IFT–Cargo Interactions and Protein Transport in Cilia
Open accessAbstract
The motile and sensory functions of cilia and flagella are indispensable for human health. Cilia assembly requires a dedicated protein shuttle, intraflagellar transport (IFT), a bidirectional motility of multi-megadalton protein arrays along ciliary microtubules. IFT functions as a protein carrier delivering hundreds of distinct proteins into growing cilia. IFT-based protein import and export continue in fully grown cilia and are required for ciliary maintenance and sensing. Large ciliary building blocks might depend on IFT to move through the transition zone, which functions as a ciliary gate. Smaller, freely diffusing proteins, such as tubulin, depend on IFT to be concentrated or removed from cilia. As I discuss here, recent work provides insights into how IFT interacts with its cargoes and how the transport is regulated.
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Progress has been made in understanding interactions between specific IFT particle polypeptides and specific ciliary cargo proteins or motor subunits during anterograde or retrograde IFT, as well as how IFT motor activity is regulated.
“Likewise, progress has been made towards understanding the interactions between specific IFT particle polypeptides and specific ciliary cargo proteins or motor subunits during anterograde or retrograde IFT, as well as how IFT motor activity is regulated 24, 48–52.”
From Cellular signalling by primary cilia in development, organ function and disease (2019) · cites this paper as [24]
The sections on cargo binding and known IFT binding sites describe specific interactions, including IFT81/IFT74 with tubulin and IFT46 with an adaptor for outer dynein arms. The building-blocks section identifies the motors for anterograde and retrograde transport, but the paper does not substantively explain how IFT motor activity is regulated or establish the claimed interactions with specific motor subunits. Page numbers were unavailable in our copy. (LLM, conf=0.82)
Experimental — accuracy not yet measuredThe intraflagellar transport system moves along axonemal microtubules to carry specific ciliary cargo proteins into or out of the organelle.
“and the intraflagellar transport (IFT) system that zips up and down axonemal microtubules to mediate the transport of specific ciliary cargo proteins into or out of the organelle 24, 25 (Figure 1).”
From Cellular signalling by primary cilia in development, organ function and disease (2019) · cites this paper as [24]
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Cites
The primary cilium: a signalling centre during vertebrate development
Goetz, S. C., & Anderson, K. V. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2774 · Cited by 1,824 · see citing works
Nonaka, S., Tanaka, Y., Okada, Y., Takeda, S., Harada, A., Kanai, Y., Kido, M. A., & Hirokawa, N. (1998) · Cell · doi:10.1016/s0092-8674(00)81705-5 · Cited by 1,619 · see citing works
Rosenbaum, J. L., & Witman, G. B. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm952 · Cited by 1,423 · see citing works
Nachury, M. V., Loktev, A. V., Zhang, Q., Westlake, C. J., Peränen, J., Merdes, A., Slusarski, D. C., Scheller, R. H., Bazan, J. F., Sheffield, V. C., et al. (2007) · Cell · doi:10.1016/j.cell.2007.03.053 · Cited by 1,384 · see citing works
The renewal of photoreceptor cell outer segments
Young, R. W. (1967) · The Journal of Cell Biology · doi:10.1083/jcb.33.1.61 · Cited by 1,184 · cited 1× · see citing works
“For example, ~2,000 opsins pass every minute through the connecting cilium into the outer segment to replace protein lost by disc shedding [38].”
BackgroundPazour, G. J., Dickert, B. L., Vucica, Y., Seeley, E. S., Rosenbaum, J. L., Witman, G. B., & Cole, D. G. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.151.3.709 · Cited by 1,147 · see citing works
Proteomic analysis of a eukaryotic cilium
Pazour, G. J., Agrin, N. S., Leszyk, J., & Witman, G. B. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200504008 · Cited by 1,028 · see citing works
A motility in the eukaryotic flagellum unrelated to flagellar beating.
