User menu

Accès à distance ? S'identifier sur le proxy UCLouvain

The Homeodomain Transcription Factor Hoxa2 Interacts with and Promotes the Proteasomal Degradation of the E3 Ubiquitin Protein Ligase RCHY1

  • Open access
  • PDF
  • 1.27 M
  1. Alexander Tara, Nolte Christof, Krumlauf Robb, Hox Genes and Segmentation of the Hindbrain and Axial Skeleton, 10.1146/annurev.cellbio.042308.113423
  2. Shah Nilay, Sukumar Saraswati, The Hox genes and their roles in oncogenesis, 10.1038/nrc2826
  3. Narita Yuichi, Rijli Filippo M., Chapter 5 Hox Genes in Neural Patterning and Circuit Formation in the Mouse Hindbrain, Current Topics in Developmental Biology (2009) ISBN:9780123745293 p.139-167, 10.1016/s0070-2153(09)88005-8
  4. Tümpel Stefan, Wiedemann Leanne M., Krumlauf Robb, Chapter 8 Hox Genes and Segmentation of the Vertebrate Hindbrain, Current Topics in Developmental Biology (2009) ISBN:9780123745293 p.103-137, 10.1016/s0070-2153(09)88004-6
  5. Mallo Moises, Wellik Deneen M., Deschamps Jacqueline, Hox genes and regional patterning of the vertebrate body plan, 10.1016/j.ydbio.2010.04.024
  6. Wellik Deneen M., Chapter 9 Hox Genes and Vertebrate Axial Pattern, Current Topics in Developmental Biology (2009) ISBN:9780123745293 p.257-278, 10.1016/s0070-2153(09)88009-5
  7. Zakany Jozsef, Duboule Denis, The role of Hox genes during vertebrate limb development, 10.1016/j.gde.2007.05.011
  8. Brison Nathalie, Tylzanowski Przemko, Debeer Philippe, Limb skeletal malformations – What the HOX is going on?, 10.1016/j.ejmg.2011.06.003
  9. Bertrand Nicolas, Roux Marine, Ryckebüsch Lucile, Niederreither Karen, Dollé Pascal, Moon Anne, Capecchi Mario, Zaffran Stéphane, Hox genes define distinct progenitor sub-domains within the second heart field, 10.1016/j.ydbio.2011.02.029
  10. Wellik Deneen M., Hox genes and kidney development, 10.1007/s00467-011-1902-1
  11. Grier David G., Thompson Alexander, Lappin Terence R.J., Halliday Henry L., Quantification of Hox and Surfactant Protein-B Transcription during Murine Lung Development, 10.1159/000201739
  12. McGonigle Glenda, J., Grappling with the HOX network in hematopoiesis and leukemia, 10.2741/3006
  13. Argiropoulos B, Humphries R K, Hox genes in hematopoiesis and leukemogenesis, 10.1038/sj.onc.1210760
  14. Moens Cecilia B., Selleri Licia, Hox cofactors in vertebrate development, 10.1016/j.ydbio.2005.10.032
  15. Ferretti E., Cambronero F., Tumpel S., Longobardi E., Wiedemann L. M., Blasi F., Krumlauf R., Hoxb1 Enhancer and Control of Rhombomere 4 Expression: Complex Interplay between PREP1-PBX1-HOXB1 Binding Sites, 10.1128/mcb.25.19.8541-8552.2005
  16. Chambers David, Wilson Leigh, Alfonsi Fabienne, Hunter Ewan, Saxena Uma, Blanc Eric, Lumsden Andrew, Rhombomere-specific analysis reveals the repertoire of genetic cues expressed across the developing hindbrain, 10.1186/1749-8104-4-6
  17. Williams Thomas M., Williams Melissa E., Kuick Rork, Misek David, McDonagh Kevin, Hanash Samir, Innis Jeffrey W., Candidate downstream regulated genes of HOX group 13 transcription factors with and without monomeric DNA binding capability, 10.1016/j.ydbio.2004.12.015
  18. Donaldson Ian J., Amin Shilu, Hensman James J., Kutejova Eva, Rattray Magnus, Lawrence Neil, Hayes Andrew, Ward Christopher M., Bobola Nicoletta, Genome-wide occupancy links Hoxa2 to Wnt–β-catenin signaling in mouse embryonic development, 10.1093/nar/gkr1240
