The DOI matches its Crossref record; 63 of the 63 references it cites were found in a registry or an index.
Binary specification of nonsense codons by splicing and cytoplasmic translation
Open accessAbstract
Premature translation termination codons resulting from nonsense or frameshift mutations are common causes of genetic disorders. Complications arising from the synthesis of C-terminally truncated polypeptides can be avoided by 'nonsense-mediated decay' of the mutant mRNAs. Premature termination codons in the beta-globin mRNA cause the common recessive form of beta-thalassemia when the affected mRNA is degraded, but the more severe dominant form when the mRNA escapes nonsense-mediated decay. We demonstrate that cells distinguish a premature termination codon within the beta-globin mRNA from the physiological translation termination codon by a two-step specification mechanism. According to the binary specification model proposed here, the positions of splice junctions are first tagged during splicing in the nucleus, defining a stop codon operationally as a premature termination codon by the presence of a 3' splicing tag. In the second step, cytoplasmic translation is required to validate the 3' splicing tag for decay of the mRNA. This model explains nonsense-mediated decay on the basis of conventional molecular mechanisms and allows us to propose a common principle for nonsense-mediated decay from yeast to man.
Overview
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
Verification
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?
The cited source says what the claim attributes to it.
In the citing paper
“The frameshift mutation leads to an ~90% reduction in cfap20 transcript abundance (Fig. 2c), presumably due to nonsense-mediated decay24–26.”
From The inner junction protein CFAP20 functions in motile and non-motile cilia and is critical for vision (2022) · cites this paper as [26]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Kozak, M. (1986) · Cell · doi:10.1016/0092-8674(86)90762-2 · Cited by 4,741
Hentze, M. W., & Kühn, L. C. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.16.8175 · Cited by 1,292
Self-citationRegulating the fate of mRNA: the control of cellular iron metabolism
Klausner, R. D., Rouault, T. A., & Harford, J. B. (1993) · Cell · doi:10.1016/0092-8674(93)90046-s · Cited by 1,210
A versatilein vivoandin vitroeukaryotic expression vector for protein engineering
Green, S., Issemann, I., & Sheer, E. (1988) · Nucleic Acids Research · doi:10.1093/nar/16.1.369 · Cited by 659
When cells stop making sense: effects of nonsense codons on RNA metabolism in vertebrate cells.
Maquat, L. E. (1995) · Europe PMC (PubMed Central) · Cited by 509
mRNA surveillance by the Caenorhabditis elegans smg genes.Preprint
Pulak, R., & Anderson, P. (1993) · Genes & Development · doi:10.1101/gad.7.10.1885 · Cited by 483
The Skipping of Constitutive Exons in Vivo Induced by Nonsense Mutations
Dietz, H. C., Valle, D., Francomano, C. A., Kendzior, R. J., Pyeritz, R. E., & Cutting, G. A. (1993) · Science · doi:10.1126/science.8430317 · Cited by 417
Nonsense Mutations in the Dihydrofolate Reductase Gene Affect RNA Processing
Urlaub, G., Mitchell, P. J., Ciudad, C. J., & Chasin, L. A. (1989) · Molecular and Cellular Biology · doi:10.1128/mcb.9.7.2868 · Cited by 358
Carter, M. S., Doskow, J., Morris, P., Li, S., Nhim, R. P., Sandstedt, S. A., & Wilkinson, M. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.48.28995 · Cited by 330
Translational termination efficiency in mammals is influenced by the base following the stop codon
McCaughan, K. K., Brown, C. M., Dalphin, M. E., Berry, M. J., & Tate, W. P. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.12.5431 · Cited by 284
Research works printed but not linked: 2
- Ausubel FM, Brent R, Kingston RI, Moore DD, Seidman JG, Smith JA and Struhl K (1994) Current Protocols in Molecular Biology. Vol. 1. John Wiley, New York.
- Konat GW, Laszkiewicz I, Grubinska B and Wiggins RC (1994) Generation of labelled DNA probes by PCR. In Griffin,H.G. and Griffin,A.M. (eds), PCR Technology. Current Innovations. CRC Press, London, pp. 37–42.
