Regulated immunoglobulin (Ig) RNA processing does not require specific cis-acting sequences: non-Ig RNA can be alternatively processed in B cells and plasma cells
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[1] R. Seipelt,et al. Alternative processing of IgA pre-mRNA responds like IgM to alterations in the efficiency of the competing splice and cleavage-polyadenylation reactions. , 1995, Molecular immunology.
[2] J. Lis,et al. The concentration of B52, an essential splicing factor and regulator of splice site choice in vitro, is critical for Drosophila development , 1994, Molecular and cellular biology.
[3] S. Rowan,et al. The A1 and A1B proteins of heterogeneous nuclear ribonucleoparticles modulate 5' splice site selection in vivo. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[4] T. Dang,et al. Role of differential mRNA stability in the regulated expression of IgM and IgD. , 1994, Journal of immunology.
[5] M. Peiter,et al. Exon size affects competition between splicing and cleavage-polyadenylation in the immunoglobulin mu gene , 1994, Molecular and cellular biology.
[6] A. Krainer,et al. General splicing factor SF2/ASF promotes alternative splicing by binding to an exonic splicing enhancer. , 1993, Genes & development.
[7] M. Rosenfeld,et al. Control of calcitonin/calcitonin gene-related peptide pre-mRNA processing by constitutive intron and exon elements , 1993, Molecular and cellular biology.
[8] Xiang-Dong Fu. Specific commitment of different pre-mRNAs to splicing by single SR proteins , 1993, Nature.
[9] A. Zahler,et al. Distinct functions of SR proteins in alternative pre-mRNA splicing. , 1993, Science.
[10] J. Nevins,et al. Alternative poly(A) site utilization during adenovirus infection coincides with a decrease in the activity of a poly(A) site processing factor , 1993, Molecular and cellular biology.
[11] Susan M. Berget,et al. Are vertebrate exons scanned during splice-site selection? , 1992, Nature.
[12] M B Roth,et al. SR proteins: a conserved family of pre-mRNA splicing factors. , 1992, Genes & development.
[13] C. Milcarek,et al. Regulated expression of the mouse gamma 2b Ig H chain gene is influenced by polyA site order and strength. , 1992, Journal of immunology.
[14] D. Toppmeyer,et al. Plasma cell-regulated polyadenylation at the Ig gamma 2b secretion-specific poly(A) site. , 1992, Journal of immunology.
[15] M. Peterson. Balanced efficiencies of splicing and cleavage-polyadenylation are required for mu-s and mu-m mRNA regulation. , 1992, Gene expression.
[16] N. Proudfoot,et al. A pause site for RNA polymerase II is associated with termination of transcription. , 1991, The EMBO journal.
[17] M. L. Peterson,et al. 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 , 1991, Molecular and cellular biology.
[18] Y. Shimura,et al. Repositioning of an alternative exon sequence of mouse IgM pre-mRNA activates splicing of the preceding intron. , 1991, Gene expression.
[19] S. Tilghman,et al. Role of alpha-fetoprotein regulatory elements in transcriptional activation in transient heterokaryons , 1990, Molecular and cellular biology.
[20] J. Manley,et al. A protein factor, ASF, controls cell-specific alternative splicing of SV40 early pre-mRNA in vitro , 1990, Cell.
[21] Adrian R. Krainer,et al. The essential pre-mRNA splicing factor SF2 influences 5′ splice site selection by activating proximal sites , 1990, Cell.
[22] C. Gorman,et al. Intervening sequences increase efficiency of RNA 3' processing and accumulation of cytoplasmic RNA. , 1990, Nucleic acids research.
[23] S. Berget,et al. Exon definition may facilitate splice site selection in RNAs with multiple exons. , 1990, Molecular and cellular biology.
[24] P. Sharp,et al. Regulation by HIV Rev depends upon recognition of splice sites , 1989, Cell.
[25] J. G. Patton,et al. Scanning from an independently specified branch point defines the 3′ splice site of mammalian introns , 1989, Nature.
[26] N. Proudfoot,et al. Definition of an efficient synthetic poly(A) site. , 1989, Genes & development.
[27] R. Perry,et al. Importance of introns for expression of mouse ribosomal protein gene rpL32 , 1989, Molecular and cellular biology.
[28] A. Buchman,et al. Comparison of intron-dependent and intron-independent gene expression , 1988, Molecular and cellular biology.
[29] T. Mitsuhashi,et al. Alternative splicing generates messages encoding rat c-erbA proteins that do not bind thyroid hormone. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[30] J. Nevins,et al. Splice site selection dominates over poly(A) site choice in RNA production from complex adenovirus transcription units. , 1988, The EMBO journal.
[31] J. Nevins,et al. 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. , 1987, Genes & development.
[32] L. J. Korn,et al. Effects of intron length on differential processing of mouse mu heavy-chain mRNA , 1987, Molecular and cellular biology.
[33] L. J. Korn,et al. Regulation of differential processing of mouse immunoglobulin mu heavy-chain mRNA. , 1987, Nucleic acids research.
[34] M. Aebi,et al. Sequence requirements for splicing of higher eukaryotic nuclear pre-mRNA , 1986, Cell.
[35] D. Lavery,et al. Cell-type-specific synthesis of murine immunoglobulin mu RNA from an adenovirus vector , 1986, Molecular and cellular biology.
[36] R. Perry,et al. Characterization of the multigene family encoding the mouse S16 ribosomal protein: strategy for distinguishing an expressed gene from its processed pseudogene counterparts by an analysis of total genomic DNA , 1985, Molecular and cellular biology.
[37] R. Grosschedl,et al. Cell-type specificity of iminunoglobulin gene expression is regulated by at least three DNA sequence elements , 1985, Cell.
[38] J. Chebath,et al. 3' end structure of the human (2'-5') oligo A synthetase gene: prediction of two distinct proteins with cell type-specific expression. , 1985, Nucleic acids research.
[39] L. Hood,et al. DNA sequence of the mouse H-2Dd transplantation antigen gene. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[40] K. Nishikura,et al. Synthesis of two mRNAs by utilization of alternate polyadenylation sites: expression of SV40‐mouse immunoglobulin mu chain gene recombinants in Cos monkey cells. , 1984, The EMBO journal.
[41] F. Blattner,et al. The molecular biology of immunoglobulin D , 1984, Nature.
[42] P Berg,et al. Transformation of mammalian cells to antibiotic resistance with a bacterial gene under control of the SV40 early region promoter. , 1982, Journal of molecular and applied genetics.
[43] F. Blattner,et al. Mouse IgA heavy chain gene sequence: implications for evolution of immunoglobulin hinge axons. , 1981, Proceedings of the National Academy of Sciences of the United States of America.
[44] D. Kemp,et al. Transcripts of the immunoglobulin C mu gene vary in structure and splicing during lymphoid development. , 1980, Proceedings of the National Academy of Sciences of the United States of America.
[45] Y. Bergman,et al. Induction of secretion of IgM from cells of the B cell line 38c-13 by somatic cell hybridization. , 1979, Journal of immunology.
[46] R. Laskov,et al. Induction of amplified synthesis and secretion of IgM by fusion of murine 'b lymphoma with myeloma cells. , 1979, Proceedings of the National Academy of Sciences of the United States of America.
[47] U. Schibler,et al. The synthesis and processing of the messenger RNAs specifying heavy and light chain immunoglobulins in MPC-11 cells , 1978, Cell.