The DOI matches its Crossref record; 101 of the 102 references it cites were found in a registry or an index.
Endosymbiotic theory for organelle origins
Abstract
Endosymbiotic theory goes back over 100 years. It explains the similarity of chloroplasts and mitochondria to free-living prokaryotes by suggesting that the organelles arose from prokaryotes through (endo)symbiosis. Gene trees provide important evidence in favour of symbiotic theory at a coarse-grained level, but the finer we get into the details of branches in trees containing dozens or hundreds of taxa, the more equivocal evidence for endosymbiotic events sometimes becomes. It seems that either the interpretation of some endosymbiotic events are wrong, or something is wrong with the interpretations of some gene trees having many leaves. There is a need for evidence that is independent of gene trees and that can help outline the course of symbiosis in eukaryote evolution. Protein import is the strongest evidence we have for the single origin of chloroplasts and mitochondria. It is probably also the strongest evidence we have to sort out the number and nature of secondary endosymbiotic events that have occurred in evolution involving the red plastid lineage. If we relax our interpretation of individual gene trees, endosymbiotic theory can tell us a lot.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“CASH lineages have plastids related to red algae, but the mechanisms by which they were acquired and the ancestors involved remain unclear [1–3].”
From Decontamination, pooling and dereplication of the 678 samples of the Marine Microbial Eukaryote Transcriptome Sequencing Project (2021) · cites this paper as [1]
Citations
Cites
Lateral gene transfer and the nature of bacterial innovation
Ochman, H., Lawrence, J. G., & Groisman, E. A. (2000) · Nature · doi:10.1038/35012500 · Cited by 3,816
Endosymbiotic gene transfer: organelle genomes forge eukaryotic chromosomes
Timmis, J. N., Ayliffe, M., Huang, C. Y., & Martin, W. F. (2004) · Nature Reviews Genetics · doi:10.1038/nrg1271 · Cited by 1,603
Self-citationGenome Sequence of an Obligate Intracellular Pathogen of Humans: Chlamydia trachomatis
Stephens, R. S., Kalman, S., Lammel, C. J., Fan, J., Marathe, R., Aravind, L., Mitchell, W., Olinger, L., Tatusov, R. L., Zhao, Q., et al. (1998) · Science · doi:10.1126/science.282.5389.754 · Cited by 1,563
The energetics of genome complexity.
Lane, N., & Martin, W. (2010) · Nature · doi:10.1038/nature09486 · Cited by 1,289
Self-citationMartin, W., Rujan, T., Richly, E., Hansen, A., Cornelsen, S., Lins, T., Leister, D., Stoebe, B., Hasegawa, M., & Penny, D. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.182432999 · Cited by 1,178 · cited 2×
“Moreover, the ‘second major’ [64], and we stress, apparent ‘source’ of prokaryotic genes in plants is not chlamydia, it is alphaproteobacteria, followed by gammaproteobacteria, then actinobacteria, deltaproteobacteria, bacilli, bacteroidetes, and betaproteobacteria, behind which chlamydiae range as another meagre appa…”
BackgroundSelf-citationEstimating the timing of early eukaryotic diversification with multigene molecular clocks
Parfrey, L. W., Lahr, D. J. G., Knoll, A. H., & Katz, L. A. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1110633108 · Cited by 899 · cited 1×
“2 billion years ago [29].”
Isoprenoid biosynthesis: The evolution of two ancient and distinct pathways across genomes
Lange, B. M., Rujan, T., Martin, W., & Croteau, R. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.240454797 · Cited by 881
Self-citationBiochemistry and Evolution of Anaerobic Energy Metabolism in Eukaryotes
Müller, M., Mentel, M., van Hellemond, J. J., Henze, K., Woehle, C., Gould, S. B., Yu, R.-Y., van der Giezen, M., Tielens, A. G. M., & Martin, W. F. (2012) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.05024-11 · Cited by 838
Self-citationGene transfer to the nucleus and the evolution of chloroplasts
Martin, W., Stoebe, B., Goremykin, V., Hansmann, S., Hasegawa, M., & Kowallik, K. V. (1998) · Nature · doi:10.1038/30234 · Cited by 772 · cited 2×
“In a study of nine plastid genomes only 11 out of 42 genes recovered the consensus tree [54].”
