Genome-wide Association of Yorkie with Chromatin and Chromatin-Remodeling Complexes
Open accessAbstract
The Hippo pathway regulates growth through the transcriptional coactivator Yorkie, but how Yorkie promotes transcription remains poorly understood. We address this by characterizing Yorkie's association with chromatin and by identifying nuclear partners that effect transcriptional activation. Coimmunoprecipitation and mass spectrometry identify GAGA factor (GAF), the Brahma complex, and the Mediator complex as Yorkie-associated nuclear protein complexes. All three are required for Yorkie's transcriptional activation of downstream genes, and GAF and the Brahma complex subunit Moira interact directly with Yorkie. Genome-wide chromatin-binding experiments identify thousands of Yorkie sites, most of which are associated with elevated transcription, based on genome-wide analysis of messenger RNA and histone H3K4Me3 modification. Chromatin binding also supports extensive functional overlap between Yorkie and GAF. Our studies suggest a widespread role for Yorkie as a regulator of transcription and identify recruitment of the chromatin-modifying GAF protein and BRM complex as a molecular mechanism for transcriptional activation by Yorkie.
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
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?
Drosophila Yki regulates transcription by binding to promoter regions of genes.
“Like YAP, Drosophila Yki is known to regulate transcription by binding to promoter regions of genes (76).”
From A Tumour-Specific Molecular Network Promotes Tumour Growth in <i>Drosophila</i> by Enforcing a JNK-YKI Feedforward Loop (2023) · cites this paper as [76]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Fast and accurate short read alignment with Burrows-Wheeler transform
Li, H., & Durbin, R. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp324 · Cited by 58,607 · see citing works
Subramanian, A., Tamayo, P., Mootha, V. K., Mukherjee, S., Ebert, B. L., Gillette, M. A., Paulovich, A., Pomeroy, S. L., Golub, T. R., Lander, E. S., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506580102 · Cited by 53,625 · see citing works
Model-based Analysis of ChIP-Seq (MACS)
Zhang, Y., Liu, T., Meyer, C. A., Eeckhoute, J., Johnson, D. S., Bernstein, B. E., Nusbaum, C., Myers, R. M., Brown, M., Li, W., et al. (2008) · Genome Biology · doi:10.1186/gb-2008-9-9-r137 · Cited by 18,386 · see citing works
Differential expression analysis for sequence count data
Anders, S., & Huber, W. (2010) · Genome Biology · doi:10.1186/gb-2010-11-10-r106 · Cited by 15,581 · see citing works
Trapnell, C., Williams, B. A., Pertea, G., Mortazavi, A., Kwan, G., van Baren, M. J., Salzberg, S. L., Wold, B. J., & Pachter, L. (2010) · Nature Biotechnology · doi:10.1038/nbt.1621 · Cited by 15,556 · see citing works
The Role of Chromatin during Transcription
Li, B., Carey, M., & Workman, J. L. (2007) · Cell · doi:10.1016/j.cell.2007.01.015 · Cited by 3,503 · see citing works
Elucidation of a universal size-control mechanism in Drosophila and mammals
Dong, J., Feldmann, G., Huang, J., Wu, S., Zhang, N., Comerford, S. A., Gayyed, M. F., Anders, R. A., Maitra, A., & Pan, D. (2007) · Cell · doi:10.1016/j.cell.2007.07.019 · Cited by 2,370 · see citing works
Brennecke, J., Hipfner, D. R., Stark, A., Russell, R. B., & Cohen, S. M. (2003) · Cell · doi:10.1016/s0092-8674(03)00231-9 · Cited by 1,721 · see citing works
Transcriptional Amplification in Tumor Cells with Elevated c-Myc
Lin, C. Y., Lovén, J., Rahl, P. B., Paranal, R. M., Burge, C. B., Bradner, J. E., Lee, T. I., & Young, R. A. (2012) · Cell · doi:10.1016/j.cell.2012.08.026 · Cited by 1,498 · see citing works
The Hippo pathway in organ size control, tissue regeneration and stem cell self-renewal
Zhao, B., Tumaneng, K., & Guan, K.-L. (2011) · Nature Cell Biology · doi:10.1038/ncb2303 · Cited by 1,205 · see citing works
c-Myc Is a Universal Amplifier of Expressed Genes in Lymphocytes and Embryonic Stem Cells
Nie, Z., Hu, G., Wei, G., Cui, K., Yamane, A., Resch, W., Wang, R., Green, D. R., Tessarollo, L., Casellas, R. C., et al. (2012) · Cell · doi:10.1016/j.cell.2012.08.033 · Cited by 1,063 · see citing works
FoxA1 Translates Epigenetic Signatures into Enhancer-Driven Lineage-Specific Transcription
