The DOI matches its Crossref record; 73 of the 73 references it cites were found in a registry or an index.
The spatial repositioning of adipogenesis genes is correlated with their expression status in a porcine mesenchymal stem cell adipogenesis model system
Abstract
Alterations in the nuclear positioning of chromosomes and specific genes during differentiation and development have suggested strongly the existence of a relationship between non-random organization of the genome and its function. In this study, we have examined the genome organization in interphase nuclei during adipogenesis, using the pig as a model organism. We hypothesized that changes in the gene expression profile and chromatin remodeling which occur during cellular differentiation would elicit repositioning of whole chromosomes, moving specific genes on them to different regions of the nucleus. We established an in vitro adipogenesis differentiation system using mesenchymal stem cells, derived from porcine bone marrow. The nuclear position of seven adipogenesis genes (PPARG, SREBF1, FABP4, CEBPA, CEBPB, CREB, and GATA2), two control genes (SOX9 and MYL1), and six chromosomes carrying these gene loci (SSC4, SSC6, SSC12, SSC13, SSC15, and SSC17) was determined. We found that during adipogenesis, using the in vitro stem cell model system, in contrast to our original hypothesis, the nuclear position of genes involved in adipogenesis was altered radically with the up-regulation of gene expression correlating with these genes becoming more internally located within nuclei. Chromosome territories, containing these genes, were also found to alter their nuclear position during the in vitro adipogenesis model, with the most dramatic repositioning being SSC4 that moved from the nuclear periphery towards the nuclear interior. We found that during in vitro adipogenesis chromosome territories decondensed and the genes were found on loops and projections of chromatin, away from the main body of the chromosomes. From our data, it appears that the temporal repositioning of genes, emanating away from chromosomes, during adipogenesis is correlated with gene activity, supporting models of the involvement of spatial genome repositioning in regulating gene expression and the nuclear interior being an important region of the nucleus for transcription.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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
“Lamina-associated domains (LADs), typically located at the nuclear periphery, are enriched in repressive chromatin marks and correlate with low transcriptional activity [74,75].”
From Origin and Evolution of Genes in Eukaryotes: Mechanisms, Dynamics, and Functional Implications (2025) · cites this paper as [75]
Citations
Cites
Adipocyte differentiation from the inside out
Rosen, E. D., & MacDougald, O. A. (2006) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2066 · Cited by 2,607
Transcriptional control of adipocyte formation
Farmer, S. R. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2006.07.001 · Cited by 1,836
Beyond the Sequence: Cellular Organization of Genome Function
Misteli, T. (2007) · Cell · doi:10.1016/j.cell.2007.01.028 · Cited by 1,140
Active genes dynamically colocalize to shared sites of ongoing transcription
Osborne, C. S., Chakalova, L., Brown, K. E., Carter, D., Horton, A., Debrand, E., Goyenechea, B., Mitchell, J. A., Lopes, S. M. C. D. S., Reik, W., et al. (2004) · Nature Genetics · doi:10.1038/ng1423 · Cited by 1,080
Differences in the Localization and Morphology of Chromosomes in the Human Nucleus
Croft, J. A., Bridger, J. M., Boyle, S., Perry, P., Teague, P., & Bickmore, W. A. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.145.6.1119 · Cited by 933
Self-citationTranscriptional repression mediated by repositioning of genes to the nuclear lamina
Reddy, K. L., Zullo, J., Bertolino, E., & Singh, H. (2008) · Nature · doi:10.1038/nature06727 · Cited by 823
