The DOI matches its Crossref record; 86 of the 87 references it cites were found in a registry or an index.
Comparative Genomics of the Eukaryotes
Open accessAbstract
A comparative analysis of the genomes of Drosophila melanogaster, Caenorhabditis elegans, and Saccharomyces cerevisiae-and the proteins they are predicted to encode-was undertaken in the context of cellular, developmental, and evolutionary processes. The nonredundant protein sets of flies and worms are similar in size and are only twice that of yeast, but different gene families are expanded in each genome, and the multidomain proteins and signaling pathways of the fly and worm are far more complex than those of yeast. The fly has orthologs to 177 of the 289 human disease genes examined and provides the foundation for rapid analysis of some of the basic processes involved in human disease.
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 cited source says what the claim attributes to it.
In the citing paper
“To our knowledge, this is the first genome-wide survey and comparison of conserved elements in different groups of eukaryotic species (excluding comparisons primarily of proteomes; e.g., Rubin et al. 2000).”
From Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes (2005) · cites this paper as Rubin et al. 2000
In the citing paper
“Comparisons (4-6) between fruit fly, nematode, and vertebrate genomes reveal greater genomic complexity in the vertebrates (and other deuterostomes (7,8)) as measured by gene content and structure, but at the same time show that many genes and networks are shared across bilaterians.”
From Sea Anemone Genome Reveals Ancestral Eumetazoan Gene Repertoire and Genomic Organization (2007) · cites this paper as [4]
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
Li, P., Nijhawan, D., Budihardjo, I., Srinivasula, S. M., Ahmad, M., Alnemri, E. S., & Wang, X. (1997) · Cell · doi:10.1016/s0092-8674(00)80434-1 · Cited by 7,289
Self-citationThe Genome Sequence of Drosophila melanogaster
Adams, M. D., Celniker, S., Holt, R. A., Evans, C. A., Gocayne, J. D., Amanatides, P. G., Scherer, S. E., Li, P. W., Hoskins, R. A., Galle, R. F., et al. (2000) · Science · doi:10.1126/science.287.5461.2185 · Cited by 5,902
Self-citationWhole-Genome Random Sequencing and Assembly of Haemophilus influenzae Rd
Fleischmann, R. D., Adams, M. D., White, O. R., Clayton, R. A., Kirkness, E. F., Kerlavage, A. R., Bult, C. J., Tomb, J.-F., Dougherty, B. A., Merrick, J. M., et al. (1995) · Science · doi:10.1126/science.7542800 · Cited by 5,731
Self-citationInduction of Apoptotic Program in Cell-Free Extracts: Requirement for dATP and Cytochrome c
Liu, X., Kim, C. N., Yang, J., Jemmerson, R., & Wang, X. (1996) · Cell · doi:10.1016/s0092-8674(00)80085-9 · Cited by 5,167
Genome Sequence of the Nematode C. elegans : A Platform for Investigating Biology
Berg, J. (1998) · Science · doi:10.1126/science.282.5396.2012 · Cited by 4,458
Goffeau, A., Barrell, B. G., Bussey, H., Davis, R. W., Dujon, B., Feldmann, H., Galibert, F., Hoheisel, J. D., Jacq, C., Johnston, M., et al. (1996) · Science · doi:10.1126/science.274.5287.546 · Cited by 4,423
Molecular characterization of mitochondrial apoptosis-inducing factor
Susin, S. A., Lorenzo, H. K., Zamzami, N., Marzo, I., Snow, B. E., Brothers, G. M., Mangion, J., Jacotot, E., Costantini, P., Loeffler, M., et al. (1999) · Nature · doi:10.1038/17135 · Cited by 4,060
BCL-2 family members and the mitochondria in apoptosisPreprint
Gross, A., McDonnell, J. M., & Korsmeyer, S. J. (1999) · Genes & Development · doi:10.1101/gad.13.15.1899 · Cited by 3,642
The SWISS-PROT protein sequence data bank and its supplement TrEMBL
Bairoch, A., & Apweiler, R. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.1.31 · Cited by 3,594
Self-citationThe SWISS-PROT protein sequence data bank and its supplement TrEMBL in 1998
Bairoch, A. (1998) · Nucleic Acids Research · doi:10.1093/nar/26.1.38 · Cited by 3,275
Research works printed but not linked: 5
- K. Weber in (29) pp. 291–293.