Lupien, M., Eeckhoute, J., Meyer, C. A., Wang, Q., Zhang, Y., Li, W., Carroll, J. S., Liu, X. S., & Brown, M. (2008) · Cell · doi:10.1016/j.cell.2008.01.018 · Cited by 983 · see citing works
Justice, R. W., Zilian, O., Woods, D. F., Noll, M., & Bryant, P. J. (1995) · Genes & Development · doi:10.1101/gad.9.5.534 · Cited by 977 · see citing works
MYC as a regulator of ribosome biogenesis and protein synthesis
van Riggelen, J., Yetil, A., & Felsher, D. W. (2010) · Nature Reviews Cancer · doi:10.1038/nrc2819 · Cited by 956 · see citing works
Xu, T., Wang, W., Zhang, S., Stewart, R. A., & Yu, W. (1995) · Development · doi:10.1242/dev.121.4.1053 · Cited by 799 · see citing works
The metazoan Mediator co-activator complex as an integrative hub for transcriptional regulation
Malik, S., & Roeder, R. G. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2901 · Cited by 730 · see citing works
Cistrome: an integrative platform for transcriptional regulation studies
Liu, T., Ortiz, J. A., Taing, L., Meyer, C. A., Lee, B. T. K., Zhang, Y., Shin, H., Wong, S. S., Ma, J., Lei, Y., et al. (2011) · Genome biology · doi:10.1186/gb-2011-12-8-r83 · Cited by 705 · see citing works
Liu, X. S., Brutlag, D. L., & Liu, J. S. (2002) · Nature Biotechnology · doi:10.1038/nbt717 · Cited by 670 · see citing works
TAZ controls Smad nucleocytoplasmic shuttling and regulates human embryonic stem-cell self-renewal
Varelas, X., Sakuma, R., Samavarchi‐Tehrani, P., Peerani, R., Rao, B. M., Dembowy, J., Yaffe, M. B., Zandstra, P. W., & Wrana, J. L. (2008) · Nature Cell Biology · doi:10.1038/ncb1748 · Cited by 666 · see citing works
Wu, S., Liu, Y., Zheng, Y., Dong, J., & Pan, D. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.01.007 · Cited by 640 · see citing works
The TEAD/TEF family of transcription factor Scalloped mediates Hippo signaling in organ size control
Zhang, L., Ren, F., Zhang, Q., Chen, Y., Wang, B., & Jiang, J. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.01.006 · Cited by 630 · see citing works
Purification and properties of an ATP-dependent nucleosome remodeling factor
Tsukiyama, T., & Wu, C. C. M. (1995) · Cell · doi:10.1016/0092-8674(95)90216-3 · Cited by 616 · see citing works
A cis-regulatory map of the Drosophila genome
Negre, N. N., Brown, C. D., Ma, L., Bristow, C. A., Miller, S. W., Wagner, U., Kheradpour, P., Eaton, M. L., Loriaux, P. M., Sealfon, R. S. G., et al. (2011) · Nature · doi:10.1038/nature09990 · Cited by 500 · see citing works
Self-citationCEAS: <i>cis</i>-regulatory element annotation system
Shin, H., Liu, T., Manrai, A. K., & Liu, X. S. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp479 · Cited by 461 · see citing works
The Trithorax-like gene encodes the Drosophila GAGA factor
Farkas, G., Gausz, J., Galloni, M., Reuter, G., Gyurkovics, H., & Karch, F. (1994) · Nature · doi:10.1038/371806a0 · Cited by 411 · see citing works
In vivo regulation of Yorkie phosphorylation and localization
Oh, H., & Irvine, K. D. (2008) · Development · doi:10.1242/dev.015255 · Cited by 404 · see citing works
Self-citationHistone H3 lysine 4 (H3K4) methylation in development and differentiation
Eissenberg, J. C., & Shilatifard, A. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.08.017 · Cited by 356 · see citing works
Recent advances in understanding chromatin remodeling by Swi/Snf complexes
Martens, J. A., & Winston, F. (2003) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(03)00022-4 · Cited by 352 · see citing works
A Comprehensive Map of Insulator Elements for the Drosophila Genome
Negre, N. N., Brown, C. D., Shah, P. K., Kheradpour, P., Morrison, C. A., Henikoff, J. G., Feng, X., Ahmad, K., Russell, S. R. H., White, R. A., et al. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1000814 · Cited by 333 · see citing works
Self-citationIn vivo analysis of Yorkie phosphorylation sites
Oh, H., & Irvine, K. D. (2009) · Oncogene · doi:10.1038/onc.2009.43 · Cited by 196 · see citing works
Self-citationPeng, H., Slattery, M. G., & Mann, R. S. (2009) · Genes & Development · doi:10.1101/gad.1820009 · Cited by 188 · see citing works
Self-citationElfring, L. K., Daniel, C., Papoulas, O., Deuring, R., Sarte, M., Moseley, S. L., Beek, S. J., Waldrip, W. R., Daubresse, G., DePace, A. H., et al. (1998) · Genetics · doi:10.1093/genetics/148.1.251 · Cited by 186 · see citing works
The Drosophila BRM complex facilitates global transcription by RNA polymerase II