BackgroundSelf-citationGene Transfer from Organelles to the Nucleus: How Much, What Happens, and Why?1
Martin, W., & Herrmann, R. G. (1998) · Plant Physiology · doi:10.1104/pp.118.1.9 · Cited by 704
Self-citation
Flagged first, then by citations
1 of the 102 references couldn’t be matched to a known paper.
Research works printed but not linked: 3
- Mereschkowsky, 1905, Über Natur und Ursprung der Chromatophoren im Pflanzenreiche, Biol Centralbl, 25, 593
- Martin, 2012, Modern endosymbiotic theory: getting lateral gene transfer into the equation, J Endocyt Cell Res, 23, 1
- Melkonian, 1996, Phylogeny of photosynthetic protists and their plastids, Verh Dtsch Zool Ges, 89, 71
Cited by
Sorted by citations
Endosymbiosis and Eukaryotic Cell Evolution
Archibald, J. M. (2015) · Current Biology · doi:10.1016/j.cub.2015.07.055 · Cited by 654
Endosymbiotic theories for eukaryote origin
Martin, W. F., Garg, S., & Zimorski, V. (2015) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2014.0330 · Cited by 583
Self-citationQuality control of the mitochondrial proteome
Song, J., Herrmann, J. M., & Becker, T. (2020) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-020-00300-2 · Cited by 501
Lamb, R., Ózsvári, B., Lisanti, C., Tanowitz, H. B., Howell, A., Martinez‐Outschoorn, U., Sotgia, F., & Lisanti, M. P. (2015) · Oncotarget · doi:10.18632/oncotarget.3174 · Cited by 484
Peiris-Pagès, M., Martinez-Outschoorn, U. E., Pestell, R. G., Sotgia, F., & Lisanti, M. P. (2016) · Breast Cancer Research · doi:10.1186/s13058-016-0712-6 · Cited by 465
Toward major evolutionary transitions theory 2.0
Szathmáry, E. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1421398112 · Cited by 415
Mitochondria: Central Organelles for Melatonin′s Antioxidant and Anti-Aging Actions
Reiter, R., Tan, D., Rosales-Corral, S., Galano, A., Zhou, X., & Xu, B. (2018) · Molecules · doi:10.3390/molecules23020509 · Cited by 393
Mitochondria: diversity in the regulation of the NLRP3 inflammasome
Gurung, P., Lukens, J. R., & Kanneganti, T.-D. (2015) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2014.11.008 · Cited by 393
Burki, F., Kaplan, M., Tikhonenkov, D. V., Zlatogursky, V., Minh, B. Q., Radaykina, L. V., Smirnov, A., Mylnikov, A. P., & Keeling, P. J. (2016) · Proceedings of the Royal Society B: Biological Sciences · doi:10.1098/rspb.2015.2802 · Cited by 301
Ladouceur, A.-M., Parmar, B. S., Biedzinski, S., Wall, J., Tope, S. G., Cohn, D. E., Kim, A., Soubry, N., Reyes‐Lamothe, R., & Weber, S. C. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2005019117 · Cited by 249
Repeated replacement of an intrabacterial symbiont in the tripartite nested mealybug symbiosis
Husník, F., & McCutcheon, J. P. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1603910113 · Cited by 245
Oatk: a de novo assembly tool for complex plant organelle genomes
Zhou, C., Brown, M. R., Blaxter, M. L., McCarthy, S., & Durbin, R. M. (2025) · Genome biology · doi:10.1186/s13059-025-03676-6 · Cited by 237
Mechanistic concepts of iron-sulfur protein biogenesis in Biology
Braymer, J. J., Freibert, S., Rakwalska‐Bange, M., & Lill, R. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2020.118863 · Cited by 240
Horizontal Gene Transfer in Eukaryotes: Not if, but How Much?