  19. Svingen T, Tonissen K F, Hox transcription factors and their elusive mammalian gene targets, 10.1038/sj.hdy.6800847
  20. RS Mann, Curr Top Dev Biol, 88, 63 (2009)
  21. Hueber Stefanie D., Lohmann Ingrid, Shaping segments:Hoxgene function in the genomic age, 10.1002/bies.20823
  22. Topisirovic I., Kentsis A., Perez J. M., Guzman M. L., Jordan C. T., Borden K. L. B., Eukaryotic Translation Initiation Factor 4E Activity Is Modulated by HOXA9 at Multiple Levels, 10.1128/mcb.25.3.1100-1112.2005
  23. Cillo Clemente, Schiavo Giulia, Cantile Monica, Bihl Michel P., Sorrentino Paolo, Carafa Vincenza, D' Armiento Maria, Roncalli Massimo, Sansano Sebastiano, Vecchione Raffaela, Tornillo Luigi, Mori Lucia, De Libero Gennaro, Zucman-Rossi Jessica, Terracciano Luigi, The HOX gene network in hepatocellular carcinoma, 10.1002/ijc.25941
  24. Rubin E., Wu X., Zhu T., Cheung J. C.Y., Chen H., Lorincz A., Pandita R. K., Sharma G. G., Ha H. C., Gasson J., Hanakahi L. A., Pandita T. K., Sukumar S., A Role for the HOXB7 Homeodomain Protein in DNA Repair, 10.1158/0008-5472.can-06-4283
  25. Chatelin Laurent, Volovitch Michel, Joliot Alain Henri, Perez Franck, Prochiantz Alain, Transcription factor Hoxa-5 is taken up by cells in culture and conveyed to their nuclei, 10.1016/0925-4773(95)00478-5
  26. Joliot A., Pernelle C., Deagostini-Bazin H., Prochiantz A., Antennapedia homeobox peptide regulates neural morphogenesis., 10.1073/pnas.88.5.1864
  27. Salsi V., Ferrari S., Ferraresi R., Cossarizza A., Grande A., Zappavigna V., HOXD13 Binds DNA Replication Origins To Promote Origin Licensing and Is Inhibited by Geminin, 10.1128/mcb.00509-09
  28. Gabellini D., Early mitotic degradation of the homeoprotein HOXC10 is potentially linked to cell cycle progression, 10.1093/emboj/cdg340
  29. Sauvageau G, Thorsteinsdottir U, Eaves C J, Lawrence H J, Largman C, Lansdorp P M, Humphries R K, Overexpression of HOXB4 in hematopoietic cells causes the selective expansion of more primitive populations in vitro and in vivo., 10.1101/gad.9.14.1753
  30. Ohno Y., Yasunaga S., Ohtsubo M., Mori S., Tsumura M., Okada S., Ohta T., Ohtani K., Kobayashi M., Takihara Y., Hoxb4 transduction down-regulates Geminin protein, providing hematopoietic stem and progenitor cells with proliferation potential, 10.1073/pnas.1011054107
  31. Gendron-Maguire Maureen, Mallo Moisés, Zhang Maobin, Gridley Thomas, Hoxa-2 mutant mice exhibit homeotic transformation of skeletal elements derived from cranial neural crest, 10.1016/0092-8674(93)90619-2
  32. Rijli Filippo M., Mark Manuel, Lakkaraju Sudhakar, Dierich Andrée, Dollé Pascal, Chambon Pierre, A homeotic transformation is generated in the rostral branchial region of the head by disruption of Hoxa-2, which acts as a selector gene, 10.1016/0092-8674(93)90620-6
  33. A Gavalas, Development, 124, 3693 (1997)
  34. Oury F., Murakami Y., Renaud J.-S., Pasqualetti M., Charnay P., Ren S.-Y., Rijli F. M., Hoxa2- and Rhombomere-Dependent Development of the Mouse Facial Somatosensory Map, 10.1126/science.1130042
  35. Kutejova E., Hoxa2 downregulates Six2 in the neural crest-derived mesenchyme, 10.1242/dev.01536
