Literature DB >> 1762910

Presence of regulatory sequences within intron 2 of the mouse thymidine kinase gene.

H Rotheneder1, M Grabner, E Wintersberger.   

Abstract

The intron 2 of the murine thymidine kinase (TK) gene was observed to contain two DNase hypersensitive site. In vitro footprinting experiments indicated specific binding sites for nuclear proteins which were characterized within the sequence of intron 2. Two GC boxes (binding sites for transcription factor SP1) and two new protein binding regions, one at the promoter proximal end of intron 2, the other one close to the border to exon 3 were found. Oligonucleotides were synthesized comprising the two new binding sites and were shown in gel mobility shift experiments to be capable of forming specific complexes with nuclear proteins. These proteins are present in growing as well as in quiescent cells suggesting that the sites described here do not contribute to growth regulation of TK expression. That they might play a role in upregulation of TK expression is, however, indicated by the results of CAT assays in which inclusion of downstream sequences of the TK gene containing parts or all of intron 2 were found to positively modulate the activity of the TK promoter.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1762910      PMCID: PMC329313          DOI: 10.1093/nar/19.24.6805

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  40 in total

1.  Genetic determinants of growth phase-dependent and adenovirus 5-responsive expression of the Chinese hamster thymidine kinase gene are contained within thymidine kinase mRNA sequences.

Authors:  J A Lewis; D A Matkovich
Journal:  Mol Cell Biol       Date:  1986-06       Impact factor: 4.272

2.  Mouse thymidine kinase: the promoter sequence and the gene and pseudogene structures in normal cells and in thymidine kinase deficient mutants.

Authors:  C Seiser; M Knöfler; I Rudelstorfer; R Haas; E Wintersberger
Journal:  Nucleic Acids Res       Date:  1989-01-11       Impact factor: 16.971

3.  DNase I- and micrococcal nuclease-hypersensitive sites in the human apolipoprotein B gene are tissue specific.

Authors:  B Levy-Wilson; C Fortier; B D Blackhart; B J McCarthy
Journal:  Mol Cell Biol       Date:  1988-01       Impact factor: 4.272

4.  Introns are inconsequential to efficient formation of cellular thymidine kinase mRNA in mouse L cells.

Authors:  M K Gross; M S Kainz; G F Merrill
Journal:  Mol Cell Biol       Date:  1987-12       Impact factor: 4.272

5.  Regulation of human thymidine kinase during the cell cycle.

Authors:  J L Sherley; T J Kelly
Journal:  J Biol Chem       Date:  1988-06-15       Impact factor: 5.157

6.  Role of the promoter in the regulation of the thymidine kinase gene.

Authors:  S Travali; K E Lipson; D Jaskulski; E Lauret; R Baserga
Journal:  Mol Cell Biol       Date:  1988-04       Impact factor: 4.272

7.  Regulation of thymidine kinase protein levels during myogenic withdrawal from the cell cycle is independent of mRNA regulation.

Authors:  M K Gross; G F Merrill
Journal:  Nucleic Acids Res       Date:  1988-12-23       Impact factor: 16.971

8.  Cell cycle regulated synthesis of stable mouse thymidine kinase mRNA is mediated by a sequence within the cDNA.

Authors:  R Hofbauer; E Müllner; C Seiser; E Wintersberger
Journal:  Nucleic Acids Res       Date:  1987-01-26       Impact factor: 16.971

9.  Nuclear posttranscriptional processing of thymidine kinase mRNA at the onset of DNA synthesis.

Authors:  J M Gudas; G B Knight; A B Pardee
Journal:  Proc Natl Acad Sci U S A       Date:  1988-07       Impact factor: 11.205

10.  Transcriptional arrest within the first exon is a fast control mechanism in c-myc gene expression.

Authors:  D Eick; G W Bornkamm
Journal:  Nucleic Acids Res       Date:  1986-11-11       Impact factor: 16.971

View more
  8 in total

1.  Interaction of Sp1 with the growth- and cell cycle-regulated transcription factor E2F.

Authors:  J Karlseder; H Rotheneder; E Wintersberger
Journal:  Mol Cell Biol       Date:  1996-04       Impact factor: 4.272

2.  A binding site for transcription factor E2F is a target for trans activation of murine thymidine kinase by polyomavirus large T antigen and plays an important role in growth regulation of the gene.

Authors:  E Ogris; H Rotheneder; I Mudrak; A Pichler; E Wintersberger
Journal:  J Virol       Date:  1993-04       Impact factor: 5.103

3.  Expression of carbonic anhydrase II (CA II) promoter-reporter fusion genes in multiple tissues of transgenic mice does not replicate normal patterns of expression indicating complexity of CA II regulation in vivo.

Authors:  R P Erickson; J Grimes; P J Venta; R E Tashian
Journal:  Biochem Genet       Date:  1995-12       Impact factor: 1.890

4.  Interaction of several related GC-box- and GT-box-binding proteins with the intronic enhancer is required for differential expression of the gb110 gene in embryonal carcinoma cells.

Authors:  L Hamann; K U Bayer; K Jensen; K Harbers
Journal:  Mol Cell Biol       Date:  1994-09       Impact factor: 4.272

5.  An S-phase specific release from a transcriptional block regulates the expression of mouse ribonucleotide reductase R2 subunit.

Authors:  S Björklund; E Skogman; L Thelander
Journal:  EMBO J       Date:  1992-12       Impact factor: 11.598

6.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1992-02-25       Impact factor: 16.971

7.  An intron mutation in the ACVRL1 may be associated with a transcriptional regulation defect in a Chinese family with hereditary hemorrhagic telangiectasia.

Authors:  Qian Yu; Xiao-Hui Shen; Ying Li; Rui-Juan Li; Ji Li; Yun-Ya Luo; Su-Fang Liu; Ming-Yang Deng; Min-Fei Pei; Guang-Sen Zhang
Journal:  PLoS One       Date:  2013-02-27       Impact factor: 3.240

8.  Presence of a regulatory element within the first intron of the human platelet-derived growth factor-A chain gene.

Authors:  Y Takimoto; A Kuramoto
Journal:  Jpn J Cancer Res       Date:  1993-12
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.