Literature DB >> 1620589

Alternative 3' processing of Xenopus alpha-tubulin mRNAs; efficient use of a CAUAAA polyadenylation signal.

K G Rabbitts1, G T Morgan.   

Abstract

The Xenopus laevis alpha-tubulin gene X alpha T14 produces two mRNAs of 1.7 and 2.15 kb and we have shown that this is due to the use, at approximately equal frequency, of alternative 3' processing sites. Unusually, the hexanucleotide polyadenylation signal responsible for use of the downstream site, pA2, is CAUAAA in contrast to the consensus AAUAAA used at the upstream site, pA1. Since such a variant hexanucleotide would normally be expected to reduce drastically the efficiency of 3' processing, we have examined the 3' flanking sequences involved in pA2 usage in injected oocytes. In deletion mutants with 40 bp or 440 bp of 3' flanking DNA use of pA2 was almost totally abolished whereas when 770 bp of the natural flank was present pA2 was used normally. This polyadenylation signal therefore requires an unexpectedly large amount of flanking DNA and we have identified in the required region a member of a novel family of 450 bp interspersed repeats that we have termed Pir elements. We speculate that because of the variant hexanucleotide efficient use of pA2 has to be potentiated by the Pir element, perhaps through an effect on transcriptional pausing or termination.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1620589      PMCID: PMC312421          DOI: 10.1093/nar/20.12.2947

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  36 in total

1.  Point mutations in AAUAAA and the poly (A) addition site: effects on the accuracy and efficiency of cleavage and polyadenylation in vitro.

Authors:  M D Sheets; S C Ogg; M P Wickens
Journal:  Nucleic Acids Res       Date:  1990-10-11       Impact factor: 16.971

2.  The complete sequence of a frog alpha-tubulin gene and its regulated expression in mouse L-cells.

Authors:  D J Smith
Journal:  Biochem J       Date:  1988-01-15       Impact factor: 3.857

3.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.

Authors:  P Chomczynski; N Sacchi
Journal:  Anal Biochem       Date:  1987-04       Impact factor: 3.365

4.  A poly(A) addition site and a downstream termination region are required for efficient cessation of transcription by RNA polymerase II in the mouse beta maj-globin gene.

Authors:  J Logan; E Falck-Pedersen; J E Darnell; T Shenk
Journal:  Proc Natl Acad Sci U S A       Date:  1987-12       Impact factor: 11.205

5.  Position-dependent sequence elements downstream of AAUAAA are required for efficient rabbit beta-globin mRNA 3' end formation.

Authors:  A Gil; N J Proudfoot
Journal:  Cell       Date:  1987-05-08       Impact factor: 41.582

6.  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

7.  Premature termination of transcription from the P1 promoter of the mouse c-myc gene.

Authors:  S Wright; L F Mirels; M C Calayag; J M Bishop
Journal:  Proc Natl Acad Sci U S A       Date:  1991-12-15       Impact factor: 11.205

8.  Mutations downstream of the polyadenylation site of a Xenopus beta-globin mRNA affect the position but not the efficiency of 3' processing.

Authors:  P J Mason; J A Elkington; M M Lloyd; M B Jones; J G Williams
Journal:  Cell       Date:  1986-07-18       Impact factor: 41.582

9.  Sequences capable of restoring poly(A) site function define two distinct downstream elements.

Authors:  M A McDevitt; R P Hart; W W Wong; J R Nevins
Journal:  EMBO J       Date:  1986-11       Impact factor: 11.598

10.  Polyadenylation of the Xenopus beta 1 globin mRNA at a downstream minor site in the absence of the major site and utilization of an AAUACA polyadenylation signal.

Authors:  P J Mason; M B Jones; J A Elkington; J G Williams
Journal:  EMBO J       Date:  1985-01       Impact factor: 11.598

View more
  7 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.  Characterization of the 3' untranslated region of the mouse homeobox gene HoxB5.

Authors:  C C Yu; C J Paige; G E Wu
Journal:  Experientia       Date:  1995-06-14

3.  Alternative polyadenylation coordinates embryonic development, sexual dimorphism and longitudinal growth in Xenopus tropicalis.

Authors:  Xiang Zhou; Yangzi Zhang; Jennifer J Michal; Lujiang Qu; Shuwen Zhang; Mark R Wildung; Weiwei Du; Derek J Pouchnik; Hui Zhao; Yin Xia; Honghua Shi; Guoli Ji; Jon F Davis; Gary D Smith; Michael D Griswold; Richard M Harland; Zhihua Jiang
Journal:  Cell Mol Life Sci       Date:  2019-02-07       Impact factor: 9.261

4.  Organization and expression of bovine TSPY.

Authors:  T Vogel; F Dechend; E Manz; C Jung; S Jakubiczka; S Fehr; J Schmidtke; F Schnieders
Journal:  Mamm Genome       Date:  1997-07       Impact factor: 2.957

5.  Genes encoding isoforms of transcription elongation factor TFIIS in Xenopus and the use of multiple unusual RNA processing signals.

Authors:  K E Plant; A Hair; G T Morgan
Journal:  Nucleic Acids Res       Date:  1996-09-15       Impact factor: 16.971

6.  Tissue specific expression and cDNA structure of a human transcript encoding a nucleic acid binding [oligo(dC)] protein related to the pre-mRNA binding protein K.

Authors:  H C Aasheim; T Loukianova; A Deggerdal; E B Smeland
Journal:  Nucleic Acids Res       Date:  1994-03-25       Impact factor: 16.971

7.  Regulatory role of the 3' untranslated region (3'UTR) of rat 5' deiodinase (D1). effects on messenger RNA translation and stability.

Authors:  Omar Arroyo-Helguera; Carmen Mejía-Viggiano; Alfredo Varela-Echavarría; Marcos Cajero-Juárez; Carmen Aceves
Journal:  Endocrine       Date:  2005-08       Impact factor: 3.925

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.