Etten, J. V., & Bhattacharya, D. (2020) · Trends in Genetics · doi:10.1016/j.tig.2020.08.006 · Cited by 233
Cavalier‐Smith, T. (2017) · PROTOPLASMA · doi:10.1007/s00709-017-1147-3 · Cited by 227
Farnie, G., Sotgia, F., & Lisanti, M. P. (2015) · Oncotarget · doi:10.18632/oncotarget.5401 · Cited by 206
Mitochondrial ROS metabolism: 10 Years later
Andreyev, A. Y., Kushnareva, Y. E., Murphy, A. N., & Starkov, A. A. (2015) · Biochemistry (Moscow) · doi:10.1134/s0006297915050028 · Cited by 196
The Symbiosome: Legume and Rhizobia Co-evolution toward a Nitrogen-Fixing Organelle?
de la Peña, T. C., Fedorova, E. E., Pueyo, J. J., & Lucas, M. M. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2017.02229 · Cited by 186
Malina, C., Larsson, C., & Nielsen, J. (2018) · FEMS Yeast Research · doi:10.1093/femsyr/foy040 · Cited by 166
Finlay, R. D., Mahmood, S., Rosenstock, N. P., Bolou‐Bi, E. B., Köhler, S. J., Fahad, Z. A., Rosling, A., Wallander, H., Belyazid, S., Bishop, K., et al. (2020) · Biogeosciences · doi:10.5194/bg-17-1507-2020 · Cited by 154
Genomic perspectives on the birth and spread of plastids
Archibald, J. M. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1421374112 · Cited by 156
The Physiology of Phagocytosis in the Context of Mitochondrial Origin
Martin, W. F., Tielens, A. G. M., Mentel, M., Garg, S. G., & Gould, S. B. (2017) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00008-17 · Cited by 157
Self-citationStreptophyte Terrestrialization in Light of Plastid Evolution.
de Vries, J., Stanton, A., Archibald, J., & Gould, S. (2016) · Trends in Plant Science · doi:10.1016/j.tplants.2016.01.021 · Cited by 145
Self-citationArtificial Mitochondria Transfer: Current Challenges, Advances, and Future Applications
Caicedo, A., Aponte, P. M., Cabrera, F., Hidalgo, C., & Khoury, M. (2017) · Stem Cells International · doi:10.1155/2017/7610414 · Cited by 150
Yi, X., Lu, Y., Lee, Y., Wei, L., Jia, J., Wang, Q., Wang, D., Bai, F., Hu, H., Hu, Q., et al. (2017) · Molecular Plant · doi:10.1016/j.molp.2017.10.011 · Cited by 148
Endosymbiotic gene transfer from prokaryotic pangenomes: Inherited chimerism in eukaryotes
Ku, C., Sathi, S. N., Roettger, M., Garg, S. G., Hazkani‐Covo, E., & Martin, W. F. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1421385112 · Cited by 143
Self-citationMartin, W. F. (2017) · BioEssays · doi:10.1002/bies.201700115 · Cited by 141
Self-citationde Vries, J., Sousa, F. L., Bölter, B., Soll, J., & Gould, S. B. (2015) · The Plant Cell · doi:10.1105/tpc.114.135541 · Cited by 128
Self-citationDGDG and Glycolipids in Plants and Algae
Kalisch, B., Dörmann, P., & Hölzl, G. (2016) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-319-25979-6_3 · Cited by 130
Effects of lipids on mitochondrial functions
Mårtensson, C. U., Doan, K. N., & Becker, T. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2016.06.015 · Cited by 135
Early Microbial Evolution: The Age of Anaerobes
Martin, W. F., & Sousa, F. L. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a018127 · Cited by 129
Self-citationAghapour, M., Remels, A. H. V., Pouwels, S. D., Bruder, D., Hiemstra, P. S., Cloonan, S. M., & Heijink, I. H. (2019) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00329.2019 · Cited by 122
Collingro, A., Köstlbacher, S., & Horn, M. (2020) · Trends in Microbiology · doi:10.1016/j.tim.2020.05.020 · Cited by 120
Eukaryogenesis, how special really?
