Repression of RNA Polymerase I Transcription by the Tumor Suppressor p53
Open accessAbstract
The tumor suppressor protein p53 is frequently inactivated in tumors. It functions as a transcriptional activator as well as a repressor for a number of viral and cellular promoters transcribed by RNA polymerase II (Pol II) and by RNA Pol III. Moreover, it appears that p53 also suppresses RNA Pol I transcription. In this study, we examined the molecular mechanism of Pol I transcriptional inhibition by p53. We show that wild-type, but not mutant, p53 can repress Pol I transcription from a human rRNA gene promoter in cotransfection assays. Furthermore, we show that recombinant p53 inhibits rRNA transcription in a cell-free transcription system. In agreement with these results, p53-null epithelial cells display an increased Pol I transcriptional activity compared to that of epithelial cells that express p53. However, both cell lines display comparable Pol I factor protein levels. Our biochemical analysis shows that p53 prevents the interaction between SL1 and UBF. Protein-protein interaction assays indicate that p53 binds to SL1, and this interaction is mostly mediated by direct contacts with TATA-binding protein and TAF(I)110. Moreover, template commitment assays show that while the formation of a UBF-SL1 complex can partially relieve the inhibition of transcription, only the assembly of a UBF-SL1-Pol I initiation complex on the rDNA promoter confers substantial protection against p53 inhibition. In summary, our results suggest that p53 represses RNA Pol I transcription by directly interfering with the assembly of a productive transcriptional machinery on the rRNA promoter.
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Induction of p53 leads to downregulation of rRNA genes and of genes that are required for import and export of ribosomal proteins from the nucleus.
“Induction of p53 leads to downregulation of rRNA genes212, 213 and of genes that are required for import and export of ribosomal proteins from the nucleus.214”
From Census and evaluation of p53 target genes (2017) · cites this paper as [213]
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Cites
p53, the cellular gatekeeper for growth and division
Levine, A. J. (1997) · Cell · doi:10.1016/s0092-8674(00)81871-1 · Cited by 7,693 · see citing works
Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours
Donehower, L. A., Harvey, M., Slagle, B. L., McArthur, M. J., Montgomery, C. A., Butel, J. S., & Bradley, A. (1992) · Nature · doi:10.1038/356215a0 · Cited by 4,649 · see citing works
Crystal Structure of a p53 Tumor Suppressor-DNA Complex: Understanding Tumorigenic Mutations
Cho, Y., Gorina, S., Jeffrey, P. D., & Pavletich, N. P. (1994) · Science · doi:10.1126/science.8023157 · Cited by 2,559 · cited 3× · see citing works
“Plasmids for the expression of glutathione Stransferase (GST) fusion human p53 fragments, pGThp53N ( 1-160 ), pGThp53C1 (160-318), pGThp53C2 (318-393), and pGThp53C (160-393), have been described previously (24).”
Backgroundp53: puzzle and paradigm.Preprint
Ko, L. J., & Prives, C. L. (1996) · Genes & Development · doi:10.1101/gad.10.9.1054 · Cited by 2,338 · see citing works
Suppression of Human Colorectal Carcinoma Cell Growth by Wild-Type p53
Baker, S. J., Markowitz, S. D., Fearon, E. R., Willson, J. K. V., & Vogelstein, B. (1990) · Science · doi:10.1126/science.2144057 · Cited by 1,742 · see citing works
Identification of p53 as a Sequence-Specific DNA-Binding Protein
Kern, S. E., Kinzler, K. W., Bruskin, A. M., Jarosz, D., Friedman, P. N., Prives, C. L., & Vogelstein, B. (1991) · Science · doi:10.1126/science.2047879 · Cited by 1,085 · see citing works
[36] Eukaryotic gene transcription with purified components
Dignam, J. D., Martin, P. L., Shastry, B. S., & Roeder, R. G. (1983) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(83)01039-3 · Cited by 963 · see citing works
Michalovitz, D., Halevy, O., & Oren, M. (1990) · Cell · doi:10.1016/0092-8674(90)90113-s · Cited by 769 · see citing works
Wild-type p53 binds to the TATA-binding protein and represses transcription.
Seto, E., Usheva, A., Zambetti, G. P., Momand, J. A., Horikoshi, N., Weinmann, R. S., Levine, A. J., & Shenk, T. E. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.24.12028 · Cited by 504 · see citing works
p53 Transcriptional Activation Mediated by Coactivators TAF II 40 and TAF II 60
Thut, C. J., Chen, J.-L., Klemm, R. D., & Tjian, R. (1995) · Science · doi:10.1126/science.7809597 · Cited by 439 · see citing works
Wild-type p53 can down-modulate the activity of various promoters.
Ginsberg, D., Mechta‐Grigoriou, F., Yaniv, M., & Oren, M. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.22.9979 · Cited by 434 · see citing works
Comai, L., Tanese, N., & Tjian, R. (1992) · Cell · doi:10.1016/0092-8674(92)90039-f · Cited by 432 · see citing works
Self-citationSequence-specific transcriptional activation is essential for growth suppression by p53.
