Literature DB >> 729004

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

J R Nevins, J E Darnell.   

Abstract

The conservation of nuclear Ad2 sequences during nucleocytoplasmic transport has been estimated from the accumulation of 3H-uridine in nuclear and cytoplasmic Ad2-specific RNA from the major late transcription unit. From 10-28% is conserved of the total Ad2 nuclear RNA synthesized from each of five regions of the genome that specify groups of 3' co-terminal mRNAs. The sum of the conservation of all the regions was equivalent to 100%, signifying the conservation of at least a part of each transcript or all of about one fifth to one sixth of the transcripts. The conservation of poly(A)+ Ad2 nuclear RNA is about 4 times greater than of total Ad2 nuclear RNA, approaching 100% conservation of poly(A)+ nuclear sequences. Since each mRNA contains three "spliced" sequences that are probably encoded only once per transcript, these data on conservation of the Ad2 sequences suggest that each transcriptional event from the 16-99 transcription unit gives rise to one of a possible 13-14 mRNA molecules with destruction of the remainder of the transcribed RNA. The portion which is conserved resides next to the region to which which poly(A) is added. Three models for the choice of poly(A) sites were considered: termination at the poly(A) site, cleavage shortly after synthesis of one of the sites before transcription was complete, and cleavage after completion of transcription. The first model was ruled out by the demonstration of equimolar synthesis over the 16-99 region. The second model is strongly supported because 3H-uridine label appears equally rapidly in the time range 2-10 min in each of the five 3' poly(A) addition sites, whereas chain completion before cleavage would lead to a faster appearance of label in the most promoter-distal site. Furthermore, briefly labeled RNA molecules extending from 16 to each of several poly(A) addition sites were the first poly(A)- terminated 3H-uridine-labeled molecules detected, demonstrating that poly(A) addition precedes splicing. The choice of which mRNA emerges from each transcriptional event would appear to depend upon first choosing one of five 3' mRNA ends followed by a 5' splicing event.

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Year:  1978        PMID: 729004     DOI: 10.1016/0092-8674(78)90071-5

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  162 in total

Review 1.  Formation of mRNA 3' ends in eukaryotes: mechanism, regulation, and interrelationships with other steps in mRNA synthesis.

Authors:  J Zhao; L Hyman; C Moore
Journal:  Microbiol Mol Biol Rev       Date:  1999-06       Impact factor: 11.056

2.  Regulated adenovirus mRNA 3'-end formation in a coupled in vitro transcription-processing system.

Authors:  S I Wilson-Gunn; J E Kilpatrick; M J Imperiale
Journal:  J Virol       Date:  1992-09       Impact factor: 5.103

3.  Differential utilization of poly (A) signals between DHFR alleles in CHL cells.

Authors:  K W Scotto; H Yang; J P Davide; P W Melera
Journal:  Nucleic Acids Res       Date:  1992-12-25       Impact factor: 16.971

4.  Intron enhancement of gene expression and the splicing efficiency of introns in maize cells.

Authors:  K R Luehrsen; V Walbot
Journal:  Mol Gen Genet       Date:  1991-01

Review 5.  Viral and cellular interactions during adenovirus DNA replication.

Authors:  Matthew Charman; Christin Herrmann; Matthew D Weitzman
Journal:  FEBS Lett       Date:  2019-12-17       Impact factor: 4.124

6.  Polyadenylation precedes splicing in vitro.

Authors:  M Niwa; S M Berget
Journal:  Gene Expr       Date:  1991-04

7.  Maturation of polycistronic pre-mRNA in Trypanosoma brucei: analysis of trans splicing and poly(A) addition at nascent RNA transcripts from the hsp70 locus.

Authors:  J Huang; L H van der Ploeg
Journal:  Mol Cell Biol       Date:  1991-06       Impact factor: 4.272

8.  Partial block to transcription of human adenovirus type 2 late genes in abortively infected monkey cells.

Authors:  J M Johnston; K P Anderson; D F Klessig
Journal:  J Virol       Date:  1985-11       Impact factor: 5.103

9.  Calcitonin mRNA polymorphism: peptide switching associated with alternative RNA splicing events.

Authors:  M G Rosenfeld; C R Lin; S G Amara; L Stolarsky; B A Roos; E S Ong; R M Evans
Journal:  Proc Natl Acad Sci U S A       Date:  1982-03       Impact factor: 11.205

10.  Structure of nuclear ribonucleoprotein: heterogeneous nuclear RNA is complexed with a major sextet of proteins in vivo.

Authors:  I V Economidis; T Pederson
Journal:  Proc Natl Acad Sci U S A       Date:  1983-03       Impact factor: 11.205

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