The DOI matches its Crossref record; 59 of the 60 references it cites were found in a registry or an index.
Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis
Open accessAbstract
Blood cell formation is classically thought to occur through a hierarchical differentiation process, although recent studies have shown that lineage commitment may occur earlier in hematopoietic stem and progenitor cells (HSPCs). The relevance to human blood diseases and the underlying regulation of these refined models remain poorly understood. By studying a genetic blood disorder, Diamond-Blackfan anemia (DBA), where the majority of mutations affect ribosomal proteins and the erythroid lineage is selectively perturbed, we are able to gain mechanistic insight into how lineage commitment is programmed normally and disrupted in disease. We show that in DBA, the pool of available ribosomes is limited, while ribosome composition remains constant. Surprisingly, this global reduction in ribosome levels more profoundly alters translation of a select subset of transcripts. We show how the reduced translation of select transcripts in HSPCs can impair erythroid lineage commitment, illuminating a regulatory role for ribosome levels in cellular differentiation.
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?
In the citing paper
“Inspired by this discovery and through functional follow up, it was shown that the more common ribosomal gene mutations impair the translation of GATA1 mRNA and thus result in impaired erythropoiesis (Khajuria et al., 2018; Ludwig et al., 2014).”
From Unraveling Hematopoiesis through the Lens of Genomics (2020) · cites this paper as Khajuria et al., 2018
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
Analysis of protein-coding genetic variation in 60,706 humans
Exome Aggregation Consortium, Lek, M., Karczewski, K. J., Minikel, E. V., Samocha, K. E., Banks, E., Fennell, T., O’Donnell-Luria, A. H., Ware, J. S., Hill, A. J., et al. (2016) · Nature · doi:10.1038/nature19057 · Cited by 9,587
Global quantification of mammalian gene expression control
Schwanhäusser, B., Busse, D., Li, N., Dittmar, G., Schuchhardt, J., Wolf, J., Chen, W., & Selbach, M. (2011) · Nature · doi:10.1038/nature10098 · Cited by 6,566 · cited 2×
“The importance of such regulation is emphasized by the observation that only a fraction of the variation in cellular protein levels can be explained through transcriptional changes (Jovanovic et al., 2015; Schwanhäusser et al., 2011).”
BackgroundCellProfiler: image analysis software for identifying and quantifying cell phenotypes
Carpenter, A. E., Jones, T. R., Lamprecht, M. R., Clarke, C., Kang, I. H., Friman, O., Guertin, D. A., Chang, J. H., Lindquist, R. A., Moffat, J., et al. (2006) · Genome biology · doi:10.1186/gb-2006-7-10-r100 · Cited by 5,212
Hematopoiesis: An Evolving Paradigm for Stem Cell Biology
Orkin, S. H., & Zon, L. I. (2008) · Cell · doi:10.1016/j.cell.2008.01.025 · Cited by 2,570
Identification and characterization of essential genes in the human genome
Wang, T., Birsoy, K., Hughes, N. W., Krupczak, K. M., Post, Y., Wei, J. J., Lander, E. S., & Sabatini, D. M. (2015) · Science · doi:10.1126/science.aac7041 · Cited by 1,617
Self-citationA unifying model for mTORC1-mediated regulation of mRNA translation
Thoreen, C. C., Chantranupong, L., Keys, H. R., Wang, T., Gray, N. S., & Sabatini, D. M. (2012) · Nature · doi:10.1038/nature11083 · Cited by 1,477