Cited by
Sorted by citations
Items 101–200 of 406
Maquat, L. E., & Li, X. (2001) · RNA · doi:10.1017/s1355838201002229 · Cited by 121
Wilkinson, M., & Shyu, A. (2001) · BioEssays · doi:10.1002/bies.1113 · Cited by 121
Sinha, R., Allemand, E., Zhang, Z., Karni, R., Myers, M. P., & Krainer, A. R. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.01270-09 · Cited by 116
Hilleren, P. J., & Parker, R. (1999) · RNA · doi:10.1017/s1355838299990519 · Cited by 115
Nonsense-Associated Altered Splicing
Wang, J., Chang, Y.-F., Hamilton, J. I., & Wilkinson, M. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00635-4 · Cited by 112
RNA surveillance by nuclear scanning?
Wilkinson, M., & Shyu, A. (2002) · Nature Cell Biology · doi:10.1038/ncb0602-e144 · Cited by 112
Precise Excision of the CAG Tract from the Huntingtin Gene by Cas9 Nickases
Dabrowska, M., Juzwa, W., Krzyżosiak, W. J., & Olejniczak, M. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00075 · Cited by 111
Ribosome‐based quality control of mRNA and nascent peptides
Simms, C. L., Thomas, E. N., & Zaher, H. S. (2016) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1366 · Cited by 108
Anczuków, O., Ware, M. D., Buisson, M., Zetoune, A. B., Stoppa‐Lyonnet, D., Sinilnikova, O. M., & Mazoyer, S. (2007) · Human Mutation · doi:10.1002/humu.20590 · Cited by 108
The Hbs1-Dom34 Protein Complex Functions in Non-stop mRNA Decay in Mammalian Cells
Saito, S., Hosoda, N., & Hoshino, S.-I. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.448977 · Cited by 116
Roignant, J., & Treisman, J. E. (2010) · Cell · doi:10.1016/j.cell.2010.09.036 · Cited by 104
SMG5-SMG7 authorize nonsense-mediated mRNA decay by enabling SMG6 endonucleolytic activity
Boehm, V., Kueckelmann, S., Gerbracht, J. V., Kallabis, S., Britto‐Borges, T., Altmüller, J., Krüger, M., Dieterich, C., & Gehring, N. H. (2021) · Nature Communications · doi:10.1038/s41467-021-24046-3 · Cited by 101
A novel phosphorylation-independent interaction between SMG6 and UPF1 is essential for human NMD
Nicholson, P., Josi, C., Kurosawa, H., Yamashita, A., & Mühlemann, O. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku645 · Cited by 103
Using the λN Peptide to Tether Proteins to RNAs
Baron-Benhamou, J., Gehring, N. H., Kulozik, A. E., & Hentze, M. W. (2004) · Humana Press eBooks · doi:10.1385/1-59259-750-5:135 · Cited by 103
Self-citationBoundary‐independent polar nonsense‐mediated decay
Wang, J., Gudikote, J. P., Olivas, O. R., & Wilkinson, M. (2002) · EMBO Reports · doi:10.1093/embo-reports/kvf036 · Cited by 103
Jonas, S., Weichenrieder, O., & Izaurralde, E. (2013) · Genes & Development · doi:10.1101/gad.206672.112 · Cited by 103
The exon junction complex: a lifelong guardian of mRNA fate
Woodward, L. A., Mabin, J. W., Gangras, P., & Singh, G. (2016) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1411 · Cited by 106
A Day in the Life of the Exon Junction Complex
Schlautmann, L. P., & Gehring, N. H. (2020) · Biomolecules · doi:10.3390/biom10060866 · Cited by 98
Translation‐coupled mRNA quality control mechanisms