Dynamic genome architecture in the nuclear space: regulation of gene expression in three dimensions
Lanctôt, C., Cheutin, T., Cremer, M., Cavalli, G., & Cremer, T. (2007) · Nature Reviews Genetics · doi:10.1038/nrg2041 · Cited by 781
Subnuclear Compartmentalization of Immunoglobulin Loci During Lymphocyte Development
Kosak, S. T., Skok, J. A., Medina, K. L., Riblet, R. J., Beau, M. M. L., Fisher, A. G., & Singh, H. (2002) · Science · doi:10.1126/science.1068768 · Cited by 722
The spatial organization of human chromosomes within the nuclei of normal and emerin-mutant cells
Boyle, S. (2001) · Human Molecular Genetics · doi:10.1093/hmg/10.3.211 · Cited by 681
Chambeyron, S., & Bickmore, W. A. (2004) · Genes & Development · doi:10.1101/gad.292104 · Cited by 618
Cited by
Sorted by citations
Mechanisms and functions of nuclear envelope remodelling
Ungricht, R., & Kutay, U. (2017) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2016.153 · Cited by 353
Harr, J. C., Luperchio, T. R., Wong, X., Cohen, E., Wheelan, S. J., & Reddy, K. L. (2015) · The Journal of Cell Biology · doi:10.1083/jcb.201405110 · Cited by 338
Mehta, I. S., Amira, M., Harvey, A., & Bridger, J. M. (2010) · Genome biology · doi:10.1186/gb-2010-11-1-r5 · Cited by 193
Self-citationMechanical Regulation of Nuclear Structure and Function
Martins, R. P., Finan, J. D., Guilak, F., & Lee, D. A. (2012) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-071910-124638 · Cited by 151
Genetics of fat tissue accumulation in pigs: a comparative approach
Switonski, M., Stachowiak, M., Cieślak, J., Bartz, M., & Grzes, M. (2010) · Journal of Applied Genetics · doi:10.1007/bf03195724 · Cited by 116
The nuclear envelope as a chromatin organizer
Zuleger, N., Robson, M. I., & Schirmer, E. C. (2011) · Nucleus · doi:10.4161/nucl.2.5.17846 · Cited by 111
The impact of chromosomal rearrangements on regulation of gene expression
Harewood, L., & Fraser, P. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu278 · Cited by 105
The effect of translocation-induced nuclear reorganization on gene expressionPreprint
Harewood, L., Schütz, F., Boyle, S., Perry, P., Delorenzi, M., Bickmore, W. A., & Reymond, A. (2010) · Genome Research · doi:10.1101/gr.103622.109 · Cited by 104
Higher order chromatin organization in cancer
Reddy, K. L., & Feinberg, A. P. (2012) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2012.12.001 · Cited by 102
Heterochromatin and gene positioning: inside, outside, any side?
Jost, K. L., Bertulat, B., & Cardoso, M. C. (2012) · Chromosoma · doi:10.1007/s00412-012-0389-2 · Cited by 88
Mehta, I. S., Eskiw, C. H., Arican-Goktas, H. D., Kill, I. R., & Bridger, J. M. (2011) · Genome biology · doi:10.1186/gb-2011-12-8-r74 · Cited by 75
Self-citationThe Nuclear Option: Evidence Implicating the Cell Nucleus in Mechanotransduction
Szczesny, S. E., & Mauck, R. L. (2016) · Journal of Biomechanical Engineering · doi:10.1115/1.4035350 · Cited by 79
Genome regulation at the peripheral zone: lamina associated domains in development and disease
Luperchio, T. R., Wong, X., & Reddy, K. L. (2014) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2013.11.021 · Cited by 72
NET gains and losses: the role of changing nuclear envelope proteomes in genome regulation
Wong, X., Luperchio, T. R., & Reddy, K. L. (2014) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2014.04.005 · Cited by 71
Chromosome territories reposition during DNA damage-repair response
Mehta, I. S., Kulashreshtha, M., Chakraborty, S., Kolthur‐Seetharam, U., & Rao, B. J. (2013) · Genome biology · doi:10.1186/gb-2013-14-12-r135 · Cited by 71
Anchoring a Leviathan: How the Nuclear Membrane Tethers the Genome
Czapiewski, R., Robson, M. I., & Schirmer, E. C. (2016) · Frontiers in Genetics · doi:10.3389/fgene.2016.00082 · Cited by 61
Gene expression, chromosome position and lamin A/C mutations
Puckelwartz, M. J., Depreux, F. F. S., & McNally, E. M. (2011) · Nucleus · doi:10.4161/nucl.2.3.16003 · Cited by 54
The nuclear lamina as a gene-silencing hub.