Pietenpol, J. A., Tokino, T., Thiagalingam, S., El‐Deiry, W. S., Kinzler, K. W., & Vogelstein, B. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.6.1998 · Cited by 406 · see citing works
Nuclear and nucleolar targeting sequences of c-erb-A, c-myb, N-myc, p53, HSP70, and HIV tat proteins
Dang, C. V., & Lee, W. M. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)84673-2 · Cited by 354 · see citing works
Bell, S. P., Learned, R. M., Jantzen, H., & Tjian, R. (1988) · Science · doi:10.1126/science.3413483 · Cited by 352 · see citing works
Activity of RNA polymerase I transcription factor UBF blocked by Rb gene product
Cavanaugh, A. H., Hempel, W. M., Taylor, L. J., Rogalsky, V., Todorov, G. I., & Rothblum, L. I. (1995) · Nature · doi:10.1038/374177a0 · Cited by 334 · see citing works
Specific repression of TATA-mediated but not initiator-mediated transcription by wild-type p53
Mack, D. H., Vartikar, J., Pipas, J. M., & Laimins, L. A. (1993) · Nature · doi:10.1038/363281a0 · Cited by 322 · see citing works
The Ribosomal L5 Protein Is Associated with mdm-2 and mdm-2-p53 Complexes
Maréchal, V., Elenbaas, B., Piette, J., Nicolas, J. C., & Levine, A. J. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.11.7414 · Cited by 318 · see citing works
Zambetti, G. P., Bargonetti, J., Walker, K. K., Prives, C. L., & Levine, A. J. (1992) · Genes & Development · doi:10.1101/gad.6.7.1143 · Cited by 311 · see citing works
[35] In Vitro transcription: Whole-cell extract
Manley, J. L., Fire, A. Z., Samuels, M. E., & Sharp, P. A. (1983) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(83)01038-1 · Cited by 294 · see citing works
Regulation of the Human hsp70 Promoter by p53
Agoff, S. N., Hou, J., Linzer, D. I., & Wu, B. (1993) · Science · doi:10.1126/science.8418500 · Cited by 292 · see citing works
Negative feedback regulation of wild‐type p53 biosynthesis.
Mosner, J., Mummenbrauer, T., Bauer, C., Sczakiel, G., Große, F., & Deppert, W. (1995) · The EMBO Journal · doi:10.1002/j.1460-2075.1995.tb00123.x · Cited by 286 · see citing works
Fries, K., Miller, W. E., & Raab‐Traub, N. (1996) · Journal of Virology · doi:10.1128/jvi.70.12.8653-8659.1996 · Cited by 253 · see citing works
Regulation of Mammalian Ribosomal Gene Transcription by RNA Polymerase I
Grummt, I. (1998) · Progress in nucleic acid research and molecular biology · doi:10.1016/s0079-6603(08)60506-1 · Cited by 237 · see citing works
Learned, R. M., Learned, T. K., Haltiner, M. M., & Tjian, R. (1986) · Cell · doi:10.1016/0092-8674(86)90559-3 · Cited by 211 · see citing works
Repression of RNA polymerase III transcription by the retinoblastoma protein
White, R. J., Trouche, D., Martin, K., Jackson, S. P., & Kouzarides, T. (1996) · Nature · doi:10.1038/382088a0 · Cited by 205 · see citing works
p53 is a general repressor of RNA polymerase III transcription
Cairns, C. A., & White, R. J. (1998) · The EMBO Journal · doi:10.1093/emboj/17.11.3112 · Cited by 190 · see citing works
Horikoshi, N., Usheva, A., Chen, J., Levine, A. J., Weinmann, R. S., & Shenk, T. E. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.1.227 · Cited by 182 · see citing works
Biochemical properties and biological effects of p53
Haffner, R., & Oren, M. (1995) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(95)90058-6 · Cited by 177 · see citing works
p21/p53, Cellular Growth Control and Genomic Integrity
El‐Deiry, W. S. (1998) · Current topics in microbiology and immunology · doi:10.1007/978-3-642-71941-7_6 · Cited by 173 · see citing works
Mechanism of Repression of RNA Polymerase I Transcription by the Retinoblastoma Protein
Voit, R., Schäfer, K., & Grummt, I. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.8.4230 · Cited by 172 · see citing works
p53-dependent repression of CDK4 translation in TGF-beta-induced G1 cell-cycle arrest.Preprint
Ewen, M. E., Oliver, C. J., Sluss, H. K., Miller, S. J., & Peeper, D. S. (1995) · Genes & Development · doi:10.1101/gad.9.2.204 · Cited by 165 · see citing works
Ragimov, N., Krauskopf, A., Navot, N., Rotter, V., Oren, M., & Aloni, Y. (1993) · PubMed · Cited by 159 · see citing works
p53 represses ribosomal gene transcription
Budde, A., & Grummt, I. (1999) · Oncogene · doi:10.1038/sj.onc.1202402 · Cited by 157 · see citing works
p53 Negatively Regulates cdc2 Transcription via the CCAAT-binding NF-Y Transcription Factor
Yun, J., Chae, H., Choy, H. E., Chung, J., Yoo, H., Han, M.-H., & Shin, D. Y. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.42.29677 · Cited by 155 · see citing works
Molecular mechanisms governing species-specific transcription of ribosomal RNA
Bell, S. P., Pikaard, C. S., Reeder, R. H., & Tjian, R. (1989) · Cell · doi:10.1016/0092-8674(89)90032-9 · Cited by 137 · see citing works
A possible mechanism for the inhibition of ribosomal RNA gene transcription during mitosis.