Armstrong, J. A., Papoulas, O., Daubresse, G., Sperling, A. S., Lis, J. T., Scott, M. P., & Tamkun, J. W. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf517 · Cited by 172 · see citing works
Yorkie: the final destination of Hippo signaling
Oh, H., & Irvine, K. D. (2010) · Trends in Cell Biology · doi:10.1016/j.tcb.2010.04.005 · Cited by 164 · see citing works
Self-citationAction of fat, four-jointed, dachsous and dachs in distal-to-proximal wing signaling
Cho, E., & Irvine, K. D. (2004) · Development · doi:10.1242/dev.01315 · Cited by 162 · see citing works
Self-citationCooperative Regulation of Growth by Yorkie and Mad through bantam
Oh, H., & Irvine, K. D. (2011) · Developmental Cell · doi:10.1016/j.devcel.2010.12.002 · Cited by 149 · see citing works
Self-citationCulí, J., & Mann, R. S. (2003) · Cell · doi:10.1016/s0092-8674(02)01279-5 · Cited by 138 · see citing works
Self-citationShimojima, T., Okada, M., Nakayama, T. W., Ueda, H., Okawa, K., Iwamatsu, A., Handa, H., & Hirose, S. (2003) · Genes & Development · doi:10.1101/gad.1086803 · Cited by 122 · see citing works
Anything else but GAGA: a nonhistone protein complex reshapes chromatin structure
Lehmann, M. (2003) · Trends in Genetics · doi:10.1016/j.tig.2003.11.005 · Cited by 86 · see citing works
Halder, G. A., & Carroll, S. B. (2001) · Development · doi:10.1242/dev.128.17.3295 · Cited by 85 · see citing works
Adkins, N. L., Hagerman, T. A., & Georgel, P. (2006) · Biochemistry and Cell Biology · doi:10.1139/o06-062 · Cited by 78 · see citing works
Vertebrate Homologue of Drosophila GAGA Factor
Matharu, N. K., Hussain, T., Sankaranarayanan, R., & Mishra, R. K. (2010) · Journal of Molecular Biology · doi:10.1016/j.jmb.2010.05.010 · Cited by 64 · see citing works
Nicolay, B., Bayarmagnai, B., Islam, A. B. M. M. K., López-Bigas, N., & Frolov, M. V. (2011) · Genes & Development · doi:10.1101/gad.1999211 · Cited by 52 · see citing works
Transcriptional activation by GAGA factor is through its direct interaction with dmTAF3
Chopra, V. S., Srinivasan, A., Kumar, R. P., Mishra, K., Basquin, D., Docquier, M., Seum, C., Pauli, D., & Mishra, R. K. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.02.008 · Cited by 50 · see citing works
Developmental Regulation of Chromatin Conformation by Hox Proteins in Drosophila
Agelopoulos, M., McKay, D. J., & Mann, R. S. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.03.003 · Cited by 48 · see citing works
Self-citationGenome-wide chromatin occupancy analysis reveals a role for ASH2 in transcriptional pausing
Pérez-Lluch, S., Blanco, E., Carbonell, A., Raha, D., Snyder, M. P., Serras, F., & Corominas, M. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkq1322 · Cited by 40 · see citing works
Blaumueller, C. M., & Mlodzik, M. (2000) · Mechanisms of Development · doi:10.1016/s0925-4773(00)00246-x · Cited by 36 · see citing works
Terriente-Félix, A., López‐Varea, A., & de Celis, J. F. (2010) · Genetics · doi:10.1534/genetics.109.113670 · Cited by 19 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Hippo pathway in organ size control, tissue homeostasis, and cancer
Yu, F.-X., Zhao, B., & Guan, K.-L. (2015) · Cell · doi:10.1016/j.cell.2015.10.044 · Cited by 2,206 · see citing works
The Biology of YAP/TAZ: Hippo Signaling and Beyond
Piccolo, S., Dupont, S., & Cordenonsi, M. (2014) · Physiological Reviews · doi:10.1152/physrev.00005.2014 · Cited by 1,797 · see citing works
Mechanisms of Hippo pathway regulation
Meng, Z., Moroishi, T., & Guan, K.-L. (2016) · Genes & Development · doi:10.1101/gad.274027.115 · Cited by 1,667 · see citing works
The Hippo Pathway: Biology and Pathophysiology
Ma, S., Meng, Z., Chen, R., & Guan, K.-L. (2019) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-013118-111829 · Cited by 1,387 · see citing works
Hippo–YAP/TAZ signalling in organ regeneration and regenerative medicine
Moya, I. M., & Halder, G. (2019) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-018-0086-y · Cited by 981 · see citing works
The Hippo Signaling Pathway in Development and Disease
Zheng, Y., & Pan, D. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.06.003 · Cited by 867 · see citing works
The two faces of Hippo: targeting the Hippo pathway for regenerative medicine and cancer treatment