  36. Bobola N., Mesenchymal patterning by Hoxa2 requires blocking Fgf-dependent activation of Ptx1, 10.1242/dev.00554
  37. Kirilenko P., He G., Mankoo B. S., Mallo M., Jones R., Bobola N., Transient Activation of Meox1 Is an Early Component of the Gene Regulatory Network Downstream of Hoxa2, 10.1128/mcb.00705-10
  38. Matis Christelle, Oury Franck, Remacle Sophie, Lampe Xavier, Gofflot Françoise, Picard Jacques J., Rijli Filippo M., Rezsohazy René, Identification ofLmo1 as part of a Hox-dependent regulatory network for hindbrain patterning, 10.1002/dvdy.21266
  39. Geisen Marc J, Meglio Thomas Di, Pasqualetti Massimo, Ducret Sebastien, Brunet Jean-François, Chedotal Alain, Rijli Filippo M, Hox Paralog Group 2 Genes Control the Migration of Mouse Pontine Neurons through Slit-Robo Signaling, 10.1371/journal.pbio.0060142
  40. Lampe Xavier, Samad Omar Abdel, Guiguen Allan, Matis Christelle, Remacle Sophie, Picard Jacques J., Rijli Filippo M., Rezsohazy René, An ultraconserved Hox–Pbx responsive element resides in the coding sequence of Hoxa2 and is active in rhombomere 4, 10.1093/nar/gkn148
  41. IJ Donaldson, Nucleic Acids Res (2012)
  42. Ravasi Timothy, Suzuki Harukazu, Cannistraci Carlo Vittorio, Katayama Shintaro, Bajic Vladimir B., Tan Kai, Akalin Altuna, Schmeier Sebastian, Kanamori-Katayama Mutsumi, Bertin Nicolas, Carninci Piero, Daub Carsten O., Forrest Alistair R.R., Gough Julian, Grimmond Sean, Han Jung-Hoon, Hashimoto Takehiro, Hide Winston, Hofmann Oliver, Kamburov Atanas, Kaur Mandeep, Kawaji Hideya, Kubosaki Atsutaka, Lassmann Timo, van Nimwegen Erik, MacPherson Cameron Ross, Ogawa Chihiro, Radovanovic Aleksandar, Schwartz Ariel, Teasdale Rohan D., Tegnér Jesper, Lenhard Boris, Teichmann Sarah A., Arakawa Takahiro, Ninomiya Noriko, Murakami Kayoko, Tagami Michihira, Fukuda Shiro, Imamura Kengo, Kai Chikatoshi, Ishihara Ryoko, Kitazume Yayoi, Kawai Jun, Hume David A., Ideker Trey, Hayashizaki Yoshihide, An Atlas of Combinatorial Transcriptional Regulation in Mouse and Man, 10.1016/j.cell.2010.01.044
  43. B Kanzler, Development, 125, 2587 (1998)
  44. Massip Laurent, Ectors Fabien, Deprez Pierre, Maleki Mehdi, Behets Catherine, Lengelé Benoît, Delahaut Philippe, Picard Jacques, Rezsöhazy René, Expression of Hoxa2 in cells entering chondrogenesis impairs overall cartilage development, 10.1111/j.1432-0436.2006.00132.x
  45. Tavella Sara, Bobola Nicoletta, Expressing Hoxa2 across the entire endochondral skeleton alters the shape of the skeletal template in a spatially restricted fashion, 10.1016/j.diff.2009.11.004
  46. Wang Monica, Doucette J. Ronald, Nazarali Adil J., Conditional Tet-Regulated Over-Expression of Hoxa2 in CG4 Cells Increases Their Proliferation and Delays Their Differentiation into Oligodendrocyte-like Cells Expressing Myelin Basic Protein, 10.1007/s10571-011-9685-2
  47. Miguez A., Ducret S., Di Meglio T., Parras C., Hmidan H., Haton C., Sekizar S., Mannioui A., Vidal M., Kerever A., Nyabi O., Haigh J., Zalc B., Rijli F. M., Thomas J.-L., Opposing Roles for Hoxa2 and Hoxb2 in Hindbrain Oligodendrocyte Patterning, 10.1523/jneurosci.0885-12.2012
  48. Cardoso Wellington V., Mitsialis S. Alex, Brody Jerome S., Williams Mary C., Retinoic acid alters the expression of pattern-related genes in the developing rat lung, 10.1002/(sici)1097-0177(199609)207:1<47::aid-aja6>3.0.co;2-w