- Blaumueller C. M., Artavanis-Tsakonas S., Perspect. Dev. Neurobiol. 4, 325 (1997);
- Park A. G., Trends Cell Biol. 10, 394 (2000);
- Miklos G. L. G., J. Am. Acad. Arts Sci. 127, 197 (1998).
- See www.sciencemag.org/feature/data/1049664.shl for complete protein domain analysis.
Cited by
Sorted by citations
Items 901–998 of 998
Abrescia, C., Sjöstrand, D., Kjaer, S., & Ibáñez, C. F. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.05.075 · Cited by 23
Evolution of Integrin I Domains
Johnson, M. S., & Chouhan, B. S. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-94-017-9153-3_1 · Cited by 22
“genomic sequence [1, 75].”
From Representational Preformationism to the Epigenesis of Openness to the World?
Moss, L. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb04920.x · Cited by 23
Hill, C. A., & Gutierrez, J. A. (2000) · Microbial & Comparative Genomics · doi:10.1089/10906590050179774 · Cited by 23
Phenotype-first screening for the identification of novel drug targets.
Austen, M., & Dohrmann, C. (2005) · Drug Discovery Today · doi:10.1016/s1359-6446(05)03368-4 · Cited by 22
Ono, Y., Fujibuchi, W., & Suwa, M. (2005) · Gene · doi:10.1016/j.gene.2005.05.038 · Cited by 23
de Rivoyre, M., Ruel, L., Varjosalo, M. T., Loubat, A., Bidet, M., Thérond, P. P., & Mus‐Veteau, I. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m512986200 · Cited by 23
Protection Effect of GDNF and Neurturin on Photosensitized Crayfish Neurons and Glial Cells
Uzdensky, A. B., Komandirov, M. A., Федоренко, Г. М., & Lobanov, A. V. (2012) · Journal of Molecular Neuroscience · doi:10.1007/s12031-012-9858-6 · Cited by 22
Adedara, A. O., Bressan, G. N., dos Santos, M. M., Fachinetto, R., Abolaji, A. O., & Barbosa, N. V. (2024) · NeuroToxicology · doi:10.1016/j.neuro.2024.02.006 · Cited by 22
Turissini, D. A., Gamez, S., & White, B. J. (2014) · Genome Biology and Evolution · doi:10.1093/gbe/evu243 · Cited by 22
Allosteric modulators of MEK1: drug design and discovery
Shang, J., Lu, S., Jiang, Y., & Zhang, J. (2016) · Chemical Biology & Drug Design · doi:10.1111/cbdd.12780 · Cited by 23
Self-citationŠkerlová, J., Lindström, H., Gonis, E., Sjödin, B., Neiers, F., Stenmark, P., & Mannervik, B. (2019) · FEBS Letters · doi:10.1002/1873-3468.13718 · Cited by 22
Post‐transcriptional suppression of pathogenic prion protein expression in Drosophila neurons
Deleault, N. R., Dolph, P. J., Feany, M. Β., Cook, M., Nishina, K. A., Harris, D. A., & Supattapone, S. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01819.x · Cited by 22
“Drosophila melanogaster has 105 neurons, and the genome of D. melanogaster contains nearly the same number of apoptosis pathway genes as Homo sapiens, and these genes are highly conserved in both sequence and function (Rubin et al. 2000).”