Weisenberger, D., & Scheer, U. (1995) · The Journal of Cell Biology · doi:10.1083/jcb.129.3.561 · Cited by 133 · see citing works
p53 Inhibits RNA Polymerase III-Directed Transcription in a Promoter-Dependent Manner
Chesnokov, I. N., Chu, W.-M., Botchan, M. R., & Schmid, C. W. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.12.7084 · Cited by 114 · see citing works
Regulation of RNA Polymerase I Transcription in Yeast and Vertebrates
Reeder, R. H. (1998) · Progress in nucleic acid research and molecular biology · doi:10.1016/s0079-6603(08)60511-5 · Cited by 109 · see citing works
p53 binds to the TATA-binding protein-TATA complex
Martin, D. W., Muñoz, R. M., Subler, M. A., & Deb, S. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)38619-3 · Cited by 107 · see citing works
The Ribosomal L5 Protein Is Associated with mdm-2 and mdm-2-p53 Complexes
Maréchal, V., Elenbaas, B., Piette, J. G., et al. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.11.7414-7420.1994 · Cited by 107 · see citing works
p53 Is Covalently Linked to 5.8S rRNA
Fontoura, B. M. A., Sorokina, E. A., David, E., & Carroll, R. B. (1992) · Molecular and Cellular Biology · doi:10.1128/mcb.12.11.5145 · Cited by 102 · see citing works
Transcription of ribosomal RNA genes by eukaryotic RNA polymerase I
Paule, M. R. (1998) · Medical Entomology and Zoology · Cited by 96 · see citing works
Wild type human p53 is antiproliferative in SV40-transformed hamster cells.
Mercer, W. E., Amin, M., Sauvé, G. J., Appella, E., Sj, U., & Romano, J. (1990) · PubMed · Cited by 91 · see citing works
Rubbi, C. P., & Milner, J. (2000) · Oncogene · doi:10.1038/sj.onc.1203378 · Cited by 74 · see citing works
RNA Polymerase III Transcription Repressed by Rb through Its Interactions with TFIIIB and TFIIIC2
Chu, W.-M., Wang, Z., Roeder, R. G., & Schmid, C. W. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.23.14755 · Cited by 73 · see citing works
Novel DNA binding of p53 mutants and their role in transcriptional activation.
Zhang, W., Funk, W. D., Wright, W. E., Shay, J. W., & Deisseroth, A. (1993) · PubMed · Cited by 64 · see citing works
Zhai, W., Tuan, J., & Comai, L. (1997) · Genes & Development · doi:10.1101/gad.11.12.1605 · Cited by 58 · see citing works
Self-citationp53 Is Covalently Linked to 5.8S rRNA
Fontoura, B. M. A., Sorokina, E. A., David, E., et al. (1992) · Molecular and Cellular Biology · doi:10.1128/mcb.12.11.5145-5151.1992 · Cited by 42 · see citing works
Mogaki, M., Hirota, M., Chaney, W. G., & Pour, P. M. (1993) · Carcinogenesis · doi:10.1093/carcin/14.12.2589 · Cited by 33 · see citing works
Zhai, W., & Comai, L. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.4.2791 · Cited by 30 · see citing works
Self-citationMartin, D. W., Subler, M. A., Munoz, R. M., Brown, D. R., Deb, S. P., & Deb, S. P. (1993) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1993.2061 · Cited by 27 · see citing works
Translocation of Retinoblastoma Protein Associated with Tumor Cell Growth Inhibition
Rogalsky, V., Todorov, G. I., & Moran, D. M. (1993) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1993.1535 · Cited by 22 · see citing works
Expression of cell cycle regulatory proteins (p53, pRB) in the human female genital tract
Bukovský, A., Caudle, M. R., KEENAN, J. A., Wimalasena, J., Foster, J. S., Upadhyaya, N. B., & Meter, S. E. V. (1995) · Journal of Assisted Reproduction and Genetics · doi:10.1007/bf02211381 · Cited by 14 · see citing works
Two different forms of p53 localized differently within cells of urogenital tumours
Benninghoff, J., Kartarius, S., Teleb, Z., Selter, H., Unteregger, G., Zwergel, T., Wullich, B., & Montenarh, M. (1999) · Cancer Letters · doi:10.1016/s0304-3835(99)00187-1 · Cited by 12 · see citing works
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Boulon, S., Westman, B. J., Hutten, S., Boisvert, F.-M., & Lamond, A. I. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.024 · Cited by 1,103 · see citing works
Census and evaluation of p53 target genes
Fischer, M. (2017) · Oncogene · doi:10.1038/onc.2016.502 · Cited by 971 · see citing works
Does the ribosome translate cancer?