  49. Leng Roger P., Lin Yunping, Ma Weili, Wu Hong, Lemmers Benedicte, Chung Stephen, Parant John M., Lozano Guillermina, Hakem Razqallah, Benchimol Samuel, Pirh2, a p53-Induced Ubiquitin-Protein Ligase, Promotes p53 Degradation, 10.1016/s0092-8674(03)00193-4
  50. Hattori T., Isobe T., Abe K., Kikuchi H., Kitagawa K., Oda T., Uchida C., Kitagawa M., Pirh2 Promotes Ubiquitin-Dependent Degradation of the Cyclin-Dependent Kinase Inhibitor p27Kip1, 10.1158/0008-5472.can-07-2033
  51. Dreze Matija, Monachello Dario, Lurin Claire, Cusick Michael E., Hill David E., Vidal Marc, Braun Pascal, High-Quality Binary Interactome Mapping, Methods in Enzymology (2010) ISBN:9780123751720 p.281-315, 10.1016/s0076-6879(10)70012-4
  52. P Lamesch, Genomics, 89, 307 (2007)
  53. Fernandez Cristina C., Gudas Lorraine J., The truncated Hoxa1 protein interacts with Hoxa1 and Pbx1 in stem cells, 10.1002/jcb.22023
  54. Lambert Barbara, Vandeputte Julie, Remacle Sophie, Bergiers Isabelle, Simonis Nicolas, Twizere Jean-Claude, Vidal Marc, Rezsohazy René, Protein interactions of the transcription factor Hoxa1, 10.1186/1471-213x-12-29
  55. Beitel L., Cloning and characterization of an androgen receptor N-terminal-interacting protein with ubiquitin-protein ligase activity, 10.1677/jme.0.0290041
  56. Logan Ian R., Sapountzi Vasileia, Gaughan Luke, Neal David E., Robson Craig N., Control of Human PIRH2 Protein Stability : INVOLVEMENT OF TIP60 AND THE PROTEASOME, 10.1074/jbc.m312712200
  57. Gehring Walter J., Qian Yan Qiu, Billeter Martin, Furukubo-Tokunaga Katsuo, Schier Alexander F., Resendez-Perez Diana, Affolter Markus, Otting Gottfried, Wüthrich Kurt, Homeodomain-DNA recognition, 10.1016/0092-8674(94)90292-5
  58. Sdek Patima, Ying Haoqiang, Chang Donny L.F., Qiu Wei, Zheng Hongwu, Touitou Robert, Allday Martin J., Jim Xiao Zhi-Xiong, MDM2 Promotes Proteasome-Dependent Ubiquitin-Independent Degradation of Retinoblastoma Protein, 10.1016/j.molcel.2005.10.017
  59. Jin Y., MDM2 promotes p21waf1/cip1 proteasomal turnover independently of ubiquitylation, 10.1093/emboj/cdg600
  60. Stewart D. P., Koss B., Bathina M., Perciavalle R. M., Bisanz K., Opferman J. T., Ubiquitin-Independent Degradation of Antiapoptotic MCL-1, 10.1128/mcb.01266-09
  61. Touitou R., A degradation signal located in the C-terminus of p21WAF1/CIP1 is a binding site for the C8 alpha-subunit of the 20S proteasome, 10.1093/emboj/20.10.2367
  62. Zheng Gang, Ning Jinying, Yang Yu-Chung, PLAGL2 controls the stability of Pirh2, an E3 ubiquitin ligase for p53, 10.1016/j.bbrc.2007.10.003
  63. Duan Shanshan, Yao Zhan, Hou Dezhi, Wu Zhengsheng, Zhu Wei-guo, Wu Mian, Phosphorylation of Pirh2 by Calmodulin-dependent kinase II impairs its ability to ubiquitinate p53, 10.1038/sj.emboj.7601749
  64. Logan I. R., Gaughan L., McCracken S. R. C., Sapountzi V., Leung H. Y., Robson C. N., Human PIRH2 Enhances Androgen Receptor Signaling through Inhibition of Histone Deacetylase 1 and Is Overexpressed in Prostate Cancer, 10.1128/mcb.00147-06
  65. Duan W., Gao L., Druhan L. J., Zhu W.-G., Morrison C., Otterson G. A., Villalona-Calero M. A., Expression of Pirh2, a Newly Identified Ubiquitin Protein Ligase, in Lung Cancer, 10.1093/jnci/djh292