Shevelyov, Y. Y., & Nurminsky, D. I. (2012) · PubMed · Cited by 52
Schistosomes and snails: a molecular encounter
Knight, M., Arican-Goktas, H. D., Ittiprasert, W., Odoemelam, E. C., Miller, A. N., & Bridger, J. M. (2014) · Frontiers in Genetics · doi:10.3389/fgene.2014.00230 · Cited by 50
Self-citationGenome architecture and the role of transcription
Papantonis, A., & Cook, P. R. (2010) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2010.03.004 · Cited by 48
Genomic loci mispositioning in Tmem120a knockout mice yields latent lipodystrophy
Czapiewski, R., Batrakou, D. G., Heras, J. I. D. L., Carter, R. N., Sivakumar, A., Sliwinska, M., Dixon, C. R., Webb, S., Lattanzi, G., Morton, N. M., et al. (2022) · Nature Communications · doi:10.1038/s41467-021-27869-2 · Cited by 48
Tremblay, D., Andrzejewski, L., Leclerc, A., & Pelling, A. E. (2013) · Cytoskeleton · doi:10.1002/cm.21148 · Cited by 46
A chromatin perspective of adipogenesis
Musri, M. M., Gomis, R., & Párrizas, M. (2010) · Organogenesis · doi:10.4161/org.6.1.10226 · Cited by 44
Knight, M., Ittiprasert, W., Arican-Goktas, H. D., & Bridger, J. M. (2016) · International Journal for Parasitology · doi:10.1016/j.ijpara.2016.03.003 · Cited by 43
Self-citationAssociation of adipogenic genes with SC-35 domains during porcine adipogenesis
Szczerbal, I., & Bridger, J. M. (2010) · Chromosome Research · doi:10.1007/s10577-010-9176-1 · Cited by 42
Self-citationGenetics of Adiposity in Large Animal Models for Human Obesity—Studies on Pigs and Dogs
Stachowiak, M., Szczerbal, I., & Switonski, M. (2016) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2016.01.001 · Cited by 39
Self-citationKnight, M., Ittiprasert, W., Odoemelam, E. C., Adema, C. M., Miller, A., Raghavan, N., & Bridger, J. M. (2010) · International Journal for Parasitology · doi:10.1016/j.ijpara.2010.07.015 · Cited by 38
Self-citationTosi, S., Kamel, Y. M., Owoka, T., Federico, C., Truong, T. H., & Saccone, S. (2015) · Biomarker Research · doi:10.1186/s40364-015-0041-4 · Cited by 37
Zappaterra, M., Gioiosa, S., Chillemi, G., Zambonelli, P., & Davoli, R. (2020) · PLoS ONE · doi:10.1371/journal.pone.0233372 · Cited by 38
Bridger, J. M., Arican-Gotkas, H. D., Foster, H. A., Godwin, L. S., Harvey, A., Kill, I. R., Knight, M., Mehta, I. S., & Ahmed, M. H. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-1-4899-8032-8_12 · Cited by 37
Self-citationFalk, M., Hausmann, M., Lukášová, E., Biswas, A., Hildenbrand, G. L., Davídková, M., Krasavin, E. A., Kleibl, Z., Falková, I., Ježková, L., et al. (2014) · Critical Reviews in Eukaryotic Gene Expression · doi:10.1615/critreveukaryotgeneexpr.v24.i3.40 · Cited by 37
Leotta, C. G., Federico, C., Brundo, M. V., Tosi, S., & Saccone, S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0105481 · Cited by 36
Elcock, L. S., & Bridger, J. M. (2010) · Biochemical Society Transactions · doi:10.1042/bst0380263 · Cited by 38
Self-citationInterphase chromosome positioning in in vitro porcine cells and ex vivo porcine tissues
Foster, H. A., Griffin, D. K., & Bridger, J. M. (2012) · BMC Cell Biology · doi:10.1186/1471-2121-13-30 · Cited by 35
Self-citationTissue-specific NETs alter genome organization and regulation even in a heterologous system
Heras, J. I. D. L., Zuleger, N., Batrakou, D. G., Czapiewski, R., Kerr, A. R. W., & Schirmer, E. C. (2017) · Nucleus · doi:10.1080/19491034.2016.1261230 · Cited by 35
