Activation of Estrogen-Responsive Genes Does Not Require Their Nuclear Co-Localization

The spatial organization of the genome in the nucleus plays a role in the regulation of gene expression. Whether co-regulated genes are subject to coordinated repositioning to a shared nuclear space is a matter of considerable interest and debate. We investigated the nuclear organization of estrogen receptor alpha (ERα) target genes in human breast epithelial and cancer cell lines, before and after transcriptional activation induced with estradiol. We find that, contrary to another report, the ERα target genes TFF1 and GREB1 are distributed in the nucleoplasm with no particular relationship to each other. The nuclear separation between these genes, as well as between the ERα target genes PGR and CTSD, was unchanged by hormone addition and transcriptional activation with no evidence for co-localization between alleles. Similarly, while the volume occupied by the chromosomes increased, the relative nuclear position of the respective chromosome territories was unaffected by hormone addition. Our results demonstrate that estradiol-induced ERα target genes are not required to co-localize in the nucleus.

[1]  Leighton J. Core,et al.  Postrecruitment Regulation of RNA Polymerase II Directs Rapid Signaling Responses at the Promoters of Estrogen Target Genes , 2008, Molecular and Cellular Biology.

[2]  J. Graham,et al.  Focal subnuclear distribution of progesterone receptor is ligand dependent and associated with transcriptional activity. , 2007, Molecular endocrinology.

[3]  Cameron S. Osborne,et al.  Myc Dynamically and Preferentially Relocates to a Transcription Factory Occupied by Igh , 2007, PLoS biology.

[4]  W. Lam,et al.  Comprehensive copy number profiles of breast cancer cell model genomes , 2006, Breast Cancer Research.

[5]  Wendy A Bickmore,et al.  Chromatin Motion Is Constrained by Association with Nuclear Compartments in Human Cells , 2002, Current Biology.

[6]  E. Liu,et al.  An Oestrogen Receptor α-bound Human Chromatin Interactome , 2009, Nature.

[7]  W. Bickmore,et al.  Chromatin decondensation and nuclear reorganization of the HoxB locus upon induction of transcription. , 2004, Genes & development.

[8]  Heike Brand,et al.  Estrogen Receptor-α Directs Ordered, Cyclical, and Combinatorial Recruitment of Cofactors on a Natural Target Promoter , 2003, Cell.

[9]  J Lippman,et al.  MCF7/LCC9: an antiestrogen-resistant MCF-7 variant in which acquired resistance to the steroidal antiestrogen ICI 182,780 confers an early cross-resistance to the nonsteroidal antiestrogen tamoxifen. , 1997, Cancer research.

[10]  Daniel R. Larson,et al.  A single molecule view of gene expression. , 2009, Trends in cell biology.

[11]  Thomas Cremer,et al.  Chromosome order in HeLa cells changes during mitosis and early G1, but is stably maintained during subsequent interphase stages , 2003, The Journal of cell biology.

[12]  H. Tanabe,et al.  Chromosomal dynamics at the Shh locus: limb bud-specific differential regulation of competence and active transcription. , 2009, Developmental cell.

[13]  J. Jones,et al.  Novel multicellular organotypic models of normal and malignant breast: tools for dissecting the role of the microenvironment in breast cancer progression , 2009, Breast Cancer Research.

[14]  J. Davie,et al.  Direct visualization of the human estrogen receptor alpha reveals a role for ligand in the nuclear distribution of the receptor. , 1999, Molecular biology of the cell.

[15]  K. Sengupta,et al.  Differential expression of VEGF-A mRNA by 17beta-estradiol in breast tumor cells lacking classical ER-alpha may be mediated through a variant form of ER-alpha. , 2004, Molecular and cellular biochemistry.

[16]  F. Stossi,et al.  Whole-Genome Cartography of Estrogen Receptor α Binding Sites , 2007, PLoS genetics.

[17]  Christopher A. Miller,et al.  A sequence-level map of chromosomal breakpoints in the MCF-7 breast cancer cell line yields insights into the evolution of a cancer genome. , 2009, Genome research.

[18]  R. Broaddus,et al.  Functional regulation of oestrogen receptor pathway by the dynein light chain 1 , 2005, EMBO reports.

