Organization of the human T cell receptor [zeta]/[eta] gene and its genetic linkage to the Fc[gamma]RII-Fc[gamma]RIII gene cluster
- DCBDC/National Cancer Institute National Institutes of Health, Bethesda, MD (United States)
- National Cancer Institute, FCRDC, National Institute of Health, Frederick, MD (United States)
- Program Resources Inc./DynCorp, FCRDC, Frederick, MD (United States)
- DCBDC/NCI NIH, Bethesda, MD (United States) DCBDC/National Cancer Institute National Institute of Health, Bethesda, MD (United States)
The [zeta]-subunit is the most recently characterized stoichiometric human TCR component. In this study the authors describe the molecular organization of the human [zeta]-gene. The [zeta] transcript is generated as the spliced product of eight exons that are separated by distances of 0.7 kb to more than 8 kb. Ribonuclease protection studies revealed multiple transcription initiation sites distributed over a range of approximately 115 bases. A variable number tandem repeat restriction fragment polymorphism contained within the structural gene has allowed for the localization of [zeta] within the human genome. Additionally, a restriction fragment polymorphism within the Fc[gamma]RII-Fc[gamma]RIII gene cluster has allowed for its localization on the map of human chromosome 1q and for the establishment of its linkage to the [zeta]-gene locus. A region that is highly homologous on a nucleotide level with the [eta]-exon of the murine [zeta]-gene is localized to the 3[prime] region of the human [zeta]-gene. Surprisingly, translation of this region into protein results in a structure that is markedly divergent from its murine counterpart. This finding has important implications regarding the potential role of [eta] in T cell function. 60 refs., 7 figs., 1 tab.
- OSTI ID:
- 6965090
- Journal Information:
- Journal of Immunology; (United States), Vol. 148:8; ISSN 0022-1767
- Country of Publication:
- United States
- Language:
- English
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550400* - Genetics