Literature DB >> 1697065

The most abundant nascent poly(A) + RNAs are transcribed by RNA polymerase III in murine tumor cells.

D A Kramerov1, S V Tillib, G P Shumyatsky, G P Georgiev.   

Abstract

Twelve to twenty percent of newly synthesized poly(A) + RNA is transcribed by RNA polymerase III in Ehrlich ascites carcinoma and P3O1 plasmocytoma mouse tumors. Most of this RNA designated as pol IIIpoly(A) + RNA has a size of 160 to 800 nucleotides with a maximum of distribution of ca. 300 nucleotides. Pol IIIpoly(A) + RNA fraction consists of two major classes of molecules corresponding to previously described B1 RNA and B2 RNA with the ratio of 1:4 to 2:3. All B2 RNAs present in poly(A) + fraction contain a long poly(A) segments at the 3' ends. Thus, RNA polymerase III transcripts can be polyadenylated. Several transcripts that hybridize with B2 probe were also observed in poly(A)- RNA. The major components consist of 180, 160, 120 and 95 nucleotides. The 180-nucleotide B2 RNA seems to be a primary transcript from B2 repeat. We suggest that other B2 RNAs are transcribed from truncated copies of B2 element.

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Year:  1990        PMID: 1697065      PMCID: PMC331270          DOI: 10.1093/nar/18.15.4499

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


  35 in total

1.  Nucleotide sequence of small polyadenylated B2 RNA.

Authors:  D A Kramerov; S V Tillib; A P Ryskov; G P Georgiev
Journal:  Nucleic Acids Res       Date:  1985-09-25       Impact factor: 16.971

2.  Sequences downstream of AAUAAA signals affect pre-mRNA cleavage and polyadenylation in vitro both directly and indirectly.

Authors:  L C Ryner; Y Takagaki; J L Manley
Journal:  Mol Cell Biol       Date:  1989-04       Impact factor: 4.272

3.  Biosynthesis and cytoplasmic distribution of small poly(A)-containing B2 RNA.

Authors:  D A Kramerov; S V Tillib; I V Lekakh; A P Ryskov; G P Georgiev
Journal:  Biochim Biophys Acta       Date:  1985-02-20

4.  RNA fingerprinting using a small horizontal agarose gel electrophoresis apparatus.

Authors:  P J Furdon; R Kole
Journal:  Anal Biochem       Date:  1987-04       Impact factor: 3.365

5.  Specificity of RNA maturation pathways: RNAs transcribed by RNA polymerase III are not substrates for splicing or polyadenylation.

Authors:  S S Sisodia; B Sollner-Webb; D W Cleveland
Journal:  Mol Cell Biol       Date:  1987-10       Impact factor: 4.272

6.  Rodent type 2 Alu family, rat identifier sequence, rabbit C family, and bovine or goat 73-bp repeat may have evolved from tRNA genes.

Authors:  K Sakamoto; N Okada
Journal:  J Mol Evol       Date:  1985       Impact factor: 2.395

7.  Polyadenylylation of an mRNA precursor occurs independently of transcription by RNA polymerase II in vivo.

Authors:  E D Lewis; J L Manley
Journal:  Proc Natl Acad Sci U S A       Date:  1986-11       Impact factor: 11.205

8.  Transcriptional regulation of two serum-induced RNAs in mouse fibroblasts: equivalence of one species to B2 repetitive elements.

Authors:  D R Edwards; C L Parfett; D T Denhardt
Journal:  Mol Cell Biol       Date:  1985-11       Impact factor: 4.272

9.  Repeat sequence families derived from mammalian tRNA genes.

Authors:  G R Daniels; P L Deininger
Journal:  Nature       Date:  1985 Oct 31-Nov 6       Impact factor: 49.962

10.  Activation of putative transposition intermediate formation in tumor cells.

Authors:  M S Grigoryan; D A Kramerov; E M Tulchinsky; E S Revasova; E M Lukanidin
Journal:  EMBO J       Date:  1985-09       Impact factor: 11.598

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  7 in total

Review 1.  RNA polymerase III transcription: its control by tumor suppressors and its deregulation by transforming agents.

Authors:  T R Brown; P H Scott; T Stein; A G Winter; R J White
Journal:  Gene Expr       Date:  2000

2.  Synthesis and processing of tRNA-related SINE transcripts in Arabidopsis thaliana.

Authors:  Thierry Pélissier; Cécile Bousquet-Antonelli; Laurence Lavie; Jean-Marc Deragon
Journal:  Nucleic Acids Res       Date:  2004-07-28       Impact factor: 16.971

3.  Transcripts synthesized by RNA polymerase III can be polyadenylated in an AAUAAA-dependent manner.

Authors:  Olga R Borodulina; Dmitri A Kramerov
Journal:  RNA       Date:  2008-07-24       Impact factor: 4.942

4.  Functional mRNA can be generated by RNA polymerase III.

Authors:  S Gunnery; M B Mathews
Journal:  Mol Cell Biol       Date:  1995-07       Impact factor: 4.272

5.  RNA polymerase III defects suppress a conditional-lethal poly(A) polymerase mutation in Saccharomyces cerevisiae.

Authors:  M W Briggs; J S Butler
Journal:  Genetics       Date:  1996-07       Impact factor: 4.562

6.  Characterization of the structure, function, and mechanism of B2 RNA, an ncRNA repressor of RNA polymerase II transcription.

Authors:  Celso A Espinoza; James A Goodrich; Jennifer F Kugel
Journal:  RNA       Date:  2007-02-16       Impact factor: 4.942

7.  In vivo analysis of the stability and transport of nuclear poly(A)+ RNA.

Authors:  S Huang; T J Deerinck; M H Ellisman; D L Spector
Journal:  J Cell Biol       Date:  1994-08       Impact factor: 10.539

  7 in total

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