Kozminski, K. G., Johnson, K. A., Forscher, P., & Rosenbaum, J. L. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.12.5519 · Cited by 1,007 · see citing works
Cole, D. G., Diener, D. R., Himelblau, A. L., Beech, P. L., Fuster, J. C., & Rosenbaum, J. L. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.141.4.993 · Cited by 898 · see citing works
Jin, H., White, S. R., Shida, T., Schulz, S., Aguiar, M., Gygi, S. P., Bazán, J. F., & Nachury, M. V. (2010) · Cell · doi:10.1016/j.cell.2010.05.015 · Cited by 594 · see citing works
PDGFRαα Signaling Is Regulated through the Primary Cilium in Fibroblasts
Schneider, L., Clement, C. A., Teilmann, S. C., Pazour, G. J., Hoffmann, E. K., Satir, P., & Christensen, S. T. (2005) · Current Biology · doi:10.1016/j.cub.2005.09.012 · Cited by 592 · see citing works
Kozminski, K. G., Beech, P. L., & Rosenbaum, J. L. (1995) · The Journal of cell biology · doi:10.1083/jcb.131.6.1517 · Cited by 586 · see citing works
Follit, J. A., Tuft, R. A., Fogarty, K. E., & Pazour, G. J. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-02-0133 · Cited by 499 · see citing works
Davenport, J. R., Watts, A. J., Roper, V. C., Croyle, M. J., van Groen, T., Wyss, J. M., Nagy, T. R., Kesterson, R. A., & Yoder, B. K. (2007) · Current Biology · doi:10.1016/j.cub.2007.08.034 · Cited by 482 · see citing works
Berbari, N. F., Lewis, J. S., Bishop, G. A., Askwith, C. C., & Mykytyn, K. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0711027105 · Cited by 474 · see citing works
The DHC1b (DHC2) Isoform of Cytoplasmic Dynein Is Required for Flagellar Assembly
Pazour, G. J., Dickert, B. L., & Witman, G. B. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.144.3.473 · Cited by 471 · see citing works
Primary cilia can both mediate and suppress Hedgehog pathway–dependent tumorigenesis
Wong, S. Y., Seol, A. D., So, P.-L., Ermilov, A. N., Bichakjian, C. K., Epstein, E. H., Dlugosz, A. A., & Reiter, J. F. (2009) · Nature Medicine · doi:10.1038/nm.2011 · Cited by 463 · see citing works
Williams, C. L., Li, C., Kida, K., Inglis, P. N., Mohan, S., Semenec, L., Bialas, N. J., Stupay, R. M., Chen, N., Blacque, O. E., et al. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201012116 · Cited by 453 · see citing works
A Proteomic Analysis of Human Cilia
Ostrowski, L. E., Blackburn, K., Radde, K. M., Moyer, M. B., Schlatzer, D., Moseley, M. A., & Boucher, R. C. (2002) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m200037-mcp200 · Cited by 441 · see citing works
Mukhopadhyay, S., Wen, X., Chih, B., Nelson, C. D., Lane, W. S., Scales, S. J., & Jackson, P. K. (2010) · Genes & Development · doi:10.1101/gad.1966210 · Cited by 435 · see citing works
Global genetic analysis in mice unveils central role for cilia in congenital heart disease
Li, Y., Klena, N., Gabriel, G. C., Liu, X., Kim, A. J., Lemke, K., Chen, Y., Chatterjee, B., Devine, W. A., Damerla, R. R., et al. (2015) · Nature · doi:10.1038/nature14269 · Cited by 433 · see citing works
Pazour, G. J., Wilkerson, C. G., & Witman, G. B. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.141.4.979 · Cited by 425 · see citing works
Functional coordination of intraflagellar transport motors
Ou, G., E. Blacque, O., Snow, J. J., Leroux, M. R., & Scholey, J. M. (2005) · Nature · doi:10.1038/nature03818 · Cited by 411 · see citing works
Deane, J. A., Cole, D. G., Seeley, E. S., Diener, D. R., & Rosenbaum, J. L. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00484-5 · Cited by 391 · see citing works
Craige, B., Tsao, C.-C., Diener, D. R., Hou, Y., Lechtreck, K. F., Rosenbaum, J. L., & Witman, G. B. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201006105 · Cited by 385 · see citing works