Booth, A., & Doolittle, W. F. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1421376112 · Cited by 118
Rogalski, M., Vieira, L. D. N., Fraga, H. P., & Guerra, M. P. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00586 · Cited by 112
Lamb, R., Fiorillo, M., Chadwick, A. L., Ózsvári, B., Reeves, K. J., Smith, D. L., Clarke, R. B., Howell, S. J., Cappello, A. R., Martinez‐Outschoorn, U., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.4159 · Cited by 114
The Molecular Machinery of Chloroplast Division1[OPEN]
Chen, C., MacCready, J. S., Ducat, D. C., & Osteryoung, K. (2017) · Plant Physiology · doi:10.1104/pp.17.01272 · Cited by 92
Pathways to balance mitochondrial translation and protein importPreprint
Priesnitz, C., & Becker, T. (2018) · Genes & Development · doi:10.1101/gad.316547.118 · Cited by 106
Rethinking evolutionary individuality
Ereshefsky, M., & Pedroso, M. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1421377112 · Cited by 108
Protein Import and the Origin of Red Complex Plastids
Gould, S. B., Maier, U., & Martin, W. F. (2015) · Current Biology · doi:10.1016/j.cub.2015.04.033 · Cited by 107
Self-citationAstRoMap European Astrobiology Roadmap
Horneck, G., Walter, N., Westall, F., Grenfell, J. L., Martin, W. F., Gómez, F., Leuko, S., Lee, N., Onofri, S., Tsiganis, K., et al. (2016) · Astrobiology · doi:10.1089/ast.2015.1441 · Cited by 107
Self-citationProline Metabolism and Its Functions in Development and Stress Tolerance
Trovato, M., Forlani, G., Signorelli, S., & Funck, D. (2019) · Springer eBooks · doi:10.1007/978-3-030-27423-8_2 · Cited by 99
Investigation of carbon and energy metabolic mechanism of mixotrophy in Chromochloris zofingiensis
Zhang, Z., Sun, D., Cheng, K., & Chen, F. (2021) · Biotechnology for Biofuels · doi:10.1186/s13068-021-01890-5 · Cited by 98
Innate immunity and tolerance toward mitochondria
Rongvaux, A. (2017) · Mitochondrion · doi:10.1016/j.mito.2017.10.007 · Cited by 115
The origin and early evolution of plants
Bowles, A. M. C., Williamson, C. J., Williams, T. A., Lenton, T. M., & Donoghue, P. C. J. (2022) · Trends in Plant Science · doi:10.1016/j.tplants.2022.09.009 · Cited by 95
How Do Quorum-Sensing Signals Mediate Algae–Bacteria Interactions?
Dow, L. (2021) · Microorganisms · doi:10.3390/microorganisms9071391 · Cited by 98
Origins, function, and regulation of the TOC–TIC general protein import machinery of plastids
Richardson, L. G. L., & Schnell, D. J. (2019) · Journal of Experimental Botany · doi:10.1093/jxb/erz517 · Cited by 89
The Role of Charge in Protein Targeting Evolution
Garg, S. G., & Gould, S. B. (2016) · Trends in Cell Biology · doi:10.1016/j.tcb.2016.07.001 · Cited by 86
Self-citationReductive evolution of chloroplasts in non-photosynthetic plants, algae and protists
Hadariová, L., Vesteg, M., Hampl, V., & Krajc̆ovic̆, J. (2017) · Current Genetics · doi:10.1007/s00294-017-0761-0 · Cited by 71
Dinoflagellates with relic endosymbiont nuclei as models for elucidating organellogenesis
Sarai, C., Tanifuji, G., Nakayama, T., Kamikawa, R., Takahashi, K., Yazaki, E., Matsuo, E., Miyashita, H., Ishida, K.-I., Iwataki, M., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1911884117 · Cited by 82
Organelles and phytohormones: a network of interactions in plant stress responses