Johnson, R. L., & Halder, G. A. (2013) · Nature Reviews Drug Discovery · doi:10.1038/nrd4161 · Cited by 884 · see citing works
YAP and TAZ: a nexus for Hippo signaling and beyond
Hansen, C. G., Moroishi, T., & Guan, K. (2015) · Trends in Cell Biology · doi:10.1016/j.tcb.2015.05.002 · Cited by 573 · see citing works
The Hippo Signaling Network and Its Biological Functions
Misra, J. R., & Irvine, K. D. (2018) · Annual Review of Genetics · doi:10.1146/annurev-genet-120417-031621 · Cited by 496 · see citing works
Self-citationYAP/TAZ Signaling and Resistance to Cancer Therapy
Nguyen, C. D. K., & Yi, C. (2019) · Trends in Cancer · doi:10.1016/j.trecan.2019.02.010 · Cited by 437 · see citing works
Couzens, A. L., Knight, J. D. R., Kean, M. J., Teo, G., Weiss, A., Dunham, W. H., Lin, Z., Bagshaw, R. D., Sicheri, F., Pawson, T. J., et al. (2013) · Science Signaling · doi:10.1126/scisignal.2004712 · Cited by 440 · see citing works
YAP1 Exerts Its Transcriptional Control via TEAD-Mediated Activation of Enhancers
Stein, C., Bardet, A. F., Roma, G., Bergling, S., Clay, I., Ruchti, A., Agarinis, C., Schmelzle, T., Bouwmeester, T., Schübeler, D., et al. (2015) · PLOS Genetics · doi:10.1371/journal.pgen.1005465 · Cited by 414 · see citing works
Integrin signalling regulates YAP/TAZ to control skin homeostasis
Elbediwy, A., Vincent‐Mistiaen, Z. I., Spencer‐Dene, B., Stone, R. K., Boeing, S., Wculek, S. K., Cordero, J., Tan, E. H., Ridgway, R., Brunton, V. G., et al. (2016) · Development · doi:10.1242/dev.133728 · Cited by 307 · see citing works
Beyer, T. A., Weiss, A., Khomchuk, Y., Huang, K., Ogunjimi, A. A., Varelas, X., & Wrana, J. L. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.11.021 · Cited by 293 · see citing works
YAP Drives Growth by Controlling Transcriptional Pause Release from Dynamic Enhancers
Galli, G. G., Carrara, M., Yuan, W.-C., Valdes-Quezada, C., Gurung, B., Pepe-Mooney, B., Zhang, T., Geeven, G., Gray, N. S., de Laat, W., et al. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.09.001 · Cited by 290 · see citing works
Transcriptional Co-repressor Function of the Hippo Pathway Transducers YAP and TAZ
Kim, M., Kim, T., Johnson, R. L., & Lim, D. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.03.015 · Cited by 285 · see citing works
The Hippo Pathway in Liver Homeostasis and Pathophysiology
Driskill, J. H., & Pan, D. (2020) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathol-030420-105050 · Cited by 232 · see citing works
Hiemer, S. E., Szymaniak, A. D., & Varelas, X. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.529115 · Cited by 227 · see citing works
The Hippo Pathway in Heart Development, Regeneration, and Diseases
Zhou, Q., Li, L., Zhao, B., & Guan, K. (2015) · Circulation Research · doi:10.1161/circresaha.116.303311 · Cited by 219 · see citing works
The Hippo Signaling Pathway Interactome
Kwon, Y. V., Vinayagam, A., Sun, X., Dephoure, N., Gygi, S. P., Hong, P., & Perrimon, N. (2013) · Science · doi:10.1126/science.1243971 · Cited by 178 · see citing works
Targeting the Hippo Pathway and Cancer through the TEAD Family of Transcription Factors
Holden, J. K., & Cunningham, C. N. (2018) · Cancers · doi:10.3390/cancers10030081 · Cited by 175 · see citing works
Transient loss of Polycomb components induces an epigenetic cancer fate
Parreno, V., Loubière, V., Schuettengruber, B., Fritsch, L., Rawal, C. C., Erokhin, M., Győrffy, B., Normanno, D., Stefano, M. D., Moreaux, J., et al. (2024) · Nature · doi:10.1038/s41586-024-07328-w · Cited by 169 · see citing works
Control of stem cell renewal and fate by YAP and TAZ
Driskill, J. H., & Pan, D. (2023) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-023-00644-5 · Cited by 165 · see citing works
Skibinski, A., Breindel, J. L., Prat, A., Galván, P., Smith, E., Rolfs, A., Gupta, P. B., LaBaer, J., & Kuperwasser, C. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.02.038 · Cited by 159 · see citing works
YAP1 and its fusion proteins in cancer initiation, progression and therapeutic resistance
Szulzewsky, F., Holland, E. C., & Vasioukhin, V. I. (2021) · Developmental Biology · doi:10.1016/j.ydbio.2020.12.018 · Cited by 154 · see citing works
The regulation and function of YAP transcription co-activator
Zhu, C., Li, L., & Zhao, B. (2014) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmu110 · Cited by 136 · see citing works
Hippo Pathway Regulation of Gastrointestinal Tissues
