W. (2007) · Trends in Genetics · doi:10.1016/j.tig.2007.01.005 · Cited by 208
Smooth muscle signalling pathways in health and disease
Kim, H. R., Appel, S., Vetterkind, S., Gangopadhyay, S. S., & Morgan, K. G. (2008) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2008.00552.x · Cited by 204
Invertebrate Muscles: Muscle Specific Genes and Proteins
Hooper, S. L., & Thuma, J. B. (2005) · Physiological Reviews · doi:10.1152/physrev.00019.2004 · Cited by 190
Larroux, C., Fahey, B., Liubicich, D., Hinman, V. F., Gauthier, M., Gongora, M., Green, K., Wörheide, G., Leys, S. P., & Degnan, B. M. (2006) · Evolution & Development · doi:10.1111/j.1525-142x.2006.00086.x · Cited by 173
Self-citationEvolution of striated muscle: Jellyfish and the origin of triploblasty
Seipel, K., & Schmid, V. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.03.032 · Cited by 172
Goodson, H. V., & Spudich, J. A. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.2.659 · Cited by 169
Torruella, G., Derelle, R., Paps, J., Lang, B. F., Roger, A. J., Shalchian-Tabrizi, K., & Ruiz-Trillo, I. (2012) · Molecular Biology and Evolution · doi:10.1093/molbev/msr185 · Cited by 169
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-citationRyan, J. F., Pang, K., Program, N. C. S., Mullikin, J. C., Martindale, M. Q., & Baxevanis, A. D. (2010) · EvoDevo · doi:10.1186/2041-9139-1-9 · Cited by 160
Hooper, S. L., Hobbs, K. H., & Thuma, J. B. (2008) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2008.06.004 · Cited by 148
Adamska, M., Larroux, C., Adamski, M., Green, K., Lovas, E., Koop, D., Richards, G. S., Zwafink, C., & Degnan, B. M. (2010) · Evolution & Development · doi:10.1111/j.1525-142x.2010.00435.x · Cited by 139
Self-citationKinetics and rhythm of body contractions in the spongeTethya wilhelma(Porifera: Demospongiae)
Nickel, M. (2004) · Journal of Experimental Biology · doi:10.1242/jeb.01289 · Cited by 120
Self-citationNakagawa, N., Hoshijima, M., Oyasu, M., Saito, N., Tanizawa, K., & Kuroda, S. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.2787 · Cited by 102
Sarcomere Formation Occurs by the Assembly of Multiple Latent Protein Complexes
Rui, Y., Bai, J., & Perrimon, N. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001208 · Cited by 102
Burkart, C., Qiu, F., Brendel, S., Beneš, V., Hååg, P., Labeit, S., Leonard, K., & Bullard, B. (2007) · Journal of Molecular Biology · doi:10.1016/j.jmb.2007.01.059 · Cited by 98
Klaavuniemi, T., Kelloniemi, A., & Ylänne, J. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m401871200 · Cited by 90
RNAs everywhere: genome‐wide annotation of structured RNAs
Backofen, R., Bernhart, S. H., Flamm, C., Fried, C., Guido Fritzsch, A., Hackermüller, J., Jana Hertel, A., Hofacker, I. L., Kristin Missal, A., Mosig, A., et al. (2006) · Journal of Experimental Zoology Part B Molecular and Developmental Evolution · doi:10.1002/jez.b.21130 · Cited by 90
The Dynamic Z Bands of Striated Muscle Cells
Sanger, J. M., & Sanger, J. W. (2008) · Science Signaling · doi:10.1126/scisignal.132pe37 · Cited by 89
Nickel, M., Scheer, C., Hammel, J. U., Herzen, J., & Beckmann, F. (2011) · Journal of Experimental Biology · doi:10.1242/jeb.049148 · Cited by 89
Self-citationPhylogenetic relationship of muscle tissues deduced from superimposition of gene trees