Monaghan, L., Longman, D., & Cáceres, J. F. (2023) · The EMBO Journal · doi:10.15252/embj.2023114378 · Cited by 98
Nonsense-Mediated Decay of MutantwaxymRNA in Rice
Isshiki, M., Yamamoto, Y., Satoh, H., & Shimamoto, K. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.125.3.1388 · Cited by 98
Sato, H., & Maquat, L. E. (2009) · Genes & Development · doi:10.1101/gad.1817109 · Cited by 98
Kashima, I., Jonas, S., Jayachandran, U., Buchwald, G., Conti, E., Lupas, A. N., & Izaurralde, E. (2010) · Genes & Development · doi:10.1101/gad.604610 · Cited by 95
Nonsense‐mediated decay of glutathione peroxidase 1 mRNA in the cytoplasm depends on intron position
Sun, X., Moriarty, P. M., & Maquat, L. E. (2000) · The EMBO Journal · doi:10.1093/emboj/19.17.4734 · Cited by 94
mRNA quality control: Marking the message for life or death
Lykke‐Andersen, J. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00036-7 · Cited by 94
Mechanism, factors, and physiological role of nonsense-mediated mRNA decay
Fatscher, T., Boehm, V., & Gehring, N. H. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-2017-9 · Cited by 93
The Meaning of NMD: Translate or Perish
Brogna, S., McLeod, T., & Petrić, M. (2016) · Trends in Genetics · doi:10.1016/j.tig.2016.04.007 · Cited by 93
Schell, T., Kulozik, A. E., & Hentze, M. W. (2002) · Genome biology · doi:10.1186/gb-2002-3-3-reviews1006 · Cited by 93
Self-citationRomão, L., Inácio, Â., Santos, S., Ávila, M. J. D. M., Faustino, P., Pacheco, P. R., & Lavinha, J. (2000) · Blood · doi:10.1182/blood.v96.8.2895 · Cited by 92
Comprehensive Mechanism of Gene Silencing and Its Role in Plant Growth and Development
El‐Sappah, A. H., Yan, K., Huang, Q., Islam, M. M., Li, Q., Wang, Y., Khan, M. S., Xianming, Z., Mir, R. R., Li, J., et al. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.705249 · Cited by 95
Boehm, V., Haberman, N., Ottens, F., Ule, J., & Gehring, N. H. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.09.012 · Cited by 89
Fatscher, T., Boehm, V., Weiche, B., & Gehring, N. H. (2014) · RNA · doi:10.1261/rna.044933.114 · Cited by 88
Nonsense-mediated RNA decay and its bipolar function in cancer
Nogueira, G., Fernandes, R. O., García-Moreno, J. F., & Romão, L. (2021) · Molecular Cancer · doi:10.1186/s12943-021-01364-0 · Cited by 93
Nonsense-Mediated Decay of Human HEXA mRNA
Rajavel, K. S., & Neufeld, E. F. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.16.5512-5519.2001 · Cited by 86
Optineurin Insufficiency Impairs IRF3 but Not NF-κB Activation in Immune Cells
Munitić, I., Torchia, M. L. G., Meena, N. P., Zhu, G., Li, C. C., & Ashwell, J. D. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1301696 · Cited by 87
The human intronless melanocortin 4-receptor gene is NMD insensitive
Brocke, K. S. (2002) · Human Molecular Genetics · doi:10.1093/hmg/11.3.331 · Cited by 84
Processing bodies are not required for mammalian nonsense-mediated mRNA decay
Stalder, L., & Mühlemann, O. (2009) · RNA · doi:10.1261/rna.1672509 · Cited by 83
The role of SMG-1 in nonsense-mediated mRNA decay