The translational landscape of mTOR signalling steers cancer initiation and metastasis
Hsieh, A. C., Liu, Y., Edlind, M. P., Ingolia, N. T., Janes, M. R., Sher, A., Shi, E. Y., Stumpf, C. R., Christensen, C., Bonham, M. J., et al. (2012) · Nature · doi:10.1038/nature10912 · Cited by 1,313
Transcriptional Heterogeneity and Lineage Commitment in Myeloid Progenitors
Paul, F., Arkin, Y., Giladi, A., Jaitin, D. A., Kenigsberg, E., Keren-Shaul, H., Winter, D., Lara-Astiaso, D., Gury, M., Weiner, A., et al. (2015) · Cell · doi:10.1016/j.cell.2015.11.013 · Cited by 1,082
Translational control by 5′-untranslated regions of eukaryotic mRNAs
Hinnebusch, A. G., Ivanov, I. P., & Sonenberg, N. (2016) · Science · doi:10.1126/science.aad9868 · Cited by 1,079
The Xist lncRNA Exploits Three-Dimensional Genome Architecture to Spread Across the X Chromosome
Engreitz, J., Pandya‐Jones, A., McDonel, P. E., Shishkin, A., Sirokman, K., Surka, C., Kadri, S., Xing, J. C., Goren, A., Lander, E. S., et al. (2013) · Science · doi:10.1126/science.1237973 · Cited by 1,008
Flagged first, then by citations
1 of the 60 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Ribosome assembly coming into focus
Klinge, S., & Woolford, J. L. (2018) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-018-0078-y · Cited by 483
Ribosomal proteins and human diseases: molecular mechanisms and targeted therapy
Kang, J., Brajanovski, N., Chan, K. T., Xuan, J., Pearson, R. B., & Sanij, E. (2021) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-021-00728-8 · Cited by 428
Deregulation of ribosomal protein expression and translation promotes breast cancer metastasis
Ebright, R. Y., Lee, S., Wittner, B. S., Niederhoffer, K., Nicholson, B. T., Bardia, A., Truesdell, S. S., Wiley, D. F., Wesley, B., Li, S. S., et al. (2020) · Science · doi:10.1126/science.aay0939 · Cited by 378
Ribosome biogenesis in disease: new players and therapeutic targets
Jiao, L., Liu, Y., Yu, X., Pan, X., Zhang, Y., Tu, J., Song, Y., & Li, Y. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01285-4 · Cited by 336
A Cell Atlas of the Adult Drosophila Midgut
Hung, R., Hu, Y., Kirchner, R., Liu, Y., Xu, C., Comjean, A., Tattikota, S. G., Li, F., Song, W., Sui, S. H., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1916820117 · Cited by 285
The Genetic Landscape of Diamond-Blackfan Anemia
Ulirsch, J. C., Verboon, J. M., Kazerounian, S., Guo, M. H., Yuan, D., Ludwig, L. S., Handsaker, R. E., Abdulhay, N. J., Fiorini, C., Genovese, G., et al. (2018) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2018.10.027 · Cited by 272
Translation deregulation in human disease
Tahmasebi, S., Khoutorsky, A., Mathews, M. B., & Sonenberg, N. (2018) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-018-0034-x · Cited by 272
Costa, L. M. D., Leblanc, T. M., & Mohandas, N. (2020) · Blood · doi:10.1182/blood.2019000947 · Cited by 240
Uncovering the assembly pathway of human ribosomes and its emerging links to disease
Bohnsack, K. E., & Bohnsack, M. T. (2019) · The EMBO Journal · doi:10.15252/embj.2018100278 · Cited by 218
Kampen, K. R., Sulima, S. O., Vereecke, S., & Keersmaecker, K. D. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz637 · Cited by 231
Interrogation of human hematopoiesis at single-cell and single-variant resolution
Ulirsch, J. C., Lareau, C. A., Bao, E. L., Ludwig, L. S., Guo, M. H., Benner, C., Satpathy, A. T., Kartha, V. K., Salem, R. M., Hirschhorn, J. N., et al. (2019) · Nature Genetics · doi:10.1038/s41588-019-0362-6 · Cited by 208
