| Autor: |
Mosier, D E, Stell, K L, Gulizia, R J, Torbett, B E, Gilmore, G L |
| Zdroj: |
The Journal of Experimental Medicine; January 1993, Vol. 177 Issue: 1 p191-194, 4p |
| Abstrakt: |
The autosomal recessive scid mutation results in defective immunoglobulin and T cell receptor gene rearrangement. The scid mutation occurred in the allotype congenic C.B-17 line, and up to 25% of C.B-17 scid mice spontaneously produce both T cells and immunoglobulin, a phenotype known as "leaky." Moreover, introduction of neonatal T cells into C.B-17 scid mice leads to immunoglobulin production by 100% of animals. We have produced mice homozygous for both the scid and beige mutations. By contrast with C.B-17 scid mice, BALB/c scid.beige mice have a < 2% incidence of "leakiness." This percentage does not increase with age, and introduction of neonatal T cells fails to rescue immunoglobulin production. This suggests that a gene (or genes) closely linked to the beige locus regulates B and/or T cell development. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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