An enhancer stimulates transcription in Trans when attached to the promoter via a protein bridge

[1]  J. Gralla Bacterial gene regulation from distant DNA sites , 1989, Cell.

[2]  K. Struhl,et al.  Yeast GCN4 transcriptional activator protein interacts with RNA polymerase II in vitro. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[3]  C. Ingles,et al.  Mutations in RNA polymerase II enhance or suppress mutations in GAL4. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[4]  R. Schüle,et al.  Many transcription factors interact synergistically with steroid receptors. , 1988, Science.

[5]  P. Nielsen,et al.  ON THE DNA BENDING BY PSORALEN INTERSTRAND CROSSLINKING. A GEL ELECTROPHORETIC STUDY , 1988, Photochemistry and photobiology.

[6]  M. Ptashne How eukaryotic transcriptional activators work , 1988, Nature.

[7]  W. Schaffner,et al.  Enhancer sequences and the regulation of gene transcription. , 1988, European journal of biochemistry.

[8]  J. Hearst,et al.  Evidence for structural deformation of the DNA helix by a psoralen diadduct but not by a monoadduct. , 1988, Nucleic acids research.

[9]  Masami Horikoshi,et al.  Transcription factor ATF interacts with the TATA factor to facilitate establishment of a preinitiation complex , 1988, Cell.

[10]  Michael R. Green,et al.  Analysis of the role of the transcription factor ATF in the assembly of a functional preinitiation complex , 1988, Cell.

[11]  H. Erickson,et al.  Detection of DNA looping due to simultaneous interaction of a DNA-binding protein with two spatially separated binding sites on DNA. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[12]  B. Judd,et al.  Transvection: Allelic cross talk , 1988, Cell.

[13]  M. Ptashne,et al.  No strict alignment is required between a transcriptional activator binding site and the "TATA box" of a yeast gene. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[14]  R. Cohen,et al.  Periodic interactions of heat shock transcriptional elements , 1988, Nature.

[15]  J. Wang,et al.  Action at a distance along a DNA. , 1988, Science.

[16]  A. Berk,et al.  Constraints on spacing between transcription factor binding sites in a simple adenovirus promoter. , 1988, Genes & development.

[17]  R. Schüle,et al.  Cooperativity of the glucocorticoid receptor and the CACCC-box binding factor , 1988, Nature.

[18]  D. Baltimore,et al.  Oligonucleotide that binds nuclear factor NF-kappa B acts as a lymphoid-specific and inducible enhancer element. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[19]  P. Sharp,et al.  The adenovirus major late transcription factor activates the rat gamma-fibrinogen promoter. , 1987, Science.

[20]  G. Schaffner,et al.  OVEC, a versatile system to study transcription in mammalian cells and cell-free extracts. , 1987, Nucleic acids research.

[21]  L. Staudt,et al.  An octamer oligonucleotide upstream of a TATA motif is sufficient for lymphoid-specific promoter activity , 1987, Nature.

[22]  E. Milgrom,et al.  Association of DNA-bound progesterone receptors , 1987, Nature.

[23]  T. Maniatis,et al.  Regulation of inducible and tissue-specific gene expression. , 1987, Science.

[24]  R. Schleif Why should DNA loop? , 1987, Nature.

[25]  B. Müller-Hill,et al.  lac repressor forms loops with linear DNA carrying two suitably spaced lac operators. , 1987, The EMBO journal.

[26]  W. Herr,et al.  Discrete elements within the SV40 enhancer region display different cell‐specific enhancer activities. , 1987, The EMBO journal.

[27]  Jun Ma,et al.  Deletion analysis of GAL4 defines two transcriptional activating segments , 1987, Cell.

[28]  W. Schaffner,et al.  The SV40 enhancer can be dissected into multiple segments, each with a different cell type specificity. , 1987, Genes & development.

[29]  B. Révet,et al.  DNA orientation using specific avidin-ferritin biotin end labelling. , 1987, Nucleic acids research.

[30]  K. Struhl,et al.  Functional dissection of a eukaryotic transcriptional activator protein, GCN4 of Yeast , 1986, Cell.

[31]  Mark Ptashne,et al.  Gene regulation by proteins acting nearby and at a distance , 1986, Nature.

