Literature DB >> 2828161

The SV40 enhancer can be dissected into multiple segments, each with a different cell type specificity.

S Schirm1, J Jiricny, W Schaffner.   

Abstract

The SV40 enhancer is known to be active in a wide variety of tissues and species. It contains a number of sequence motifs that can be bound by protein factors and whose integrity is essential for full enhancer activity. We have individually analyzed three synthetic oligonucleotides derived from sequences present within the SV40 enhancer: two oligonucleotides contain variants of the enhancer "core" sequence (designated corePVUII and coreC) and the third represents a region containing a decanucleotide homology to the immunoglobulin promoters/enhancers (designated SPHI). The oligonucleotides were multimerized and linked to a beta-globin test gene. Transcripts of the test gene were analyzed following transient expression in 10 cell lines representing a broad spectrum of tissues. We show that each of the three short segments can individually act as an enhancer when present in multiple copies. None of these enhancers is ubiquitously active; however, each shows activity in a distinctive subpopulation of cell lines. This cell type specificity is most remarkable in the case of the two oligonucleotide segments containing the core sequences. One of these is primarily active in CV-1 cells, whereas the other exhibits a cell type specificity identical to that of the entire enhancer, possibly identifying it as the most important sequence element within the native SV40 enhancer. Our data suggest that a particular cell type specificity is typical for individual enhancer segments, and that enhancers of differing specificity can be assembled from the individual sequence motifs by combining them in different patterns.

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Year:  1987        PMID: 2828161     DOI: 10.1101/gad.1.1.65

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  118 in total

1.  The Pea rbcS-3A Promoter Mediates Light Responsiveness but not Organ Specificity.

Authors:  C. Kuhlemeier; G. Strittmatter; K. Ward; N. H. Chua
Journal:  Plant Cell       Date:  1989-04       Impact factor: 11.277

2.  The SV40 early transcriptional regulatory element is unable to direct gene expression in pituitary GH-3 cells.

Authors:  T A Coleman; Y T Hou; J J Kopchick
Journal:  Gene Expr       Date:  1992

3.  Activation of a late H2B histone gene in blastula-stage sea urchin embryos by an unusual enhancer element located 3' of the gene.

Authors:  A Z Zhao; A M Colin; J Bell; M Baker; B R Char; R Maxson
Journal:  Mol Cell Biol       Date:  1990-12       Impact factor: 4.272

4.  Lymphoid-specific transcriptional activation by components of the IgH enhancer: studies on the E2/E3 and octanucleotide elements.

Authors:  G P Cook; M S Neuberger
Journal:  Nucleic Acids Res       Date:  1990-06-25       Impact factor: 16.971

5.  Characterization of the human p53 gene promoter.

Authors:  S P Tuck; L Crawford
Journal:  Mol Cell Biol       Date:  1989-05       Impact factor: 4.272

6.  Individual protein-binding domains of the insulin gene enhancer positively activate beta-cell-specific transcription.

Authors:  O Karlsson; M D Walker; W J Rutter; T Edlund
Journal:  Mol Cell Biol       Date:  1989-02       Impact factor: 4.272

7.  Multiple basal elements of a human hsp70 promoter function differently in human and rodent cell lines.

Authors:  J M Greene; Z Larin; I C Taylor; H Prentice; K A Gwinn; R E Kingston
Journal:  Mol Cell Biol       Date:  1987-10       Impact factor: 4.272

8.  Activation of mutated simian virus 40 enhancers by amplification of wild-type enhancer elements.

Authors:  J Clarke; W Herr
Journal:  J Virol       Date:  1987-11       Impact factor: 5.103

9.  The -6.1-kilobase chicken lysozyme enhancer is a multifactorial complex containing several cell-type-specific elements.

Authors:  T Grewal; M Theisen; U Borgmeyer; T Grussenmeyer; R A Rupp; A Stief; F Qian; A Hecht; A E Sippel
Journal:  Mol Cell Biol       Date:  1992-05       Impact factor: 4.272

10.  The human M creatine kinase gene enhancer contains multiple functional interacting domains.

Authors:  R V Trask; J C Koster; M E Ritchie; J J Billadello
Journal:  Nucleic Acids Res       Date:  1992-05-11       Impact factor: 16.971

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