Literature DB >> 2842435

Abundant 5 kb RNA of human cytomegalovirus without a major translational reading frame.

B Plachter1, B Traupe, J Albrecht, G Jahn.   

Abstract

Although all herpesviruses are similar in their temporal regulation of gene expression, the organization of the immediate early (IE) genes varies markedly between the different members of the group. Most of the IE transcripts of human cytomegalovirus originate from a restricted region within the long unique segment of its linear dsDNA genome of 235 kb. One of the predominant transcripts from the IE region is a 5 kb RNA. Northern blot analyses revealed that this class of RNA is continuously present in infected cells. It was detected at high levels in IE and late RNA preparations, and in low amounts in early RNA preparations. It was not confined to the poly(A)+ fraction upon oligo(dT) selection, but also appeared in similar amounts in poly(A)- fractions. Fine mapping of this transcript was done by nuclease protection and primer extension. The RNA appeared to be unspliced, and no signals such as TATA or CCAAT, known to be important elements in eukaryotic RNA polymerase II promoters, were found close to the 5' end. Sequence analysis revealed multiple stop codons throughout the AT-rich potential coding region. Since no splicing was found to occur, the largest protein deduced from the DNA sequence would be of not more than 12,000 Mr. However, a computer program designed to detect protein-coding DNA sequences by codon usage did not reveal significant evidence for a protein encoded in this region. Therefore this RNA is likely to represent an unprecedented case of a large non-coding transcript present in cells that are lytically infected by an animal virus.

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Year:  1988        PMID: 2842435     DOI: 10.1099/0022-1317-69-9-2251

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  10 in total

1.  Coding potential of laboratory and clinical strains of human cytomegalovirus.

Authors:  Eain Murphy; Dong Yu; Jane Grimwood; Jeremy Schmutz; Mark Dickson; Michael A Jarvis; Gabriele Hahn; Jay A Nelson; Richard M Myers; Thomas E Shenk
Journal:  Proc Natl Acad Sci U S A       Date:  2003-12-01       Impact factor: 11.205

2.  Human cytomegalovirus with IE-2 (UL122) deleted fails to express early lytic genes.

Authors:  A Marchini; H Liu; H Zhu
Journal:  J Virol       Date:  2001-02       Impact factor: 5.103

3.  Human cytomegalovirus immediate-early two protein region involved in negative regulation of the major immediate-early promoter.

Authors:  T W Hermiston; C L Malone; M F Stinski
Journal:  J Virol       Date:  1990-07       Impact factor: 5.103

4.  Murine cytomegalovirus encodes a stable intron that facilitates persistent replication in the mouse.

Authors:  Caroline A Kulesza; Thomas Shenk
Journal:  Proc Natl Acad Sci U S A       Date:  2006-11-14       Impact factor: 11.205

5.  Sequences in the human cytomegalovirus 2.7-kilobase RNA promoter which mediate its regulation as an early gene.

Authors:  K M Klucher; D K Rabert; D H Spector
Journal:  J Virol       Date:  1989-12       Impact factor: 5.103

6.  Identification of binding sites for the 86-kilodalton IE2 protein of human cytomegalovirus within an IE2-responsive viral early promoter.

Authors:  H Arlt; D Lang; S Gebert; T Stamminger
Journal:  J Virol       Date:  1994-07       Impact factor: 5.103

7.  Human cytomegalovirus UL36-38 and US3 immediate-early genes: temporally regulated expression of nuclear, cytoplasmic, and polysome-associated transcripts during infection.

Authors:  D J Tenney; A M Colberg-Poley
Journal:  J Virol       Date:  1991-12       Impact factor: 5.103

8.  Discrete clusters of virus-encoded micrornas are associated with complementary strands of the genome and the 7.2-kilobase stable intron in murine cytomegalovirus.

Authors:  Amy H Buck; Javier Santoyo-Lopez; Kevin A Robertson; Diwakar S Kumar; Martin Reczko; Peter Ghazal
Journal:  J Virol       Date:  2007-10-10       Impact factor: 5.103

9.  In vivo and in vitro analysis of transcriptional activation mediated by the human cytomegalovirus major immediate-early proteins.

Authors:  K M Klucher; M Sommer; J T Kadonaga; D H Spector
Journal:  Mol Cell Biol       Date:  1993-02       Impact factor: 4.272

10.  Human cytomegalovirus 5-kilobase immediate-early RNA is a stable intron.

Authors:  Caroline A Kulesza; Thomas Shenk
Journal:  J Virol       Date:  2004-12       Impact factor: 5.103

  10 in total

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