BackgroundEvolution of discrete Notch‐like receptors from a distant gene duplication in Caenorhabditis
Rudel, D., & Kimble, J. E. (2002) · Evolution & Development · doi:10.1046/j.1525-142x.2002.02027.x · Cited by 22
de Oliveira-Neto, O. B., Batista, J. A. N., Rigden, D. J., Fragoso, R. D. R., Silva, R. O. S., Gomes, E. A., Franco, O. L., Dias, S. C., Cordeiro, C. M. T., Monnerat, R. G., et al. (2004) · Insect Biochemistry and Molecular Biology · doi:10.1016/j.ibmb.2004.06.001 · Cited by 22
Drosophila p53: meeting the Grim Reaper
Steller, H. (2000) · Nature Cell Biology · doi:10.1038/35014093 · Cited by 22
Differential properties of the two Drosophila γ-tubulin isotypes
Raynaud‐Messina, B., Debec, A., Tollon, Y., Garès, M., & Wright, M. (2001) · European Journal of Cell Biology · doi:10.1078/0171-9335-00195 · Cited by 22
The human genome and the future of medicine
Mattick, J. S. (2003) · The Medical Journal of Australia · doi:10.5694/j.1326-5377.2003.tb05505.x · Cited by 22
Celniker, S. (2000) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(00)00140-4 · Cited by 22
Self-citationThe cloning, genomic organization and expression of the focal contact protein paxillin in Drosophila
Wheeler, G. N., & Hynes, R. O. (2001) · Gene · doi:10.1016/s0378-1119(00)00512-6 · Cited by 22
Self-citationIdentification and characterization of protein subcomplexes in yeast
Hollunder, J., Beyer, A., & Wilhelm, T. E. (2005) · PROTEOMICS · doi:10.1002/pmic.200401121 · Cited by 22
Computational prediction of gene structure and regulation in the genome of Drosophila melanogaster
Rubin, G. M., Preiss, A., & Genetik, A. (2000) · Cited by 21
Self-citationNoree, C., Sirinonthanawech, N., & Wilhelm, J. E. (2019) · Scientific Reports · doi:10.1038/s41598-018-36719-z · Cited by 21
Jia, Y., Xu, M., Hu, H., Chapman, B., Watt, C., Buerte, B., Han, N., Zhu, M., Bian, H., Li, C., et al. (2023) · BMC Biology · doi:10.1186/s12915-022-01503-z · Cited by 21
“Comparative genomics analyses across different life forms have revealed that gene families are generally conserved [11, 13], leading to the suggestion that gene duplication, instead of gene invention, is the major driving force underlying genome evolution [6, 14].”
BackgroundBinding Mechanism of the N-Terminal SH3 Domain of CrkII and Proline-Rich Motifs in cAbl
Bhatt, V. S., Zeng, D., Krieger, I. V., Sacchettini, J. C., & Cho, J. (2016) · Biophysical Journal · doi:10.1016/j.bpj.2016.05.008 · Cited by 21
Uzdensky, A. B., Berezhnaya, E. V., Khaitin, A. M., Kovaleva, V. D., Komandirov, M. A., Neginskaya, M. A., Rudkovskii, M. V., & Sharifulina, S. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9237-8 · Cited by 21
Drosophila as a model for antiviral immunity.
Wang, J.-H., Valanne, S., & Rämet, M. (2010) · World Journal of Biological Chemsitry · doi:10.4331/wjbc.v1.i5.151 · Cited by 19
Grassi, L., Fusco, D., Sellerio, A. L., Corà, D., Bassetti, B., Caselle, M., & Lagomarsino, M. C. (2010) · Molecular BioSystems · doi:10.1039/c003507f · Cited by 22
“Genomes possess a high degree of redundancy in the information they encode for [1, 2, 3, 4, 5].”
BackgroundLin, C., Hovhannisyan, V., Wu, J., Lin, C., Chen, J., Lin, S., & Dong, C. (2008) · Journal of Biomedical Optics · doi:10.1117/1.2981817 · Cited by 21
Choudhary, M., Fu, Y., Mackenzie, C., & Kaplan, S. (2004) · Journal of Bacteriology · doi:10.1128/jb.186.7.2019-2027.2004 · Cited by 22
“Genomes of most prokaryotic (20) and eukaryotic ( 34 ) species examined to date show a high degree of gene duplication, which is an ongoing process.”
BackgroundIntracellular infections in Drosophila melanogaster: Host defense and mechanisms of pathogenesis
Péan, C. B., & Dionne, M. (2013) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2013.04.013 · Cited by 23
Nozawa, M., Aotsuka, T., & Tamura, K. (2005) · Genetics · doi:10.1534/genetics.105.041699 · Cited by 20
“Many genes sharing common functional domains in different combinations (e.g., Rubin et al. 2000; Li et al. 2001) indicate a substantial contribution of exon shuffling to the diversity of genes and gene functions in genomes.”