Bridger, J. M., Arican-Gotkas, H. D., Foster, H. A., Godwin, L. S., Harvey, A., Kill, I. R., Knight, M., Mehta, I. S., & Ahmed, M. H. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-1-4899-8032-8_28 · Cited by 35
Self-citationChromosomal aneuploidies induced upon Lamin B2 depletion are mislocalized in the interphase nucleus
Ranade, D., Koul, S., Thompson, J. J., Prasad, K. B., & Sengupta, K. (2016) · Chromosoma · doi:10.1007/s00412-016-0580-y · Cited by 33
The Nuclear Lamina as a Gene-silencing Hub
(2012) · Current Issues in Molecular Biology · doi:10.21775/cimb.014.027 · Cited by 32
Nuclear Envelope: Connecting Structural Genome Organization to Regulation of Gene Expression
Stancheva, I., & Schirmer, E. C. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-1-4899-8032-8_10 · Cited by 31
Gene regulation through dynamic actin control of nuclear structure
Sankaran, J. S., Uzer, G., van Wijnen, A. J., & Rubin, J. E. (2019) · Experimental Biology and Medicine · doi:10.1177/1535370219850079 · Cited by 31
Structural Variation and Its Effect on Expression
Harewood, L., Chaignat, E., & Reymond, A. (2011) · Methods in molecular biology · doi:10.1007/978-1-61779-507-7_8 · Cited by 28
Dog obesity – The need for identifying predisposing genetic markers
Switonski, M., & Mankowska, M. (2013) · Research in Veterinary Science · doi:10.1016/j.rvsc.2013.08.015 · Cited by 28
Arican-Goktas, H. D., Ittiprasert, W., Bridger, J. M., & Knight, M. (2014) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0003013 · Cited by 34
Self-citationSpatial organization of chromosome territories in the interphase nucleus of trisomy 21 cells
Kemeny, S., Tatout, C., Salaün, G., Pebrel‐Richard, C., Goumy, C., Ollier, N., Maurin, E., Pereira, B., Vago, P., & Gouas, L. (2017) · Chromosoma · doi:10.1007/s00412-017-0653-6 · Cited by 30
Malashicheva, A., Bogdanova, M., Zabirnyk, A., Smolina, N., Ignatieva, E. V., Фрейлихман, О. А., Fedorov, A. V., Dmitrieva, R. I., Sjöberg, G., Sejersen, T., et al. (2015) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2015.04.006 · Cited by 27
Male Fertility, Chromosome Abnormalities, and Nuclear Organization
Ioannou, D., & Griffin, D. K. (2010) · Cytogenetic and Genome Research · doi:10.1159/000322060 · Cited by 27
Hierarchical radial and polar organisation of chromosomes in human sperm
Millan, N., Lau, P. E., Hann, M., Ioannou, D., Hoffman, D. I., Barrionuevo, M. R., Maxson, W., Ory, S. J., & Tempest, H. G. (2012) · Chromosome Research · doi:10.1007/s10577-012-9323-y · Cited by 26
Chromobility: the rapid movement of chromosomes in interphase nuclei
Bridger, J. M. (2011) · Biochemical Society Transactions · doi:10.1042/bst20110696 · Cited by 26
Self-citationOrganization of nuclear architecture during adipocyte differentiation
Charó, N. L., Ceschan, M. I. R., Galigniana, N. M., Toneatto, J., & Piwien‐Pilipuk, G. (2016) · Nucleus · doi:10.1080/19491034.2016.1197442 · Cited by 27
Stachecka, J., Nowacka‐Woszuk, J., Kolodziejski, P. A., & Szczerbal, I. (2019) · Chromosome Research · doi:10.1007/s10577-019-09604-2 · Cited by 24
Self-citationStachecka, J., Kolodziejski, P. A., Noak, M., & Szczerbal, I. (2021) · Scientific Reports · doi:10.1038/s41598-020-79384-x · Cited by 23
Self-citationThe first case of 38,XX (SRY-positive) disorder of sex development in a cat
Szczerbal, I., Stachowiak, M., Dzimira, S., Sliwa, K., & Switonski, M. (2015) · Molecular Cytogenetics · doi:10.1186/s13039-015-0128-5 · Cited by 23
Self-citationTranscriptomic and nuclear architecture of immune cells after LPS activation