Self-citationBerbari, N. F., Johnson, A. D., Lewis, J. S., Askwith, C. C., & Mykytyn, K. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-09-0942 · Cited by 352 · see citing works
Lechtreck, K.-F., Johnson, E. C., Sakai, T., Cochran, D., Ballif, B. A., Rush, J., Pazour, G. J., Ikebe, M., & Witman, G. B. (2009) · Journal of Cell Biology · doi:10.1083/jcb.200909183 · Cited by 347 · see citing works
Self-citationBlacque, O. E., Reardon, M. J., Li, C., McCarthy, J., Mahjoub, M. R., Ansley, S. J., Badano, J. L., Mah, A. K., Beales, P. L., Davidson, W. S., et al. (2004) · Genes & Development · doi:10.1101/gad.1194004 · Cited by 347 · see citing works
Cytoplasmic Dynein Heavy Chain 1b Is Required for Flagellar Assembly in<i>Chlamydomonas</i>
Porter, M. E., Bower, R., Knott, J. A., Byrd, P., & Dentler, W. (1999) · Molecular Biology of the Cell · doi:10.1091/mbc.10.3.693 · Cited by 333 · see citing works
Molecular Basis of Tubulin Transport Within the Cilium by IFT74 and IFT81
Bhogaraju, S., Cajanek, L., Fort, C., Blisnick, T., Weber, K., Taschner, M., Mizuno, N., Lamla, S., Bastin, P., Nigg, E. A., et al. (2013) · Science · doi:10.1126/science.1240985 · Cited by 317 · see citing works
Kee, H. L., Dishinger, J. F., Blasius, T. L., Liu, C., Margolis, B. L., & Verhey, K. J. (2012) · Nature Cell Biology · doi:10.1038/ncb2450 · Cited by 311 · see citing works
Wallingford, J. B., & Mitchell, B. J. (2011) · Genes & Development · doi:10.1101/gad.2008011 · Cited by 304 · see citing works
Signor, D., Wedaman, K. P., Orozco, J. T., Dwyer, N. D., Bargmann, C. I., Rose, L. S., & Scholey, J. M. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.147.3.519 · Cited by 301 · see citing works
FLAGELLAR REGENERATION IN PROTOZOAN FLAGELLATES
Rosenbaum, J. L., & Child, F. M. (1967) · The Journal of Cell Biology · doi:10.1083/jcb.34.1.345 · Cited by 296 · see citing works
Role of Primary Cilia in the Pathogenesis of Polycystic Kidney Disease
Yoder, B. K. (2007) · Journal of the American Society of Nephrology · doi:10.1681/asn.2006111215 · Cited by 288 · see citing works
Jonassen, J. A., Agustin, J. T. S., Follit, J. A., & Pazour, G. J. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200808137 · Cited by 278 · see citing works
IFT27 Links the BBSome to IFT for Maintenance of the Ciliary Signaling Compartment
Eguether, T., San Agustin, J. T., Keady, B. T., Jonassen, J. A., Liang, Y., Francis, R., Tobita, K., Johnson, C. A., Abdelhamed, Z. A., Lo, C. W., et al. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.09.011 · Cited by 260 · see citing works
Polarity of flagellar assembly in Chlamydomonas.
Johnson, K. A., & Rosenbaum, J. L. (1992) · The Journal of Cell Biology · doi:10.1083/jcb.119.6.1605 · Cited by 255 · see citing works
Ciliary disorder of the skeleton
Huber, C., & Cormier‐Daire, V. (2012) · American Journal of Medical Genetics Part C Seminars in Medical Genetics · doi:10.1002/ajmg.c.31336 · Cited by 249 · see citing works
Protein Particles inChlamydomonasFlagella Undergo a Transport Cycle Consisting of Four Phases
Iomini, C., Babaev-Khaimov, V., Sassaroli, M., & Piperno, G. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.153.1.13 · Cited by 241 · see citing works
The Cilium Secretes Bioactive Ectosomes
Wood, C. R., Huang, K., Diener, D. R., & Rosenbaum, J. L. (2013) · Current Biology · doi:10.1016/j.cub.2013.04.019 · Cited by 233 · see citing works
An ARL3–UNC119–RP2 GTPase cycle targets myristoylated NPHP3 to the primary ciliumPreprint
Wright, K. J., Baye, L. M., Olivier-Mason, A., Mukhopadhyay, S., Sang, L., Kwong, M., Wang, W., Pretorius, P. R., Sheffield, V. C., Sengupta, P., et al. (2011) · Genes & Development · doi:10.1101/gad.173443.111 · Cited by 229 · see citing works
Hou, Y., Qin, H., Follit, J. A., Pazour, G. J., Rosenbaum, J. L., & Witman, G. B. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200608041 · Cited by 226 · see citing works