Bittner, A., Cieśla, A., Gruden, K., Lukan, T., Mahmud, S., Teige, M., Vothknecht, U. C., & Wurzinger, B. (2022) · Journal of Experimental Botany · doi:10.1093/jxb/erac384 · Cited by 82
Genomic Changes Associated with the Evolutionary Transitions of Nostoc to a Plant Symbiont
Warshan, D., Liaimer, A., Pederson, E. R. A., Kim, S.-Y., Shapiro, N., Woyke, T., Altermark, B., Pawlowski, K., Weyman, P. D., Dupont, C. L., et al. (2018) · Molecular Biology and Evolution · doi:10.1093/molbev/msy029 · Cited by 77
Tension and Resolution: Dynamic, Evolving Populations of Organelle Genomes within Plant Cells
Johnston, I. G. (2018) · Molecular Plant · doi:10.1016/j.molp.2018.11.002 · Cited by 74
Advancing organelle genome transformation and editing for crop improvement
Li, S., Chang, L., & Zhang, J. (2021) · Plant Communications · doi:10.1016/j.xplc.2021.100141 · Cited by 52
Coupling of import and assembly pathways in mitochondrial protein biogenesis
Grevel, A., Pfanner, N., & Becker, T. (2019) · Biological Chemistry · doi:10.1515/hsz-2019-0310 · Cited by 71
New insights in cyanobacterial cold stress responses: Genes, sensors, and molecular triggers
Sinetova, M. A., & Los, D. A. (2016) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2016.07.006 · Cited by 70
Evolutionary dynamics of cryptophyte plastid genomes
Kim, J. I., Moore, C. E., Archibald, J. M., Bhattacharya, D., Yi, G., Yoon, H. S., & Shin, W. (2017) · Genome Biology and Evolution · doi:10.1093/gbe/evx123 · Cited by 70
Human Mitochondrial DNA: Particularities and Diseases
Habbane, M., Montoya, J., Rhouda, T., Sbaoui, Y., Radallah, D., & Emperador, S. (2021) · Biomedicines · doi:10.3390/biomedicines9101364 · Cited by 86
The monoplastidic bottleneck in algae and plant evolution
de Vries, J., & Gould, S. B. (2017) · Journal of Cell Science · doi:10.1242/jcs.203414 · Cited by 70
Self-citationMechanistic connections between mitochondrial biology and regulated cell death
Chipuk, J. E., Mohammed, J. N., Gelles, J. D., & Chen, Y. (2021) · Developmental Cell · doi:10.1016/j.devcel.2021.03.033 · Cited by 69
Zhang, X., Chen, H.-M., Ni, Y., Wu, B., Li, J.-L., Burzyński, A., & Liu, C. (2024) · Molecular Ecology Resources · doi:10.1111/1755-0998.13952 · Cited by 64
Energy metabolism in anaerobic eukaryotes and Earth's late oxygenation
Zimorski, V., Mentel, M., Tielens, A. G. M., & Martin, W. F. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.03.030 · Cited by 69
Self-citationSmall One-Helix Proteins Are Essential for Photosynthesis in Arabidopsis
Beck, J., Lohscheider, J. N., Albert, S., Andersson, U., Mendgen, K. W., Rojas-Stütz, M., Adamska, I., & Funck, D. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00007 · Cited by 64
Archaeal ancestors of eukaryotes: not so elusive any more
Koonin, E. V. (2015) · BMC Biology · doi:10.1186/s12915-015-0194-5 · Cited by 68
Endosymbiosis and its implications for evolutionary theory
O’Malley, M. A. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1421389112 · Cited by 69
Impact of the plastidial stringent response in plant growth and stress responses
Maekawa, M., Honoki, R., Ihara, Y., Sato, R., Oikawa, A., Kanno, Y., Ohta, H., Seo, M., Saito, K., & Masuda, S. (2015) · Nature Plants · doi:10.1038/nplants.2015.167 · Cited by 63
Engineered mitochondria in diseases: mechanisms, strategies, and applications