Solinhac, R., Mompart, F., Martin, P. G. P., Robelin, D., Pinton, P., Iannuccelli, E., Lahbib-Mansais, Y., Oswald, I. P., & Martine Yerle, B. (2011) · Chromosoma · doi:10.1007/s00412-011-0328-7 · Cited by 22
Gatticchi, L., Petricciuolo, M., Scarpelli, P., Macchioni, L., Corazzi, L., & Roberti, R. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2020.118897 · Cited by 23
Ioannou, D., Meershoek, E. J., Christopikou, D., Ellis, M., Thornhill, A. R., & Griffin, D. K. (2011) · Chromosome Research · doi:10.1007/s10577-011-9238-z · Cited by 23
Rozwadowska, N., Kolanowski, T. J., Wiland, E., Siatkowski, M., Pawlak, P., Malcher, A., Miętkiewski, T., Olszewska, M., & Kurpisz, M. K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0073231 · Cited by 21
Arnandis, T., Vicens, I. F., Torres, L., Garcı́a, C., García–Trevijano, E. R., Zaragozá, R., & Vinã, J. R. (2014) · Biochemical Journal · doi:10.1042/bj20130847 · Cited by 20
Spatial segregation of heterochromatin: Uncovering functionality in a multicellular organism
Cabianca, D. S., & Gasser, S. M. (2016) · Nucleus · doi:10.1080/19491034.2016.1187354 · Cited by 19
Naito, M., Omoteyama, K., Mikami, Y., Takagi, M., & Takahashi, T. (2011) · Histochemistry and Cell Biology · doi:10.1007/s00418-011-0890-3 · Cited by 18
Stachecka, J., Walczak, A., Kociucka, B., Ruszczycki, B., Wilczynski, G. M., & Szczerbal, I. (2017) · Histochemistry and Cell Biology · doi:10.1007/s00418-017-1618-9 · Cited by 19
Self-citationLeBlanc, S. E., Wu, Q., Barutcu, A. R., Xiao, H., Ohkawa, Y., & Imbalzano, A. N. (2014) · PLoS ONE · doi:10.1371/journal.pone.0086140 · Cited by 18
Three-Dimensional Segmentation and Reconstruction of Neuronal Nuclei in Confocal Microscopic Images
Ruszczycki, B., Pels, K. K., Walczak, A., Zamłyńska, K., Such, M., Szczepankiewicz, A. A., Hall, M. H., Magalska, A., Magnowska, M., Wolny, A., et al. (2019) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2019.00081 · Cited by 17
Significance of higher-order chromatin architecture for neuronal function and dysfunction
Wilczynski, G. M. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.01.016 · Cited by 17
Physical Signals May Affect Mesenchymal Stem Cell Differentiation via Epigenetic Controls
Rubin, J. E., Styner, M., & Uzer, G. (2017) · Exercise and Sport Sciences Reviews · doi:10.1249/jes.0000000000000129 · Cited by 16
Chromosomal Rearrangements and Altered Nuclear Organization: Recent Mechanistic Models in Cancer
Federico, C., Bruno, F., Ragusa, D., Clements, C. S., Brancato, D., Henry, M. P., Bridger, J. M., Tosi, S., & Saccone, S. (2021) · Cancers · doi:10.3390/cancers13225860 · Cited by 17
Self-citationX monosomy in a Virilized Female Cat
Szczerbal, I., Niżański, W., Dzimira, S., Nowacka‐Woszuk, J., Ochota, M., & Switonski, M. (2015) · Reproduction in Domestic Animals · doi:10.1111/rda.12483 · Cited by 16
Self-citationKociucka, B., Flisikowska, T., Mróz, D., & Szczerbal, I. (2016) · Journal of Applied Genetics · doi:10.1007/s13353-016-0350-9 · Cited by 16
Self-citationOrigin and Evolution of Genes in Eukaryotes: Mechanisms, Dynamics, and Functional Implications
Saccone, S., Brancato, D., Bruno, F., Coniglio, E., Sturiale, V., & Federico, C. (2025) · Genes · doi:10.3390/genes16060702 · Cited by 17
“Lamina-associated domains (LADs), typically located at the nuclear periphery, are enriched in repressive chromatin marks and correlate with low transcriptional activity [74,75].”