BackgroundSystematic gene targeting on the X chromosome of Drosophila melanogaster
Beinert, N., Werner, M., Dowe, G., Chung, H., J�ckle, H., & Sch�fer, U. (2004) · Chromosoma · doi:10.1007/s00412-004-0313-5 · Cited by 21
The Vision and Challenges of the Gene Ontology
Lewis, S. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-3743-1_21 · Cited by 20
Self-citationDrosophila as a Model for Tumor-Induced Organ Wasting
Saavedra, P. H. V., & Perrimon, N. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-23629-8_11 · Cited by 20
Robustness of microbiome function
Lee, K. K., Park, Y., & Kuehn, S. (2023) · Current Opinion in Systems Biology · doi:10.1016/j.coisb.2023.100479 · Cited by 20
Alaraby, M., Villacorta, A., Abass, D., Hernández, A., & Marcos, R. (2023) · Environmental Pollution · doi:10.1016/j.envpol.2023.122968 · Cited by 20
Dhar, R., Bergmiller, T., & Wagner, A. (2014) · Evolution · doi:10.1111/evo.12373 · Cited by 22
“…in Taylor and Raes 2004), only the genomic era revealed its full extent, showing that about 20–60% of a genome’s genes can have duplicates (Himmelreich et al. 1996; Klenk et al. 1997; Tomb et al. 1997; Arabidopsis Genome Initiative, 2000; Rubin et al. 2000; Li et al. 2001; Kellis et al. 2004).”
BackgroundExperimental Evolution of Gene Duplicates in a Bacterial Plasmid Model
Holloway, A. K., Palzkill, T. G., & Bull, J. J. (2007) · Journal of Molecular Evolution · doi:10.1007/s00239-006-0087-x · Cited by 21
Muraille, É. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00223 · Cited by 20
Rosch, R. E., Burrows, D. R. W., Jones, L., Peters, C. H., Ruben, P. C., & Samarut, É. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00556 · Cited by 24
Genetic Approaches to Analyzing Mitochondrial Outer Membrane Permeability
Graham, B. H., & Craigen, W. J. (2004) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(04)59004-x · Cited by 20
Senescence in adipose-derived stem cells and its implications in nerve regeneration
Mantovani, C., Terenghi, G., & Magnaghi, V. (2014) · Neural Regeneration Research · doi:10.4103/1673-5374.125324 · Cited by 20
Медведева, А. В., Molotkov, D. A., Nikitina, E. A., Popov, A. V., Karagodin, D. A., Baricheva, E. M., & Savvateeva-Popova, E. V. (2008) · Russian Journal of Genetics · doi:10.1134/s1022795408060069 · Cited by 20
“The projects of sequencing the human genome [2] and the genomes of Drosophila [3], nematode Caenorhabditis elegans [ 4 ], and Arabidopsis thaliana [5] have shown high evolutionary conservation of genes, which provided the development of a new approach, comparative genomics.”
BackgroundCharacterization of Drosophila palmitoyl-protein thioesterase 1
Glaser, R. L., Hickey, A. J., Chotkowski, H. L., & Chu‐LaGraff, Q. (2003) · Gene · doi:10.1016/s0378-1119(03)00623-1 · Cited by 20
Src proteins/src genes: from sponges to mammals
Ćetković, H., Grebenjuk, V. A., Müller, W. E. G., & Gamulin, V. (2004) · Gene · doi:10.1016/j.gene.2004.07.044 · Cited by 20
Functional genomics in Drosophila models of human disease
Chen, K.-F., & Crowther, D. C. (2012) · Briefings in Functional Genomics · doi:10.1093/bfgp/els038 · Cited by 21
Corronc, H. L., Alix, P., & Hue, B. (2002) · Journal of Insect Physiology · doi:10.1016/s0022-1910(02)00061-6 · Cited by 20
Ara, G., Afzal, M., Jyoti, S., Naz, F., Rahul, R., & Siddique, Y. H. (2019) · Current Drug Therapy · doi:10.2174/1574885513666180529114546 · Cited by 20
Solution structure and binding specificity of FBP11/HYPA WW domain as Group‐II/III
Kato, Y. S., Hino, Y., Nagata, K., & Tanokura, M. (2006) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.20880 · Cited by 20
Amid, C., Bahr, A., Mujica, A. O., Sampson, N., Bikar, S.-E., Winterpacht, A., Zabel, B., Hankeln, T., & Schmidt, E. (2001) · Cytogenetic and Genome Research · doi:10.1159/000056999 · Cited by 20
