The DOI matches its Crossref record; 41 of the 43 references it cites were found in a registry or an index.
Genome-wide Analysis of PTB-RNA Interactions Reveals a Strategy Used by the General Splicing Repressor to Modulate Exon Inclusion or Skipping
Open accessAbstract
Recent transcriptome analysis indicates that > 90% of human genes undergo alternative splicing, underscoring the contribution of differential RNA processing to diverse proteomes in higher eukaryotic cells. The polypyrimidine tract-binding protein PTB is a well-characterized splicing repressor, but PTB knockdown causes both exon inclusion and skipping. Genome-wide mapping of PTB-RNA interactions and construction of a functional RNA map now reveal that dominant PTB binding near a competing constitutive splice site generally induces exon inclusion, whereas prevalent binding close to an alternative site often causes exon skipping. This positional effect was further demonstrated by disrupting or creating a PTB-binding site on minigene constructs and testing their responses to PTB knockdown or overexpression. These findings suggest a mechanism for PTB to modulate splice site competition to produce opposite functional consequences, which may be generally applicable to RNA-binding splicing factors to positively or negatively regulate alternative splicing in mammalian cells.
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
“known splicing regulators, including RBFOX and PTB family members4, were associated with preferential exon inclusion or exclusion in a manner that correlated with the expression and binding location of the RBP”
From A compendium of RNA-binding motifs for decoding gene regulation (2013) · cites this paper as [34]
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
Alternative isoform regulation in human tissue transcriptomes
Wang, E. T., Sandberg, R., Luo, S., Khrebtukova, I., Zhang, L., Mayr, C., Kingsmore, S. F., Schroth, G. P., & Burge, C. B. (2008) · Nature · doi:10.1038/nature07509 · Cited by 5,181
The M2 splice isoform of pyruvate kinase is important for cancer metabolism and tumour growth
Christofk, H. R., Vander Heiden, M. G., Harris, M. H., Ramanathan, A., Gerszten, R. E., Wei, R., Fleming, M. D., Schreiber, S. L., & Cantley, L. C. (2008) · Nature · doi:10.1038/nature06734 · Cited by 2,820
Mechanisms of Alternative Pre-Messenger RNA Splicing
Black, D. L. (2003) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.72.121801.161720 · Cited by 2,704
Self-citationThe UCSC Genome Browser Database
Karolchik, D. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg129 · Cited by 1,890
HITS-CLIP yields genome-wide insights into brain alternative RNA processing
Licatalosi, D. D., Mele, A., Fak, J. J., Ule, J., Kayikci, M., Chi, S. W., Clark, T. A., Schweitzer, A. C., Blume, J. E., Wang, X., et al. (2008) · Nature · doi:10.1038/nature07488 · Cited by 1,352 · cited 9×
“However, splicing regulators can often affect alternative splicing in a position-dependent manner, as has recently emerged from genomewide analysis of RNA-binding splicing regulators (Licatalosi et al., 2008; Yeo et al., 2009).”