Federico, C., Pappalardo, A. M., Ferrito, V., Tosi, S., & Saccone, S. (2017) · Chromosome Research · doi:10.1007/s10577-017-9560-1 · Cited by 15
Gatticchi, L., Heras, J. I. D. L., Sivakumar, A., Zuleger, N., Roberti, R., & Schirmer, E. C. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.592573 · Cited by 14
Rizzotto, A., & Schirmer, E. C. (2017) · Biochemical Society Transactions · doi:10.1042/bst20170153 · Cited by 14
Kociucka, B., Cieślak, J., & Szczerbal, I. (2012) · Cytogenetic and Genome Research · doi:10.1159/000338255 · Cited by 13
Self-citationJost, K. L., Bertulat, B., Rapp, A. W., Brero, A., Hardt, T., Domaing, P., Gösele, C., Schulz, H., Hübner, N., & Cardoso, M. C. (2015) · Epigenetics & Chromatin · doi:10.1186/s13072-015-0025-5 · Cited by 13
Sarusi-Portuguez, A., Schwartz, M., Siersbæk, R., Nielsen, R., Sung, M., Mandrup, S., Kaplan, T., & Hakim, O. (2017) · FEBS Journal · doi:10.1111/febs.14183 · Cited by 13
Federico, C., Owoka, T., Ragusa, D., Sturiale, V., Caponnetto, D., Leotta, C. G., Bruno, F., Foster, H. A., Rigamonti, S., Giudici, G., et al. (2019) · Cancers · doi:10.3390/cancers11040585 · Cited by 12
Self-citationIoannou, D., Kandukuri, L. R., Ameer, Q., Victor, B., Simpson, J. L., & Tempest, H. G. (2015) · PLoS ONE · doi:10.1371/journal.pone.0118886 · Cited by 12
Chromosome territory repositioning induced by PHA-activation of lymphocytes: A 2D and 3D appraisal
Ioannou, D., Kandukuri, L. R., Simpson, J. L., & Tempest, H. G. (2015) · Molecular Cytogenetics · doi:10.1186/s13039-015-0146-3 · Cited by 11
Adipogenesis is under surveillance of Hsp90 and the high molecular weight Immunophilin FKBP51
Toneatto, J., Charó, N. L., Galigniana, N. M., & Piwien‐Pilipuk, G. (2015) · Adipocyte · doi:10.1080/21623945.2015.1049401 · Cited by 11
Meet the neighbours: tools to dissect nuclear structure and function
Osborne, C. S., Ewels, P., & Young, A. (2011) · Briefings in Functional Genomics · doi:10.1093/bfgp/elq034 · Cited by 9
Interphase Chromosome Behavior in Normal and Diseased Cells
Bourne, G., Moir, C. A., Bikkul, M. U., Ahmed, M. H., Kill, I. R., Eskiw, C. H., Tosi, S., & Bridger, J. M. (2013) · Springer eBooks · doi:10.1007/978-1-4614-6558-4_2 · Cited by 9
Self-citationRole of Nuclear Lamina in Gene Repression and Maintenance of Chromosome Architecture in the Nucleus
Shevelyov, Y. Y., & Ulianov, S. V. (2018) · Biochemistry (Moscow) · doi:10.1134/s0006297918040077 · Cited by 9
Mehta, I. S., Chakraborty, S., & Rao, B. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061386 · Cited by 9
Pérez‐Serrano, R. M., González‐Dávalos, L., Lozano‐Flores, C., Shimada, A. S., Antaramián, A., Varela‐Echavarría, A., & Mora, O. (2016) · Cells Tissues Organs · doi:10.1159/000447628 · Cited by 8
Maldonado, V. V., Jensen, H., Barnes, C. L., & Samsonraj, R. M. (2025) · Biochimie · doi:10.1016/j.biochi.2025.04.002 · Cited by 7
Kociucka, B., Sosnowski, J., Kubiak, A., Nowak, A., Pawlak, P., & Szczerbal, I. (2013) · Cytogenetic and Genome Research · doi:10.1159/000348434 · Cited by 7
Self-citationAksoy, M. O., Bilinska, A., Stachowiak, M., Flisikowska, T., & Szczerbal, I. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252312677 · Cited by 6
Self-citationTagged Chromosomal Insertion Site System
Harr, J. C., & Reddy, K. L. (2015) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2015.09.028 · Cited by 5
O molekularnej patogenezie stresu i depresji
Pels, K. K. (2020) · Kosmos · doi:10.36921/kos.2020_2619 · Cited by 5
