Literature DB >> 501800

Synthesis and processing of adenoviral RNA in isolated nuclei.

V W Yang, S J Flint.   

Abstract

Adenoviral RNA sequences synthesized in nuclei isolated during the late phase of productive infection comprise, besides virus-associated, VA, RNA, five major species, ranging in size from approximately 13S to 55S. The latter RNA species is of the length predicted if the major transcriptional unit expressed during the late phase were completely copied in vitro. Some 30% of the RNA sequences labeled in vitro are polyadenylated, and about one-third of the polyadenylated RNA is virus specific. Hybridization analysis of the sequences immediately adjacent to polyadenylic acid in late RNA labeled in isolated nuclei suggests that polyadenylation in vitro occurs at the same sites recognized within the cell. The polyadenylic acid-containing viral RNA sequences made in isolated nuclei are found in three major species of RNA, sedimenting at approximately 28S, 18S, and 13S. These sizes are remarkably similar to those reported for late mRNA species, suggesting that additional processing steps can occur in isolated nuclei. Hybridization of RNA to XhoI fragments of adenovirus type 2 DNA transferred to nitrocellulose filters reveals that sequences complementary to the region from 22.0 to 26.5 units present in 55S RNA are absent from all smaller species, suggesting that the smaller RNA species labeled in isolated nuclei are generated by splicing. The splicing events necessary to generate the 5' leader segment common to the majority of late adenoviral mRNA species are shown to be performed correctly in isolated nuclei.

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Year:  1979        PMID: 501800      PMCID: PMC353570     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  45 in total

1.  RNA aggregation during sulfhydryl-agarose chromatography of mercurated RNA.

Authors:  D A Konkel; V M Ingram
Journal:  Nucleic Acids Res       Date:  1977-06       Impact factor: 16.971

2.  Detection of two restriction endonuclease activities in Haemophilus parainfluenzae using analytical agarose--ethidium bromide electrophoresis.

Authors:  P A Sharp; B Sugden; J Sambrook
Journal:  Biochemistry       Date:  1973-07-31       Impact factor: 3.162

3.  Alpha-amanitin: a specific inhibitor of one of two DNA-pendent RNA polymerase activities from calf thymus.

Authors:  C Kedinger; M Gniazdowski; J L Mandel; F Gissinger; P Chambon
Journal:  Biochem Biophys Res Commun       Date:  1970-01-06       Impact factor: 3.575

4.  Size distribution of polyadenylated adenovirus 2 RNA synthesized in isolated nuclei.

Authors:  S G Zimmer; C J Goldenberg; D P Carlson; E A Craig; H J Raskas
Journal:  Biochemistry       Date:  1978-10-03       Impact factor: 3.162

5.  Coincidence of the promoter and capped 5' terminus of RNA from the adenovirus 2 major late transcription unit.

Authors:  E B Ziff; R M Evans
Journal:  Cell       Date:  1978-12       Impact factor: 41.582

6.  Steps in the processing of Ad2 mRNA: poly(A)+ nuclear sequences are conserved and poly(A) addition precedes splicing.

Authors:  J R Nevins; J E Darnell
Journal:  Cell       Date:  1978-12       Impact factor: 41.582

7.  RNA synthesis in isolated nuclei: in vitro initiation of adenovirus 2 major late mRNA precursor.

Authors:  J L Manley; P A Sharp; M L Gefter
Journal:  Proc Natl Acad Sci U S A       Date:  1979-01       Impact factor: 11.205

8.  Mapping of adenovirus late promoters with nascent mercurated RNA.

Authors:  R Weinmann; L O Aiello
Journal:  Proc Natl Acad Sci U S A       Date:  1978-04       Impact factor: 11.205

9.  Mercurated nucleotides: assessment of a new tool to study RNA synthesis and processing in isolated nuclei.

Authors:  K P Schäfer
Journal:  Nucleic Acids Res       Date:  1977-12       Impact factor: 16.971

10.  Spliced segments at the 5' terminus of adenovirus 2 late mRNA.

Authors:  S M Berget; C Moore; P A Sharp
Journal:  Proc Natl Acad Sci U S A       Date:  1977-08       Impact factor: 11.205

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  11 in total

1.  Nuclei of adenovirus 2-infected cells contain an RNA species that corresponds to an intron excised intact from mRNA precursors.

Authors:  R Rosenthal; H J Raskas
Journal:  Mol Cell Biol       Date:  1985-05       Impact factor: 4.272

2.  Splice junctions in adenovirus 2 early region 4 mRNAs: multiple splice sites produce 18 to 24 RNAs.

Authors:  M A Tigges; H J Raskas
Journal:  J Virol       Date:  1984-04       Impact factor: 5.103

3.  Assembly of nuclear ribonucleoprotein particles during in vitro transcription.

Authors:  I V Economidis; T Pederson
Journal:  Proc Natl Acad Sci U S A       Date:  1982-03       Impact factor: 11.205

4.  RNA metabolism in isolated nuclei: processing and transport of immunoglobulin light chain sequences.

Authors:  C Otegui; R J Patterson
Journal:  Nucleic Acids Res       Date:  1981-09-25       Impact factor: 16.971

5.  Could poly(A) align the splicing sites of messenger RNA precursors?

Authors:  M Bina; R J Feldmann; R G Deeley
Journal:  Proc Natl Acad Sci U S A       Date:  1980-03       Impact factor: 11.205

6.  A small nuclear ribonucleoprotein is required for splicing of adenoviral early RNA sequences.

Authors:  V W Yang; M R Lerner; J A Steitz; S J Flint
Journal:  Proc Natl Acad Sci U S A       Date:  1981-03       Impact factor: 11.205

7.  Transcription and processing of adenoviral RNA by extracts from HeLa cells.

Authors:  B Weingärtner; W Keller
Journal:  Proc Natl Acad Sci U S A       Date:  1981-07       Impact factor: 11.205

8.  Deletion of the nontransforming Epstein-Barr virus strain P3HR-1 causes fusion of the large internal repeat to the DSL region.

Authors:  G W Bornkamm; J Hudewentz; U K Freese; U Zimber
Journal:  J Virol       Date:  1982-09       Impact factor: 5.103

9.  Effect of adenovirus infection on expression of human histone genes.

Authors:  S J Flint; M A Plumb; U C Yang; G S Stein; J L Stein
Journal:  Mol Cell Biol       Date:  1984-07       Impact factor: 4.272

10.  Expression of adenovirus-2 early region 4: assignment of the early region 4 polypeptides to their respective mRNAs, using in vitro translation.

Authors:  M A Tigges; H J Raskas
Journal:  J Virol       Date:  1982-12       Impact factor: 5.103

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