Yamashita, A., Kashima, I., & Ohno, S. (2005) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2005.10.002 · Cited by 88
Role of SMG ‐1‐mediated U pf1 phosphorylation in mammalian nonsense‐mediated m RNA decay
Yamashita, A. (2013) · Genes to Cells · doi:10.1111/gtc.12033 · Cited by 84
Danckwardt, S., Gehring, N. H., Neu‐Yilik, G., Hundsdoerfer, P., Pförsich, M., Frede, U., Hentze, M. W., & Kulozik, A. E. (2004) · Blood · doi:10.1182/blood-2003-08-2894 · Cited by 82
Self-citationNew insights into the formation of active nonsense-mediated decay complexes
Singh, G., & Lykke‐Andersen, J. (2003) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(03)00176-2 · Cited by 82
CDS Annotation in Full-Length cDNA SequencePreprint
Furuno, M., Kasukawa, T., Saito, R., Adachi, J., Suzuki, H., Baldarelli, R. M., Hayashizaki, Y., & Okazaki, Y. (2003) · Genome Research · doi:10.1101/gr.1060303 · Cited by 82
Genetic association analysis of 77,539 genomes reveals rare disease etiologies
Greene, D. J., Pirri, D., Frudd, K., Sackey, E., Al‐Owain, M. A., Giese, A. P. J., Ramzan, K., Riaz, S., Yamanaka, I., Boeckx, N., et al. (2023) · Nature Medicine · doi:10.1038/s41591-023-02211-z · Cited by 80
Danckwardt, S., Neu‐Yilik, G., Thermann, R., Frede, U., Hentze, M. W., & Kulozik, A. E. (2002) · Blood · doi:10.1182/blood.v99.5.1811 · Cited by 80
Self-citationAn Efficient System for Cap- and Poly(A)-Dependent Translation In Vitro
Svitkin, Y. V., & Sonenberg, N. (2004) · Humana Press eBooks · doi:10.1385/1-59259-750-5:155 · Cited by 80
Ribosome dynamics and mRNA turnover, a complex relationship under constant cellular scrutiny
Morris, C., Cluet, D., & Ricci, E. P. (2021) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1658 · Cited by 82
Xu, M., Xie, Y., Abouzeid, H., Gordon, C. T., Fiorentino, A., Sun, Z., Lehman, A., Osman, I. S., Dharmat, R., Riveiro-Álvarez, R., et al. (2017) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2017.02.008 · Cited by 77
Zebrafish bmp4 functions during late gastrulation to specify ventroposterior cell fates
Stickney, H. L., Imai, Y., Draper, B. W., Moens, C. B., & Talbot, W. S. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.07.027 · Cited by 78
Asselta, R., Duga, S., Spena, S., Santagostino, E., Peyvandi, F., Piseddu, G., Targhetta, R., Malcovati, M., Mannucci, P. M., & Tenchini, M. L. (2001) · Blood · doi:10.1182/blood.v98.13.3685 · Cited by 78
ICP0 Gene Expression Is a Herpes Simplex Virus Type 1 Apoptotic Trigger
Sanfilippo, C. M., & Blaho, J. A. (2006) · Journal of Virology · doi:10.1128/jvi.00334-06 · Cited by 77
Bühler, M. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh651 · Cited by 79
Gómez‐Lozano, N., Estefanía, E., Williams, F., Halfpenny, I. A., Middleton, D., Solís, R., & Vilches, C. (2004) · European Journal of Immunology · doi:10.1002/eji.200425493 · Cited by 75
Wang, J., Vock, V. M., Li, S., Olivas, O. R., & Wilkinson, M. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m111781200 · Cited by 74
Sato, H., Hosoda, N., & Maquat, L. E. (2008) · Molecular Cell · doi:10.1016/j.molcel.2007.12.009 · Cited by 75