Ruggero, D., & Pandolfi, P. P. (2003) · Nature reviews. Cancer · doi:10.1038/nrc1015 · Cited by 924 · see citing works
Rubbi, C. P., & Milner, J. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg579 · Cited by 811 · see citing works
Ribosomal proteins: functions beyond the ribosome
Zhou, X. Y., Liao, W.-J., Liao, J., Liao, P., & Lu, H. (2015) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjv014 · Cited by 740 · see citing works
Regulation of HDM2 activity by the ribosomal protein L11
Lohrum, M. A. E., Ludwig, R. L., Kubbutat, M. H. G., Hanlon, M., & Vousden, K. H. (2003) · Cancer Cell · doi:10.1016/s1535-6108(03)00134-x · Cited by 626 · see citing works
Drygin, D., Lin, A. H., Bliesath, J., Ho, C., O’Brien, S., Proffitt, C., Omori, M., Haddach, M., Schwaebe, M. K., Siddiqui-Jain, A., et al. (2010) · Cancer Research · doi:10.1158/0008-5472.can-10-1728 · Cited by 622 · see citing works
Divorcing ARF and p53: an unsettled case
Sherr, C. J. (2006) · Nature reviews. Cancer · doi:10.1038/nrc1954 · Cited by 595 · see citing works
Anticancer activity of CX-3543: a direct inhibitor of rRNA biogenesis.
Drygin, D., Siddiqui-Jain, A., O'Brien, S., Schwaebe, M., Lin, A., Bliesath, J., Ho, C., Proffitt, C., Trent, K., Whitten, J., et al. (2009) · Cancer Research · doi:10.1158/0008-5472.can-09-1304 · Cited by 534 · see citing works
The expanding universe of p53 targets
Menendez, D., Inga, A., & Resnick, M. A. (2009) · Nature Reviews Cancer · doi:10.1038/nrc2730 · Cited by 568 · see citing works
Transcriptional Regulation by P53
Beckerman, R., & Prives, C. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a000935 · Cited by 569 · see citing works
Life on a planet of its own: Regulation of RNA polymerase I transcription in the nucleolus
Grummt, I. (2003) · Genes & Development · doi:10.1101/gad.1098503r · Cited by 540 · see citing works
Transcriptional regulation by p53: one protein, many possibilities
Laptenko, O., & Prives, C. L. (2006) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401916 · Cited by 500 · see citing works
Dai, M., Zeng, S. X., Jin, Y., Sun, X., David, L. L., & Lu, H. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.17.7654-7668.2004 · Cited by 495 · see citing works
Chemotherapeutic Drugs Inhibit Ribosome Biogenesis at Various Levels
Burger, K., Mühl, B., Thomas, H., Michaela, R., Anastassia, M., Orban, M., Kellner, M., Anita, G.-E., Kremmer, E., Hölzel, M., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.074211 · Cited by 461 · see citing works
Nucleolus, Ribosomes, and Cancer
Montanaro, L., Treré, D., & Derenzini, M. (2008) · American Journal Of Pathology · doi:10.2353/ajpath.2008.070752 · Cited by 456 · see citing works
Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function
Jones, N. C., Lynn, M. L., Gaudenz, K., Sakai, D., Aoto, K., Rey, J., Glynn, E. F., Ellington, L. R., Du, C., Dixon, J., et al. (2008) · Nature Medicine · doi:10.1038/nm1725 · Cited by 426 · see citing works
The RNA Polymerase I Transcription Machinery: An Emerging Target for the Treatment of Cancer
Drygin, D., Rice, W. G., & Grummt, I. (2010) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.010909.105844 · Cited by 419 · see citing works
Marcel, V., Ghayad, S. E., Belin, S., Thérizols, G., Morel, A., Solano-Gonzàlez, E., Vendrell, J. A., Hacot, S., Mertani, H. C., Albaret, M. A., et al. (2013) · Cancer Cell · doi:10.1016/j.ccr.2013.08.013 · Cited by 361 · see citing works
RNA polymerases I and III, growth control and cancer
White, R. J. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1551 · Cited by 330 · see citing works
French, S. L., Osheim, Y. N., Cioci, F., Nomura, M., & Beyer, A. L. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.5.1558-1568.2003 · Cited by 321 · see citing works
Ribosome Biogenesis: A Central Player in Cancer Metastasis and Therapeutic Resistance
Elhamamsy, A. R., Metge, B. J., Alsheikh, H. A., Shevde, L. A., & Samant, R. S. (2022) · Cancer Research · doi:10.1158/0008-5472.can-21-4087 · Cited by 320 · see citing works
A Targeting Modality for Destruction of RNA Polymerase I that Possesses Anticancer Activity
Peltonen, K., Colis, L. C., Liu, H., Trivedi, R. K., Moubarek, M. S., Moore, H. M., Bai, B., Rudek, M. A., Bieberich, C. J., & Laiho, M. (2014) · Cancer Cell · doi:10.1016/j.ccr.2013.12.009 · Cited by 317 · see citing works
A housekeeper with power of attorney: the rRNA genes in ribosome biogenesis
Moss, T., Langlois, F., Gagnon-Kugler, T., & Stefanovsky, V. Y. (2006) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-006-6278-1 · Cited by 310 · see citing works