Li, M., Wu, L., Si, H., Wu, Y., Liu, Y., Zeng, Y., & Shen, B. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-02081-y · Cited by 71
LEA Proteins and the Evolution of the WHy Domain
Mertens, J., Aliyu, H., & Cowan, D. A. (2018) · Applied and Environmental Microbiology · doi:10.1128/aem.00539-18 · Cited by 61
Essential and Detrimental — an Update on Intracellular Iron Trafficking and Homeostasis
Vigani, G., Solti, Ï., Thomine, S. ⁄. B., & Philippar, K. (2019) · Plant and Cell Physiology · doi:10.1093/pcp/pcz091 · Cited by 62
Subcellular compartmentalization in the biosynthesis and engineering of plant natural products
Yao, L., Wu, X., Jiang, X., SHAN, M. I., Zhang, Z., Li, Y., Yang, A., Li, Y., & Yang, C. (2023) · Biotechnology Advances · doi:10.1016/j.biotechadv.2023.108258 · Cited by 59
Liu, X., Hempel, F., Stork, S., Bolte, K., Moog, D., Heimerl, T., Maier, U. G., & Zauner, S. (2016) · Algal Research · doi:10.1016/j.algal.2016.10.018 · Cited by 59
A non-photosynthetic diatom reveals early steps of reductive evolution in plastids
Kamikawa, R., Moog, D., Zauner, S., Tanifuji, G., Ishida, K.-I., Miyashita, H., Mayama, S., Hashimoto, T., Maier, U. G., Archibald, J. M., et al. (2017) · Molecular Biology and Evolution · doi:10.1093/molbev/msx172 · Cited by 59
Plant Organelle Genome Replication
Morley, S. A., Ahmad, N., & Nielsen, B. L. (2019) · Plants · doi:10.3390/plants8100358 · Cited by 58
A mitochondrial based oncology platform for targeting cancer stem cells (CSCs): MITO-ONC-RX
Sotgia, F., Ózsvári, B., Fiorillo, M., Francesco, E. M. D., Bonuccelli, G., & Lisanti, M. P. (2018) · Cell Cycle · doi:10.1080/15384101.2018.1515551 · Cited by 57
Moog, D., Rensing, S. A., Archibald, J. M., Maier, U. G., & Ullrich, K. K. (2015) · Genome Biology and Evolution · doi:10.1093/gbe/evv190 · Cited by 56
Plastid establishment did not require a chlamydial partner
Domman, D., Horn, M., Embley, T. M., & Williams, T. A. (2015) · Nature Communications · doi:10.1038/ncomms7421 · Cited by 51
Jiang, P., Shi, F., Li, M., Liu, B., Wen, J., Xiao, H., & Li, L. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.00359 · Cited by 54
Cenci, U., Sibbald, S. J., Curtis, B. A., Kamikawa, R., Eme, L., Moog, D., Henrissat, B., Maréchal, E., Chabi, M., Djemiel, C., et al. (2018) · BMC Biology · doi:10.1186/s12915-018-0593-5 · Cited by 53
de Vries, J., & Archibald, J. M. (2018) · Current Biology · doi:10.1016/j.cub.2018.01.027 · Cited by 52
Evolution and Design Principles of the Diverse Chloroplast Transit Peptides.
Lee, D. W., & Hwang, I. (2018) · PubMed Central · doi:10.14348/molcells.2018.0033 · Cited by 52
The DnaJ proteins DJA6 and DJA5 are essential for chloroplast iron–sulfur cluster biogenesis
Zhang, J., Bai, Z., Ouyang, M., Xu, X., Xiong, H., Wang, Q., Grimm, B., Rochaix, J., & Zhang, L. (2021) · The EMBO Journal · doi:10.15252/embj.2020106742 · Cited by 52
Zhao, L., Wang, P., Li, K., Zhang, Q.-B., He, F.-Y., Li, C., Su, H., Chen, X., Liu, L., & Zhang, Y. (2023) · The Plant Cell · doi:10.1093/plcell/koad087 · Cited by 50
A Novel Prokaryote-Type ECF/ABC Transporter Module in Chloroplast Metal Homeostasis
von Voithenberg, L. V., Park, J., Stübe, R., Lux, C., Lee, Y., & Philippar, K. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01264 · Cited by 50
Mechanisms and pathways of mitochondrial outer membrane protein biogenesis.