Self-citationTranslational control of stem cell function
Saba, J. A., Liakath‐Ali, K., Green, R., & Watt, F. M. (2021) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-021-00386-2 · Cited by 205
Ribosomopathies: Old Concepts, New Controversies
Farley‐Barnes, K. I., Ogawa, L. M., & Baserga, S. J. (2019) · Trends in Genetics · doi:10.1016/j.tig.2019.07.004 · Cited by 193
Targeting the RNA Polymerase I Transcription for Cancer Therapy Comes of Age
Ferreira, R., Schneekloth, J. S., Panov, K. I., Hannan, K. M., & Hannan, R. D. (2020) · Cells · doi:10.3390/cells9020266 · Cited by 188
Transcriptional States and Chromatin Accessibility Underlying Human Erythropoiesis
Ludwig, L. S., Lareau, C. A., Bao, E. L., Nandakumar, S. K., Muus, C., Ulirsch, J. C., Chowdhary, K., Buenrostro, J. D., Mohandas, N., An, X., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.05.046 · Cited by 167
Unraveling Hematopoiesis through the Lens of Genomics
Liggett, L. A., & Sankaran, V. G. (2020) · Cell · doi:10.1016/j.cell.2020.08.030 · Cited by 163
Structures of translationally inactive mammalian ribosomes
Brown, A., Baird, M. R., Yip, M.-C.-J., Murray, J., & Shao, S. (2018) · eLife · doi:10.7554/elife.40486 · Cited by 138
Genetic predisposition to MDS: clinical features and clonal evolution
Kennedy, A. L., & Shimamura, A. (2019) · Blood · doi:10.1182/blood-2018-10-844662 · Cited by 152
N6-methyladenosine (m6A) in 18S rRNA promotes fatty acid metabolism and oncogenic transformation
Peng, H., Chen, B., Wei, W., Guo, S., Han, H., Yang, C., Ma, J., Wang, L., Peng, S., Kuang, M., et al. (2022) · Nature Metabolism · doi:10.1038/s42255-022-00622-9 · Cited by 147
Human hematopoietic stem cell vulnerability to ferroptosis
Zhao, J., Jia, Y., Mahmut, D., Deik, A., Jeanfavre, S., Clish, C. B., & Sankaran, V. G. (2023) · Cell · doi:10.1016/j.cell.2023.01.020 · Cited by 144
Translational control through ribosome heterogeneity and functional specialization
Gay, D. M., Lund, A. H., & Jansson, M. D. (2022) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2021.07.001 · Cited by 141
Cheng, Z., Mugler, C. F., Keskin, A., Hodapp, S. J., Chan, L. Y., Weis, K., Mertins, P., Regev, A., Jovanović, M., & Brar, G. A. (2018) · Molecular Cell · doi:10.1016/j.molcel.2018.10.032 · Cited by 135
Regulation of GATA1 levels in erythropoiesis
Gutiérrez, L., Caballero, N., Fernández‐Calleja, L., Karkoulia, E., & Strouboulis, J. (2019) · IUBMB Life · doi:10.1002/iub.2192 · Cited by 138
Proteotoxicity from aberrant ribosome biogenesis compromises cell fitness
Tye, B., Commins, N., Ryazanova, L. V., Wühr, M., Springer, M., Pincus, D., & Churchman, L. S. (2019) · eLife · doi:10.7554/elife.43002 · Cited by 143
Does functional specialization of ribosomes really exist?
Ferretti, M., & Karbstein, K. (2019) · RNA · doi:10.1261/rna.069823.118 · Cited by 145
Germline NPM1 mutations lead to altered rRNA 2′-O-methylation and cause dyskeratosis congenita
Nachmani, D., Bothmer, A., Grisendi, S., Mele, A., Bothmer, D., Lee, J. D., Monteleone, E., Cheng, K., Zhang, Y., Bester, A. C., et al. (2019) · Nature Genetics · doi:10.1038/s41588-019-0502-z · Cited by 140
Integrated stress response activity marks stem cells in normal hematopoiesis and leukemia
van Galen, P., Mbong, N., Kreso, A., Schoof, E. M., Wagenblast, E., Ng, S. W. K., Krivdova, G., Jin, L., Nakauchi, H., & Dick, J. E. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.10.021 · Cited by 131