Ribosome biogenesis surveillance: probing the ribosomal protein-Mdm2-p53 pathway
Deisenroth, C., & Zhang, Y. (2010) · Oncogene · doi:10.1038/onc.2010.189 · Cited by 303 · see citing works
Nucleolar Arf Tumor Suppressor Inhibits Ribosomal RNA Processing
Sugimoto, M., Kuo, M.-L., Roussel, M. F., & Sherr, C. J. (2003) · Molecular Cell · doi:10.1016/s1097-2765(03)00057-1 · Cited by 273 · see citing works
What the nucleolus says to a tumour pathologist
Derenzini, M., Montanaro, L., & Treré, D. (2009) · Histopathology · doi:10.1111/j.1365-2559.2008.03168.x · Cited by 260 · see citing works
The nucleolus: an emerging target for cancer therapy
Hein, N., Hannan, K. M., George, A. J., Sanij, E., & Hannan, R. D. (2013) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2013.07.005 · Cited by 245 · see citing works
Wang, X., Kua, H.-Y., Hu, Y., Guo, K., Zeng, Q., Wu, Q., Ng, H., Karsenty, G., Crombrugghe, B. D., Yeh, J. K., et al. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200507106 · Cited by 250 · see citing works
p53 and ribosome biogenesis stress: The essentials
Golomb, L., Volarević, S., & Oren, M. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.04.014 · Cited by 242 · see citing works
Stefanovsky, V. Y., Pelletier, G., Hannan, R. D., Gagnon-Kugler, T., Rothblum, L. I., & Moss, T. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00384-7 · Cited by 242 · see citing works
Targeting the nucleolus for cancer intervention
Quin, J. E., Devlin, J. R., Cameron, D. P., Hannan, K. M., Pearson, R. B., & Hannan, R. D. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2013.12.009 · Cited by 224 · see citing works
Wang, W., Nag, S. A., Zhang, X., Wang, M., Wang, H., Zhou, J., & Zhang, R. (2014) · Medicinal Research Reviews · doi:10.1002/med.21327 · Cited by 224 · see citing works
Dysregulation of the basal RNA polymerase transcription apparatus in cancer
Bywater, M. J., Pearson, R. B., McArthur, G. A., & Hannan, R. D. (2013) · Nature reviews. Cancer · doi:10.1038/nrc3496 · Cited by 219 · see citing works
Impaired ribosome biogenesis: mechanisms and relevance to cancer and aging
Turi, Z., Lacey, M., Mistrík, M., & Moudrý, P. (2019) · Aging · doi:10.18632/aging.101922 · Cited by 209 · see citing works
At the Center of Eukaryotic Life
Moss, T., & Stefanovsky, V. Y. (2002) · Cell · doi:10.1016/s0092-8674(02)00761-4 · Cited by 215 · see citing works
Conventional and nonconventional roles of the nucleolus
Olson, M. O. J., Hingorani, K., & Szebeni, A. (2002) · International review of cytology · doi:10.1016/s0074-7696(02)19014-0 · Cited by 214 · see citing works
RNA polymerase III transcription and cancer
White, R. J. (2004) · Oncogene · doi:10.1038/sj.onc.1207547 · Cited by 207 · see citing works
Basic mechanisms in RNA polymerase i transcription of the ribosomal RNA genes
Goodfellow, S. J., & Zomerdijk, J. C. B. M. (2013) · Subcellular Biochemistry · doi:10.1007/978-94-007-4525-4_10 · Cited by 197 · see citing works
RNA polymerases I and III, non-coding RNAs and cancer
White, R. J. (2008) · Trends in Genetics · doi:10.1016/j.tig.2008.10.003 · Cited by 190 · see citing works
How Ribosomes Translate Cancer
Sulima, S. O., Hofman, I. J., Keersmaecker, K. D., & Dinman, J. D. (2017) · Cancer Discovery · doi:10.1158/2159-8290.cd-17-0550 · Cited by 174 · see citing works
IMP dehydrogenase-2 drives aberrant nucleolar activity and promotes tumorigenesis in glioblastoma
Kofuji, S., Hirayama, A., Eberhardt, A. O., Kawaguchi, R. K., Sugiura, Y., Sampetrean, O., Ikeda, Y., Warren, M., Sakamoto, N., Kitahara, S., et al. (2019) · Nature Cell Biology · doi:10.1038/s41556-019-0363-9 · Cited by 171 · see citing works
Haddach, M., Schwaebe, M. K., Michaux, J., Nagasawa, J. Y., O’Brien, S., Whitten, J. P., Pierre, F., Kerdoncuff, P., Darjania, L., Stansfield, R. K., et al. (2012) · ACS Medicinal Chemistry Letters · doi:10.1021/ml300110s · Cited by 165 · see citing works
Regulation of NF‐κB and p53 through activation of ATR and Chk1 by the ARF tumour suppressor
Rocha, S., Garrett, M. D., Campbell, K. J., Schumm, K., & Perkins, N. D. (2005) · The EMBO Journal · doi:10.1038/sj.emboj.7600608 · Cited by 161 · see citing works
miR-10 in development and cancer
Lund, A. H. (2009) · Cell Death and Differentiation · doi:10.1038/cdd.2009.58 · Cited by 161 · see citing works
At the crossroads of growth control; making ribosomal RNA
Moss, T. (2004) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2004.02.005 · Cited by 157 · see citing works
Ribosomes and marrow failure: coincidental association or molecular paradigm?