Light-driven translocation of signaling proteins in vertebrate photoreceptors
Calvert, P. D., Strissel, K. J., Schiesser, W. E., Pugh, E. N., & Arshavsky, V. Y. (2006) · Trends in Cell Biology · doi:10.1016/j.tcb.2006.09.001 · Cited by 224 · see citing works
Domire, J. S., Green, J. A., Lee, K. G., Johnson, A. D., Askwith, C. C., & Mykytyn, K. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-010-0603-4 · Cited by 217 · see citing works
The IFT-A complex regulates Shh signaling through cilia structure and membrane protein trafficking
Liem, K. F., Ashe, A., He, M., Satir, P., Moran, J., Beier, D., Wicking, C., & Anderson, K. V. (2012) · Journal of Cell Biology · doi:10.1083/jcb.201110049 · Cited by 214 · see citing works
The BBSome controls IFT assembly and turnaround in cilia
Wei, Q., Zhang, Y., Li, Y., Zhang, Q., Ling, K., & Hu, J. (2012) · Nature Cell Biology · doi:10.1038/ncb2560 · Cited by 208 · see citing works
Qin, H., Burnette, D. T., Bae, Y.-K., Forscher, P., Barr, M. M., & Rosenbaum, J. L. (2005) · Current Biology · doi:10.1016/j.cub.2005.08.047 · Cited by 206 · see citing works
Electron-tomographic analysis of intraflagellar transport particle trains in situ
Pigino, G., Geimer, S., Lanzavecchia, S., Paccagnini, E., Cantele, F., Diener, D. R., Rosenbaum, J. L., & Lupetti, P. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200905103 · Cited by 204 · see citing works
Tam, B. M., Moritz, O. L., Hurd, L. B., & Papermaster, D. S. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.151.7.1369 · Cited by 202 · see citing works
The Role of Preassembled Cytoplasmic Complexes in Assembly of Flagellar Dynein Subunits
Fowkes, M. E., & Mitchell, D. R. (1998) · Molecular Biology of the Cell · doi:10.1091/mbc.9.9.2337 · Cited by 199 · see citing works
Tubulin transport by IFT is upregulated during ciliary growth by a cilium-autonomous mechanism
Weghe, J. C. V. D., Harris, J. A., Hyman, S., Kner, P., & Lechtreck, K. F. (2015) · The Journal of Cell Biology · doi:10.1083/jcb.201409036 · Cited by 197 · see citing works
Self-citationLiew, G. M., Ye, F., Nager, A. R., Murphy, J. P., Lee, J. S., Aguiar, M., Breslow, D. K., Gygi, S. P., & Nachury, M. V. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.09.004 · Cited by 193 · see citing works
Function and dynamics of PKD2 in Chlamydomonas reinhardtii flagella
Huang, K., Diener, D. R., Mitchell, A. P., Pazour, G. J., Witman, G. B., & Rosenbaum, J. L. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200704069 · Cited by 192 · see citing works
Architecture and function of IFT complex proteins in ciliogenesis
Taschner, M. J., Bhogaraju, S., & Lorentzen, E. (2011) · Differentiation · doi:10.1016/j.diff.2011.11.001 · Cited by 190 · see citing works
Intraflagellar transport delivers tubulin isotypes to sensory cilium middle and distal segments
Hao, L., Thein, M. C., Brust‐Mascher, I., Civelekoglu‐Scholey, G., Lu, Y., Açar, Ş., Prevo, B., Shaham, S., & Scholey, J. M. (2011) · Nature Cell Biology · doi:10.1038/ncb2268 · Cited by 188 · see citing works
Yen, H.-J., Tayeh, M. K., Mullins, R. F., Stone, E. M., Sheffield, V. C., & Slusarski, D. C. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddi468 · Cited by 180 · see citing works
Dissecting the Molecular Mechanisms of Intraflagellar Transport in Chlamydomonas
Pedersen, L. B., Geimer, S., & Rosenbaum, J. L. (2006) · Current Biology · doi:10.1016/j.cub.2006.02.020 · Cited by 174 · see citing works
An in vitro assay for entry into cilia reveals unique properties of the soluble diffusion barrier
Breslow, D. K., Koslover, E. F., Seydel, F., Spakowitz, A. J., & Nachury, M. V. (2013) · The Journal of Cell Biology · doi:10.1083/jcb.201212024 · Cited by 173 · see citing works