Understanding the molecular responses to hypoxia using Drosophila as a genetic model
Farahani, R., & Haddad, G. G. (2003) · Respiratory Physiology & Neurobiology · doi:10.1016/s1569-9048(03)00049-1 · Cited by 20
Neurobiology of anxiety and fear: challenges for genomic science of the new millennium
Moldin, S. O. (2000) · Biological Psychiatry · doi:10.1016/s0006-3223(00)00943-4 · Cited by 20
Watanabe, Y., Zenke, K., Itoh, N., & Yoshinaga, T. (2021) · Aquaculture · doi:10.1016/j.aquaculture.2021.736657 · Cited by 19
Mozer, B. A. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0229 · Cited by 19
C. elegans models of neuromuscular diseases expedite translational research
Sleigh, J. N., & Sattelle, D. B. (2010) · Translational Neuroscience · doi:10.2478/v10134-010-0032-9 · Cited by 19
Evolutionary Patterns of Recently Emerged Animal Duplogs
Ezawa, K., Ikeo, K., Gojobori, T., & Saitou, N. (2011) · Genome Biology and Evolution · doi:10.1093/gbe/evr074 · Cited by 19
Lamping, E., Zhu, J., Niimi, M., & Cannon, R. D. (2017) · Genetics · doi:10.1534/genetics.116.194811 · Cited by 19
“%) of genes in all kingdoms of life are generated by gene duplication (Rubin et al. 2000; Li et al. 2001; Zhang 2002).”
BackgroundMethylmercury Exposure Induces Sexual Dysfunction in Male and Female Drosophila Melanogaster
Chauhan, V. P. S., Srikumar, S., Aamer, S., Pandareesh, M. D., & Chauhan, A. (2017) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph14101108 · Cited by 19
The Power of Drosophila Genetics: The Discovery of the Hippo Pathway
Gokhale, R. H., & Pfleger, C. M. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-8910-2_1 · Cited by 21
Contributive Role of Hyperglycemia and Hypoglycemia Towards the Development of Alzheimer’s Disease
Chakrabarty, R., Yousuf, S., & Singh, M. P. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02846-y · Cited by 20
Modeling Dilated Cardiomyopathies in Drosophila
Wolf, M. J. (2012) · Trends in Cardiovascular Medicine · doi:10.1016/j.tcm.2012.06.012 · Cited by 19
Modular assembly of genes and the evolution of new functions
Patthy, L. (2003) · Contemporary issues in genetics and evolution · doi:10.1007/978-94-010-0229-5_11 · Cited by 19
Small flies—Big discoveries: Nearly a century of Drosophila genetics and development
Letsou, A., & Bohmann, D. (2005) · Developmental Dynamics · doi:10.1002/dvdy.20307 · Cited by 19
“Indeed, when compared with mammalian proteins and expressed sequence tags, more than half of the fly proteins have similar mammalian counterparts at a statistical cutoff of E 10 10, com- pared with 36% and 38% for worm and yeast, respectively (Rubin et al., 2000).”
BackgroundAnalyzing the Function of Tumor Suppressor Genes Using a Drosophila Model
Pagliarini, R. A., Quiñones, A. T., & Xu, T. (2003) · Humana Press eBooks · doi:10.1385/1-59259-329-1:349 · Cited by 19
Proteomics methods for probing molecular mechanisms in signal transduction1
Sheffield, L. G., & Gavinski, J. J. (2003) · Journal of Animal Science · doi:10.2527/2003.81suppl_348x · Cited by 19
Current advances in molecular genetics of autosomal-dominant polycystic kidney disease
Wu, G. (2001) · Current Opinion in Nephrology & Hypertension · doi:10.1097/00041552-200101000-00005 · Cited by 19
Chen, J., Yu, Q., Zhang, T., Ma, Y., Xiao, M., Zhang, C., & Ge, Y. (2025) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2025.137959 · Cited by 18
Insect Models in Nutrition Research
Tonk, M., Vilcinskas, A., & Wagner, A. E. (2022) · Biomolecules · doi:10.3390/biom12111668 · Cited by 19
“Even so, >60% of human disease genes have homologs or even orthologs in the fruit fly genome [23].”