Yu, F., Meng, Z., Plouffe, S. W., & Guan, K. (2014) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021014-071733 · Cited by 138 · see citing works
Cellular Organization and Cytoskeletal Regulation of the Hippo Signaling Network
Sun, S., & Irvine, K. D. (2016) · Trends in Cell Biology · doi:10.1016/j.tcb.2016.05.003 · Cited by 135 · see citing works
Self-citationZhu, C., Li, L., Zhang, Z., Bi, M., Wang, H., Su, W., Hernandez, K., Liu, P., Chen, J., Chen, M., et al. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.06.010 · Cited by 120 · see citing works
The transcriptional response to tumorigenic polarity loss in Drosophila
Bunker, B. D., Nellimoottil, T. T., Boileau, R. M., Classen, A. K., & Bilder, D. (2015) · eLife · doi:10.7554/elife.03189 · Cited by 114 · see citing works
Broad‐complex, tramtrack, and bric‐à‐brac (BTB) proteins: Critical regulators of development
Chaharbakhshi, E. O., & Jemc, J. C. (2016) · genesis · doi:10.1002/dvg.22964 · Cited by 106 · see citing works
Role of the Hippo pathway and mechanisms for controlling cellular localization of YAP/TAZ
Kwon, H., Kim, J.-Y., & Jho, E. (2021) · FEBS Journal · doi:10.1111/febs.16091 · Cited by 101 · see citing works
The Roles of YAP/TAZ and the Hippo Pathway in Healthy and Diseased Skin
Rognoni, E., & Walko, G. (2019) · Cells · doi:10.3390/cells8050411 · Cited by 100 · see citing works
Role of YAP/TAZ transcriptional regulators in resistance to anti-cancer therapies
Kim, M. H., & Kim, J. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2412-x · Cited by 98 · see citing works
The Hippo signal transduction network in skeletal and cardiac muscle
Wackerhage, H., Del Re, D. P., Judson, R. N., Sudol, M., & Sadoshima, J. (2014) · Science Signaling · doi:10.1126/scisignal.2005096 · Cited by 92 · see citing works
Wu, B.-K., Mei, S.-C., Chen, E. H., Zheng, Y., & Pan, D. (2022) · Nature Genetics · doi:10.1038/s41588-022-01119-7 · Cited by 90 · see citing works
Dynamic Fluctuations in Subcellular Localization of the Hippo Pathway Effector Yorkie In Vivo
Manning, S. A., Dent, L., Kondo, S., Zhao, Z., Plachta, N., & Harvey, K. F. (2018) · Current Biology · doi:10.1016/j.cub.2018.04.018 · Cited by 90 · see citing works
GAGA-associated factor fosters loop formation in the Drosophila genome
Li, X., Tang, X., Bing, X., Catalano, C., Li, T., Dolsten, G. A., Wu, C., & Levine, M. (2023) · Molecular Cell · doi:10.1016/j.molcel.2023.03.011 · Cited by 77 · see citing works
Yorkie Promotes Transcription by Recruiting a Histone Methyltransferase Complex
Oh, H., Slattery, M. G., Ma, L., White, K. P., Mann, R. S., & Irvine, K. D. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.06.017 · Cited by 77 · see citing works
Self-citationQing, Y., Yin, F., Wang, W., Zheng, Y., Guo, P., Schozer, F., Deng, H., & Pan, D. (2014) · eLife · doi:10.7554/elife.02564 · Cited by 72 · see citing works
Hippo Gains Weight: Added Insights and Complexity to Pathway Control
Enderle, L., & McNeill, H. (2013) · Science Signaling · doi:10.1126/scisignal.2004208 · Cited by 70 · see citing works
The Roles of Hippo Signaling Transducers Yap and Taz in Chromatin Remodeling
Hillmer, R. E., & Link, B. A. (2019) · Cells · doi:10.3390/cells8050502 · Cited by 70 · see citing works
YAP promotes breast cancer metastasis by repressing growth differentiation factor-15
Wang, T., Mao, B., Cheng, C., Zou, Z., Gao, J., Yang, Y., Lei, T., Qi, X., Yuan, Z., Xu, W., et al. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2018.02.020 · Cited by 66 · see citing works
Jin, Y., Xu, J., Yin, M.-X., Lu, Y., Hu, L., Li, P., Zhang, P., Yuan, Z., Ho, M. S.-C., Ji, H., et al. (2013) · eLife · doi:10.7554/elife.00999 · Cited by 65 · see citing works
Targeting the Hippo pathway in cancer
Harvey, K. F., & Tang, T. T.-L. (2025) · Nature Reviews Drug Discovery · doi:10.1038/s41573-025-01234-0 · Cited by 64 · see citing works
Emerging Principles in the Transcriptional Control by YAP and TAZ
Lopez-Hernandez, A., Sberna, S., & Campaner, S. (2021) · Cancers · doi:10.3390/cancers13164242 · Cited by 59 · see citing works
Pfleger, C. M. (2017) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2016.12.001 · Cited by 61 · see citing works
Ikmi, A., Gaertner, B., Seidel, C. W., Srivastava, M., Zeitlinger, J., & Gibson, M. C. (2014) · Molecular Biology and Evolution · doi:10.1093/molbev/msu071 · Cited by 55 · see citing works
