Literature DB >> 3923370

An immunoglobulin promoter displays cell-type specificity independently of the enhancer.

J Foster, J Stafford, C Queen.   

Abstract

Recent studies in which cloned immunoglobulin genes were introduced into cultured cells have produced two significant findings. First, the genes are expressed after transfection into lymphoid cells but not non-lymphoid cells. Second, transcription of an immunoglobulin gene requires, in addition to the promoter region, an enhancer element located downstream of the transcription start site. These findings raise the question of whether it is the promoter or the enhancer region that is responsible for the observed cell-type specificity. It has, in fact, been shown that immunoglobulin enhancers function only in lymphoid cells. We show here that the promoter for an immunoglobulin kappa light-chain gene also is strongly specific for lymphoid cells. Our result reemphasizes the importance of promoters relative to enhancers in determining which cells express which genes.

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Year:  1985        PMID: 3923370     DOI: 10.1038/315423a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  60 in total

1.  Promoters with the octamer DNA motif (ATGCAAAT) can be ubiquitous or cell type-specific depending on binding affinity of the octamer site and Oct-factor concentration.

Authors:  I Kemler; E Bucher; K Seipel; M M Müller-Immerglück; W Schaffner
Journal:  Nucleic Acids Res       Date:  1991-01-25       Impact factor: 16.971

2.  Identification of a novel factor that interacts with an immunoglobulin heavy-chain promoter and stimulates transcription in conjunction with the lymphoid cell-specific factor OTF2.

Authors:  B K Yoza; R G Roeder
Journal:  Mol Cell Biol       Date:  1990-05       Impact factor: 4.272

3.  Regulation of kappa immunoglobulin gene transcription in vitro.

Authors:  R A Currie
Journal:  Nucleic Acids Res       Date:  1990-05-25       Impact factor: 16.971

4.  Identification of an octamer-binding site in the human kappa light-chain enhancer.

Authors:  K Nelms; B Van Ness
Journal:  Mol Cell Biol       Date:  1990-07       Impact factor: 4.272

5.  Interaction of a nuclear protein with a palindromic sequence of the mouse immunoglobulin lambda 2-chain gene promoter is important for its transcription.

Authors:  L A Chang; H Murialdo
Journal:  Mol Cell Biol       Date:  1990-11       Impact factor: 4.272

6.  Tissue preferential expression of the hepatitis B virus (HBV) surface antigen gene in two lines of HBV transgenic mice.

Authors:  R D Burk; J A DeLoia; M K elAwady; J D Gearhart
Journal:  J Virol       Date:  1988-02       Impact factor: 5.103

7.  Every enhancer works with every promoter for all the combinations tested: could new regulatory pathways evolve by enhancer shuffling?

Authors:  M Kermekchiev; M Pettersson; P Matthias; W Schaffner
Journal:  Gene Expr       Date:  1991-04

8.  The endogenous Mtv-8 provirus resides within the V kappa locus.

Authors:  J N Yang; J P Dudley
Journal:  J Virol       Date:  1991-07       Impact factor: 5.103

9.  Structural differences in a single gene encoding the V kappa Ser group of light chains explain the existence of two mouse light-chain genetic markers.

Authors:  R T Boyd; M M Goldrick; P D Gottlieb
Journal:  Proc Natl Acad Sci U S A       Date:  1986-12       Impact factor: 11.205

10.  B-lymphocyte targeting of gene expression in transgenic mice with the immunoglobulin heavy-chain enhancer.

Authors:  P Gerlinger; M LeMeur; C Irrmann; P Renard; C Wasylyk; B Wasylyk
Journal:  Nucleic Acids Res       Date:  1986-08-26       Impact factor: 16.971

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