Williams, C. L., McIntyre, J. C., Norris, S. R., Jenkins, P. M., Zhang, L., Pei, Q., Verhey, K. J., & Martens, J. R. (2014) · Nature Communications · doi:10.1038/ncomms6813 · Cited by 171 · see citing works
A Differential Cargo-Loading Model of Ciliary Length Regulation by IFT
Wren, K. N., Weghe, J. C. V. D., Tritschler, D., Schauer, A., Patel, D. K., Smith, E. F., Porter, M. E., Kner, P., & Lechtreck, K. F. (2013) · Current Biology · doi:10.1016/j.cub.2013.10.044 · Cited by 164 · see citing works
Self-citationAhmed, N. T., Gao, C., Lucker, B. F., Cole, D. G., & Mitchell, D. R. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200802025 · Cited by 164 · see citing works
Wang, Q., Pan, J., & Snell, W. J. (2006) · Cell · doi:10.1016/j.cell.2006.02.044 · Cited by 154 · see citing works
Evolution of modular intraflagellar transport from a coatomer-like progenitor
van Dam, T. J. P., Townsend, M. J., Turk, M., Schlessinger, A., Šali, A., Field, M. C., & Huynen, M. A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1221011110 · Cited by 152 · see citing works
Chapter 5 Targeting Proteins to the Ciliary Membrane
Pazour, G. J., & Bloodgood, R. A. (2008) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(08)00805-3 · Cited by 145 · see citing works
Lechtreck, K. F., Brown, J. M., Sampaio, J. L., Craft, J. M., Shevchenko, A., Evans, J. E., & Witman, G. B. (2013) · Journal of Cell Biology · doi:10.1083/jcb.201207139 · Cited by 140 · see citing works
Self-citationYe, F., Breslow, D. K., Koslover, E. F., Spakowitz, A. J., Nelson, W. J., & Nachury, M. V. (2013) · eLife · doi:10.7554/elife.00654 · Cited by 138 · see citing works
Mueller, J. M., Perrone, C. A., Bower, R., Cole, D. G., & Porter, M. E. (2004) · Molecular Biology of the Cell · doi:10.1091/mbc.e04-10-0931 · Cited by 134 · see citing works
Brazelton, W. J., Amundsen, C. D., Silflow, C. D., & Lefebvre, P. A. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00485-7 · Cited by 128 · see citing works
Cao, M., Ning, J., Hernandez-Lara, C. I., Belzile, O., Wang, Q., Dutcher, S. K., Liu, Y., & Snell, W. J. (2015) · eLife · doi:10.7554/elife.05242 · Cited by 127 · see citing works
Brown, J., Marsala, C., Kosoy, R., & Gaertig, J. (1999) · Molecular Biology of the Cell · doi:10.1091/mbc.10.10.3081 · Cited by 124 · see citing works
Taschner, M. J., Kotsis, F., Bräuer, P., Kuehn, E. W., & Lorentzen, E. (2014) · The Journal of Cell Biology · doi:10.1083/jcb.201408002 · Cited by 120 · see citing works
Liang, Y., Pang, Y., Wu, Q., Hu, Z., Han, X., Xu, Y., Deng, H., & Pan, J. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.07.019 · Cited by 116 · see citing works
Wang, H., Gau, B. C., Slade, W. O., Juergens, M., Li, P., & Hicks, L. M. (2014) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m114.038281 · Cited by 115 · see citing works
Intraflagellar transport proteins cycle between the flagellum and its base
Buisson, J., Chenouard, N., Lagache, T., Blisnick, T., Olivo‐Marín, J., & Bastin, P. (2012) · Journal of Cell Science · doi:10.1242/jcs.117069 · Cited by 113 · see citing works
THE SITE OF IN VIVO ASSEMBLY OF FLAGELLAR MICROTUBULES*
Witman, G. B. (1975) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1975.tb19199.x · Cited by 112 · see citing works
The role of retrograde intraflagellar transport in flagellar assembly, maintenance, and function
Engel, B. D., Ishikawa, H., Wemmer, K. A., Geimer, S., Wakabayashi, K., Hirono, M., Craige, B., Pazour, G. J., Witman, G. B., Kamiya, R., et al. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201206068 · Cited by 111 · see citing works
Intraflagellar transport complex structure and cargo interactions
Bhogaraju, S., Engel, B. D., & Lorentzen, E. (2013) · Cilia · doi:10.1186/2046-2530-2-10 · Cited by 111 · see citing works