Boone, É., Colombani, J., Andersen, D. S., & Léopold, P. (2016) · Nature Communications · doi:10.1038/ncomms13505 · Cited by 55 · see citing works
Changes in chromatin accessibility ensure robust cell cycle exit in terminally differentiated cells
Ma, Y., McKay, D. J., & Buttitta, L. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000378 · Cited by 52 · see citing works
GAGA factor: a multifunctional pioneering chromatin protein
Chetverina, D., Erokhin, M., & Schedl, P. D. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03776-z · Cited by 52 · see citing works
Regulation of Tissue Growth by the Mammalian Hippo Signaling Pathway
Watt, K. I., Harvey, K. F., & Gregorevic, P. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00942 · Cited by 52 · see citing works
Grendler, J., Lowgren, S., Mills, M. T., & Losick, V. P. (2018) · Development · doi:10.1242/dev.173005 · Cited by 40 · see citing works
Hippo‐Yap/Taz signaling: Complex network interactions and impact in epithelial cell behavior
van Soldt, B. J., & Cardoso, W. V. (2019) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.371 · Cited by 50 · see citing works
Tsai, S., Chang, Y.-L., Swamy, K. B. S., Chiang, R.-L., & Huang, D.-H. (2016) · Epigenetics & Chromatin · doi:10.1186/s13072-016-0082-4 · Cited by 47 · see citing works
Yap regulates skeletal muscle fatty acid oxidation and adiposity in metabolic disease
Watt, K., Henstridge, D., Ziemann, M., Sim, C., Montgomery, M., Samocha-Bonet, D., Parker, B., Dodd, G., Bond, S., Salmi, T. M., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-23240-7 · Cited by 38 · see citing works
Valencia-Sama, I., Zhao, Y., Lai, D., van Rensburg, H. J. J., Hao, Y., & Yang, X. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.642363 · Cited by 46 · see citing works
Integration of mechanical and chemical signals by YAP and TAZ transcription coactivators
Guo, X., & Zhao, B. (2013) · Cell & Bioscience · doi:10.1186/2045-3701-3-33 · Cited by 45 · see citing works
Organ of Corti size is governed by Yap/Tead-mediated progenitor self-renewal
Gnedeva, K., Wang, X., McGovern, M. M., Barton, M., Tao, L., Trecek, T., Monroe, T. O., Llamas, J., Makmura, W., Martin, J. F., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2000175117 · Cited by 46 · see citing works
SWI/SNF chromatin remodeling controls Notch-responsive enhancer accessibility
Pillidge, Z., & Bray, S. (2018) · bioRxiv · doi:10.15252/embr.201846944 · Cited by 41 · see citing works
Slattery, M. G., Voutev, R., Ma, L., Negre, N. N., White, K. P., & Mann, R. S. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003753 · Cited by 41 · see citing works
Self-citationIncreased ACTL6A occupancy within mSWI/SNF chromatin remodelers drives human squamous cell carcinoma
Chang, C.-Y., Shipony, Z., Lin, S. G., Kuo, A., Xiong, X., Loh, K. M., Greenleaf, W. J., & Crabtree, G. R. (2021) · Molecular Cell · doi:10.1016/j.molcel.2021.10.005 · Cited by 41 · see citing works
Organ Size Control Is Dominant over Rb Family Inactivation to Restrict Proliferation In Vivo
Ehmer, U., Zmoos, A., Auerbach, R. K., Vaka, D., Butte, A. J., Kay, M. A., & Sage, J. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.06.025 · Cited by 39 · see citing works
Zhang, P., Pei, C., Wang, X., Xiang, J., Sun, B.-F., Cheng, Y., Qi, X., Marchetti, M., Xu, J.-W., Sun, Y.-P., et al. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.10.033 · Cited by 36 · see citing works
Lorberbaum, D. S., Ramos, A. I., Peterson, K. A., Carpenter, B. S., Parker, D. S., De, S., Hillers‐Ziemer, L. E., Blake, V. M., Nishi, Y., McFarlane, M., et al. (2016) · eLife · doi:10.7554/elife.13550 · Cited by 38 · see citing works
Zhu, Y., Li, D., Wang, Y., Pei, C., Liu, S., Zhang, L., Yuan, Z., & Zhang, P. (2014) · Cellular Signalling · doi:10.1016/j.cellsig.2014.12.002 · Cited by 37 · see citing works
Valipour, E., Kowsari, A., Bayat, H., Banan, M., Kazeminasab, S., Mohammadparast, S., & Ohadi, M. (2013) · Gene · doi:10.1016/j.gene.2013.09.032 · Cited by 37 · see citing works
Shavenbaby and Yorkie mediate Hippo signaling to protect adult stem cells from apoptosis
Bohere, J. G., Mancheno-Ferris, A., Hayek, S. A., Zanet, J., Valenti, P., Akino, K., Yamabe, Y., Inagaki, S., Chanut-Delalande, H., Plaza, S., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-07569-0 · Cited by 36 · see citing works
