Home LiteratureArticle Details
PMID: 2565533 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

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.

Molecular and cellular biology ·Vol. 9 ·No. 2 ·1989-02-00 ·Pages 726-38

Peterson ML, Perry RP

Abstract

The relative abundance of the mRNAs encoding the membrane (mu m) and secreted (mu s) forms of immunoglobulin mu heavy chain is regulated during B-cell maturation by a change in the mode of RNA processing. Current models to explain this regulation involve either competition between cleavage-polyadenylation at the proximal (mu s) poly(A) site and cleavage-polyadenylation at the distal (mu m) poly(A) site [poly(A) site model] or competition between cleavage-polyadenylation at the mu s poly(A) site and splicing of the C mu 4 and M1 exons, which eliminates the mu s site (mu s site-splice model). To test certain predictions of these models and to determine whether there is a unique structural feature of the mu s poly(A) site that is essential for regulation, we constructed modified mu genes in which the mu s or mu m poly(A) site was replaced by other poly(A) sites and then studied the transient expression of these genes in cells representative of both early- and late-stage lymphocytes. Substitutions at the mu s site dramatically altered the relative usage of this site and caused corresponding reciprocal changes in the usage of the mu m site. Despite these changes, use of the proximal site was still usually higher in plasmacytomas than in pre-B cells, indicating that regulation does not depend on a unique feature of the mu s poly(A) site. Replacement of the distal (mu m) site had no detectable effect on the usage of the mu s site in either plasmacytomas or pre-B cells. These findings are inconsistent with the poly(A) site model. In addition, we noted that in a wide variety of organisms, the sequence at the 5' splice junction of the C mu 4-to-M1 intron is significantly different from the consensus 5' splice junction sequence and is therefore suboptimal with respect to its complementary base pairing with U1 small nuclear RNA. When we mutated this suboptimal sequence into the consensus sequence, the mu mRNA production in plasmacytoma cells was shifted from predominantly mu s to exclusively mu m. This result unequivocally demonstrated that splicing of the C mu 4-to-M1 exon is in competition with usage of the mu s poly(A) site. A key feature of this regulatory phenomenon appears to be the appropriately balanced efficiencies of these two processing reactions. Consistent with predictions of the mu s site-splice model, B cells were found to contain mu m precursor RNA that had undergone the C mu 4-to-M1 splice but had not yet been polyadenylated at the mu m site.