Liu, J. M., & Ellis, S. R. (2006) · Blood · doi:10.1182/blood-2005-12-4831 · Cited by 154 · see citing works
The nucleolus and transcription of ribosomal genes
Raška, I., Koberna, K., Malínský, J., Fidlerová, H., & Mašata, M. (2004) · Biology of the Cell · doi:10.1016/j.biolcel.2004.04.015 · Cited by 153 · see citing works
Crighton, D., Woiwode, A., Zhang, C., Mandavia, N., Morton, J. P., Warnock, L. J., Milner, J., White, R. J., & Johnson, D. L. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg265 · Cited by 141 · see citing works
Dysregulation of RNA polymerase I transcription during disease
Hannan, K. M., Sanij, E., Rothblum, L. I., Hannan, R. D., & Pearson, R. B. (2012) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2012.10.014 · Cited by 137 · see citing works
Importin 7 and Exportin 1 Link c-Myc and p53 to Regulation of Ribosomal Biogenesis
Golomb, L., Bublik, D. R., Wilder, S., Nevo, R., Kiss, V., Grabusic, K., Volarevic, S., & Oren, M. (2012) · Molecular Cell · doi:10.1016/j.molcel.2011.11.022 · Cited by 137 · see citing works
Regulation of ribosome biogenesis within the nucleolus
Leary, D. J., & Huang, S. (2001) · FEBS Letters · doi:10.1016/s0014-5793(01)03143-x · Cited by 132 · see citing works
Li, F., Li, G., Liu, G., Lee, S. W., & Aaronson, S. A. (2001) · The EMBO Journal · doi:10.1093/emboj/20.8.1931 · Cited by 132 · see citing works
Cancer nucleus: Morphology and beyond
Dey, P. (2009) · Diagnostic Cytopathology · doi:10.1002/dc.21234 · Cited by 130 · see citing works
Wang, M., & Lemos, B. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1006994 · Cited by 129 · see citing works
Kao, C.-F., Chen, S.-Y., Chen, J., & Lee, Y. W. (2004) · Oncogene · doi:10.1038/sj.onc.1207368 · Cited by 129 · see citing works
The ribosome, (slow) beating heart of cancer (stem) cell
Bastide, A., & David, A. (2018) · Oncogenesis · doi:10.1038/s41389-018-0044-8 · Cited by 119 · see citing works
Ribosome biogenesis and cancer
Derenzini, M., Montanaro, L., & Treré, D. (2017) · Acta Histochemica · doi:10.1016/j.acthis.2017.01.009 · Cited by 119 · see citing works
Ribosomopathies: Global process, tissue specific defects
Yelick, P. C., & Trainor, P. A. (2015) · Rare Diseases · doi:10.1080/21675511.2015.1025185 · Cited by 117 · see citing works
The nucleolus as a fundamental regulator of the p53 response and a new target for cancer therapy
Woods, S. J., Hannan, K. M., Pearson, R. B., & Hannan, R. D. (2014) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2014.10.007 · Cited by 116 · see citing works
Ho, Y., & Gasch, A. P. (2015) · Current Genetics · doi:10.1007/s00294-015-0491-0 · Cited by 110 · see citing works
Regulation of RNA Polymerase I Transcription in Development, Disease, and Aging
Sharifi, S., & Bierhoff, H. (2018) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-062917-012612 · Cited by 106 · see citing works
LAS1L interacts with the mammalian Rix1 complex to regulate ribosome biogenesis
Castle, C. D., Cassimere, E. K., & Denicourt, C. (2011) · Molecular Biology of the Cell · doi:10.1091/mbc.e11-06-0530 · Cited by 105 · see citing works
Signal Transduction in Ribosome Biogenesis: A Recipe to Avoid Disaster
Piazzi, M., Bavelloni, A., Gallo, A., Faenza, I., & Blalock, W. L. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20112718 · Cited by 102 · see citing works
PTEN Represses RNA Polymerase I Transcription by Disrupting the SL1 Complex
Zhang, C., Comai, L., & Johnson, D. L. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.16.6899-6911.2005 · Cited by 101 · see citing works
Self-citationHE4 (WFDC2) gene overexpression promotes ovarian tumor growth
Moore, R. G., Hill, E. K., Horan, T. C., Yano, N., Kim, K., MacLaughlan, S. D., Lambert-Messerlian, G. M., Tseng, Y., Padbury, J. F., Miller, M. C., et al. (2014) · Scientific Reports · doi:10.1038/srep03574 · Cited by 100 · see citing works
Regulation of the p53 transcriptional activity
Liu, G., & Chen, X. (2005) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20700 · Cited by 99 · see citing works
Arf induces p53-dependent and -independent antiproliferative genes.