InfluentialAlternative pre-mRNA splicing and proteome expansion in metazoans
Maniatis, T., & Tasic, B. (2002) · Nature · doi:10.1038/418236a · Cited by 774
Systematic Identification and Analysis of Exonic Splicing Silencers
Wang, Z., Rolish, M. E., Yeo, G. W.-M., Tung, V., Mawson, M., & Burge, C. B. (2004) · Cell · doi:10.1016/j.cell.2004.11.010 · Cited by 678
Self-citationBoutz, P. L., Stoilov, P., Li, Q., Lin, C.-H., Chawla, G., Ostrow, K., Shiue, L., Ares, M., & Black, D. L. (2007) · Genes & Development · doi:10.1101/gad.1558107 · Cited by 577
Self-citationYeo, G. W., Coufal, N. G., Liang, T. Y., Peng, G. E., Fu, X.-D., & Gage, F. H. (2009) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1545 · Cited by 572
Self-citationSingh, R., Valcárcel, J., & Green, M. R. (1995) · Science · doi:10.1126/science.7761834 · Cited by 539
Flagged first, then by citations
2 of the 43 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 301–400 of 469
The combinatorial control of alternative splicing in C. elegans
Tan, J. H., & Fraser, A. G. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1007033 · Cited by 18
Self-Attention Based Neural Network for Predicting RNA-Protein Binding Sites
Wang, X., Zhang, M., Long, C., Yao, L., & Zhu, M. (2022) · IEEE Transactions on Computational Biology and Bioinformatics · doi:10.1109/tcbb.2022.3204661 · Cited by 18
Simpson, C. G., Lewandowska, D., Liney, M., Davidson, D., Chapman, S. N., Fuller, J., McNicol, J., Shaw, P. D., & Brown, J. W. S. (2014) · New Phytologist · doi:10.1111/nph.12821 · Cited by 18
RNA Pol II inhibition activates cell death independently from the loss of transcription
Harper, N. W., Birdsall, G. A., Honeywell, M. E., Ward, K. M., Pai, A. A., & Lee, M. J. (2025) · Cell · doi:10.1016/j.cell.2025.07.034 · Cited by 18
Hinman, M. N., Zhou, H.-L., Sharma, A., & Lou, H. J. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt166 · Cited by 18
Bahrami‐Samani, E., Vo, D. T., Araujo, P. R. D., Vogel, C., Smith, A. D., Penalva, L. O. F., & Uren, P. J. (2014) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1274 · Cited by 15
Therapeutic Potential of PTB Inhibition Through Converting Glial Cells to Neurons in the Brain
Fu, X.-D., & Mobley, W. C. (2023) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-083022-113120 · Cited by 16
Self-citationJoshi, A., Esteve, V., Buckroyd, A., Blatter, M., Allain, F. H. ‐., & Curry, S. (2014) · PeerJ · doi:10.7717/peerj.305 · Cited by 15
RNA-binding protein research with transcriptome-wide technologies in neural development
Yano, M., Ohtsuka, T., & Okano, H. (2014) · Cell and Tissue Research · doi:10.1007/s00441-014-1923-8 · Cited by 16
A developmentally regulated spliced variant of PTBP1 is upregulated in type 1 diabetic hearts
Belanger, K. K., Nutter, C. A., Li, J., Yu, P., & Kuyumcu‐Martinez, M. N. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.12.150 · Cited by 17
Hotspot exons are common targets of splicing perturbations
Glidden, D. T., Buerer, J. L., Saueressig, C. F., & Fairbrother, W. G. (2021) · Nature Communications · doi:10.1038/s41467-021-22780-2 · Cited by 16
Diverse regulation of 3′ splice site usage
Sohail, M., & Xie, J. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-2037-5 · Cited by 18
Díaz‐Muñoz, M. D., Bell, S. E., & Turner, M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0116899 · Cited by 17
Inflammatory Microenvironment Modulation of Alternative Splicing in Cancer: A Way to Adapt
Silva, A. L., Faria, M., & Matos, P. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-34025-4_13 · Cited by 16
Sadée, C., Hagler, L. D., Becker, W. R., Jarmoskaite, I., Vaidyanathan, P. P., Denny, S. K., Greenleaf, W. J., & Herschlag, D. (2022) · Nature Communications · doi:10.1038/s41467-022-31968-z · Cited by 16
SRSF2 is required for mRNA splicing during spermatogenesis