MeSH Terms
Animals B-Lymphocytes/immunology,metabolism Base Sequence Cell Line Chimera Gene Expression Regulation Immunoglobulin mu-Chains/genetics Models, Biological Mutation Poly A/genetics,metabolism RNA Processing, Post-Transcriptional RNA Splicing RNA, Messenger/biosynthesis,genetics,metabolism
Chemicals
Immunoglobulin mu-Chains RNA, Messenger Poly A
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Peterson M L
Institue for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
Perry R P
References (59)
59 references, click to expand
  1. Changes in size and secondary structure of the ribosomal transcription unit during vertebrate evolution.
    J Mol Biol. 1975 May 25;94(3):503-17 PMID: 809590
  2. A novel RNA in which the 5' end is generated by cleavage at the poly(A) site of immunoglobulin heavy-chain secreted mRNA.
    Mol Cell Biol. 1986 Dec;6(12):4749-52 PMID: 2879225
  3. Steps in the processing of Ad2 mRNA: poly(A)+ nuclear sequences are conserved and poly(A) addition precedes splicing.
    Cell. 1978 Dec;15(4):1477-93 PMID: 729004
  4. The synthesis and processing of the messenger RNAs specifying heavy and light chain immunoglobulins in MPC-11 cells.
    Cell. 1978 Dec;15(4):1495-509 PMID: 103631
  5. Synthesis of secreted and membrane-bound immunoglobulin mu heavy chains is directed by mRNAs that differ at their 3' ends.
    Cell. 1980 Jun;20(2):293-301 PMID: 6771018
  6. Two mRNAs can be produced from a single immunoglobulin mu gene by alternative RNA processing pathways.
    Cell. 1980 Jun;20(2):313-9 PMID: 6771020
  7. An adenovirus mutant defective in splicing RNA from early region 1A.
    Nature. 1981 Jun 11;291(5815):508-10 PMID: 6262659
  8. Nuclear RNA is spliced in the absence of poly(A) addition.
    Cell. 1981 Oct;26(1 Pt 1):39-46 PMID: 6976837
  9. Correlation of hnRNP structure and nascent transcript cleavage.
    Cell. 1981 Oct;26(2 Pt 2):155-65 PMID: 6174239
  10. Characterization of productive and sterile transcripts from the immunoglobulin heavy-chain locus: processing of micron and muS mRNA.
    Mol Cell Biol. 1983 Jul;3(7):1317-32 PMID: 6412070
  11. Nucleotide sequence of the constant region of a chicken mu heavy chain immunoglobulin mRNA.
    Nucleic Acids Res. 1983 Aug 25;11(16):5381-9 PMID: 6310496
  12. Functional immunoglobulin M production after transfection of cloned immunoglobulin heavy and light chain genes into lymphoid cells.
    Proc Natl Acad Sci U S A. 1983 Oct;80(20):6351-5 PMID: 6312453
  13. Mode of regulation of immunoglobulin mu- and delta-chain expression varies during B-lymphocyte maturation.
    Cell. 1984 Feb;36(2):329-38 PMID: 6319016
  14. The molecular biology of immunoglobulin D.
    Nature. 1984 Feb 2-8;307(5950):417-22 PMID: 6420708
  15. Transcriptional regulation of the mu-delta heavy chain locus in normal murine B lymphocytes.
    J Exp Med. 1984 Aug 1;160(2):564-83 PMID: 6206182
  16. The sequence of the human immunoglobulin mu-delta intron reveals possible vestigial switch segments.
    Nucleic Acids Res. 1984 Aug 24;12(16):6523-35 PMID: 6089118
  17. Transcription termination and 3' processing: the end is in site!
    Cell. 1985 Jun;41(2):349-59 PMID: 2580642
  18. 3' end structure of the human (2'-5') oligo A synthetase gene: prediction of two distinct proteins with cell type-specific expression.
    Nucleic Acids Res. 1985 Feb 25;13(4):1267-81 PMID: 2860635
  19. The "spliceosome": yeast pre-messenger RNA associates with a 40S complex in a splicing-dependent reaction.
    Science. 1985 May 24;228(4702):963-7 PMID: 3890181
  20. Splice commitment dictates neuron-specific alternative RNA processing in calcitonin/CGRP gene expression.
    Cell. 1987 Feb 13;48(3):517-24 PMID: 2879637
  21. Splicing of messenger RNA precursors.
    Science. 1987 Feb 13;235(4790):766-71 PMID: 3544217
  22. Regulation of differential processing of mouse immunoglobulin mu heavy-chain mRNA.
    Nucleic Acids Res. 1987 Jun 11;15(11):4603-15 PMID: 3108856
  23. Effects of intron length on differential processing of mouse mu heavy-chain mRNA.
    Mol Cell Biol. 1987 Jul;7(7):2602-5 PMID: 2886909
  24. RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression.
    Nucleic Acids Res. 1987 Sep 11;15(17):7155-74 PMID: 3658675
  25. The natural 5' splice site of simian virus 40 large T antigen can be improved by increasing the base complementarity to U1 RNA.
    Mol Cell Biol. 1987 Aug;7(8):3018-20 PMID: 2823114
  26. 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.
    Genes Dev. 1987 Jul;1(5):471-81 PMID: 3119424
  27. 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.
    Proc Natl Acad Sci U S A. 1987 Dec;84(23):8306-10 PMID: 3479794
  28. Protein-binding site at the immunoglobulin mu membrane polyadenylylation signal: possible role in transcription termination.
    Proc Natl Acad Sci U S A. 1987 Dec;84(24):9160-4 PMID: 3122214
  29. Nuclear factors in B lymphoma enhance splicing of mouse membrane-bound mu mRNA in Xenopus oocytes.
    Science. 1988 Jan 29;239(4839):494-7 PMID: 3124268
  30. The coupling between enhancer activity and hypomethylation of kappa immunoglobulin genes is developmentally regulated.
