Literature DB >> 2411548

Formation of the 3' end of U1 snRNA is directed by a conserved sequence located downstream of the coding region.

N Hernandez.   

Abstract

U1 is a small non-polyadenylated nuclear RNA that is transcribed by RNA polymerase II and is known to play a role in mRNA splicing. The mature 3' end of U1 snRNA is formed in at least two steps. The first step generates precursors of U1 RNA with a few extra nucleotides at the 3' end; in the second step, these precursors are shortened to mature U1 RNA. Here, I have determined the sequences required for the first step. Human U1 genes with various deletions and substitutions near the 3' end of the coding region were constructed and introduced into HeLa cells by DNA transfection. The structure of the RNA synthesized during transient expression of the exogenous U1 gene was analyzed by S1 mapping. The results show that a 13 nucleotide sequence located downstream from the U1 coding region and conserved among U1, U2 and U3 genes of different species is the only sequence required to direct the first step in the formation of the 3' end of U1 snRNA.

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Year:  1985        PMID: 2411548      PMCID: PMC554424          DOI: 10.1002/j.1460-2075.1985.tb03857.x

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


  60 in total

1.  Small RNAs in the nucleus and cytoplasm of HeLa cells.

Authors:  G L Eliceiri; M S Sayavedra
Journal:  Biochem Biophys Res Commun       Date:  1976-09-20       Impact factor: 3.575

2.  Small RNA species of the HeLa cell: metabolism and subcellular localization.

Authors:  G Zieve; S Penman
Journal:  Cell       Date:  1976-05       Impact factor: 41.582

3.  Structure of the sea urchin U1 RNA repeat.

Authors:  D T Brown; G F Morris; N Chodchoy; C Sprecher; W F Marzluff
Journal:  Nucleic Acids Res       Date:  1985-01-25       Impact factor: 16.971

4.  Short-lived, small RNAs in the cytoplasm of HeLa cells.

Authors:  G L Eliceiri
Journal:  Cell       Date:  1974-09       Impact factor: 41.582

5.  Metabolism of small molecular weight monodisperse nuclear RNA.

Authors:  R Weinberg; S Penman
Journal:  Biochim Biophys Acta       Date:  1969-09-17

6.  Transcription of the mouse dihydrofolate reductase gene proceeds unabated through seven polyadenylation sites and terminates near a region of repeated DNA.

Authors:  E G Frayne; E J Leys; G F Crouse; A G Hook; R E Kellems
Journal:  Mol Cell Biol       Date:  1984-12       Impact factor: 4.272

7.  The primary transcription unit of the mouse beta-major globin gene.

Authors:  E Hofer; J E Darnell
Journal:  Cell       Date:  1981-02       Impact factor: 41.582

8.  The consensus sequence YGTGTTYY located downstream from the AATAAA signal is required for efficient formation of mRNA 3' termini.

Authors:  J McLauchlan; D Gaffney; J L Whitton; J B Clements
Journal:  Nucleic Acids Res       Date:  1985-02-25       Impact factor: 16.971

9.  The conserved CAAGAAAGA spacer sequence is an essential element for the formation of 3' termini of the sea urchin H3 histone mRNA by RNA processing.

Authors:  O Georgiev; M L Birnstiel
Journal:  EMBO J       Date:  1985-02       Impact factor: 11.598

10.  Human U2 and U1 RNA genes use similar transcription signals.

Authors:  G Westin; E Lund; J T Murphy; U Pettersson; J E Dahlberg
Journal:  EMBO J       Date:  1984-12-20       Impact factor: 11.598

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  96 in total

Review 1.  The 3' end formation in small RNAs.

Authors:  Karthika Perumal; Ram Reddy
Journal:  Gene Expr       Date:  2002

2.  Effect of 3' terminal adenylic acid residue on the uridylation of human small RNAs in vitro and in frog oocytes.

Authors:  Y Chen; K Sinha; K Perumal; R Reddy
Journal:  RNA       Date:  2000-09       Impact factor: 4.942

3.  Transcription of the human U2 snRNA genes continues beyond the 3' box in vivo.

Authors:  P Cuello; D C Boyd; M J Dye; N J Proudfoot; S Murphy
Journal:  EMBO J       Date:  1999-05-17       Impact factor: 11.598

4.  3'-box-dependent processing of human pre-U1 snRNA requires a combination of RNA and protein co-factors.

Authors:  Patricia Uguen; Shona Murphy
Journal:  Nucleic Acids Res       Date:  2004-06-01       Impact factor: 16.971

5.  Formation of the 3' end of sea urchin U1 small nuclear RNA occurs independently of the conserved 3' box and on transcripts initiated from a histone promoter.

Authors:  B J Wendelburg; W F Marzluff
Journal:  Mol Cell Biol       Date:  1992-09       Impact factor: 4.272

6.  3'-End polishing of the kinetoplastid spliced leader RNA is performed by SNIP, a 3'-->5' exonuclease with a Motley assortment of small RNA substrates.

Authors:  Gusti M Zeiner; Robert A Hitchcock; Nancy R Sturm; David A Campbell
Journal:  Mol Cell Biol       Date:  2004-12       Impact factor: 4.272

7.  In vitro analysis of a transcription termination site for RNA polymerase II.

Authors:  D K Wiest; D K Hawley
Journal:  Mol Cell Biol       Date:  1990-11       Impact factor: 4.272

8.  A subset of Drosophila integrator proteins is essential for efficient U7 snRNA and spliceosomal snRNA 3'-end formation.

Authors:  Nader Ezzeddine; Jiandong Chen; Bernhard Waltenspiel; Brandon Burch; Todd Albrecht; Ming Zhuo; William D Warren; William F Marzluff; Eric J Wagner
Journal:  Mol Cell Biol       Date:  2010-11-15       Impact factor: 4.272

9.  Identification of the major spliceosomal RNAs in Dictyostelium discoideum reveals developmentally regulated U2 variants and polyadenylated snRNAs.

Authors:  Andrea Hinas; Pontus Larsson; Lotta Avesson; Leif A Kirsebom; Anders Virtanen; Fredrik Söderbom
Journal:  Eukaryot Cell       Date:  2006-06

10.  UACUAAC is the preferred branch site for mammalian mRNA splicing.

Authors:  Y A Zhuang; A M Goldstein; A M Weiner
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

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