Control of tissue morphogenesis by the HOX gene Ultrabithorax
Díaz-de-la-Loza, M.-D.-C., Loker, R., Mann, R. S., & Thompson, B. J. (2020) · Development · doi:10.1242/dev.184564 · Cited by 36 · see citing works
Self-citationMst1 positively regulates B-cell receptor signaling via CD19 transcriptional levels
Bai, X., Huang, L., Niu, L., Zhang, Y., Wang, J., Sun, X., Jiang, H., Zhang, Z., Miller, H. E., Tao, W., et al. (2016) · Blood Advances · doi:10.1182/bloodadvances.2016000588 · Cited by 35 · see citing works
Atrophin controls developmental signaling pathways via interactions with Trithorax-like
Yeung, K., Boija, A., Karlsson, E., Holmqvist, P.-H., Tsatskis, Y., Nisoli, I., Yap, D., Lorzadeh, A., Moksa, M., Hirst, M., et al. (2017) · eLife · doi:10.7554/elife.23084 · Cited by 34 · see citing works
Türkel, N., Sahota, V. K., Bolden, J. E., Goulding, K. R., Doggett, K., Willoughby, L. F., Blanco, E., Martı́n-Blanco, E., Corominas, M., Ellul, J., et al. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003627 · Cited by 33 · see citing works
Diverse patterns of genomic targeting by transcriptional regulators in Drosophila melanogasterPreprint
Slattery, M., Ma, L., Spokony, R. F., Arthur, R. K., Kheradpour, P., Kundaje, A., Nègre, N., Crofts, A., Ptashkin, R., Zieba, J., et al. (2014) · Genome Research · doi:10.1101/gr.168807.113 · Cited by 33 · see citing works
Self-citationScalloped and Yorkie are required for cell cycle re-entry of quiescent cells after tissue damage
Meserve, J. H., & Duronio, R. J. (2015) · Development · doi:10.1242/dev.119339 · Cited by 32 · see citing works
Hsu, T.-H., Yang, C.-Y., Yeh, T.-H., Huang, Y.-C., Wang, T., & Yu, J. (2017) · Scientific Reports · doi:10.1038/s41598-017-04052-6 · Cited by 32 · see citing works
Heuberger, J., Grinat, J., Kosel, F., Liu, L., Kunz, S., Vidal, R. O., Keil, M., Haybaeck, J., Robine, S., Louvard, D., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2019699118 · Cited by 31 · see citing works
Jeibmann, A., Eikmeier, K., Linge, A., Kool, M., Koos, B., Schulz, J., Albrecht, S., Bartelheim, K., Frühwald, M. C., Pfister, S. M., et al. (2014) · Nature Communications · doi:10.1038/ncomms5005 · Cited by 30 · see citing works
Paul, S., Xie, S., Yao, X., & Dey, A. (2022) · Cells · doi:10.3390/cells11142225 · Cited by 25 · see citing works
Howard, A., Bojko, J., Flynn, B. P., Bowen, S., Jungwirth, U., & Walko, G. (2022) · Experimental Dermatology · doi:10.1111/exd.14655 · Cited by 26 · see citing works
Small-Molecule Cyanamide Pan-TEAD·YAP1 Covalent Antagonists
Bum‐Erdene, K., Yeh, I., González-Gutiérrez, G., Ghozayel, M. K., Pollok, K. E., & Meroueh, S. O. (2022) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.2c01189 · Cited by 24 · see citing works
Natural compounds targeting YAP/TAZ axis in cancer: Current state of art and challenges
Kumar, A., BharathwajChetty, B., Manickasamy, M. K., Unnikrishnan, J., Alqahtani, M. S., Abbas, M., Almubarak, H. A., Sethi, G., & Kunnumakkara, A. B. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2024.107167 · Cited by 23 · see citing works
Metabolic control of progenitor cell propagation during Drosophila tracheal remodeling
Li, Y., Dong, P., Yang, Y., Guo, T., Zhao, Q., Miao, D., Li, H., Lu, T., Xia, F., Lyu, J., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-30492-4 · Cited by 23 · see citing works
Hippo signaling in epithelial stem cells
Yin, M.-X., & Zhang, L. (2014) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmu111 · Cited by 22 · see citing works
Emamalizadeh, B., Movafagh, A., Darvish, H., Kazeminasab, S., Andarva, M., Namdar‐Aligoodarzi, P., & Ohadi, M. (2017) · Molecular Genetics and Genomics · doi:10.1007/s00438-017-1294-4 · Cited by 21 · see citing works
Li, X., Liu, M., Ren, X., Loncle, N., Wang, Q., Hemba-Waduge, R.-U.-S., Yu, S. H., Boube, M., Bourbon, H.-M. G., Ni, J., et al. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1008832 · Cited by 20 · see citing works
Hippo signaling suppresses tumor cell metastasis via a Yki-Src42A positive feedback loop
Ding, Y., Wang, G., Zhan, M., Sun, X., Deng, Y., Zhao, Y., Liu, B., Liu, Q., Wu, S., & Zhou, Z. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-04423-y · Cited by 19 · see citing works
A Variably Occupied CTCF Binding Site in the Ultrabithorax Gene in the Drosophila Bithorax Complex
