Multiple immunoglobulin heavy-chain gene transcripts in Abelson murine leukemia virus-transformed lymphoid cell lines

Author:

Alt F W,Rosenberg N,Enea V,Siden E,Baltimore D

Abstract

Lymphoid cells transformed by Abelson murine leukemia virus (A-MuLV) contain three classes of RNA transcripts from immunoglobulin mu genes. P mu-mRNAs (productive) correspond to the normal 2.7-kilobase (kb) membrane (mu m) and 2.4-kb secreted (mu s) mu mRNA species both in size and coding capacity and occur at approximately equal abundance in most mu-positive (pre-B-like) A-MuLV transformants. A mu-mRNAs (aberrant) generally fall into one of two categories--aberrantly small 2.3-kb mu m and 2.0-kb mu s mRNAs which encode aberrantly small mu polypeptide chains, or normal-sized, V H-containing mu RNAs which do not encode immunologically identifiable mu polypeptide chains. In one case, the latter type of A mu-mRNA was demonstrated to result from an in-phase termination codon in the D segment of the mu mRNA. Also, most, if not all, A-MuLV transformants express members of a 3.0 to 1.9-kb set of C mu-containing, but V H-negative S mu-RNAs (for sterile), the expression of which may occur simultaneously with but independently of P mu-mRNAs or A mu-mRNAs. The S mu-RNA sequences do not encode immunologically identifiable mu chains and can be produced by cells with unrearranged heavy-chain alleles, such as T-lymphocytes, although the structure of the S mu-RNAs from T-lymphoid cells appears to be different from that of B-lymphoid cell S mu-RNAs. Certain A-MuLV transformants also express gamma-RNA sequences that are probably analogous to the three different forms of mu RNA. These data support the concept that heavy-chain allelic exclusion, like that of light chains, is not mediated by control at the DNA or RNA levels but is probably a consequence of feedback control from cytoplasmic mu chains.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

Reference53 articles.

1. Synthesis of secreted and membrane-bound immunoglobulin mu heavy chains is directed by mRNAs that differ at their 3'- ends;Alt F. W.;Cell,1980

2. Alt F. W. V. Enea A. L. M. Bothwell and D. Baltimore. 1979. Probes for specific mRNAs by subtractive hybridization: anomalous expression of immunoglobulin genes p. 407-419. In T. Maniatis R. Axel and C. F. Fox (ed.) Eukaryotic gene regulation vol. 14. Academic Press Inc. New York.

3. Activity of multiple light chain genes in murine myeloma lines expressing a single, functional light chain;Alt F. W.;Cell,1980

4. Alt F. W. N. Rosenberg R. Casanova E. Thomas and D. Balimore. 1982. Immunoglobulin heavy chain class switching and lipopolysaccharide-dependent heavy chain expression in derivatives of an Abelson murine leukemia virus-transformed cell line. Nature (London) in press.

5. Alt F. W. N. E. Rosenberg S. Lewis R. J. Casanova and D. Baltimore. 1981. Variation in immunoglobulin heavy and light chain gene expression in a cloned Abelson murine leukemia virus-transformed cell line p. 33-41. In N. Klinman D. Mosier I. Scher and E. S. Vitetta (ed.) B Iymphocytes in the immune response. Elsevier/North Holland New York.

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