The DOI matches its Crossref record; 29 of the 29 references it cites were found in a registry or an index.
RAG-1 and RAG-2, Adjacent Genes That Synergistically Activate V(D)J Recombination
Abstract
The vast repertoire of immunoglobulins and T cell receptors is generated, in part, by V(D)J recombination, a series of genomic rearrangements that occur specifically in developing lymphocytes. The recombination activating gene, RAG-1, which is a gene expressed exclusively in maturing lymphoid cells, was previously isolated. RAG-1 inefficiently induced V(D)J recombinase activity when transfected into fibroblasts, but cotransfection with an adjacent gene, RAG-2, has resulted in at least a 1000-fold increase in the frequency of recombination. The 2.1-kilobase RAG-2 complementary DNA encodes a putative protein of 527 amino acids whose sequence is unrelated to that of RAG-1. Like RAG-1, RAG-2 is conserved between species that carry out V(D)J recombination, and its expression pattern correlates precisely with that of V(D)J recombinase activity. In addition to being located just 8 kilobases apart, these convergently transcribed genes are unusual in that most, if not all, of their coding and 3′ untranslated sequences are contained in single exons. RAG-1 and RAG-2 might activate the expression of the V(D)J recombinase but, more likely, they directly participate in the recombination reaction.
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Metadata
- Authors
- Oettinger, M. A., Schatz, D. G., Gorka, C., & Baltimore, D.
- Venue
- Science
- Published
- 1990-06-22
- Volume
- 248
- Issue
- 4962
- Pages
- 1517-1523
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2068012172
- Cited by
- 1,456
- References
- 29
- FWCI
- 23.64
- Type
- journal article
- Language
- en
- Open access
- closed
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- Oettinger, M. A., Schatz, D. G., Gorka, C., & Baltimore, D. (1990). RAG-1 and RAG-2, Adjacent Genes That Synergistically Activate V(D)J Recombination. Science. https://doi.org/10.1126/science.2360047
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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