Lei, W., Du, Z., Meng, T., Su, R., Li, Y., Liu, W., Sun, S., Liu, M., Hou, Y., Zhang, C., et al. (2023) · BMC Biology · doi:10.1186/s12915-023-01736-6 · Cited by 16
Self-citationYavarpour‐Bali, H., Ghasemi‐Kasman, M., & Shojaei, A. (2019) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2019.109820 · Cited by 15
Wang, Y., Chembazhi, U. V., Yee, D., Chen, S., Ji, J., Wang, Y., Nguyen, K. L., Lin, P.-C. P., Ratti, A., Hess, R. A., et al. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae862 · Cited by 14
Nishtala, S., Neelamraju, Y., & Janga, S. C. (2016) · Scientific Reports · doi:10.1038/srep25711 · Cited by 14
RNA Processing: Redrawing the Map of Charted Territory
Corrionero, A., & Valcárcel, J. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.12.004 · Cited by 15
Multiple roles of RBM4 in muscle cell differentiation
Lin, J.-C. (2011) · Frontiers in Bioscience-Scholar · doi:10.2741/260 · Cited by 17
Pomella, S., Melaiu, O., Cifaldi, L., Bei, R., GARGARI, M., Campanella, V., & Barillari, G. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25168929 · Cited by 18
Assessing Computational Steps for CLIP-Seq Data Analysis
Liu, Q., Zhong, X. Y., Madison, B., Rustgi, A. K., & Shyr, Y. (2015) · BioMed Research International · doi:10.1155/2015/196082 · Cited by 13
Davis‐Turak, J., Johnson, T., & Hoffmann, A. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky870 · Cited by 13
Lu, X., Zhong, J., Liu, L., Zhang, W., Zhao, S., Chen, L., Wei, Y., Zhang, H., Wu, J., Chen, W., et al. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.929037 · Cited by 13
mRNA isoform balance in neuronal development and disease
LaForce, G. R., Philippidou, P., & Schaffer, A. E. (2022) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1762 · Cited by 15
Neural Differentiation Modulates the Vertebrate Brain Specific Splicing Program
Madgwick, A., Fort, P., Hanson, P. S., Thibault, P., Gaudreau, M., Lutfalla, G., Möröy, T., Elela, S. A., Chaudhry, B., Elliott, D. J., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0125998 · Cited by 14
Decoding Abnormal Splicing Code in Human Diseases
Ohno, K. (2015) · Journal of Investigative Genomics · doi:10.15406/jig.2015.02.00016 · Cited by 12
Co-profiling of in situ RNA-protein interactions and transcriptome in single cells and tissues
Cheng, Q., Xie, G., Zhang, X., Wang, J., Ding, S., Wu, Y., Shi, M., Duan, F., Wan, Z.-L., Wei, J.-J., et al. (2025) · Nature Methods · doi:10.1038/s41592-025-02774-4 · Cited by 12
Post-transcriptional mechanisms controlling neurogenesis and direct neuronal reprogramming
Papadimitriou, E., & Thomaidou, D. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.390976 · Cited by 14
Butler, N., & Hannapel, D. J. (2012) · Planta · doi:10.1007/s00425-012-1726-7 · Cited by 12
Chen, L. (2012) · Statistics in Biosciences · doi:10.1007/s12561-012-9064-7 · Cited by 14
Min De, Z. E. N. G., Yi, S., Xiao, Y., & Chen, Z. (2022) · Cytokine · doi:10.1016/j.cyto.2022.155812 · Cited by 12
Rationally designed stapled peptides allosterically inhibit PTBP1–RNA-binding
Schmeing, S., Amrahova, G., Bigler, K., Chang, J., Openy, J., Pal, S., Posada, L., Gasper, R., & Hart, P. ‘. (2023) · Chemical Science · doi:10.1039/d3sc00985h · Cited by 12
Alternatively spliced MBNL1 isoforms exhibit differential influence on enhancing brown adipogenesis
Hung, C.-S., & Lin, J.-C. (2019) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2019.194437 · Cited by 12
Brain Repair by Cell Replacement via In Situ Neuronal Reprogramming
Qian, H., & Fu, X. (2021) · Annual Review of Genetics · doi:10.1146/annurev-genet-071719-023616 · Cited by 14
Self-citationZhou, Q., Kong, D., Li, W., Shi, Z., Liu, Y., Sun, R., Ma, X., Qiu, C., Liu, Z., Hou, Y., et al. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121512 · Cited by 11