[19]  S. Lakhani,et al.  Comparative genomic hybridization reveals extensive variation among different MCF-7 cell stocks. , 2000, Cancer genetics and cytogenetics.

[20]  P. Mombaerts,et al.  Local and cis Effects of the H Element on Expression of Odorant Receptor Genes in Mouse , 2007, Cell.

[21]  Anne E Carpenter,et al.  Long-Range Directional Movement of an Interphase Chromosome Site , 2006, Current Biology.

[22]  Cameron S. Osborne,et al.  Active genes dynamically colocalize to shared sites of ongoing transcription , 2004, Nature Genetics.

[23]  Wen-Lin Kuo,et al.  A collection of breast cancer cell lines for the study of functionally distinct cancer subtypes. , 2006, Cancer cell.

[24]  Xiang-Dong Fu,et al.  Enhancing nuclear receptor-induced transcription requires nuclear motor and LSD1-dependent gene networking in interchromatin granules , 2008, Proceedings of the National Academy of Sciences.

[25]  Michelle L Bowie,et al.  Interferon-regulatory factor-1 is critical for tamoxifen-mediated apoptosis in human mammary epithelial cells , 2004, Oncogene.

[26]  T. Cremer,et al.  Maintenance of imprinting and nuclear architecture in cycling cells , 2007, Proceedings of the National Academy of Sciences.

[27]  R. van Driel,et al.  Nuclear distribution of transcription factors in relation to sites of transcription and RNA polymerase II. , 1997, Journal of cell science.

[28]  S. Bautista,et al.  CCND1 and FGFR1 coamplification results in the colocalization of 11q13 and 8p12 sequences in breast tumor nuclei , 1998, Genes, chromosomes & cancer.

[29]  Rakesh Kumar,et al.  An inherent role of microtubule network in the action of nuclear receptor , 2006, Proceedings of the National Academy of Sciences.

[30]  Chia-Lun Tsai,et al.  Transient Homologous Chromosome Pairing Marks the Onset of X Inactivation , 2006, Science.

[31]  Michael M. Wang,et al.  p150/glued modifies nuclear estrogen receptor function. , 2009, Molecular endocrinology.

[32]  Céline Lefebvre,et al.  From the Cover: Location analysis of estrogen receptor alpha target promoters reveals that FOXA1 defines a domain of the estrogen response. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[33]  T. Ikemura,et al.  Relative locations of the centromere and imprinted SNRPN gene within chromosome 15 territories during the cell cycle in HL60 cells. , 2000, Journal of cell science.

[34]  E. Heard,et al.  The ins and outs of gene regulation and chromosome territory organisation. , 2007, Current opinion in cell biology.

[35]  Vincent T. Lombardi,et al.  Acquisition of Hormone-independent Growth in MCF-7 Cells Is Accompanied by Increased Expression of Estrogen-regulated Genes but Without Detectable DNA Amplifications , 2007 .

[36]  H. Richard-Foy,et al.  Eliminating epigenetic barriers induces transient hormone-regulated gene expression in estrogen receptor negative breast cancer cells , 2008, Oncogene.

[37]  Clifford A. Meyer,et al.  Genome-wide analysis of estrogen receptor binding sites , 2006, Nature Genetics.

[38]  C. Larsson,et al.  Chromosomal alterations in 15 breast cancer cell lines by comparative genomic hybridization and spectral karyotyping , 2000, Genes, chromosomes & cancer.

[39]  Roland Eils,et al.  Transient colocalization of X-inactivation centres accompanies the initiation of X inactivation , 2006, Nature Cell Biology.

[40]  Johan Staaf,et al.  High‐resolution genomic profiles of breast cancer cell lines assessed by tiling BAC array comparative genomic hybridization , 2007, Genes, chromosomes & cancer.

[41]  Wendy A. Bickmore,et al.  The Radial Positioning of Chromatin Is Not Inherited through Mitosis but Is Established De Novo in Early G1 , 2004, Current Biology.

[42]  Marina Bibikova,et al.  Sensitive ChIP-DSL technology reveals an extensive estrogen receptor α-binding program on human gene promoters , 2007, Proceedings of the National Academy of Sciences.