    Mol Cell Biol. 1988 Feb;8(2):930-7 PMID: 3127693
  31. Amino acid sequence of heavy chain from Xenopus laevis IgM deduced from cDNA sequence: implications for evolution of immunoglobulin domains.
    Proc Natl Acad Sci U S A. 1988 Apr;85(7):2245-9 PMID: 2451244
  32. Poly(A) site choice rather than splice site choice governs the regulated production of IgM heavy-chain RNAs.
    Proc Natl Acad Sci U S A. 1988 Apr;85(8):2439-43 PMID: 3128787
  33. A functional mRNA polyadenylation signal is required for transcription termination by RNA polymerase II.
    Genes Dev. 1988 Apr;2(4):440-52 PMID: 2836265
  34. Alternative expression of secreted and membrane forms of immunoglobulin mu-chain is regulated by transcriptional termination in stable plasmacytoma transfectants.
    J Immunol. 1988 Jun 1;140(11):3988-94 PMID: 3131424
  35. Processing at immunoglobulin polyadenylation sites in lymphoid cell extracts.
    EMBO J. 1988 May;7(5):1421-9 PMID: 2900759
  36. Complete structure and organization of immunoglobulin heavy chain constant region genes in a phylogenetically primitive vertebrate.
    EMBO J. 1988 Jul;7(7):1979-88 PMID: 3138109
  37. Splice site selection dominates over poly(A) site choice in RNA production from complex adenovirus transcription units.
    EMBO J. 1988 Jul;7(7):2107-16 PMID: 3416835
  38. Splice site selection, rate of splicing, and alternative splicing on nascent transcripts.
    Genes Dev. 1988 Jun;2(6):754-65 PMID: 3138163
  39. Transcription of the unrearranged mouse C kappa locus: sequence of the initiation region and comparison of activity with a rearranged V kappa-C kappa gene.
    Cell. 1981 Dec;27(3 Pt 2):593-602 PMID: 6101210
  40. Organization and reorganization of immunoglobulin genes in A-MULV-transformed cells: rearrangement of heavy but not light chain genes.
    Cell. 1981 Dec;27(2 Pt 1):381-90 PMID: 6277505
  41. Mouse IgA heavy chain gene sequence: implications for evolution of immunoglobulin hinge axons.
    Proc Natl Acad Sci U S A. 1981 Dec;78(12):7684-8 PMID: 6801659
  42. Production of RNA for secreted immunoglobulin mu chains does not require transcriptional termination 5' to the microM exons.
    Nature. 1983 Jan 6;301(5895):84-6 PMID: 6185845
  43. Human beta-globin pre-mRNA synthesized in vitro is accurately spliced in Xenopus oocyte nuclei.
    Cell. 1983 Mar;32(3):681-94 PMID: 6550524
  44. Specific transcription and RNA splicing defects in five cloned beta-thalassaemia genes.
    Nature. 1983 Apr 14;302(5909):591-6 PMID: 6188062
  45. Cell-type specificity of immunoglobulin gene expression is regulated by at least three DNA sequence elements.
    Cell. 1985 Jul;41(3):885-97 PMID: 3924411
  46. Human 2-5A synthetase: characterization of a novel cDNA and corresponding gene structure.
    EMBO J. 1985 Jul;4(7):1761-8 PMID: 2411547
  47. Phylogenetic conservation of immunoglobulin heavy chains: direct comparison of hamster and mouse Cmu genes.
    Nucleic Acids Res. 1985 Aug 12;13(15):5611-28 PMID: 2994005
  48. RNP particles at splice junction sequences on Drosophila chorion transcripts.
    Cell. 1985 Nov;43(1):143-51 PMID: 3935315
  49. Role of an RNA cleavage/poly(A) addition site in the production of membrane-bound and secreted IgM mRNA.
    Proc Natl Acad Sci U S A. 1985 Dec;82(24):8658-62 PMID: 3936040
  50. Tandem kappa immunoglobulin promoters are equally active in the presence of the kappa enhancer: implications for models of enhancer function.
    Cell. 1986 Jul 18;46(2):253-62 PMID: 3087628
  51. Transcriptional and posttranscriptional control of immunoglobulin mRNA production during B lymphocyte development.
    Nucleic Acids Res. 1986 Jul 11;14(13):5431-47 PMID: 3090517
  52. A compensatory base change in U1 snRNA suppresses a 5' splice site mutation.
    Cell. 1986 Sep 12;46(6):827-35 PMID: 3757028
  53. Procedures for in vitro DNA mutagenesis of human leukocyte interferon sequences.
    Methods Enzymol. 1986;119:403-15 PMID: 3762406
  54. Immunoelectron microscope visualization of nuclear ribonucleoprotein antigens within spread transcription complexes.
    J Cell Biol. 1986 Oct;103(4):1153-7 PMID: 2945824
  55. Cell-type-specific synthesis of murine immunoglobulin mu RNA from an adenovirus vector.
    Mol Cell Biol. 1986 Jan;6(1):123-33 PMID: 3097501
  56. The role of nucleotide sequences in splice site selection in eukaryotic pre-messenger RNA.
    Nature. 1986 Nov 20-26;324(6094):280-2 PMID: 2946960
  57. 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.
    Proc Natl Acad Sci U S A. 1986 Dec;83(23):8883-7 PMID: 3097638
  58. Alpha-thalassaemia caused by a poly(A) site mutation reveals that transcriptional termination is linked to 3' end processing in the human alpha 2 globin gene.
    EMBO J. 1986 Nov;5(11):2915-22 PMID: 3024968
  59. The genome of simian virus 40.
    Science. 1978 May 5;200(4341):494-502 PMID: 205947
Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1989-02-00
Pages
726-38
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC362650
Subset
IM
Grants
NIAID NIH HHS · AI-17330 · United States
NCI NIH HHS · CA-06927 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com