Intraflagellar transport drives flagellar surface motility
Shih, S. M., Engel, B. D., Kocabaş, F., Bilyard, T., Gennerich, A., Marshall, W. F., & Yıldız, A. (2013) · eLife · doi:10.7554/elife.00744 · Cited by 109 · see citing works
Bitter and sweet taste receptors in the respiratory epithelium in health and disease
Lee, R. J., & Cohen, N. A. (2014) · Journal of Molecular Medicine · doi:10.1007/s00109-014-1222-6 · Cited by 109 · see citing works
Crystal structure of the intraflagellar transport complex 25/27
Bhogaraju, S., Taschner, M. J., Morawetz, M., Minard‐Basquin, C., & Lorentzen, E. (2011) · The EMBO Journal · doi:10.1038/emboj.2011.110 · Cited by 104 · see citing works
Establishing a connection between cilia and Bardet–Biedl Syndrome
Mykytyn, K., & Sheffield, V. C. (2004) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2004.01.003 · Cited by 101 · see citing works
Immune synapse targeting of specific recycling receptors by the intraflagellar transport system
Finetti, F., Patrussi, L., Masi, G., Onnis, A., Galgano, D., Lucherini, O. M., Pazour, G. J., & Baldari, C. T. (2014) · Journal of Cell Science · doi:10.1242/jcs.139337 · Cited by 98 · see citing works
Broekhuis, J. R., Verhey, K. J., & Jansen, G. (2014) · PLoS ONE · doi:10.1371/journal.pone.0108470 · Cited by 97 · see citing works
Structural basis for membrane targeting of the BBSome by ARL6
Mourão, A., Nager, A. R., Nachury, M. V., & Lorentzen, E. (2014) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2920 · Cited by 86 · see citing works
Assembly of IFT Trains at the Ciliary Base Depends on IFT74
Brown, J., Cochran, D. A., Craige, B., Kubo, T., & Witman, G. B. (2015) · Current Biology · doi:10.1016/j.cub.2015.04.060 · Cited by 82 · see citing works
A Migrating Ciliary Gate Compartmentalizes the Site of Axoneme Assembly in Drosophila Spermatids
Basiri, M. L., Ha, A., Chadha, A., Clark, N. M., Polyanovsky, A. D., Cook, B., & Avidor‐Reiss, T. (2014) · Current Biology · doi:10.1016/j.cub.2014.09.047 · Cited by 74 · see citing works
Compartmentalized Calcium Signaling in Cilia Regulates Intraflagellar Transport
Collingridge, P. W., Brownlee, C., & Wheeler, G. L. (2013) · Current Biology · doi:10.1016/j.cub.2013.09.059 · Cited by 68 · see citing works
Uncoordinated (UNC)119: Coordinating the trafficking of myristoylated proteins
Constantine, R., Zhang, H., Gerstner, C. D., Frederick, J. M., & Baehr, W. (2012) · Vision Research · doi:10.1016/j.visres.2012.08.012 · Cited by 65 · see citing works
Hilton, L. K., Gunawardane, K., Kim, J. W., et al. (2013) · Current Biology · doi:10.1016/j.cub.2013.09.038 · Cited by 63 · see citing works
Sequential assembly of flagellar radial spokes
Diener, D. R., Yang, P., Geimer, S., et al. (2011) · Cytoskeleton · doi:10.1002/cm.20520 · Cited by 62 · see citing works
Belzile, O., Hernandez-Lara, C. I., Wang, Q., & Snell, W. J. (2013) · Current Biology · doi:10.1016/j.cub.2013.06.025 · Cited by 59 · see citing works
ParameciumBBS genes are key to presence of channels in Cilia
Valentine, M. S., Rajendran, A., Yano, J., Weeraratne, S. D., Beisson, J., Cohen, J., Koll, F., & Houten, J. V. (2012) · Cilia · doi:10.1186/2046-2530-1-16 · Cited by 58 · see citing works
Li, W., Yi, P., & Ou, G. (2015) · The Journal of Cell Biology · doi:10.1083/jcb.201411041 · Cited by 54 · see citing works
Proteins of the Ciliary Axoneme Are Found on Cytoplasmic Membrane Vesicles during Growth of Cilia
Wood, C. R., & Rosenbaum, J. L. (2014) · Current Biology · doi:10.1016/j.cub.2014.03.047 · Cited by 48 · see citing works
Fok, A. K., Wang, H., Katayama, A., et al. (1994) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.970290304 · Cited by 47 · see citing works
The Retrograde IFT Machinery of C. elegans Cilia: Two IFT Dynein Complexes?