Neu‐Yilik, G., Gehring, N. H., Thermann, R., Frede, U., Hentze, M. W., & Kulozik, A. E. (2001) · The EMBO Journal · doi:10.1093/emboj/20.3.532 · Cited by 74
Self-citationPABPC1——mRNA stability, protein translation and tumorigenesis
Qi, Y., Wang, M., & Jiang, Q. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.1025291 · Cited by 72
Splicing repression allows the gradual emergence of new Alu-exons in primate evolution
Attig, J., Mozos, I. R. D. L., Haberman, N., Wang, Z., Emmett, W., Zarnack, K., König, J., & Ule, J. (2016) · eLife · doi:10.7554/elife.19545 · Cited by 70
Splicing‐dependent NMD does not require the EJC in Schizosaccharomyces pombe
Wen, J., & Brogna, S. (2010) · The EMBO Journal · doi:10.1038/emboj.2010.48 · Cited by 77
Chowdhury, B., Tsokos, C. G., Krishnan, S. K., Robertson, J., Fisher, C. U., Warke, R. G., Warke, V. G., Nambiar, M. P., & Tsokos, G. C. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m501048200 · Cited by 72
Transcriptional Silencing of Nonsense Codon-Containing Immunoglobulin Minigenes
Bühler, M., Mohn, F., Stalder, L., & Mühlemann, O. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.03.030 · Cited by 73
van Wijk, R., Nieuwenhuis, H. K., van den Berg, H. M., Huizinga, E. G., van der Meijden, B. B., Kraaijenhagen, R. J., & van Solinge, W. W. (2001) · Blood · doi:10.1182/blood.v98.2.358 · Cited by 72
Brendel, V., & Kleffe, J. (1998) · Nucleic Acids Research · doi:10.1093/nar/26.20.4748 · Cited by 72
Neu‐Yilik, G., & Kulozik, A. E. (2008) · Advances in genetics · doi:10.1016/s0065-2660(08)00604-4 · Cited by 74
Self-citationWodrich, H. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.4.901 · Cited by 71
5‐azacytidine inhibits nonsense‐mediated decay in a MYC‐dependent fashion
Bhuvanagiri, M., Lewis, J., Putzker, K., Becker, J. P., Leicht, S., Krijgsveld, J., Batra, R., Turnwald, B., Jovanovic, B., Hauer, C., et al. (2014) · EMBO Molecular Medicine · doi:10.15252/emmm.201404461 · Cited by 76
Self-citationPremature termination codons enhance mRNA decapping in human cells
Couttet, P. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh218 · Cited by 70
Georgieva, T. G., Dunkov, B. C., Harizanova, N., Ralchev, K. H., & Law, J. H. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.6.2716 · Cited by 70
Dominant optic atrophy: correlation between clinical and molecular genetic studies
Puomila, A., Huoponen, K., Mäntyjärvi, M., Hämäläinen, P., Paananen, R., Sankila, E., Savontaus, M., Somer, M., & Nikoskelainen, E. K. (2005) · Acta Ophthalmologica Scandinavica · doi:10.1111/j.1600-0420.2005.00448.x · Cited by 69
mRNA surveillance mitigates genetic dominance in Caenorhabditis elegans
Cali, B. M., & Anderson, P. (1998) · Molecular and General Genetics MGG · doi:10.1007/s004380050883 · Cited by 66
Suppression of Nonsense Mutations by New Emerging Technologies
Morais, P., Adachi, H., & Yu, Y. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21124394 · Cited by 65
IS IT DOMINANTLY INHERITED β THALASSAEMIA OR JUST A β‐CHAIN VARIANT THAT IS HIGHLY UNSTABLE?