Massively parallel base editing to map variant effects in human hematopoiesis
Martin-Rufino, J. D., Castano, N., Pang, M., Grody, E. I., Joubran, S. R., Caulier, A., Wahlster, L., Li, T., Qiu, X., Riera-Escandell, A. M., et al. (2023) · Cell · doi:10.1016/j.cell.2023.03.035 · Cited by 123
Pre-Ribosomal RNA Processing in Human Cells: From Mechanisms to Congenital Diseases
Aubert, M., O’Donohue, M.-F., Lebaron, S., & Gleizes, P. (2018) · Biomolecules · doi:10.3390/biom8040123 · Cited by 128
Rare ribosomopathies: insights into mechanisms of cancer
Aspesi, A., & Ellis, S. R. (2019) · Nature reviews. Cancer · doi:10.1038/s41568-019-0105-0 · Cited by 121
Ribosome heterogeneity in stem cells and development
Li, D., & Wang, J. (2020) · The Journal of Cell Biology · doi:10.1083/jcb.202001108 · Cited by 115
Wu, J., Subbaiah, K. C. V., Xie, L. H., Jiang, F., Khor, E.-S., Mickelsen, D. M., Myers, J. R., Tang, W. H. W., & Yao, P. (2020) · Circulation Research · doi:10.1161/circresaha.119.315999 · Cited by 115
Generally applicable transcriptome-wide analysis of translation using anota2seq
Oertlin, C., Lorent, J., Murie, C., Furic, L., Topisirovic, I., & Larsson, O. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz223 · Cited by 107
Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation
Basak, A., Munschauer, M., Lareau, C. A., Montbleau, K. E., Ulirsch, J. C., Hartigan, C. R., Schenone, M., Lian, J., Wang, Y., Huang, Y., et al. (2020) · Nature Genetics · doi:10.1038/s41588-019-0568-7 · Cited by 105
A single-cell survey of cellular hierarchy in acute myeloid leukemia
Wu, J., Xiao, Y., Sun, J., Sun, H., Chen, H., Zhu, Y., Fu, H., Yu, C., Weigao, E., Lai, S., et al. (2020) · Journal of Hematology & Oncology · doi:10.1186/s13045-020-00941-y · Cited by 114
Gillespie, M. A., Palii, C. G., Sanchez-Taltavull, D., Shannon, P., Longabaugh, W. J. R., Downes, D. J., Sivaraman, K., Espinoza, H. M., Hughes, J. R., Price, N. D., et al. (2020) · Molecular Cell · doi:10.1016/j.molcel.2020.03.031 · Cited by 110
RNA-binding proteins balance brain function in health and disease
Schieweck, R., Ninkovic, J., & Kiebler, M. A. (2020) · Physiological Reviews · doi:10.1152/physrev.00047.2019 · Cited by 110
Structure, Dynamics and Function of the 26S Proteasome
Mao, Y. (2020) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-030-58971-4_1 · Cited by 110
Molecular and cellular mechanisms that regulate human erythropoiesis
Caulier, A., & Sankaran, V. G. (2021) · Blood · doi:10.1182/blood.2021011044 · Cited by 113
Shen, S., Faouzi, S., Bastide, A., Martineau, S., Malka-Mahieu, H., Fu, Y., Sun, X., Mateus, C., Routier, É., Roy, S., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-13360-6 · Cited by 113
Heme-regulated eIF2α kinase in erythropoiesis and hemoglobinopathies
Chen, J.-J., & Zhang, S. (2019) · Blood · doi:10.1182/blood.2019001915 · Cited by 96
Ribosome Stoichiometry: From Form to Function
Emmott, E., Jovanović, M., & Slavov, N. (2018) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2018.10.009 · Cited by 102
DNA-PKcs has KU-dependent function in rRNA processing and haematopoiesis
Shao, Z., Flynn, R. A., Crowe, J. L., Zhu, Y., Liang, J., Jiang, W., Aryan, F., Aoude, P., Bertozzi, C. R., Estes, V. M., et al. (2020) · Nature · doi:10.1038/s41586-020-2041-2 · Cited by 95
Translation elongation rate varies among organs and decreases with age