Kuo, M.-L., Duncavage, E. J., Mathew, R., den Besten, W., Pei, D., Naeve, D., Yamamoto, T. S., Cheng, C., Sherr, C. J., & Roussel, M. F. (2003) · PubMed · Cited by 99 · see citing works
Donati, G., Bertoni, S., Brighenti, E., Vici, M., Treré, D., Volarević, S., Montanaro, L., & Derenzini, M. (2011) · Oncogene · doi:10.1038/onc.2011.48 · Cited by 95 · see citing works
Suppression of Cardiomyocyte Hypertrophy by Inhibition of the Ubiquitin-Proteasome System
Meiners, S., Dreger, H., Fechner, M., Bieler, S., Rother, W., Günther, C., Baumann, G., Stangl, V., & Stangl, K. (2007) · Hypertension · doi:10.1161/hypertensionaha.107.097816 · Cited by 98 · see citing works
Guarding the ‘translation apparatus’: defective ribosome biogenesis and the p53 signaling pathway
Chakraborty, A., Uechi, T., & Kenmochi, N. (2011) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.73 · Cited by 96 · see citing works
Grewal, S. (2014) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2014.12.005 · Cited by 95 · see citing works
Montanaro, L., Treré, D., & Derenzini, M. (2011) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2011.10.006 · Cited by 93 · see citing works
Connecting the nucleolus to the cell cycle and human disease
Tsai, R. Y. L., & Pederson, T. (2014) · The FASEB Journal · doi:10.1096/fj.14-254680 · Cited by 95 · see citing works
Horton, L. E., Bushell, M., Baus, D., Tilleray, V. J., Clemens, M. J., & Hensold, J. O. (2002) · Oncogene · doi:10.1038/sj.onc.1205662 · Cited by 92 · see citing works
Barkić, M., Crnomarković, S., Grabušić, K., Bogetić, I., Panić, L., Tamarut, S., Brdovčak, M. C., Jerić, I., Vidak, S., & Volarević, S. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.01588-08 · Cited by 92 · see citing works
Ribosomal DNA and the Nucleolus as Keystones of Nuclear Architecture, Organization, and Function
Cerqueira, A. V., & Lemos, B. (2019) · Trends in Genetics · doi:10.1016/j.tig.2019.07.011 · Cited by 89 · see citing works
Small Molecule BMH-Compounds That Inhibit RNA Polymerase I and Cause Nucleolar Stress
Peltonen, K., Colis, L. C., Liu, H., Jäämaa, S., Zhang, Z., af Hällström, T., Moore, H. M., Sirajuddin, P., & Laiho, M. (2014) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-14-0256 · Cited by 90 · see citing works
p53 Represses the Oncogenic Sno-MiR-28 Derived from a SnoRNA
Yu, F., Bracken, C. P., Pillman, K. A., Lawrence, D., Goodall, G. J., Callen, D. F., & Neilsen, P. M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0129190 · Cited by 89 · see citing works
p8-deficient fibroblasts grow more rapidly and are more resistant to adriamycin-induced apoptosis
Vasseur, S., Hoffmeister, A., García‐Montero, A. C., Mallo, G. V., Feil, R., Kühbandner, S., Dagorn, J., & Iovanna, J. (2002) · Oncogene · doi:10.1038/sj.onc.1205222 · Cited by 89 · see citing works
p53, a translational regulator: contribution to its tumour-suppressor activity
Marcel, V., Catez, F., & Diaz, J. (2015) · Oncogene · doi:10.1038/onc.2015.25 · Cited by 88 · see citing works
Srivenugopal, K. S., Shou, J., Mullapudi, S., Lang, F. F., Rao, J. S., & Ali‐Osman, F. (2001) · PubMed · Cited by 88 · see citing works
Schneider, D. A. (2011) · Gene · doi:10.1016/j.gene.2011.08.006 · Cited by 87 · see citing works
p53 activation during ribosome biogenesis regulates normal erythroid differentiation
Goff, S. L., Boussaid, I., Floquet, C., Raimbault, A., Hatin, I., Andrieu‐Soler, C., Salma, M., Leduc, M., Gautier, E., Guyot, B., et al. (2020) · Blood · doi:10.1182/blood.2019003439 · Cited by 85 · see citing works
Rrn3 Phosphorylation Is a Regulatory Checkpoint for Ribosome Biogenesis
Cavanaugh, A. H., Hirschler‐Laszkiewicz, I., Hu, Q., Dundr, M., Smink, T., Misteli, T., & Rothblum, L. I. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m201232200 · Cited by 86 · see citing works
Ribosomal proteins as novel players in tumorigenesis
Heras-Rubio, A. D. L., Perucho, L., Paciucci, R., Vilardell, J., & LLeonart, M. E. (2013) · Cancer and Metastasis Reviews · doi:10.1007/s10555-013-9460-6 · Cited by 86 · see citing works
The Nucleolus: In Genome Maintenance and Repair