BackgroundLv, Y., Pan, Y., Li, J., Ding, Y., Yu, Z., Yan, K., & Shang, Q. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.126765 · Cited by 18
Self-citationvan Kesteren, R. E., Gagatek, J. S., Hagendorf, A., Gouwenberg, Y., Smit, A. B., & Syed, N. I. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06189.x · Cited by 18
“…studies predict the presence of neurotrophin-like molecules in some invertebrate species (Bothwell, 2006; Burke et al., 2006; Kassabov et al., 2007), genome sequence data suggest that genuine neurotrophins are absent in invertebrates (Chao, 2000; Rubin et al., 2000; Jaaro & Fainzilber, 2006).”
BackgroundPhytoremediation: A Green Technology
Jan, S., & Parray, J. A. (2016) · Springer eBooks · doi:10.1007/978-981-10-1693-6_5 · Cited by 18
Molecular Mechanisms of Tight Binding through Fuzzy Interactions
Shen, Q., Shi, J., Zeng, D., Zhao, B., Li, P., Hwang, W., & Cho, J. (2018) · Biophysical Journal · doi:10.1016/j.bpj.2018.01.031 · Cited by 18
Self-citationmiRNAs in Insects Infected by Animal and Plant Viruses
Monsanto‐Hearne, V., & Johnson, K. N. (2018) · Viruses · doi:10.3390/v10070354 · Cited by 19
“melanogaster exhibits genetic pathways and life cycles similar to mosquitoes [18,61,122,123].”
BackgroundDynamical binding of proline-rich peptides to their recognition domains
Gu, W., & Helms, V. (2005) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2005.07.033 · Cited by 18
Neurotrophic and Gliatrophic Contexts in Drosophila
Hidalgo, A., Learte, A. R., McQuilton, P., Pennack, J. A., & Zhu, B. (2006) · Brain Behavior and Evolution · doi:10.1159/000094086 · Cited by 18
Evolution of insect proteomes: insights into synapse organization and synaptic vesicle life cycle
Yanay, C., Morpurgo, N., & Michal Linial, B. (2008) · Genome biology · doi:10.1186/gb-2008-9-2-r27 · Cited by 18
Tandem Duplicate Genes in Maize Are Abundant and Date to Two Distinct Periods of Time
Kono, T. J. Y., Brohammer, A. B., McGaugh, S. E., & Hirsch, C. N. (2018) · G3 Genes Genomes Genetics · doi:10.1534/g3.118.200580 · Cited by 18
“Many protein coding genes in eukaryotes are part of large families of genes with related function and are consistent with origins in gene duplication (Rubin 2000).”
BackgroundLeão, M. B., da Rosa, P. C. C., Wagner, C., Lugokenski, T. H., & Corte, C. L. D. (2018) · Environmental Science and Pollution Research · doi:10.1007/s11356-018-2293-7 · Cited by 18
Fragoso, R. D. R., Batista, J. A. N., Neto, O. B. D. O., & Grossi‐de‐Sá, M. F. (2005) · Experimental Parasitology · doi:10.1016/j.exppara.2005.02.010 · Cited by 18
“In the D. melanogaster genome, these enzymes constitute the second largest gene family, with 377 diVerent sequences, whereas in the C. elegans genome serine proteinases are encoded by just 18 genes (Rubin et al., 2000).”
BackgroundSpring, J. (2003) · Springer eBooks · doi:10.1007/978-94-010-0263-9_2 · Cited by 18
Genome comparisons highlight similarity and diversity within the eukaryotic kingdoms
Ball, C. A., & Cherry, J. M. (2001) · Current Opinion in Chemical Biology · doi:10.1016/s1367-5931(00)00172-1 · Cited by 18
Self-citationA comparative genomic analysis of ESTs from Ustilago maydis
Austin, R. E., Provart, N. J., Sacadura, N. T., Nugent, K. G., Babu, M., & Saville, B. (2004) · Functional & Integrative Genomics · doi:10.1007/s10142-004-0118-x · Cited by 18
“elegans (Rubin et al. 2000).”