An Optimized Adaptation of DamID for NGS Applications
Reddy, K. L., & Wong, X. (2024) · Methods in molecular biology · doi:10.1007/978-1-0716-4192-7_14 · Cited by 3
Alterations to Genome Organisation in Stem Cells, Their Differentiation and Associated Diseases
Bridger, J. M., Pereira, R. T., Pina, C., Tosi, S., & Lewis, A. (2022) · Results and problems in cell differentiation · doi:10.1007/978-3-031-06573-6_3 · Cited by 3
Self-citationFederico, C., Brancato, D., Bruno, F., Galvano, D., Caruso, M., & Saccone, S. (2024) · Genes · doi:10.3390/genes15060722 · Cited by 3
Chromosomal dynamics of cell cycle regulator gene p21 during transcriptional activation
Philimonenko, A. A., Janáček, J., Snyers, L., Almeder, M., Berger, W., Schmidt, W. M., Schöfer, C., Hozák, P., & Weipoltshammer, K. (2010) · Journal of Structural Biology · doi:10.1016/j.jsb.2010.10.010 · Cited by 3
Odoemelam, E. C. (2009) · Brunel University Research Archive (BURA) (Brunel University London) · Cited by 2
Hong, E. P., Rhee, K. H., Kim, D. H., & Park, J. W. (2017) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-017-0892-x · Cited by 1
Corticosteroid Receptors, Their Chaperones and Cochaperones: How Do They Modulate Adipogenesis?
Toneatto, J., Charó, N. L., Naselli, A., Muñoz-Bernart, M., Lombardi, A., & Piwien‐Pilipuk, G. (2014) · Nuclear Receptor Research · doi:10.11131/2014/101092 · Cited by 1
Role of the Nucleolus in Rearrangements of the IGH Locus
Iarovaia, O. V., Ioudinkova, E. S., Razin, S. V., & Vassetzky, Y. S. (2018) · Molecular Biology · doi:10.1134/s0026893317050211 · Cited by 1
The Nuclear Lamina as a Chromatin Organizer
Zuleger, N., & Schirmer, E. C. (2011) · doi:10.1002/9783527639991.ch8 · Cited by 1
Inner nuclear membrane proteins: targeting and influence on genome organization
Zuleger, N. (2012) · ERA
The role of lamin A and emerin in mediating genome organisation
Godwin, L. S. (2010) · Brunel University Research Archive (BURA) (Brunel University London)
Gene positioning and genome function
Vishnoi, N., & Yao, J. (2014) · Frontiers in Biology · doi:10.1007/s11515-014-1313-3
Metadata
- Authors
- Szczerbal, I., Foster, H. A., & Bridger, J. M.
- Affiliations
- Poznań University of Life Sciences (PL)
- Brunel University of London (GB)
- Corresponding author
- Szczerbal, Izabela
- Bridger, Joanna M.
- Venue
- Chromosoma
- Published
- 2009-07-08
- Volume
- 118
- Issue
- 5
- Pages
- 647-663
- ISSN
- 0009-5915 (ISSN-L)
- 1432-0886
- OpenAlex
- W2049017075
- Cited by
- 107
- References
- 73
- Citations by year
- 2025: 4 · 2024: 3 · 2022: 2 · 2021: 2 · 2020: 4 · 2019: 5 · 2018: 4 · 2017: 9 · 2016: 9 · 2015: 10 · 2014: 15 · 2013: 8 · 2012: 9
- FWCI
- 4.28
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Chromosoma (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Brunel University London
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
- Keywords
- adipogenesis, chromosome territories, interphase nuclei, mesenchymal stem cells, gene expression regulation, chromatin looping, chromatin decondensation, PPARγ, SREBF1, FABP4, C/EBP, GATA2, SOX9, spatial genome organization
- MeSH terms
- Animals, Cell Differentiation, Genes, Swine, Gene Expression, CCAAT-Enhancer-Binding Proteins, Chromatin Assembly and Disassembly, PPAR gamma, Adipogenesis, GATA2 Transcription Factor, Sterol Regulatory Element Binding Protein 1, Mesenchymal Stem Cells
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