Literature DB >> 16453705

The suffix sequence is involved in processing the 3' ends of different mRNAs in Drosophila melanogaster.

Nickolai A Tchurikov1, Alexander K Ebralidze, Georgii P Georgiev.   

Abstract

We describe here the nucleotide sequences of several genomic and mRNA copies of the suffix, a short dispersed actively transcribed repeat located at the 3' ends of many different genes of Drosophila melanogaster. Only one strand of the suffix is transcribed. The patterns of suffix-containing mRNAs vary during development. The five randomly selected genomic copies of the suffix are 265 bp long and quite conservative in their sequence. The non-transcribed strand is terminated with oligo(A) preceded by AATAAA sequence. No repetitive flanking sequences can be detected. The three other genomic copies selected by hybridization with suffix-containing cDNA clones are less conservative, especially in the 5' part. In particular, they contain short insertions carrying a polyadenylation signal AATAAA at exactly the same position of the suffix. Comparison of genomic and cDNA clones shows that mRNAs are polyadenylated at the last nucleotide of these insertions. The cDNA clones include the same part of the suffix, from the 39th to 112th nucleotide. Thus, a segment of the suffix forms the last exon for both genes. In one case, the beginning of the last intron coincides with the beginning of suffix, creating a very unusual donor splicing site. We conclude that the suffix sequence is directly involved in the formation of the last splicing site and 3'-end maturation of mRNA, at least in the case of the two genes analysed.

Entities:  

Year:  1986        PMID: 16453705      PMCID: PMC1167118          DOI: 10.1002/j.1460-2075.1986.tb04502.x

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  32 in total

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Authors:  K A Wharton; B Yedvobnick; V G Finnerty; S Artavanis-Tsakonas
Journal:  Cell       Date:  1985-01       Impact factor: 41.582

2.  On the structural organization of operon and the regulation of RNA synthesis in animal cells.

Authors:  G P Georgiev
Journal:  J Theor Biol       Date:  1969-12       Impact factor: 2.691

3.  Gene regulation for higher cells: a theory.

Authors:  R J Britten; E H Davidson
Journal:  Science       Date:  1969-07-25       Impact factor: 47.728

4.  The homeo box: a key to the understanding of development?

Authors:  W J Gehring
Journal:  Cell       Date:  1985-01       Impact factor: 41.582

5.  Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose.

Authors:  P S Thomas
Journal:  Proc Natl Acad Sci U S A       Date:  1980-09       Impact factor: 11.205

6.  The sequence 5'-AAUAAA-3'forms parts of the recognition site for polyadenylation of late SV40 mRNAs.

Authors:  M Fitzgerald; T Shenk
Journal:  Cell       Date:  1981-04       Impact factor: 41.582

7.  Message sequences and short repetitive sequences are interspersed in sea urchin egg poly(A)+ RNAs.

Authors:  F D Costantini; R J Britten; E H Davidson
Journal:  Nature       Date:  1980-09-11       Impact factor: 49.962

8.  Role of the conserved AAUAAA sequence: four AAUAAA point mutants prevent messenger RNA 3' end formation.

Authors:  M Wickens; P Stephenson
Journal:  Science       Date:  1984-11-30       Impact factor: 47.728

9.  Inhibition of RNA cleavage but not polyadenylation by a point mutation in mRNA 3' consensus sequence AAUAAA.

Authors:  C Montell; E F Fisher; M H Caruthers; A J Berk
Journal:  Nature       Date:  1983 Oct 13-19       Impact factor: 49.962

10.  Repetitive DNA sequences cotranscribed with developmentally regulated Dictyostelium discoideum mRNAs.

Authors:  C Zuker; H F Lodish
Journal:  Proc Natl Acad Sci U S A       Date:  1981-09       Impact factor: 11.205

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  9 in total

1.  NMR structure of a parallel-stranded DNA duplex at atomic resolution.

Authors:  V Rani Parvathy; Sukesh R Bhaumik; Kandala V R Chary; Girjesh Govil; Keliang Liu; Frank B Howard; H Todd Miles
Journal:  Nucleic Acids Res       Date:  2002-04-01       Impact factor: 16.971

2.  On the possibility of origin of a short element of Drosophila (suffix) from a related long retroelement (F element).

Authors:  O V Kretova; N A Tchurikov
Journal:  Dokl Biochem Biophys       Date:  2005 Jul-Aug       Impact factor: 0.788

3.  Mobile elements and transposition events in the cut locus of Drosophila melanogaster.

Authors:  N A Tchurikov; T I Gerasimova; T K Johnson; N I Barbakar; A L Kenzior; G P Georgiev
Journal:  Mol Gen Genet       Date:  1989-10

4.  Molecular analysis of transcription start sites of separate copies of the suffix short retroelement in genome of Drosophila.

Authors:  O S Zenina; D M Fedoseeva; O V Kretova; N A Tchurikov
Journal:  Dokl Biochem Biophys       Date:  2013-05-09       Impact factor: 0.788

5.  Characterization of transcribed dispersed repetitive DNAs in the nuclear genome of the green alga Chlamydomonas reinhardtii.

Authors:  A Day; J D Rochaix
Journal:  Curr Genet       Date:  1989-09       Impact factor: 3.886

6.  Related polypeptides are encoded by Drosophila F elements, I factors, and mammalian L1 sequences.

Authors:  P P Di Nocera; G Casari
Journal:  Proc Natl Acad Sci U S A       Date:  1987-08       Impact factor: 11.205

7.  Structural properties of g,t-parallel duplexes.

Authors:  Anna Aviñó; Elena Cubero; Raimundo Gargallo; Carlos González; Modesto Orozco; Ramon Eritja
Journal:  J Nucleic Acids       Date:  2010-02-21

8.  Both piRNA and siRNA pathways are silencing transcripts of the suffix element in the Drosophila melanogaster germline and somatic cells.

Authors:  Nickolai A Tchurikov; Olga V Kretova
Journal:  PLoS One       Date:  2011-07-14       Impact factor: 3.240

9.  Suffix-specific RNAi leads to silencing of F element in Drosophila melanogaster.

Authors:  Nickolai A Tchurikov; Olga V Kretova
Journal:  PLoS One       Date:  2007-05-30       Impact factor: 3.240

  9 in total

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