  66. Chen M., Cortay J.-C., Logan I. R., Sapountzi V., Robson C. N., Gerlier D., Inhibition of Ubiquitination and Stabilization of Human Ubiquitin E3 Ligase PIRH2 by Measles Virus Phosphoprotein, 10.1128/jvi.79.18.11824-11836.2005
  67. V Zuckerman, J Pathol, 219, 3 (2009)
  68. Yang Xiu, Zhou Yuefang, Barcarse Erin A., O’Gorman Stephen, Altered neuronal lineages in the facial ganglia of Hoxa2 mutant mice, 10.1016/j.ydbio.2007.11.032
  69. Sengupta Sagar, Harris Curtis C., p53: traffic cop at the crossroads of DNA repair and recombination, 10.1038/nrm1546
  70. Pachkowski Brian F., Guyton Kathryn Z., Sonawane Babasaheb, DNA repair during in utero development: A review of the current state of knowledge, research needs, and potential application in risk assessment, 10.1016/j.mrrev.2011.05.003
  71. Jung Y.-S., Liu G., Chen X., Pirh2 E3 Ubiquitin Ligase Targets DNA Polymerase Eta for 20S Proteasomal Degradation, 10.1128/mcb.01198-09
  72. Jung Y.-S., Hakem A., Hakem R., Chen X., Pirh2 E3 Ubiquitin Ligase Monoubiquitinates DNA Polymerase Eta To Suppress Translesion DNA Synthesis, 10.1128/mcb.05808-11
  73. Hakem Anne, Bohgaki Miyuki, Lemmers Bénédicte, Tai Elisabeth, Salmena Leonardo, Matysiak-Zablocki Elzbieta, Jung Yong-Sam, Karaskova Jana, Kaustov Lilia, Duan Shili, Madore Jason, Boutros Paul, Sheng Yi, Chesi Marta, Bergsagel P. Leif, Perez-Ordonez Bayardo, Mes-Masson Anne-Marie, Penn Linda, Squire Jeremy, Chen Xinbin, Jurisica Igor, Arrowsmith Cheryl, Sanchez Otto, Benchimol Samuel, Hakem Razqallah, Role of Pirh2 in Mediating the Regulation of p53 and c-Myc, 10.1371/journal.pgen.1002360
  74. Barrios-Rodiles M., High-Throughput Mapping of a Dynamic Signaling Network in Mammalian Cells, 10.1126/science.1105776
  75. Rual Jean-François, Venkatesan Kavitha, Hao Tong, Hirozane-Kishikawa Tomoko, Dricot Amélie, Li Ning, Berriz Gabriel F., Gibbons Francis D., Dreze Matija, Ayivi-Guedehoussou Nono, Klitgord Niels, Simon Christophe, Boxem Mike, Milstein Stuart, Rosenberg Jennifer, Goldberg Debra S., Zhang Lan V., Wong Sharyl L., Franklin Giovanni, Li Siming, Albala Joanna S., Lim Janghoo, Fraughton Carlene, Llamosas Estelle, Cevik Sebiha, Bex Camille, Lamesch Philippe, Sikorski Robert S., Vandenhaute Jean, Zoghbi Huda Y., Smolyar Alex, Bosak Stephanie, Sequerra Reynaldo, Doucette-Stamm Lynn, Cusick Michael E., Hill David E., Roth Frederick P., Vidal Marc, Towards a proteome-scale map of the human protein–protein interaction network, 10.1038/nature04209
  76. Lamesch Philippe, Li Ning, Milstein Stuart, Fan Changyu, Hao Tong, Szabo Gabor, Hu Zhenjun, Venkatesan Kavitha, Bethel Graeme, Martin Paul, Rogers Jane, Lawlor Stephanie, McLaren Stuart, Dricot Amélie, Borick Heather, Cusick Michael E., Vandenhaute Jean, Dunham Ian, Hill David E., Vidal Marc, hORFeome v3.1: A resource of human open reading frames representing over 10,000 human genes, 10.1016/j.ygeno.2006.11.012
  77. Chen Dz-Chi, Yang Bei-Chang, Kuo Tsong-Teh, One-step transformation of yeast in stationary phase, 10.1007/bf00318659
Bibliographic reference Bergiers, Isabelle ; Bridoux, Laure ; Nguyen, Nathan ; Twizere, Jean-Claude ; Rezsohazy, René. The Homeodomain Transcription Factor Hoxa2 Interacts with and Promotes the Proteasomal Degradation of the E3 Ubiquitin Protein Ligase RCHY1. In: PLoS ONE, Vol. 8, no.11, p. e80387 (2013)
Permanent URL http://hdl.handle.net/2078.1/139533