Gerashchenko, M. V., Peterfi, Z., Yim, S. H., & Gladyshev, V. N. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkaa1103 · Cited by 98
Downregulation of ribosome biogenesis during early forebrain development
Chau, K. F., Shannon, M. L., Fame, R. M., Fonseca, E., Mullan, H., Johnson, M. B., Sendamarai, A. K., Springel, M. W., Laurent, B., & Lehtinen, M. K. (2018) · eLife · doi:10.7554/elife.36998 · Cited by 95
An update on the pathogenesis and diagnosis of Diamond–Blackfan anemia
Costa, L. M. D., Narla, A., & Mohandas, N. (2018) · F1000Research · doi:10.12688/f1000research.15542.1 · Cited by 94
Luan, Y., Tang, N., Yang, J., Liu, S., Cheng, C., Wang, Y., Chen, C., Guo, Y., Wang, H., Zhao, W., et al. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac053 · Cited by 95
Translational Control in Stem Cells
Tahmasebi, S., Amiri, M., & Sonenberg, N. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2018.00709 · Cited by 94
Post-Transcriptional Regulation of Homeostatic, Stressed, and Malignant Stem Cells
Chua, B. A., van der Werf, I. M., Jamieson, C. H. M., & Signer, R. A. J. (2020) · Cell stem cell · doi:10.1016/j.stem.2020.01.005 · Cited by 96
Quiescence Entry, Maintenance, and Exit in Adult Stem Cells
Mohammad, K., Dakik, P., Medkour, Y., Mitrofanova, D., & Titorenko, V. I. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20092158 · Cited by 93
Pauli, C., Liu, Y., Rohde, C., Cui, C., Fijałkowska, D., Gerloff, D., Walter, C., Krijgsveld, J., Dugas, M., Edemir, B., et al. (2020) · Blood · doi:10.1182/blood.2019004121 · Cited by 96
Cell-type-specific quantification of protein synthesis in vivo
Jose, L. H. S., & Signer, R. A. J. (2019) · Nature Protocols · doi:10.1038/s41596-018-0100-z · Cited by 95
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
UFMylation: a ubiquitin-like modification
Zhou, X., Mahdizadeh, S. J., Gallo, M. L., Eriksson, L. A., Chevet, É., & Lafont, É. (2023) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2023.10.004 · Cited by 86
The homeostatic regulation of ribosome biogenesis
Ni, C., & Buszczak, M. (2022) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2022.03.043 · Cited by 86
Broeck, A. V., & Klinge, S. (2024) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-030222-113611 · Cited by 86
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 85
A rare codon-based translational program of cell proliferation
Guimaraes, J. C., Mittal, N., Gnann, A., Jedlinski, D., Riba, A., Buczak, K., Schmidt, A., & Zavolan, M. (2020) · Genome biology · doi:10.1186/s13059-020-1943-5 · Cited by 73
Specialized ribosomes and the control of translation
Guo, H. (2018) · Biochemical Society Transactions · doi:10.1042/bst20160426 · Cited by 80
How I manage children with Diamond‐Blackfan anaemia
Bartels, M., & Bierings, M. (2018) · British Journal of Haematology · doi:10.1111/bjh.15701 · Cited by 75
Dysregulated Ribosome Biogenesis Reveals Therapeutic Liabilities in Cancer
Bursać, S., Prodan, Y., Pullen, N., Bártek, J., & Volarević, S. (2020) · Trends in cancer · doi:10.1016/j.trecan.2020.08.003 · Cited by 74
A Dynamic rRNA Ribomethylome Drives Stemness in Acute Myeloid Leukemia
Zhou, F., Aroua, N., Liu, Y., Rohde, C., Cheng, J., Wirth, A.-K., Fijałkowska, D., Göllner, S., Lotze, M., Yun, H., et al. (2022) · Cancer Discovery · doi:10.1158/2159-8290.cd-22-0210 · Cited by 81
Ribosomal RNA 2′-O-methylation dynamics impact cell fate decisions