MethodLarge-scale mutagenesis and functional genomics in yeast
Que, Q. Q., & Winzeler, E. A. (2002) · Functional & Integrative Genomics · doi:10.1007/s10142-002-0057-3 · Cited by 18
Miao, Y., Chen, R., Wang, X., Zhang, J., Tang, W., Zhang, Z., Liu, Y., & Xu, Q. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.953490 · Cited by 18
“The fruit fly has obvious advantages as a diabetes model: (1) it is small and can be easily raised in large quantities in the laboratory (8); (2) it has a short life-cycle (10–12 days) and thus it is the data results of certain studies based on it that can be obtained quickly; (3) it has complex neuropils and neural c…”
BackgroundSelf-citationKembro, J. M., Flesia, A. G., Nieto, P. S., Caliva, J. M., Lloyd, D., Cortassa, S. C., & Aon, M. A. (2023) · Scientific Reports · doi:10.1038/s41598-023-32286-0 · Cited by 16
Drosophila as a Robust Model System for Assessing Autophagy: A Review
Demir, E., & Kacew, S. (2023) · Toxics · doi:10.3390/toxics11080682 · Cited by 18
Berglund, E. C., Kuklinski, N. J., Karagündüz, E., Ucar, K., Hanrieder, J., & Ewing, A. G. (2013) · Analytical Chemistry · doi:10.1021/ac303377x · Cited by 17
Galea, C. A., Mobli, M., McNeil, K. A., Mulhern, T. D., Wallace, J. C., King, G. F., Forbes, B. E., & Norton, R. S. (2011) · Biochimie · doi:10.1016/j.biochi.2011.09.012 · Cited by 17
Molecular Alterations in Sporadic Primary Hyperparathyroidism
Alvelos, M. I., Mendes, M., & Soares, P. (2011) · Genetics Research International · doi:10.4061/2011/275802 · Cited by 17
Castillo-Morales, A., Monzón‐Sandoval, J., Urrutia, A. O., & Gutiérrez, H. (2013) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2013.2428 · Cited by 17
Gene duplication in the genome of parasitic Giardia lamblia
Sun, J., Jiang, H., Flores, R., & Wen, J. (2010) · BMC Evolutionary Biology · doi:10.1186/1471-2148-10-49 · Cited by 18
Picchio, L., Legagneux, V., Deschamps, S., Renaud, Y., Chauveau, S., Paillard, L., & Jagla, K. (2018) · Disease Models & Mechanisms · doi:10.1242/dmm.031849 · Cited by 17
Strategies for Engineering and Rewiring Kinase Regulation
McCormick, J. W., Pincus, D., Resnekov, O., & Reynolds, K. A. (2019) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2019.11.005 · Cited by 17
The Globin Gene Family in Arthropods: Evolution and Functional Diversity
Prothmann, A., Hoffmann, F. G., Opazo, J. C., Herbener, P., Storz, J. F., Burmester, T., & Hankeln, T. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.00858 · Cited by 17
“Thus, in contrast to early interpretations of comparative genome analyses (Rubin et al., 2000), our results indicate that globins are part of the standard gene repertoire of the arthropod genome.”
ResultExploring the alternative: Fish, flies and worms as preclinical models for ALS
Braems, E., Tziortzouda, P., & Bosch, L. V. D. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.136041 · Cited by 20
Mingione, V. R., Foda, Z. H., Paung, Y., Philipose, H., Rangwala, A. M., Shan, Y., & Seeliger, M. A. (2022) · Journal of Molecular Biology · doi:10.1016/j.jmb.2022.167628 · Cited by 13
Collins, A. G. (2000) · doi:10.1666/0094-8373(2000)026
Metadata
- Authors
- Rubin, G. M., Yandell, M. D., Wortman, J. R., Gabor, G. L., Miklos, Nelson, C. R., Hariharan, I. K., Fortini, M. E., Li, P. W., Apweiler, R., Fleischmann, W., Cherry, J. M., Henikoff, S., Skupski, M. P., Misra, S., Ashburner, M., Birney, E., Boguski, M. S., Brody, T., Brokstein, P., Celniker, S. E., Chervitz, S. A., Coates, D., Cravchik, A., Gabrielian, A., Galle, R. F., Gelbart, W. M., George, R. A., Goldstein, L. S. B., Gong, F., Guan, P., Harris, N. L., Hay, B. A., Hoskins, R. A., Li, J., Li, Z., Hynes, R. O., Jones, S. J. M., Kuehl, P. M., Lemaitre, B., Littleton, J. T., Morrison, D. K., Mungall, C., O'Farrell, P. H., Pickeral, O. K., Shue, C., Vosshall, L. B., Zhang, J., Zhao, Q., Zheng, X. H., Zhong, F., Zhong, W., Gibbs, R., Venter, J. C., Adams, M. D., & Lewis, S.