[32]  Mark Ptashne,et al.  DNA loops induced by cooperative binding of λ repressor , 1986, Nature.

[33]  S. Plon,et al.  Transcription of the human β-globin gene is stimulated by an SV40 enhancer to which it is physically linked but topologically uncoupled , 1986, Cell.

[34]  S. Plon,et al.  The use of psoralen-modified DNA to probe the mechanism of enhancer action , 1986, Cell.

[35]  M. Ptashne,et al.  Cooperative binding of λ repressors to sites separated by integral turns of the DNA helix , 1986, Cell.

[36]  C. Cantor,et al.  Molecular cloning and nucleotide sequence of the streptavidin gene. , 1986, Nucleic acids research.

[37]  M. Vigneron,et al.  Requirement of stereospecific alignments for initiation from the simian virus 40 early promoter , 1986, Nature.

[38]  H. Schöler,et al.  Cell type‐specific transcriptional enhancement in vitro requires the presence of trans‐acting factors. , 1985, The EMBO journal.

[39]  W. Schaffner,et al.  Simian virus 40 enhancer increases RNA polymerase density within the linked gene , 1985, Nature.

[40]  R. Treisman,et al.  Simian virus 40 enhancer increases number of RNA polymerase II molecules on linked DNA , 1985, Nature.

[41]  R. Kamen,et al.  Polyomavirus enhancer contains multiple redundant sequence elements that activate both DNA replication and gene expression , 1985, Molecular and cellular biology.

[42]  R. Sinden,et al.  Interstrand psoralen cross-links do not introduce appreciable bends in DNA. , 1984, Biochemistry.

[43]  H. Zentgraf,et al.  A transcription enhancer acts in vitro over distances of hundreds of base-pairs on both circular and linear templates but not on chromatin-reconstituted DNA. , 1984, Journal of molecular biology.

[44]  R. Brent,et al.  A bacterial repressor protein or a yeast transcriptional terminator can block upstream activation of a yeast gene , 1984, Nature.

[45]  P. Chambon,et al.  Stimulation of in vitro transcription from the SV40 early promoter by the enhancer involves a specific trans‐acting factor. , 1984, The EMBO journal.

[46]  R. Parish,et al.  Psoralen-crosslinking of DNA as a probe for the structure of active nucleolar chromatin. , 1984, Journal of molecular biology.

[47]  T. Dunn,et al.  An operator at -280 base pairs that is required for repression of araBAD operon promoter: addition of DNA helical turns between the operator and promoter cyclically hinders repression. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[48]  R. Roeder,et al.  Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei. , 1983, Nucleic acids research.

[49]  J. Reiser,et al.  Three regions upstream from the cap site are required for efficient and accurate transcription of the rabbit β-globin gene in mouse 3T6 cells , 1983, Cell.

[50]  J. Banerji,et al.  Expression of a β-globin gene is enhanced by remote SV40 DNA sequences , 1981, Cell.

[51]  P. Chambon,et al.  The SV40 72 base repair repeat has a striking effect on gene expression both in SV40 and other chimeric recombinants. , 1981, Nucleic acids research.

[52]  M. Goldberg,et al.  The Drosophila zeste gene and transvection. , 1989, Trends in genetics : TIG.

[53]  P. Hagerman Flexibility of DNA. , 1988, Annual review of biophysics and biophysical chemistry.

[54]  M. Gellert,et al.  Communication between segments of DNA during site-specific recombination , 1987, Nature.

[55]  Susan M. Gasser,et al.  A glimpse at chromosomal order , 1987 .

[56]  D. Picard Viral and cellular transcription enhancers. , 1985, Oxford surveys on eukaryotic genes.

[57]  Walter Schaffner,et al.  Enhancers and eukaryotic gene transcription , 1985 .

[58]  P. Chambon,et al.  Stimulation of in vitro transcription from heterologous promoters by the simian virus 40 enhancer. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[59]  F. J. Wolf,et al.  THE PROPERTIES OF STREPTAVIDIN, A BIOTIN-BINDING PROTEIN PRODUCED BY STREPTOMYCETES. , 1964, Archives of biochemistry and biophysics.