RNA structure, binding, and coordination in Arabidopsis
Foley, S. W., Kramer, M. C., & Gregory, B. D. (2017) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1426 · Cited by 10
SMARTIV: combined sequence and structure de-novo motif discovery for in-vivo RNA binding data
Polishchuk, M. S., Paz, I., Yakhini, Z., & Mandel‐Gutfreund, Y. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky453 · Cited by 11
Mapping of In Vivo RNA-Binding Sites by Ultraviolet (UV)-Cross-Linking Immunoprecipitation (CLIP)Preprint
Darnell, J. C., Mele, A., Hung, K. Y. S., & Darnell, R. B. (2018) · Cold Spring Harbor Protocols · doi:10.1101/pdb.top097931 · Cited by 12
Yangǂ, D., Huai-yun, Z., Peng, K., Chen, L., He, H., Huang, X., Qin, J., He, G., & Zhang, D. (2016) · International Journal of Agriculture and Biology · doi:10.17957/ijab/15.0218 · Cited by 11
RNA Secondary Structure Representation Network for RNA-proteins Binding Prediction
Liu, Z., Luo, F., & Du, B. (2021) · Proceedings of the AAAI Conference on Artificial Intelligence · doi:10.1609/aaai.v35i1.16112 · Cited by 10
A Posttranscriptional Mechanism That Controls Ptbp1 Abundance in the Xenopus Epidermis
Méreau, A., Anquetil, V., Lerivray, H., Viet, J., Schirmer, C., Audic, Y., Legagneux, V., Hardy, S., & Paillard, L. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.01040-14 · Cited by 9
Community effects in regulation of translation
Macdonald, P. M., Kanke, M., & Kenny, A. (2016) · eLife · doi:10.7554/elife.10965 · Cited by 9
Shang, M., Weng, L., Wu, S., Liu, B., Yin, X., Wang, Z., & Mao, A. (2021) · PubMed Central · Cited by 9
Distinct and Modular Organization of Protein Interacting Sites in Long Non-coding RNAs
Jalali, S., Gandhi, S., & Scaria, V. (2018) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2018.00027 · Cited by 9
Research progress of cell treatment strategy in Parkinson's disease
Peng, Y., Chen, J., Hu, H., Liu, W., Liang, W., & Wang, J. (2024) · Neuroscience Applied · doi:10.1016/j.nsa.2024.104061 · Cited by 8
SOX2 interacts with hnRNPK to modulate alternative splicing in mouse embryonic stem cells
Huang, Y., Liu, Y., Pu, M., Zhang, Y., Cao, Q., Li, S., Wei, Y., & Hou, L. (2024) · Cell & Bioscience · doi:10.1186/s13578-024-01284-8 · Cited by 7
Self-citationAngulo, J., Cáceres, C. J., Contreras, N., Fernández-García, L., Chamond, N., Ameur, M., Sargueil, B., & López‐Lastra, M. (2022) · Viruses · doi:10.3390/v15010008 · Cited by 7
Pirmoradi, S., Khatibi, S. M. H., Vahed, S. Z., Rad, H. H., Khamaneh, A. M., Akbarpour, Z., Seyedrezazadeh, E., Teshnehlab, M., Chapman, K. R., & Ansarin, K. (2023) · Scientific Reports · doi:10.1038/s41598-023-42581-5 · Cited by 7
The chloroplast RNA–binding protein CP29A supports rbcL expression during cold acclimation
Lenzen, B., Rösch, F., Legen, J., Ruwe, H., Kachariya, N. N., Sattler, M., Small, I., & Schmitz‐Linneweber, C. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2403969122 · Cited by 8
Transcriptome analysis reveals PTBP1 as a key regulator of circRNA biogenesis
Wang, M., Zheng, S., Zhang, Y., Zhang, J., Lai, F., Zhou, C., Zhou, Q., Li, X., & Li, G. (2025) · BMC Biology · doi:10.1186/s12915-025-02233-8 · Cited by 7
Self-citationAlternative splicing regulation and its therapeutic potential in bladder cancer
Li, L., Jin, T., Hu, L., & Ding, J. (2024) · Frontiers in Oncology · doi:10.3389/fonc.2024.1402350 · Cited by 6
PTBP1 and Cancer: From RNA Regulation to Therapeutic Potential
Ji, C., Zhu, J., Hou, X., Zhou, C., Zhao, J., Zheng, X., & Tang, Y. (2025) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.70675 · Cited by 13
Structural insights reveal the specific recognition of meiRNA by the Mei2 protein
Shen, S., Jian, Y., Cai, Z., Li, F., Lv, M., Liu, Y., Wu, J., Fu, C., & Shi, Y. (2022) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjac029 · Cited by 6
