Diversity of murine gamma genes and expression in fetal and adult T lymphocytes
Abstract
The search for the genes encoding the T-cell receptor alpha and chains revealed a third gene, T gamma (ref. 1), which shares with t T alpha (refs 2-7) and T beta (refs 8-15) genes a number of structure features, including somatic rearrangement during T-cell development. T gamma gene expression appears to be unnecessary in son mature T cells and is at its greatest in fetal thymocytes encouraging speculation that T gamma has a role in T-cell development and may be involved in the recognition of polymorphic major histocompatibility complex (MHC) products during thymic education. One argument against the participation of T gamma in such a process has been its apparently limited diversity, due to the small number of gene segments available for rearrangement. We here describe the identification of additional T gamma V-gene segments and demonstrate that they can be rearranged to previously identified J- and C-gene segments and are expressed in fetal thymocytes. In addition we describe a variety of patterns of T gamma mRNA processing which may be significant for T gamma gene regulation.
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Heilig and Tonegawa's nomenclature proposed in 1986 segregated mouse γδ T cells into six distinct subsets: Vγ1, Vγ2, Vγ4, Vγ5, Vγ6, and Vγ7.
“Heilig and Tonegawa’s nomenclature proposed in 1986 segregated mouse γδ T cells into six distinct subsets: Vγ1, Vγ2, Vγ4, Vγ5, Vγ6, and Vγ7 (3).”
From Comparing Mouse and Human Tissue-Resident γδ T Cells (2022) · cites this paper as [3]
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References 49 · Cited by 448
- Authors
- Heilig, J. S., & Tonegawa, S.
- Affiliations
- Massachusetts Institute of Technology (US)
- ORCID
- Tonegawa, Susumu
- Venue
- Nature
- Published
- 1986-08
- Volume
- 322
- Issue
- 6082
- Pages
- 836-840
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2056615300
- Cited by
- 448
- References
- 49
- Citations by year
- 2026: 19 · 2025: 22 · 2024: 13 · 2023: 17 · 2022: 18 · 2021: 24 · 2020: 34 · 2019: 14 · 2018: 22 · 2017: 18 · 2016: 20 · 2015: 17 · 2014: 17 · 2013: 15 · 2012: 12
- FWCI
- 6.41
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (CA 28900, P30-CA14051-14, P30CA014051)
- National Institute of Allergy and Infectious Diseases (AII7879)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
- Keywords
- T cell receptor gamma chain, V gene segments, somatic rearrangements, fetal thymocytes, T cell development, thymic selection, major histocompatibility complex, gene expression, mRNA processing, gene expression regulation
- MeSH terms
- Animals, Base Sequence, DNA, Genes, Peptide Fragments, Receptors, Antigen, T-Cell, RNA Splicing, T-Lymphocytes, Thymus Gland, Receptors, Antigen, T-Cell, gamma-delta, Receptors, Antigen, T-Cell, alpha-beta, Mice
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