Thein, S. L. (1999) · British Journal of Haematology · doi:10.1046/j.1365-2141.1999.01492.x · Cited by 65
Sharma, N., Evans, T. A., Pellicore, M. J., Davis-Marcisak, E. F., Aksit, M. A., McCague, A. F., Joynt, A. T., Lu, Z., Han, S. T., Anzmann, A. F., et al. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007723 · Cited by 64
Buisson, M., Anczuków, O., Zetoune, A. B., Ware, M. D., & Mazoyer, S. (2006) · Human Mutation · doi:10.1002/humu.20384 · Cited by 64
Wilson, G. M., Sun, Y. M., Sellers, J. A., Lu, H., Penkar, N., Dillard, G., & Brewer, G. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.6.4056 · Cited by 63
Cheruiyot, A., Li, S., Srivatsan, S. N., Ahmed, T., Chen, Y., Lemacon, D. S., Li, Y., Yang, Z., Wadugu, B. A., Warner, W. A., et al. (2021) · Cancer Research · doi:10.1158/0008-5472.can-20-4016 · Cited by 61
Alston, C. L., Heidler, J., Dibley, M. G., Kremer, L. S., Taylor, L. S., Fratter, C., French, C. E., Glasgow, R. I. C., Feichtinger, R. G., Delon, I., et al. (2018) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2018.08.013 · Cited by 61
Neural tube defects and the 13q deletion syndrome: Evidence for a critical region in 13q33-34
Luo, J., Balkin, N. E., Stewart, J. F., Sarwark, J. F., Charrow, J., & Nye, J. S. (2000) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(20000320)91:3 · Cited by 102
Self-citationDenecke, J., Kranz, C., Kemming, D., Koch, H.-G., & Marquardt, T. (2004) · Human Mutation · doi:10.1002/humu.20026 · Cited by 61
CASC3 promotes transcriptome-wide activation of nonsense-mediated decay by the exon junction complex
Gerbracht, J. V., Boehm, V., Britto‐Borges, T., Kallabis, S., Wiederstein, J. L., Ciriello, S., Aschemeier, D., Krüger, M., Frese, C. K., Altmüller, J., et al. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa564 · Cited by 58
Failsafe nonsense-mediated mRNA decay does not detectably target eIF4E-bound mRNA
Matsuda, D., Hosoda, N., Kim, Y. K., & Maquat, L. E. (2007) · Nature Structural & Molecular Biology · doi:10.1038/nsmb1297 · Cited by 59
Human INT6/eIF3e is required for nonsense‐mediated mRNA decay
Morris, C., Wittmann, J., Jäck, H., & Jalinot, P. (2007) · EMBO Reports · doi:10.1038/sj.embor.7400955 · Cited by 62
Shigeoka, T. (2005) · Nucleic Acids Research · doi:10.1093/nar/gni022 · Cited by 59
A chemiluminescence-based reporter system to monitor nonsense-mediated mRNA decay
Boelz, S., Neu‐Yilik, G., Gehring, N. H., Hentze, M. W., & Kulozik, A. E. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.08.017 · Cited by 58
Self-citationmRNA surveillance in mammalian cells: The relationship between introns and translation termination
Sun, X., & Maquat, L. E. (2000) · RNA · doi:10.1017/s1355838200991660 · Cited by 56
Dagenais, S. L., Adam, A. N., Innis, J. W., & Glover, T. W. (2001) · The American Journal of Human Genetics · doi:10.1086/321290 · Cited by 55
Intranuclear degradation of nonsense codon‐containing mRNA
Bühler, M., Wilkinson, M., & Mühlemann, O. (2002) · EMBO Reports · doi:10.1093/embo-reports/kvf129 · Cited by 55
mRNP quality control goes regulatory
Mühlemann, O., & Jensen, T. H. (2011) · Trends in Genetics · doi:10.1016/j.tig.2011.11.001 · Cited by 54
Control of human -globin mRNA stability and its impact on beta-thalassemia phenotype
Peixeiro, I., Silva, A. L., & Romao, L. (2011) · Haematologica · doi:10.3324/haematol.2010.039206 · Cited by 51
Persuy, M. A., Printz, C., Medrano, J. F. F., & Mercier, J. (1999) · Animal Genetics · doi:10.1046/j.1365-2052.1999.00547.x · Cited by 53
The uORF-containing thrombopoietin mRNA escapes nonsense-mediated decay (NMD)
Stockklausner, C. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl277 · Cited by 53