Tsekrekou, M., Stratigi, K., & Chatzinikolaou, G. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18071411 · Cited by 82 · see citing works
Cancer Biogenesis in Ribosomopathies
Sulima, S. O., Kampen, K. R., & Keersmaecker, K. D. (2019) · Cells · doi:10.3390/cells8030229 · Cited by 85 · see citing works
Nucleolar Size and Activity Are Related to pRb and p53 Status in Human Breast Cancer
Treré, D., Ceccarelli, C., Montanaro, L., Tosti, E., & Derenzini, M. (2004) · Journal of Histochemistry & Cytochemistry · doi:10.1369/jhc.4a6454.2004 · Cited by 85 · see citing works
Methylation of the ribosomal RNA gene promoter is associated with aging and age‐related decline
D’Aquila, P., Montesanto, A., Mandalà, M., Garasto, S., Mari, V., Corsonello, A., Bellizzi, D., & Passarino, G. (2017) · Aging Cell · doi:10.1111/acel.12603 · Cited by 84 · see citing works
Ayrault, O., Andrique, L., Fauvin, D., Eymin, B., Gazzéri, S., & Seité, P. (2006) · Oncogene · doi:10.1038/sj.onc.1209743 · Cited by 84 · see citing works
Therapeutic Approaches Targeting Nucleolus in Cancer
Carotenuto, P., Pecoraro, A., Palma, G., Russo, G., & Russo, A. (2019) · Cells · doi:10.3390/cells8091090 · Cited by 80 · see citing works
Transcriptional Repression: Conserved and Evolved Features
Payankaulam, S., Li, L. M., & Arnosti, D. N. (2010) · Current Biology · doi:10.1016/j.cub.2010.06.037 · Cited by 79 · see citing works
Emerging Role of Eukaryote Ribosomes in Translational Control
Venezia, N. D., Vincent, A., Marcel, V., Catez, F., & Diaz, J. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20051226 · Cited by 77 · see citing works
Scission of the p53-MDM2 Loop by Ribosomal Proteins
Zhou, X. Y., Liao, J.-M., Liao, W.-J., & Lu, H. (2012) · Genes & Cancer · doi:10.1177/1947601912455200 · Cited by 78 · see citing works
Porter, J. R., Fisher, B. E., Baranello, L., Liu, J. C., Kambach, D. M., Nie, Z., Koh, W. S., Luo, J., Stommel, J. M., Levens, D., et al. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.07.028 · Cited by 78 · see citing works
Mechanisms of translational deregulation in human tumors and therapeutic intervention strategies
Bilanges, B., & Stokoe, D. (2007) · Oncogene · doi:10.1038/sj.onc.1210431 · Cited by 77 · see citing works
Las1L Is a Nucleolar Protein Required for Cell Proliferation and Ribosome Biogenesis
Castle, C. D., Cassimere, E. K., Lee, J., & Denicourt, C. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.00358-10 · Cited by 75 · see citing works
The Evolution of the Ribosomal Protein–MDM2–p53 PathwayPreprint
Deisenroth, C., Franklin, D. A., & Zhang, Y. (2016) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a026138 · Cited by 74 · see citing works
Baltanás, F. C., Casafont, Í., Weruaga, E., Alonso, J. R., Berciano, M. T., & Lafarga, M. (2010) · Brain Pathology · doi:10.1111/j.1750-3639.2010.00461.x · Cited by 73 · see citing works
- Authors
- Zhai, W., & Comai, L.
- Affiliations
- University of Southern California (US)
- Corresponding author
- Comai, Lucio
- ORCID
- Comai, Lucio
- Venue
- Molecular and Cellular Biology
- Publisher
- Informa UK Limited
- Published
- 2000-08
- Volume
- 20
- Issue
- 16
- Pages
- 5930-5938
- ISSN
- 0270-7306 (ISSN-L)
- 1098-5549
- PMC
- PMC86070
- OpenAlex
- W2146842824
- Cited by
- 289
- References
- 53
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 8 · 2023: 9 · 2022: 10 · 2021: 14 · 2020: 7 · 2019: 14 · 2018: 13 · 2017: 13 · 2016: 6 · 2015: 14 · 2014: 24 · 2013: 21 · 2012: 7
- FWCI
- 2.53
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Molecular and Cellular Biology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute of General Medical Sciences (R01GM053949, R01 GM53949)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
- Keywords
- p53, RNA polymerase I transcription, transcriptional repression, UBF, TATA-binding protein, protein-protein interaction, transcription initiation complex, tumor suppressor
- MeSH terms
- HeLa Cells, Humans, Plasmids, RNA Polymerase I, Transcription, Genetic, Transfection, Genes, Tumor Suppressor, Genes, p53, Tumor Suppressor Protein p53
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