Oota, S., & Saitou, N. (1999) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a026170 · Cited by 88
Molecular Architecture in Muscle Contractile Assemblies
Squire, J. M., AL-Khayat, H. A., Knupp, C., & Luther, P. K. (2005) · Advances in protein chemistry · doi:10.1016/s0065-3233(04)71002-5 · Cited by 86
Coevolution of head, neck, and tail domains of myosin heavy chains
Korn, E. D. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.230441597 · Cited by 77
Chevalier, S., Martin, A., Leclère, L., Amiel, A., & Houliston, E. (2006) · Development Genes and Evolution · doi:10.1007/s00427-006-0103-6 · Cited by 75
Self-citationChapman, D. M. F. (1974) · Elsevier eBooks · doi:10.1016/b978-0-12-512150-7.50006-2 · Cited by 73
Boelsterli, U. (1977) · Journal of Morphology · doi:10.1002/jmor.1051540206 · Cited by 69
Insights from diploblasts; the evolution of mesoderm and muscle
Burton, P. M. (2007) · Journal of Experimental Zoology Part B Molecular and Developmental Evolution · doi:10.1002/jez.b.21150 · Cited by 69
Structure and function of the prehensile tentilla of Euplokamis (Ctenophora, Cydippida)
Mackie, G. O., Mills, C. E., & Singla, C. L. (1988) · Zoomorphology · doi:10.1007/bf00312216 · Cited by 67
Molecular evolution of immunoglobulin and fibronectin domains in titin and related muscle proteins
Kenny, P. A., Liston, E. M., & Higgins, D. G. (1999) · Gene · doi:10.1016/s0378-1119(99)00122-5 · Cited by 66
In Situ Hybridization of Starlet Sea Anemone (Nematostella vectensis) Embryos, Larvae, and PolypsPreprint
Genikhovich, G., & Technau, U. (2009) · Cold Spring Harbor Protocols · doi:10.1101/pdb.prot5282 · Cited by 66
Self-citationNebulin: A Study of Protein Repeat Evolution
Björklund, Å. K., Light, S., Sagit, R., & Elofsson, A. (2010) · Journal of Molecular Biology · doi:10.1016/j.jmb.2010.07.011 · Cited by 61
Sutter, S. B., Raeker, M. Ö., Borisov, A. B., & Russell, M. W. W. (2004) · Development Genes and Evolution · doi:10.1007/s00427-004-0413-5 · Cited by 47
Fontdevila, A. (2011) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780199541379.001.0001 · Cited by 42
Life stage specific expression of a myosin heavy chain in the hydrozoan Podocoryne carnea
Schuchert, P., Reber-Müller, S., & Schmid, V. (1993) · Differentiation · doi:10.1111/j.1432-0436.1993.tb00654.x · Cited by 41
Nickel, M., Donath, T., Schweikert, M., & Beckmann, F. (2006) · Zoomorphology · doi:10.1007/s00435-006-0021-1 · Cited by 41
Self-citationHammel, J. U., Herzen, J., Beckmann, F., & Nickel, M. (2009) · Frontiers in Zoology · doi:10.1186/1742-9994-6-19 · Cited by 38
Self-citationAyme-Southgate, A., Southgate, R., Philipp, R. A., Sotka, E. E., & Kramp, C. R. (2008) · Journal of Molecular Evolution · doi:10.1007/s00239-008-9177-2 · Cited by 23
Whole-Mount In Situ Hybridization in AmphimedonPreprint
Larroux, C., Fahey, B., Adamska, M., Richards, G. S., Gauthier, M., Green, K., Lovas, E. M., & Degnan, B. M. (2008) · Cold Spring Harbor Protocols · doi:10.1101/pdb.prot5096 · Cited by 21
Self-citationStructure of the amphioxus nebulin gene and evolution of the nebulin family genes
Hanashima, A., Kubokawa, K., & Kimura, S. (2009) · Gene · doi:10.1016/j.gene.2009.04.020 · Cited by 10
Hammel, R. N., & Ulrich, J. (2011) · Cited by 1
Flagged first, then by citations
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
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