Häfner, S. J., Jansson, M., Altinel, K., Andersen, K. L., Abay-Nørgaard, Z., Ménard, P., Fontenas, M., Sørensen, D. M., Gay, D. M., Arendrup, F. S., et al. (2023) · Developmental Cell · doi:10.1016/j.devcel.2023.06.007 · Cited by 72
Iskander, D., Wang, G., Heuston, E. F., Christodoulidou, C., Psaila, B., Ponnusamy, K., Ren, H., Mokhtari, Z., Robinson, M. E., Chaidos, A., et al. (2021) · Science Translational Medicine · doi:10.1126/scitranslmed.abf0113 · Cited by 72
The impact of ribosome biogenesis in cancer: from proliferation to metastasis
Hwang, S.-P., & Denicourt, C. (2024) · NAR Cancer · doi:10.1093/narcan/zcae017 · Cited by 78
Ribosome biogenesis and function in development and disease
Ni, C., & Buszczak, M. (2023) · Development · doi:10.1242/dev.201187 · Cited by 67
Cortés-López, M., Chamely, P., Hawkins, A. G., Stanley, R. F., Swett, A. D., Ganesan, S., Mouhieddine, T. H., Dai, X., Kluegel, L., Chen, C. Y., et al. (2023) · Cell stem cell · doi:10.1016/j.stem.2023.07.012 · Cited by 69
Cenik, E. S., Meng, X., Tang, N. H., Hall, R. N., Arribere, J. A., Cenik, C., Jin, Y., & Fire, A. Z. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.01.019 · Cited by 57
Zhang, S., Macias-Garcia, A., Ulirsch, J. C., Velazquez, J. G., Butty, V. L., Levine, S. S., Sankaran, V. G., & Chen, J.-J. (2019) · eLife · doi:10.7554/elife.46976 · Cited by 64
Venturi, G., & Montanaro, L. (2020) · Cells · doi:10.3390/cells9102300 · Cited by 62
A stem cell roadmap of ribosome heterogeneity reveals a function for RPL10A in mesoderm production
Genuth, N. R., Shi, Z., Kunimoto, K., Hung, V., Xu, A., Kerr, C. H., Tiu, G. C., Osés-Prieto, J. A., Salomon, R. E. A., Axelrod, J. D., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-33263-3 · Cited by 62
Tiu, G. C., Kerr, C. H., Forester, C. M., Krishnarao, P. S., Rosenblatt, H. D., Raj, N., Lantz, T. C., Zhulyn, O., Bowen, M. E., Shokat, L., et al. (2021) · Developmental Cell · doi:10.1016/j.devcel.2021.06.013 · Cited by 59
Jia, Y., Li, L., Lin, Y.-H., Gopal, P., Shen, S., Zhou, K., Yu, X., Sharma, T., Zhang, Y., Siegwart, D. J., et al. (2022) · Cell Stem Cell · doi:10.1016/j.stem.2022.01.001 · Cited by 59
RNA Polymerases I and III in development and disease
Watt, K. E. N., Macintosh, J., Bernard, G., & Trainor, P. A. (2022) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2022.03.027 · Cited by 62
A disease-linked lncRNA mutation in RNase MRP inhibits ribosome synthesis
Robertson, N., Shchepachev, V., Wright, D., Turowski, T. W., Spanos, C., Helwak, A., Zamoyska, R., & Tollervey, D. W. (2022) · Nature Communications · doi:10.1038/s41467-022-28295-8 · Cited by 57
The role of bile acid receptor TGR5 in regulating inflammatory signalling
Ye, D., He, J., & He, X. (2024) · Scandinavian Journal of Immunology · doi:10.1111/sji.13361 · Cited by 61
Translational Control during Cellular Senescence
Payea, M. J., Anerillas, C., Tharakan, R., & Gorospe, M. (2020) · Molecular and Cellular Biology · doi:10.1128/mcb.00512-20 · Cited by 56
Excess ribosomal protein production unbalances translation in a model of Fragile X Syndrome
Seo, S. S., Louros, S. R., Anstey, N. J., Gonzalez‐Lozano, M. A., Harper, C. B., Verity, N., Dando, O., Thomson, S. R., Darnell, J. C., Kind, P. C., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-30979-0 · Cited by 50
Single-cell analyses demonstrate that a heme–GATA1 feedback loop regulates red cell differentiation