Gupta, A., & Becker, T. (2020) · Biochimica et Biophysica Acta - Bioenergetics · doi:10.1016/j.bbabio.2020.148323 · Cited by 44
Did some red alga‐derived plastids evolve via kleptoplastidy? A hypothesis
Bodył, A. (2017) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12340 · Cited by 48
Sorting of nuclear-encoded chloroplast membrane proteins
Lee, D. W., Lee, J., & Hwang, I. (2017) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2017.06.011 · Cited by 47
Compartmentalized metabolic engineering for biochemical and biofuel production
Huttanus, H. M., & Feng, X. (2017) · Biotechnology Journal · doi:10.1002/biot.201700052 · Cited by 45
Mitochondrial retrograde signaling in the nervous system
Hunt, R. J., & Bateman, J. M. (2017) · FEBS Letters · doi:10.1002/1873-3468.12890 · Cited by 45
Speijer, D. (2015) · BioEssays · doi:10.1002/bies.201500107 · Cited by 44
Versatility of hydrocarbon production in cyanobacteria
Xie, M., Wang, W., Zhang, W., Chen, L., & Lü, X. (2016) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-016-8064-9 · Cited by 45
Engineering artificial photosynthetic life-forms through endosymbiosis
Cournoyer, J. E., Altman, S. D., Gao, Y.-L., Wallace, C. L., Zhang, D., Lo, G.-H., Haskin, N. T., & Mehta, A. P. (2022) · Nature Communications · doi:10.1038/s41467-022-29961-7 · Cited by 47
Role of Mitochondrial Dysfunctions in Neurodegenerative Disorders: Advances in Mitochondrial Biology
Kathiresan, D. S., Balasubramani, R., Marudhachalam, K., Jaiswal, P., Ramesh, N., Suruthi, G. S., Moorthi, P. V., & Vijayan, M. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04469-x · Cited by 48
Amaroli, A., Ravera, S., Zekiy, A. O., Benedicenti, S., & Pasquale, C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031372 · Cited by 44
Phase separation in plants: New insights into cellular compartmentalization
Xu, X., Zheng, C., Lu, D., Song, C., & Zhang, L. (2021) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13152 · Cited by 43
A unifying model for membrane protein biogenesis
Hegde, R. S., & Keenan, R. J. (2024) · Nature Structural & Molecular Biology · doi:10.1038/s41594-024-01296-5 · Cited by 41
Antibiotics May Trigger Mitochondrial Dysfunction Inducing Psychiatric Disorders
Stefano, G. B., Samuel, J., & Kream, R. M. (2017) · Medical Science Monitor · doi:10.12659/msm.899478 · Cited by 42
Kim, L. J., Tsuyuki, K. M., Hu, F., Park, E. Y., Zhang, J., Iraheta, J. G., Chia, J., Huang, R., Tucker, A. E., Clyne, M., et al. (2021) · The Plant Journal · doi:10.1111/tpj.15286 · Cited by 45
Cryo-EM structures of the plant plastid-encoded RNA polymerase
Wu, X., Mu, W., Li, F., Shu-yi, S., Cui, C.-J., Kim, C., Zhou, F., & Zhang, Y. (2024) · Cell · doi:10.1016/j.cell.2024.01.026 · Cited by 42
A sea slug’s guide to plastid symbiosis
de Vries, J., Rauch, C., Christa, G., & Gould, S. B. (2014) · Acta Societatis Botanicorum Poloniae · doi:10.5586/asbp.2014.042 · Cited by 39
Self-citationÓzsvári, B., Fiorillo, M., Bonuccelli, G., Cappello, A. R., Frattaruolo, L., Sotgia, F., Trowbridge, R., Foster, R., & Lisanti, M. P. (2017) · Oncotarget · doi:10.18632/oncotarget.19084 · Cited by 42
Metadata
- Authors
- Zimorski, V., Ku, C., Martin, W. F., & Gould, S. B.
- Affiliations
- Heinrich Heine University Düsseldorf (DE)
- Venue
- Current Opinion in Microbiology
- Publisher
- Elsevier BV
- Published
- 2014-12
- Volume
- 22
- Pages
- 38-48
- ISSN
- 1369-5274 (ISSN-L)
- OpenAlex
- W2060804705
- Semantic Scholar
- 13afd83e6ec98416549a7dd120f485251fbb892d
- Cited by
- 453
- References
- 102
- Citations by year
- 2026: 27 · 2025: 50 · 2024: 53 · 2023: 23 · 2022: 44 · 2021: 40 · 2020: 36 · 2019: 39 · 2018: 35 · 2017: 39 · 2016: 30 · 2015: 31 · 2014: 6
- FWCI
- 3.33
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Current Opinion in Microbiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- European Research Council (232975)
- Deutsche Forschungsgemeinschaft (GO1825/4-1)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Protist diversity and phylogeny
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Chromosomal and Genetic Variations
- Keywords
- endosymbiotic theory, organelle origin, chloroplasts, mitochondria, secondary endosymbiosis, gene trees, protein import, eukaryotic evolution, symbiosis
- MeSH terms
- Adenosine Triphosphate, Cyanobacteria, Eukaryotic Cells, Mitochondria, Prokaryotic Cells, Symbiosis, Organelles, Protein Transport
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