Vorobeva, M. A., Skvortsov, D. A., & Pervouchine, D. D. (2024) · Acta Naturae · doi:10.32607/actanaturae.26826 · Cited by 6
Wu, Y., Yang, M., Wu, S., Luo, P.-Q., Zhang, C., Ruan, C.-S., Cui, W., Zhao, Q.-R., Chen, L., Meng, J.-J., et al. (2024) · Diabetologia · doi:10.1007/s00125-024-06224-2 · Cited by 6
Self-citationUnraveling the Mechanism of Action of Ubiquitin-Specific Protease 5 and Its Inhibitors in Tumors
Wang, J., Fang, S., Jiang, Y., & Hua, Q. (2024) · Clinical Medicine Insights Oncology · doi:10.1177/11795549241281932 · Cited by 6
Heimiller, J., Sridharan, V., Huntley, J., Wesley, C. S., & Singh, R. (2014) · PLoS ONE · doi:10.1371/journal.pone.0098585 · Cited by 6
Burgardt, R., Lambert, D., Heuwieser, C., Sack, M., Wagner, G., Weinberg, Z., & Wachter, A. (2024) · The Plant Journal · doi:10.1111/tpj.16739 · Cited by 5
Illuminating the Transcriptome through the Genome
Elliott, D. J. (2014) · Genes · doi:10.3390/genes5010235 · Cited by 7
Predicting Alternative Splicing
Barash, Y., & Vaquero-Garcia, J. (2014) · Methods in molecular biology · doi:10.1007/978-1-62703-980-2_28 · Cited by 6
Identification and Characterization of a Minimal Functional Splicing Regulatory Protein, PTBP1
Ontiveros, R. J., Hernandez, L. C., Nguyen, H., Lopez, A. L. H., Shankar, A., Kim, E., & Keppetipola, N. (2020) · Biochemistry · doi:10.1021/acs.biochem.0c00664 · Cited by 7
PTBP1 correlates with HER2 positivity, lymph node spread and metastasis in breast cancer
Tabatabaeian, S., Sadeghi, S., & Tabatabaeian, H. (2020) · Gene Reports · doi:10.1016/j.genrep.2020.100659 · Cited by 5
Chen, W., Chen, X., Cheng, C., She, S., Li, X., Shan, L., Zhang, X., Dan, S., Wang, Y., Zhou, Y.-W., et al. (2025) · Stem Cell Research & Therapy · doi:10.1186/s13287-025-04229-1 · Cited by 7
Self-citationDiscovery of microRNA Regulatory Networks by Integrating Multidimensional High-Throughput Data
Yang, J., & Qu, L. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-94-007-5590-1_13 · Cited by 5
A Novel Deep Learning Method for Predicting RNA-Protein Binding Sites
Zhao, X., Chang, F., Lv, H., Zou, G., & Zhang, B. (2023) · Applied Sciences · doi:10.3390/app13053247 · Cited by 5
Two Faces of Evil: Cancer and Neurodegeneration
Curran, T., & Christen, Y. (2010) · Research and perspectives in Alzheimer's disease · doi:10.1007/978-3-642-16602-0 · Cited by 5
A new method to identify global targets of RNA-binding proteins in plantsPreprint
Cheng, Y.-L., Hsieh, H., & Tu, S. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.06.11.448000 · Cited by 5
Re-Activation of Neurogenic Niches in Aging BrainPreprint
Maimon, R., Chillón-Marinas, C., Vazquez‐Sanchez, S., Kern, C., Jenie, I., Malukhina, K., Moore, S. R., Cui, J., Goginashvili, A., Moghadami, S., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.27.575940 · Cited by 6
Ye, R., Hu, N., & Xue, Y. (2023) · STAR Protocols · doi:10.1016/j.xpro.2023.102401 · Cited by 4
Self-citationYang, J., Feng, J. H., Lv, J. G., Chu, X., Wei, Y., Zhang, Y., Li, J., Sun, Y., Li, G., Jiang, T., et al. (2024) · Functional & Integrative Genomics · doi:10.1007/s10142-024-01412-0 · Cited by 5
Self-citationRecursive splicing is a rare event in the mouse brain
Moon, S., & Zhao, Y.-T. (2022) · PLoS ONE · doi:10.1371/journal.pone.0263082 · Cited by 4
PTBP1 enforces ATR-CHK1 signaling determining the potency of CDC7 inhibitors
Göder, A., Quinlan, A., Rainey, M. D., Bennett, D., Shamavu, D., Corso, J., & Santocanale, C. (2023) · iScience · doi:10.1016/j.isci.2023.106951 · Cited by 5
Therapeutic strategies for aberrant splicing in cancer and genetic disorders
Shi, W., Tang, J., & Xiang, J. (2024) · Clinical Genetics · doi:10.1111/cge.14478 · Cited by 4
An alternative simple method in laryngoscope blade decontamination.
