Literature DB >> 1826045

The developmentally regulated shift from membrane to secreted mu mRNA production is accompanied by an increase in cleavage-polyadenylation efficiency but no measurable change in splicing efficiency.

M L Peterson1, E R Gimmi, R P Perry.   

Abstract

To determine whether there are any developmental changes in the efficiencies of cleavage-polyadenylation or splicing reactions that could affect the usage of weak (suboptimal) processing signals and thus provide a basis for the regulated production of mu m versus mu s mRNA during B-lymphocyte maturation, we studied the expression of transfected mu genes in which the natural competition between cleavage-polyadenylation and splicing was replaced by alternative usage of tandem weak and strong poly(A) sites or by competition between suboptimal and optimal 5' splice junctions. Our results indicate that there is a 50 to 100% increase in cleavage-polyadenylation efficiency but no measurable change in splicing efficiency as maturation proceeds from the B-cell to plasma cell stage.

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Year:  1991        PMID: 1826045      PMCID: PMC359942          DOI: 10.1128/mcb.11.4.2324-2327.1991

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  12 in total

1.  Regulated production of mu m and mu s mRNA requires linkage of the poly(A) addition sites and is dependent on the length of the mu s-mu m intron.

Authors:  M L Peterson; R P Perry
Journal:  Proc Natl Acad Sci U S A       Date:  1986-12       Impact factor: 11.205

2.  A role for exon sequences and splice-site proximity in splice-site selection.

Authors:  R Reed; T Maniatis
Journal:  Cell       Date:  1986-08-29       Impact factor: 41.582

3.  The regulated production of mu m and mu s mRNA is dependent on the relative efficiencies of mu s poly(A) site usage and the c mu 4-to-M1 splice.

Authors:  M L Peterson; R P Perry
Journal:  Mol Cell Biol       Date:  1989-02       Impact factor: 4.272

4.  Regulation of differential processing of mouse immunoglobulin mu heavy-chain mRNA.

Authors:  N Tsurushita; N M Avdalovic; L J Korn
Journal:  Nucleic Acids Res       Date:  1987-06-11       Impact factor: 16.971

5.  Transcriptional and posttranscriptional control of immunoglobulin mRNA production during B lymphocyte development.

Authors:  D E Kelley; R P Perry
Journal:  Nucleic Acids Res       Date:  1986-07-11       Impact factor: 16.971

6.  Relative position and strengths of poly(A) sites as well as transcription termination are critical to membrane versus secreted mu-chain expression during B-cell development.

Authors:  G Galli; J W Guise; M A McDevitt; P W Tucker; J R Nevins
Journal:  Genes Dev       Date:  1987-07       Impact factor: 11.361

7.  A secondary structure at the 3' splice site affects the in vitro splicing reaction of mouse immunoglobulin mu chain pre-mRNAs.

Authors:  A Watakabe; K Inoue; H Sakamoto; Y Shimura
Journal:  Nucleic Acids Res       Date:  1989-10-25       Impact factor: 16.971

8.  A compensatory base change in U1 snRNA suppresses a 5' splice site mutation.

Authors:  Y Zhuang; A M Weiner
Journal:  Cell       Date:  1986-09-12       Impact factor: 41.582

9.  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

10.  Alternative expression of secreted and membrane forms of immunoglobulin mu-chain is regulated by transcriptional termination in stable plasmacytoma transfectants.

Authors:  J W Guise; P L Lim; D Yuan; P W Tucker
Journal:  J Immunol       Date:  1988-06-01       Impact factor: 5.422

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  26 in total

1.  hnRNP F influences binding of a 64-kilodalton subunit of cleavage stimulation factor to mRNA precursors in mouse B cells.

Authors:  K L Veraldi; G K Arhin; K Martincic; L H Chung-Ganster; J Wilusz; C Milcarek
Journal:  Mol Cell Biol       Date:  2001-02       Impact factor: 4.272

Review 2.  Developmental regulation of immunoglobulin mRNA processing and the IgA response: establishing a paradigm.

Authors:  D A Lebman; J H Coyle
Journal:  Immunol Res       Date:  1999       Impact factor: 2.829

3.  Regulation of nuclear poly(A) addition controls the expression of immunoglobulin M secretory mRNA.

Authors:  C Phillips; S Jung; S I Gunderson
Journal:  EMBO J       Date:  2001-11-15       Impact factor: 11.598

4.  Balanced efficiencies of splicing and cleavage-polyadenylation are required for mu-s and mu-m mRNA regulation.

Authors:  M L Peterson
Journal:  Gene Expr       Date:  1992

5.  B-cell and plasma-cell splicing differences: a potential role in regulated immunoglobulin RNA processing.

Authors:  Shirley R Bruce; R W Cameron Dingle; Martha L Peterson
Journal:  RNA       Date:  2003-10       Impact factor: 4.942

6.  Two distant upstream regions containing cis-acting signals regulating splicing facilitate 3'-end processing of avian sarcoma virus RNA.

Authors:  J T Miller; C M Stoltzfus
Journal:  J Virol       Date:  1992-07       Impact factor: 5.103

7.  U1A inhibits cleavage at the immunoglobulin M heavy-chain secretory poly(A) site by binding between the two downstream GU-rich regions.

Authors:  Catherine Phillips; Niseema Pachikara; Samuel I Gunderson
Journal:  Mol Cell Biol       Date:  2004-07       Impact factor: 4.272

8.  Non-snRNP U1A levels decrease during mammalian B-cell differentiation and release the IgM secretory poly(A) site from repression.

Authors:  Jianglin Ma; Samuel I Gunderson; Catherine Phillips
Journal:  RNA       Date:  2006-01       Impact factor: 4.942

9.  Polypyrimidine tract binding protein prevents activity of an intronic regulatory element that promotes usage of a composite 3'-terminal exon.

Authors:  Vincent Anquetil; Caroline Le Sommer; Agnès Méreau; Sandra Hamon; Hubert Lerivray; Serge Hardy
Journal:  J Biol Chem       Date:  2009-09-17       Impact factor: 5.157

Review 10.  Alternative poly(A) site selection in complex transcription units: means to an end?

Authors:  G Edwalds-Gilbert; K L Veraldi; C Milcarek
Journal:  Nucleic Acids Res       Date:  1997-07-01       Impact factor: 16.971

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