Doty, R. T., Yan, X. S., Lausted, C. G., Munday, A. D., Yang, Z., Yi, D., Jabbari, N., Liu, L., Keel, S., Tian, Q., et al. (2018) · Blood · doi:10.1182/blood-2018-05-850412 · Cited by 59
Dynamic Regulation of Proteasome Expression
Motosugi, R., & Murata, S. (2019) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2019.00030 · Cited by 53
Translational Regulations in Response to Endoplasmic Reticulum Stress in Cancers
Jaud, M., Philippe, C., Bella, D. D., Tang, W., Pyronnet, S., Laurell, H., Mazzolini, L., Rouault‐Pierre, K., & Touriol, C. (2020) · Cells · doi:10.3390/cells9030540 · Cited by 58
Altered translation elongation contributes to key hallmarks of aging in the killifish brain
Fraia, D. D., Marino, A., Lee, J. H., Sacramento, E. K., Baumgart, M., Bagnoli, S., Balla, T., Schalk, F., Kamrad, S., Guan, R., et al. (2025) · Science · doi:10.1126/science.adk3079 · Cited by 56
Yoshinaga, M., Han, K., Morgens, D. W., Horii, T., Kobayashi, R., Tsuruyama, T., Hia, F., Yasukura, S., Kajiya, A., Cai, T., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-34078-y · Cited by 52
Fine‐Tuning of Cholesterol Homeostasis Controls Erythroid Differentiation
Lu, Z., Huang, L., Li, Y., Xu, Y., Zhang, R., Zhou, Q., Sun, Q., Lu, Y., Chen, J., Shen, Y., et al. (2021) · Advanced Science · doi:10.1002/advs.202102669 · Cited by 47
GATA1 mutations in red cell disorders
Ling, T., & Crispino, J. D. (2019) · IUBMB Life · doi:10.1002/iub.2177 · Cited by 47
Drosophila RpS12 controls translation, growth, and cell competition through Xrp1
Ji, Z., Kiparaki, M., Folgado-Marco, V., Kumar, A., Blanco, J., Rimesso, G., Chuen, J., Liu, Y., Zheng, D., & Baker, N. E. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1008513 · Cited by 46
Kiparaki, M., Khan, C., Folgado-Marco, V., Chuen, J., Moulos, P., & Baker, N. E. (2022) · eLife · doi:10.7554/elife.71705 · Cited by 47
James, C. C., & Smyth, J. W. (2018) · Life Sciences · doi:10.1016/j.lfs.2018.09.054 · Cited by 46
Bolze, A., Boisson, B., Bosch, B., Antipenko, A., Bouaziz, M., Sackstein, P. E., Chaker-Margot, M., Barlogis, V., Briggs, T. A., Colino, E., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1805437115 · Cited by 44
Gaikwad, S., Ghobakhlou, F., Young, D. J., Visweswaraiah, J., Zhang, H., & Hinnebusch, A. G. (2021) · eLife · doi:10.7554/elife.64283 · Cited by 41
Li, Q., Yang, H., Stroup, E. K., Wang, H., & Ji, Z. (2022) · Genome Research · doi:10.1101/gr.276139.121 · Cited by 46
The genetics of human hematopoiesis and its disruption in disease
Bao, E. L., Cheng, A. N., & Sankaran, V. G. (2019) · EMBO Molecular Medicine · doi:10.15252/emmm.201910316 · Cited by 46
Spevak, C. C., Elias, H. K., Kannan, L., Ali, M. A., Martin, G. H., Selvaraj, S., Eng, W. S., Ernlund, A. W., Rajasekhar, V. K., Woolthuis, C. M., et al. (2020) · Cell stem cell · doi:10.1016/j.stem.2019.12.006 · Cited by 44
Specialized Ribosomes in Health and Disease
Miller, S. C., MacDonald, C. C., Kellogg, M. K., Karamysheva, Z. N., & Karamyshev, A. L. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076334 · Cited by 42
Bhoopalan, S. V., Yen, J. S., Mayuranathan, T., Mayberry, K. D., Yao, Y., Osuna, M. Á. L., Jang, Y., Liyanage, J. S. S., Blanc, L., Ellis, S. R., et al. (2022) · JCI Insight · doi:10.1172/jci.insight.161810 · Cited by 42
Ashley, R. J., Yan, H., Wang, N., Hale, J., Dulmovits, B. M., Papoin, J., Olive, M. E., Udeshi, N. D., Carr, S. A., Vlachos, A., et al. (2020) · Journal of Clinical Investigation · doi:10.1172/jci132284 · Cited by 45