Hao, L., Efimenko, E., Swoboda, P., & Scholey, J. M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020995 · Cited by 47 · see citing works
The blind leading the obese: the molecular pathophysiology of a human obesity syndrome.
Sheffield, V. C. (2010) · PubMed · Cited by 46 · see citing works
Getting tubulin to the tip of the cilium: One IFT train, many different tubulin cargo‐binding sites?
Bhogaraju, S., Weber, K., Engel, B. D., Lechtreck, K. F., & Lorentzen, E. (2014) · BioEssays · doi:10.1002/bies.201400007 · Cited by 42 · see citing works
Self-citationViswanadha, R., Hunter, E. L., Yamamoto, R., Wirschell, M., Alford, L. M., Dutcher, S. K., & Sale, W. S. (2014) · Cytoskeleton · doi:10.1002/cm.21192 · Cited by 41 · see citing works
NPHP proteins: gatekeepers of the ciliary compartment
Omran, H. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201008080 · Cited by 38 · see citing works
The sterols and fatty acids from purified flagella ofChlamydomonas reinhardi
Gealt, M. A., Adler, J. H., & Nes, W. R. (1981) · Lipids · doi:10.1007/bf02535687 · Cited by 33 · see citing works
The Chlamydomonas mutant pf27 reveals novel features of ciliary radial spoke assembly
Alford, L. M., Mattheyses, A. L., Hunter, E. L., Lin, H., Dutcher, S. K., & Sale, W. S. (2013) · Cytoskeleton · doi:10.1002/cm.21144 · Cited by 22 · see citing works
Lefebvre, P. A. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-370873-1.00042-3 · Cited by 17 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Cellular signalling by primary cilia in development, organ function and disease
Anvarian, Z., Mykytyn, K., Mukhopadhyay, S., Pedersen, L. B., & Christensen, S. T. (2019) · Nature Reviews Nephrology · doi:10.1038/s41581-019-0116-9 · Cited by 845 · see citing works
Structure of the Decorated Ciliary Doublet Microtubule
Ma, M., Stoyanova, M., Rademacher, G., Dutcher, S. K., Brown, A., & Zhang, R. (2019) · Cell · doi:10.1016/j.cell.2019.09.030 · Cited by 290 · see citing works
BBSome trains remove activated GPCRs from cilia by enabling passage through the transition zone
Ye, F., Nager, A. R., & Nachury, M. V. (2018) · Journal of Cell Biology · doi:10.1083/jcb.201709041 · Cited by 256 · see citing works
Intraflagellar transport: mechanisms of motor action, cooperation, and cargo delivery
Prevo, B., Scholey, J. M., & Peterman, E. J. G. (2017) · The FEBS Journal · doi:10.1111/febs.14068 · Cited by 203 · see citing works
Christensen, S. T., Morthorst, S. K., Mogensen, J. B., & Pedersen, L. B. (2017) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a028167 · Cited by 125 · see citing works
Multiciliated Cells in Animals
Meunier, A., & Azimzadeh, J. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a028233 · Cited by 117 · see citing works
Propulsive nanomachines: the convergent evolution of archaella, flagella and cilia
Beeby, M., Ferreira, J. L., Tripp, P., Albers, S.-V., & Mitchell, D. R. (2020) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaa006 · Cited by 110 · see citing works
Role for the IFT-A Complex in Selective Transport to the Primary Cilium
Fu, W., Wang, L., Kim, S., Li, J., & Dynlacht, B. D. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.10.018 · Cited by 86 · see citing works
Toropova, K., Mladenov, M., & Roberts, A. J. (2017) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.3391 · Cited by 85 · see citing works
The intraflagellar transport machinery in ciliary signaling