[43]  Anne E Carpenter,et al.  Alteration of Large-Scale Chromatin Structure by Estrogen Receptor , 2002, Molecular and Cellular Biology.

[44]  B. Steensel,et al.  Nuclear organization of active and inactive chromatin domains uncovered by chromosome conformation capture–on-chip (4C) , 2006, Nature Genetics.

[45]  A. Krystosek Repositioning of human interphase chromosomes by nucleolar dynamics in the reverse transformation of HT1080 fibrosarcoma cells. , 1998, Experimental cell research.

[46]  Juliet A. Ellis,et al.  The spatial organization of human chromosomes within the nuclei of normal and emerin-mutant cells. , 2001, Human molecular genetics.

[47]  Richard Axel,et al.  Interchromosomal Interactions and Olfactory Receptor Choice , 2006, Cell.

[48]  Y. Ruan,et al.  ChIP‐based methods for the identification of long‐range chromatin interactions , 2009, Journal of cellular biochemistry.

[49]  M. Mancini,et al.  Subnuclear trafficking of estrogen receptor-alpha and steroid receptor coactivator-1. , 2000, Molecular endocrinology.

[50]  F. Iborra,et al.  Association between active genes occurs at nuclear speckles and is modulated by chromatin environment , 2008, The Journal of cell biology.

[51]  D. Thanos,et al.  Virus Infection Induces NF-κB-Dependent Interchromosomal Associations Mediating Monoallelic IFN-β Gene Expression , 2008, Cell.

[52]  Andrew G. Clark,et al.  Genomic Analyses of Transcription Factor Binding, Histone Acetylation, and Gene Expression Reveal Mechanistically Distinct Classes of Estrogen-Regulated Promoters , 2007, Molecular and Cellular Biology.

[53]  R. Flavell,et al.  Interchromosomal associations between alternatively expressed loci , 2005, Nature.

[54]  J. LaSalle,et al.  Homologous Association of Oppositely Imprinted Chromosomal Domains , 1996, Science.

[55]  K. Sengupta,et al.  Differential expression of VEGF-A mRNA by 17β-estradiol in breast tumor cells lacking classical ER-α may be mediated through a variant form of ER-α , 2004, Molecular and Cellular Biochemistry.

[56]  P. Fraser,et al.  Nuclear organization of the genome and the potential for gene regulation , 2007, Nature.

[57]  W. Bickmore,et al.  Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization. , 1992, American journal of human genetics.

[58]  Giacomo Cavalli,et al.  Chromosome kissing. , 2007, Current opinion in genetics & development.

[59]  A. Pombo,et al.  Intermingling of Chromosome Territories in Interphase Suggests Role in Translocations and Transcription-Dependent Associations , 2006, PLoS biology.

[60]  Carolyn L. Smith,et al.  Subnuclear Trafficking of Estrogen Receptor-α and Steroid Receptor Coactivator-1 , 2000 .

[61]  Peter R. Cook,et al.  Similar active genes cluster in specialized transcription factories , 2008, The Journal of cell biology.

[62]  C. Osborne,et al.  Biological differences among MCF-7 human breast cancer cell lines from different laboratories , 2005, Breast Cancer Research and Treatment.

[63]  Helena Fidlerová,et al.  Chromatin position in human HepG2 cells: Although being non-random, significantly changed in daughter cells , 2009, Journal of structural biology.

[64]  Wendy A Bickmore,et al.  Nuclear reorganisation and chromatin decondensation are conserved, but distinct, mechanisms linked to Hox gene activation , 2007, Development.

[65]  N. Nowak,et al.  Molecular characterization of the t(3;9) associated with immortalization in the MCF10A cell line. , 2005, Cancer genetics and cytogenetics.

[66]  Thomas Cremer,et al.  Multicolor 3D fluorescence in situ hybridization for imaging interphase chromosomes. , 2008, Methods in molecular biology.

[67]  Myles Brown,et al.  Cofactor Dynamics and Sufficiency in Estrogen Receptor–Regulated Transcription , 2000, Cell.

[68]  Wendy A. Bickmore,et al.  Transcription factories: gene expression in unions? , 2009, Nature Reviews Genetics.