Orhan, M. E., Saygun, O., & Güzeldemir, M. E. (2002) · PubMed · Cited by 4
Altina, N. H., Maranon, D. G., Anderson, J. R., Donaldson, M. K., Elmegerhi, S., Clair, L. A. S., Perera, R. M., Geiss, B. J., & Wilusz, J. (2024) · Virology · doi:10.1016/j.virol.2024.109986 · Cited by 3
RNA-protein interaction techniques - A historical and comparative analysis
Chakrabarty, S., Roy, S., Sarkar, S., & Singh, K. K. (2025) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2025.195115 · Cited by 3
RBPMS and RBPMS2 Cooperate to Safeguard Cardiac Splicing
Wu, T., Chen, Z., Gao, C., Stanley, E. V., Zhang, Z., Gu, Y., Zhou, X., & Chen, J. (2025) · Circulation Research · doi:10.1161/circresaha.125.326948 · Cited by 3
Self-citationA cutting-edge strategy for spinal cord injury treatment: resident cellular transdifferentiation
Fang, Y.-M., Chen, W.-C., Zheng, W.-J., Yang, Y.-S., Zhang, Y., Chen, X.-L., Pei, M.-Q., Lin, S., & He, H. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1237641 · Cited by 3
Self-citationPAIP1 binds to pre-mRNA and regulates alternative splicing of cancer pathway genes including VEGFA
Zheng, J., Zhang, X., Xue, Y., Shao, W., Wei, Y., Mi, S., Yang, X., Hu, L., Zhang, Y., & Ming, L. (2024) · BMC Genomics · doi:10.1186/s12864-024-10530-9 · Cited by 4
Self-citationArias, M. A., Ke, S., & Chasin, L. A. (2010) · Nature Biotechnology · doi:10.1038/nbt0710-686 · Cited by 3
Lee, J. S., Bae, J. S., Kim, J., Kim, Y., Park, T. J., Pasaje, C. F. A., Park, B., Cheong, H. S., Uh, S., Park, J., et al. (2012) · Respiratory Care · doi:10.4187/respcare.01480 · Cited by 3
My road to alternative splicing control: from simple paths to loops and interconnections
Chabot, B. (2015) · Biochemistry and Cell Biology · doi:10.1139/bcb-2014-0161 · Cited by 3
Lorkovic, Z. (2012) · CRC Press eBooks · doi:10.1201/9781498713368-7 · Cited by 3
Dissecting Splicing Regulatory Network by Integrative Analysis of CLIP-Seq Data
Zhang, M. Q. (2011) · Springer eBooks · doi:10.1007/978-1-4614-0782-9_12 · Cited by 2
Kremsky, I., Bellora, N., & Eyras, E. (2015) · PLoS ONE · doi:10.1371/journal.pone.0132448 · Cited by 3
König, J., McGlincy, N. J., & Ule, J. (2011) · Wiley eBooks · doi:10.1002/9783527644582.ch10 · Cited by 3
Rio, D. C. (2014) · Cold Spring Harbor Protocols · doi:10.1101/pdb.prot080705 · Cited by 3
Data Science Issues in Understanding Protein-RNA InteractionsPreprint
Chakrabarti, A. M., Haberman, N., Praznik, A., Luscombe, N. M., & Ule, J. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/208124 · Cited by 3
Gavilan, C. M., Murata-Nakamura, Y., Porter, R. S., Cutler, B., Rai, S., Kim, H., & Iwase, S. (2025) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-025-01584-8 · Cited by 2
Genetic variation within ABCE1 is associated with the chicken L blood system
Fulton, J. E., McCarron, A. M., Wolc, A., Mullen, A., Foerstner, C., Sparling, B. A. T. E., Drobik-Czwarno, W., & Taylor, R. L. (2025) · Poultry Science · doi:10.1016/j.psj.2025.106027 · Cited by 2