Magbanua, J., Runneburger, E., Russell, S., & White, R. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.01061-14 · Cited by 22 · see citing works
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 19 · see citing works
Spatial regulation of expanded transcription in the Drosophila wing imaginal disc
Wang, L.-H., & Baker, N. E. (2018) · PLoS ONE · doi:10.1371/journal.pone.0201317 · Cited by 18 · see citing works
A Drosophila model of oral peptide therapeutics for adult intestinal stem cell tumors
Bajpai, A., Ahmad, Q. T., Tang, H.-W., Manzar, N., Singh, V. P., Thakur, A. K., Ateeq, B., Perrimon, N., & Sinha, P. (2020) · Disease Models & Mechanisms · doi:10.1242/dmm.044420 · Cited by 17 · see citing works
Nuclear receptors connect progenitor transcription factors to cell cycle control
Neto, M., Naval-Sánchez, M., Potier, D., Pereira, P. S., Geerts, D., Aerts, S., & Casares, F. (2017) · Scientific Reports · doi:10.1038/s41598-017-04936-7 · Cited by 16 · see citing works
Song, S., Herranz, H., & Cohen, S. M. (2017) · Disease Models & Mechanisms · doi:10.1242/dmm.030122 · Cited by 15 · see citing works
Mohammadi, S., Arefnezhad, R., Danaii, S., & Yousefi, M. (2020) · BioFactors · doi:10.1002/biof.1634 · Cited by 14 · see citing works
Cabut/dTIEG associates with the transcription factor Yorkie for growth control
Ruiz‐Romero, M., Blanco, E., Paricio, N., Serras, F., & Corominas, M. (2015) · EMBO Reports · doi:10.15252/embr.201439193 · Cited by 14 · see citing works
Jahanshahi, M., Hsiao, K., Jenny, A., & Pfleger, C. M. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006198 · Cited by 14 · see citing works
Wang, X., Guo, Y., Lin, P., Yu, M., Song, S., Xu, W., Kong, D., Wang, Y., Zhang, Y., Lu, F., et al. (2024) · The EMBO Journal · doi:10.1038/s44318-024-00290-3 · Cited by 13 · see citing works
TAZ Represses the Neuronal Commitment of Neural Stem Cells
Robledinos-Antón, N., Escoll, M., Guan, K., & Cuadrado, A. (2020) · Cells · doi:10.3390/cells9102230 · Cited by 13 · see citing works
Zraly, C. B., Zakkar, A., Perez, J. H., Ng, J. K., White, K. P., Slattery, M. G., & Dingwall, A. K. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa082 · Cited by 12 · see citing works
Self-citationChauhan, C., Zraly, C. B., & Dingwall, A. K. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.05.018 · Cited by 11 · see citing works
Pérez-Lluch, S., Klein, C. C., Breschi, A., Ruiz‐Romero, M., Abad, A., Palumbo, E., Bekish, L., Arnan, C., & Guigó, R. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1009245 · Cited by 11 · see citing works
- Authors
- Oh, H., Slattery, M., Ma, L., Crofts, A., White, K. P., Mann, R. S., & Irvine, K. D.
- Affiliations
- Rutgers, The State University of New Jersey (US)
- University of Chicago (US)
- Columbia University (US)
- Corresponding author
- Irvine, Kenneth D.
- Venue
- Cell Reports
- Publisher
- Elsevier BV
- Published
- 2013-02
- Volume
- 3
- Issue
- 2
- Pages
- 309-318
- ISSN
- 2211-1247 (ISSN-L)
- PMC
- PMC3633442
- OpenAlex
- W2090698584
- Cited by
- 145
- References
- 48
- Citations by year
- 2026: 7 · 2025: 8 · 2024: 10 · 2023: 7 · 2022: 5 · 2021: 12 · 2020: 11 · 2019: 15 · 2018: 9 · 2017: 9 · 2016: 12 · 2015: 12 · 2014: 17 · 2013: 11
- FWCI
- 10.05
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Cell Reports (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Howard Hughes Medical Institute
- National Human Genome Research Institute (U01HG004264)
- National Institute of General Medical Sciences (R01GM058575, P50GM081892, R01GM054510, GM078620, R01GM078620)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Hippo pathway signaling and YAP/TAZ
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Keywords
- Yorkie, Hippo signaling pathway, transcriptional activation, GAGA factor, Moira, Mediator complex, chromatin remodeling, chromatin binding, histone H3K4me3, transcriptional coactivator, growth regulation
- MeSH terms
- YAP-Signaling Proteins, Animals, Chromatin, DNA-Binding Proteins, Drosophila, Histones, Nuclear Proteins, Protein Binding, RNA, Messenger, Transcription Factors, Wings, Animal, Transcriptional Activation, Trans-Activators, Genome, Cell Cycle Proteins, Drosophila Proteins, RNA Interference, RNA, Small Interfering, Chromatin Assembly and Disassembly, Mediator Complex
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