NMD inhibition by 5-azacytidine augments presentation of immunogenic frameshift-derived neoepitopes
Becker, J. P., Helm, D., Rettel, M., Stein, F., Hernandez‐Sanchez, A., Urban, K., Gebert, J. F., Kloor, M., Neu‐Yilik, G., Doeberitz, M. V. K., et al. (2021) · iScience · doi:10.1016/j.isci.2021.102389 · Cited by 50
Self-citationA versatile cis-acting inverter module for synthetic translational switches
Endo, K., Hayashi, K., Inoue, T., & Saito, H. (2013) · Nature Communications · doi:10.1038/ncomms3393 · Cited by 51
Raimondeau, E., Bufton, J. C., & Schaffitzel, C. (2018) · Biochemical Society Transactions · doi:10.1042/bst20170427 · Cited by 50
Luhmann, U. F. O., Carvalho, L. S., Holthaus, S.-M. K., Cowing, J. A., Greenaway, S., Chu, C. J., Herrmann, P., Smith, A. J., Munro, P., Potter, P. K., et al. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu424 · Cited by 49
Nuclear mRNA Binding Proteins Couple Pre-mRNA Splicing and Post-splicing Events
Kim, V. N., & Dreyfuss, G. (2001) · Molecules and Cells · doi:10.1016/s1016-8478(23)17055-5 · Cited by 49
Caspases shutdown nonsense-mediated mRNA decay during apoptosis
Jia, J., Furlan, A., Gonzalez-Hilarion, S., Leroy, C., Gruenert, D. C., Tulasne, D., & Lejeune, F. (2015) · Cell Death and Differentiation · doi:10.1038/cdd.2015.18 · Cited by 47
Gušić, M., Schottmann, G., Feichtinger, R. G., Du, C., Scholz, C., Wagner, M., Mayr, J. A., Lee, C.-Y., Yépez, V. A., Lorenz, N., et al. (2019) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2019.12.005 · Cited by 53
A Single-nucleotide Deletion Leads to Rapid Degradation ofTAP-1 mRNA in a Melanoma Cell Line
Yang, T., McNally, B. A., Ferrone, S., Liu, Y., & Zheng, P. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m300954200 · Cited by 48
Raczyńska, K. D., Ruepp, M., Brzęk, A., Reber, S., Romeo, V., Rindlisbacher, B., Heller, M., Szweykowska-Kulińska, Z., Jarmołowski, A., & Schümperli, D. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv794 · Cited by 47
The RNA helicase DHX34 functions as a scaffold for SMG1-mediated UPF1 phosphorylation
Melero, R., Hug, N., López‐Perrote, A., Yamashita, A., Cáceres, J. F., & Llorca, Ó. (2016) · Nature Communications · doi:10.1038/ncomms10585 · Cited by 48
Metadata
- Authors
- Thermann, R., Neu‐Yilik, G., Deters, A., Frede, U., Wehr, K., Hagemeier, C., Hentze, M. W., & Kulozik, A. E.
- Affiliations
- Humboldt-Universität zu Berlin (DE)
- European Molecular Biology Laboratory (DE)
- Corresponding author
- Hentze, Matthias W.
- Kulozik, Andreas E.
- Venue
- The EMBO Journal
- Published
- 1998-06-15
- Volume
- 17
- Issue
- 12
- Pages
- 3484-3494
- ISSN
- 0261-4189 (ISSN-L)
- 1460-2075
- PMC
- PMC1170685
- OpenAlex
- W2036625038
- Cited by
- 406
- References
- 59
- Citations by year
- 2026: 8 · 2025: 9 · 2024: 3 · 2023: 12 · 2022: 15 · 2021: 17 · 2020: 15 · 2019: 14 · 2018: 15 · 2017: 12 · 2016: 15 · 2015: 15 · 2014: 8 · 2013: 19 · 2012: 8
- FWCI
- 7.69
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The EMBO Journal (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Deutsche Forschungsgemeinschaft
- Chinese Academy of Agricultural Sciences
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Health Sciences › Medicine › Genetics (clinical) › Hemoglobinopathies and Related Disorders
- Keywords
- nonsense-mediated mRNA decay, stop codon, premature stop codon, beta-globin mRNA, beta-thalassemia, splicing, splice junctions, cytoplasmic translation, mRNA degradation, frameshift mutation
- MeSH terms
- HeLa Cells, Humans, RNA, Messenger, Protein Biosynthesis, Codon, Terminator, Codon, Nonsense, Fluorescent Antibody Technique, Indirect
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