Literature DB >> 106887

Purification and preparation of antibody to RNA polymerase II stimulatory factors from Ehrlich ascites tumor cells.

K Sekimizu, Y Nakanishi, D Mizuno, S Natori.   

Abstract

An improved method was developed for purification of the protein termed S-II that specifically stimulates RNA polymerase II of Ehrlich ascites tumor cells. The specific activity of the final preparation was 400 000 units/mg of protein, which is about 30-fold higher than that of the previous preparation [Sekimizu, K., et al. (1976) Biochemistry 15, 5064]. The final preparation gave a single band on both sodium dodecyl sulfate and nondenaturing gel electrophoresis, and the protein extracted from the band on nondenaturing gel had stimulatory activity. S-II is a basic protein with a molecular weight of 40 500. The fundamental characteristics of S-II determined with the previous preparation were confirmed with completely purified S-II. A specific antibody to S-II was prepared. This antibody inhibited only the stimulatory activity of S-II and did not affect the activity of RNA polymerase II itself. Thus, S-II is probably not a component of the multimeric proteins of RNA polymerase II.

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Year:  1979        PMID: 106887     DOI: 10.1021/bi00575a031

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  13 in total

1.  Drosophila RNA polymerase II elongation factor DmS-II has homology to mouse S-II and sequence similarity to yeast PPR2.

Authors:  T K Marshall; H Guo; D H Price
Journal:  Nucleic Acids Res       Date:  1990-11-11       Impact factor: 16.971

2.  Control of formation of two distinct classes of RNA polymerase II elongation complexes.

Authors:  N F Marshall; D H Price
Journal:  Mol Cell Biol       Date:  1992-05       Impact factor: 4.272

3.  Cloning, expression and characterization of the human transcription elongation factor, TFIIS.

Authors:  O J Yoo; H S Yoon; K H Baek; C J Jeon; K Miyamoto; A Ueno; K Agarwal
Journal:  Nucleic Acids Res       Date:  1991-03-11       Impact factor: 16.971

4.  Purification of two transcription factors required for initiation by mammalian RNA polymerase II.

Authors:  T Kawaguchi; S Kitajima; Y Niho; T Oda; J Germino; S M Weissman; Y Yasukochi
Journal:  Proc Natl Acad Sci U S A       Date:  1990-09       Impact factor: 11.205

5.  TFIIS binds to mouse RNA polymerase I and stimulates transcript elongation and hydrolytic cleavage of nascent rRNA.

Authors:  G Schnapp; B R Graveley; I Grummt
Journal:  Mol Gen Genet       Date:  1996-09-25

6.  Inhibition of DNA-dependent transcription by the leader RNA of vesicular stomatitis virus: role of specific nucleotide sequences and cell protein binding.

Authors:  B W Grinnell; R R Wagner
Journal:  Mol Cell Biol       Date:  1985-10       Impact factor: 4.272

7.  The Rpb6 subunit of fission yeast RNA polymerase II is a contact target of the transcription elongation factor TFIIS.

Authors:  A Ishiguro; Y Nogi; K Hisatake; M Muramatsu; A Ishihama
Journal:  Mol Cell Biol       Date:  2000-02       Impact factor: 4.272

8.  Identification of rpo30, a vaccinia virus RNA polymerase gene with structural similarity to a eucaryotic transcription elongation factor.

Authors:  B Y Ahn; P D Gershon; E V Jones; B Moss
Journal:  Mol Cell Biol       Date:  1990-10       Impact factor: 4.272

9.  Stimulatory proteins of RNA polymerase II from Ehrlich ascites tumor cells.

Authors:  S Natori
Journal:  Mol Cell Biochem       Date:  1982-08-06       Impact factor: 3.396

10.  Genetic interactions of DST1 in Saccharomyces cerevisiae suggest a role of TFIIS in the initiation-elongation transition.

Authors:  Francisco Malagon; Amy H Tong; Brenda K Shafer; Jeffrey N Strathern
Journal:  Genetics       Date:  2004-03       Impact factor: 4.562

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