KIS counteracts PTBP2 and regulates alternative exon usage in neurons
Moreno-Aguilera, M., Mendoza, M. B., Neher, A. M., Dodel, M., Mardakheh, F. K., Ortiz, R., & Gallego, C. (2024) · eLife · doi:10.7554/elife.96048 · Cited by 1
Profiling genetically driven alternative splicing across the Indonesian archipelago
Ibeh, N., Kusuma, P., Darusallam, C. C., Malik, S. G., Sudoyo, H., McCarthy, D. J., & Romero, I. G. (2024) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2024.09.004 · Cited by 2
Liu, W., Li, X., Liao, S., Dou, K., & Zhang, Y. (2017) · Gene · doi:10.1016/j.gene.2017.03.023 · Cited by 2
Self-citationMammalian Cis-Acting RNA Sequence Elements
Louis, I. V.-S., & Sagarsky, C. (2018) · InTech eBooks · doi:10.5772/intechopen.72124 · Cited by 3
Alternative Splice Site Selection
Coelho, M. B., & Smith, C. W. J. (2012) · Wiley eBooks · doi:10.1002/9783527636778.ch8 · Cited by 2
Evsyukova, I. Y. (2012) · Cited by 2
The function and regulation of the U11-48K protein in U12-dependent splicing
Turunen, J. J. (2012) · Työväentutkimus Vuosikirja · Cited by 2
Pilaka, P. P., Sadek, N. H., Fusca, D. D., Cutter, A. D., & Calarco, J. A. (2025) · Genetics · doi:10.1093/genetics/iyaf025 · Cited by 2
Metadata
- Authors
- Xue, Y., Zhou, Y., Wu, T., Zhu, T., Ji, X., Kwon, Y.-S., Zhang, C., Yeo, G., Black, D. L., Sun, H., Fu, X.-D., & Zhang, Y.
- Affiliations
- Wuhan University (CN)
- University of California San Diego (US)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Fu, Xiang-Dong
- Zhang, Yi
- ORCID
- Venue
- Molecular Cell
- Publisher
- Elsevier BV
- Published
- 2009-12
- Volume
- 36
- Issue
- 6
- Pages
- 996-1006
- ISSN
- 1097-2765 (ISSN-L)
- PMC
- PMC2807993
- OpenAlex
- W1974898488
- Cited by
- 469
- References
- 43
- Citations by year
- 2026: 14 · 2025: 17 · 2024: 23 · 2023: 28 · 2022: 25 · 2021: 19 · 2020: 22 · 2019: 15 · 2018: 35 · 2017: 24 · 2016: 25 · 2015: 34 · 2014: 44 · 2013: 35 · 2012: 43
- FWCI
- 14.24
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Molecular Cell (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National High-tech Research and Development Program
- National Key Research and Development Program of China
- National Human Genome Research Institute (HG004659, R01HG004659)
- National Institute of General Medical Sciences (R01GM084317, GM049369, R01GM049369, GM084317)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Keywords
- polypyrimidine tract-binding protein, PTB, alternative splicing, exon skipping, exon inclusion, RNA-binding proteins, splicing repressor, minigene constructs, splice site selection
- MeSH terms
- Animals, Binding Sites, Exons, HeLa Cells, Humans, Molecular Sequence Data, Protein Binding, RNA, Genome, Human, Alternative Splicing, Gene Expression Profiling, Polypyrimidine Tract-Binding Protein
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