Literature DB >> 8259677

Analysis of figwort mosaic virus (plant pararetrovirus) polyadenylation signal.

H Sanfaçon1.   

Abstract

Analysis of the cauliflower mosaic virus (CaMV) polyadenylation (poly(A)) signal has revealed several striking differences to poly(A) signals from animal genes such as the absence of activating sequences downstream from the cleavage site. Instead, upstream sequences were shown to induce recognition of an AAUAAA sequence. To test whether these features are representative of other plant pararetrovirus poly(A) signals, a characterization of the figwort mosaic virus (FMV) poly(A) signal is presented here. The FMV RNAs were isolated from infected plants and mapped, and the different elements composing the FMV poly(A) signal were identified. Multiple upstream sequences were found to be essential for efficient processing at the FMV poly(A) site and could be replaced by the CaMV upstream elements. The FMV upstream sequences showed homologies to other characterized upstream sequences from CaMV, from animal viruses, and from plant poly(A) signals. Surprisingly, neither the FMV nor the CaMV upstream elements could induce recognition of an AAUAAA sequence present in the FMV poly(A) signal, instead a UAUAAA sequence 55 nucleotides further downstream was utilized. It is proposed that additional features may be required for appropriate cleavage such as the context of the AAUAAA-like sequence or perhaps the cleavage site itself.

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Year:  1994        PMID: 8259677     DOI: 10.1006/viro.1994.1006

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  16 in total

1.  Patterns of variant polyadenylation signal usage in human genes.

Authors:  E Beaudoing; S Freier; J R Wyatt; J M Claverie; D Gautheret
Journal:  Genome Res       Date:  2000-07       Impact factor: 9.043

2.  A near-upstream element in a plant polyadenylation signal consists of more than six nucleotides.

Authors:  Q Li; A G Hunt
Journal:  Plant Mol Biol       Date:  1995-08       Impact factor: 4.076

3.  Alternatively spliced mRNA variants of chloroplast ascorbate peroxidase isoenzymes in spinach leaves.

Authors:  K Yoshimura; Y Yabuta; M Tamoi; T Ishikawa; S Shigeoka
Journal:  Biochem J       Date:  1999-02-15       Impact factor: 3.857

Review 4.  Plant mRNA 3'-end formation.

Authors:  H M Rothnie
Journal:  Plant Mol Biol       Date:  1996-10       Impact factor: 4.076

5.  A composite polyadenylation signal with TATA box function.

Authors:  N Paran; A Ori; I Haviv; Y Shaul
Journal:  Mol Cell Biol       Date:  2000-02       Impact factor: 4.272

6.  Efficient transcription from the rice tungro bacilliform virus promoter requires elements downstream of the transcription start site.

Authors:  G Chen; H M Rothnie; X He; T Hohn; J Fütterer
Journal:  J Virol       Date:  1996-12       Impact factor: 5.103

7.  Molecular cloning and expression of a cDNA sequence encoding histidinol phosphate aminotransferase from Nicotiana tabacum.

Authors:  F El Malki; V Frankard; M Jacobs
Journal:  Plant Mol Biol       Date:  1998-08       Impact factor: 4.076

8.  Sequence and spatial requirements for the tissue- and species-independent 3'-end processing mechanism of plant mRNA.

Authors:  L Wu; T Ueda; J Messing
Journal:  Mol Cell Biol       Date:  1994-10       Impact factor: 4.272

Review 9.  Genetic elements of plant viruses as tools for genetic engineering.

Authors:  A R Mushegian; R J Shepherd
Journal:  Microbiol Rev       Date:  1995-12

10.  The Epstein-Barr virus (EBV) SM protein enhances pre-mRNA processing of the EBV DNA polymerase transcript.

Authors:  S C Key; T Yoshizaki; J S Pagano
Journal:  J Virol       Date:  1998-11       Impact factor: 5.103

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