Angiogenin (ANG)—Ribonuclease Inhibitor (RNH1) System in Protein Synthesis and Disease
Sarangdhar, M. A., & Allam, R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22031287 · Cited by 41
Germline SAMD9L truncation variants trigger global translational repression
Allenspach, E. J., Soveg, F. W., Finn, L. S., So, L., Gorman, J. A., Rosen, A. B. I., Skoda‐Smith, S., Wheeler, M. M., Barrow, K. A., Rich, L. M., et al. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20201195 · Cited by 41
Du, C., Liu, C., Yu, K., Zhang, S., Fu, Z., Chen, X., Liao, W., Chen, J., Zhang, Y., Wang, X., et al. (2024) · Cell stem cell · doi:10.1016/j.stem.2024.07.009 · Cited by 42
Ivanov, I. P., Saba, J. A., Fan, C., Wang, J., Firth, A. E., Cao, C., Green, R., & Dever, T. E. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2117226119 · Cited by 41
Metadata
- Authors
- Khajuria, R. K., Munschauer, M., Ulirsch, J. C., Fiorini, C., Ludwig, L. S., McFarland, S. K., Abdulhay, N. J., Specht, H., Keshishian, H., Mani, D. R., Jovanovic, M., Ellis, S. R., Fulco, C. P., Engreitz, J. M., Schütz, S., Lian, J., Gripp, K. W., Weinberg, O. K., Pinkus, G. S., Gehrke, L., Regev, A., Lander, E. S., Gazda, H. T., Lee, W. Y., Panse, V. G., Carr, S. A., & Sankaran, V. G.
- Affiliations
- Broad Institute (US)
- University of Louisville (US)
- University of Zurich (CH)
- Harvard University (US)
- Alfred I. duPont Hospital for Children (US)
- Boston Children's Hospital (US)
- Brigham and Women's Hospital (US)
- Corresponding author
- Sankaran, Vijay G.
- ORCID
- Khajuria, Rajiv K.
- Munschauer, Mathias
- Ulirsch, Jacob C.
- Fiorini, Claudia
- Ludwig, Leif S.
- Abdulhay, Nour J.
- Specht, Harrison
- Keshishian, Hasmik
- Mani, D.R.
- Ellis, Steven R.
- Fulco, Charles P.
- Engreitz, Jesse M.
- Lian, John
- Gripp, Karen W.
- Weinberg, Olga K.
- Gehrke, Lee
- Regev, Aviv
- Lander, Eric S.
- Gazda, Hanna T.
- Panse, Vikram G.
- Carr, Steven A.
- Sankaran, Vijay G.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2018-03
- Volume
- 173
- Issue
- 1
- Pages
- 90-103.e19
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC5866246
- OpenAlex
- W2793800931
- Cited by
- 416
- References
- 60
- Citations by year
- 2026: 40 · 2025: 35 · 2024: 47 · 2023: 48 · 2022: 52 · 2021: 51 · 2020: 71 · 2019: 46 · 2018: 26
- FWCI
- 17.88
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Zurich Open Repository and Archive (University of Zurich) (submittedVersion)
- Funders
- Boehringer Ingelheim
- NIH (T32 HL007574, R01 DK103794, R33 HL120791)
- Swiss National Science Foundation
- Novartis Foundation
- Olga Mayenfisch Stiftung
- European Research Council (EURIBIO260676)
- DBA Foundation
- March of Dimes
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
- Health Sciences › Medicine › Hematology › Blood disorders and treatments
- Keywords
- translational regulation, lineage commitment, hematopoiesis, hematopoietic stem and progenitor cells, Diamond-Blackfan anemia, ribosomal proteins, erythroid differentiation, ribosome composition, blood cell differentiation
- MeSH terms
- Bone Marrow Cells, Cells, Cultured, Female, Hematopoietic Stem Cells, Humans, Male, Ribosomal Proteins, Ribosomes, Transcription Factors, 5' Untranslated Regions, Mutation, Missense, Anemia, Diamond-Blackfan, RNA Interference, RNA, Small Interfering, GATA1 Transcription Factor, Apoptosis Regulatory Proteins
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