Mourão, A., Christensen, S. T., & Lorentzen, E. (2016) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2016.06.009 · Cited by 83 · see citing works
Interaction of heterotrimeric kinesin-II with IFT-B–connecting tetramer is crucial for ciliogenesis
Funabashi, T., Katoh, Y., Okazaki, M., Sugawa, M., & Nakayama, K. (2018) · Journal of Cell Biology · doi:10.1083/jcb.201801039 · Cited by 65 · see citing works
Kunova Bosakova, M., Varecha, M., Hampl, M., Duran, I., Nita, A., Buchtova, M., Dosedelova, H., Machat, R., Xie, Y., Ni, Z., et al. (2018) · Human Molecular Genetics · doi:10.1093/hmg/ddy031 · Cited by 50 · see citing works
Regulation of ciliary membrane protein trafficking and signalling by kinesin motor proteins
Morthorst, S. K., Christensen, S. T., & Pedersen, L. B. (2018) · The FEBS Journal · doi:10.1111/febs.14583 · Cited by 49 · see citing works
Scheidel, N., Kennedy, J., & Blacque, O. E. (2018) · The EMBO Journal · doi:10.15252/embj.201798248 · Cited by 38 · see citing works
Ryan, R., Failler, M., Reilly, M. L., Garfa-Traore, M., Delous, M., Filhol, E., Reboul, T., Bole-Feysot, C., Nitschké, P., Baudouin, V., et al. (2018) · Human Molecular Genetics · doi:10.1093/hmg/ddx396 · Cited by 48 · see citing works
Compartmentalization of Photoreceptor Sensory Cilia
Barnes, C. L., Malhotra, H., & Calvert, P. D. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.636737 · Cited by 44 · see citing works
The primary cilia are associated with the axon initial segment in neurons
Wang, H., Li, Y., Li, X., Sun, Z., Yu, F., Pashang, A., Kulasiri, D., Li, H. W., Chen, H., Hou, H., et al. (2025) · Advanced Science · doi:10.1002/advs.202407405 · Cited by 13 · see citing works
Primary cilia in the mature brain: emerging roles in Alzheimer's disease pathogenesis
Huang, A. S., Li, A. S. M., & Hor, C. H. H. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1650884 · Cited by 4 · see citing works
“Between the basal body and the axoneme, a region called transition zone serves as gatekeeper to control proteins in or out of the cilium (Lechtreck, 2015).”
- Authors
- Lechtreck, K. F.
- Affiliations
- University of Georgia (US)
- Corresponding author
- Lechtreck, Karl F.
- ORCID
- Lechtreck, Karl F.
- Venue
- Trends in Biochemical Sciences
- Publisher
- Elsevier BV
- Published
- 2015-12
- Volume
- 40
- Issue
- 12
- Pages
- 765-778
- ISSN
- 0968-0004 (ISSN-L)
- PMC
- PMC4661101
- OpenAlex
- W1809267070
- Cited by
- 316
- References
- 104
- Citations by year
- 2026: 8 · 2025: 17 · 2024: 24 · 2023: 35 · 2022: 28 · 2021: 37 · 2020: 42 · 2019: 32 · 2018: 32 · 2017: 35 · 2016: 24 · 2015: 1 · 2014: 1
- FWCI
- 3.94
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Trends in Biochemical Sciences (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of General Medical Sciences (R01GM110413, GM110413)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and Kidney Cyst Diseases
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Cystic Fibrosis Research Advances
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Hereditary Neurological Disorders
- Keywords
- intraflagellar transport, cilia, flagella, transition zone, ciliary microtubules, ciliary assembly, transport regulation
- MeSH terms
- Animals, Cilia, Humans, Microtubules, Proteins, 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.
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