- Affiliations
- Howard Hughes Medical Institute (US)
- Celera Genomics, Rockville, MD, 20850 USA.
- GenetixXpress, 78 Pacific Road, Palm Beach, Sydney, Australia 2108.
- University of California, Berkeley (US)
- Harvard University (US)
- University of Pennsylvania (US)
- European Bioinformatics Institute (GB)
- Stanford University (US)
- Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa (ZA)
- National Institutes of Health (US)
- Lawrence Berkeley National Laboratory (US)
- Neomorphic, 2612 Eighth Street, Berkeley, CA 94710, USA.
- University of Leeds (GB)
- California Institute of Technology (US)
- BC Cancer Agency (CA)
- University of Maryland, Baltimore (US)
- Centre de Génétique Moléculaire, CNRS, 91198 Gif-sur-Yvette, France.
- Massachusetts Institute of Technology (US)
- Department of Biochemistry and Biophysics, University of California, San Francisco, CA 94143, USA.
- Columbia University (US)
- Baylor College of Medicine (US)
- ORCID
- Rubin, Gerald M.
- Yandell, Mark D.
- Wortman, Jennifer R.
- Nelson, Catherine R.
- Hariharan, Iswar K.
- Apweiler, Rolf
- Cherry, J. Michael
- Henikoff, Steven
- Ashburner, Michael
- Birney, Ewan
- Celniker, Susan E.
- Chervitz, Stephen A.
- Gabrielian, Andrei
- George, Reed A.
- Goldstein, Lawrence S. B.
- Guan, Ping
- Harris, Nomi L.
- Hay, Bruce A.
- Li, Jiayin
- Hynes, Richard O.
- Jones, S. J. M.
- Littleton, J. Troy
- Morrison, Deborah K.
- Mungall, Chris
- Vosshall, Leslie B.
- Zhang, Jiong
- Zhao, Qi
- Zhong, Fei
- Zhong, Wenyan
- Gibbs, Richard
- Venter, J. Craig
- Adams, Mark D.
- Lewis, Suzanna
- Venue
- Science
- Published
- 2000-03-24
- Volume
- 287
- Issue
- 5461
- Pages
- 2204-2215
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC2754258
- OpenAlex
- W2106013076
- Cited by
- 1,698
- References
- 87
- Citations by year
- 2026: 19 · 2025: 26 · 2024: 18 · 2023: 24 · 2022: 30 · 2021: 29 · 2020: 37 · 2019: 33 · 2018: 36 · 2017: 34 · 2016: 34 · 2015: 38 · 2014: 34 · 2013: 45 · 2012: 55
- FWCI
- 75.40
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- CaltechAUTHORS (California Institute of Technology) (submittedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion, cc-by-nc-nd)
- Funders
- National Human Genome Research Institute (P50HG000750, P4IHG00739, P50-HG00750)
- National Institute of General Medical Sciences (R01GM037193, R01GM060988)
- National Institute of Neurological Disorders and Stroke (R01NS040296)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- comparative genomics, eukaryotic genomes, Drosophila melanogaster, Caenorhabditis elegans, Saccharomyces cerevisiae, gene family expansion, multidomain proteins, signaling pathways, orthologs, human disease genes, model organisms
- MeSH terms
- Animals, Cell Adhesion, Cell Cycle, Drosophila melanogaster, Biological Evolution, Fungal Proteins, Multigene Family, Genetics, Medical, Humans, Immunity, Neoplasms, Saccharomyces cerevisiae, Signal Transduction, Helminth Proteins, Genome, Caenorhabditis elegans, Apoptosis, Protein Structure, Tertiary, Insect Proteins, Genes, Duplicate, Proteome, Genetic Diseases, Inborn
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