التفاصيل البيبلوغرافية
| العنوان: |
V(D)J Recombinase-Mediated TCR β Locus Gene Usage and Coding Joint Processing in Peripheral T Cells during Perinatal and Pediatric Development. |
| المؤلفون: |
Murray, Janet M.1, Messier, Terri2, Rivers, Jami2, O'Neill, J. Patrick2, Walker, Vernon E.3, Vacek, Pamela M.4, Finette, Barry A.1,5 barry.finette@uvm.edu |
| المصدر: |
Journal of Immunology. 9/1/2012, Vol. 189 Issue 5, p2356-2364. 9p. |
| مصطلحات موضوعية: |
*RECOMBINASES, *T cell receptors, *NUCLEOTIDE sequence, *GENE rearrangement, *ETIOLOGY of diseases, *CHILD development, LEUKEMIA immunology |
| مستخلص: |
The generation of TCR proteins is the result of V(D)J recombinase-mediated genomic rearrangements at recombination signal sequences (RSS) in human lymphocytes. V(D)J recombinase can also mediate rearrangements at nonimmune or "cryptic" RSS in normal and leukemic human peripheral T cells. We previously demonstrated age- and gender-specific developmental differences in V(D)J coding joint processing at cryptic RSS within the HPRT locus in peripheral T cells from healthy children (Murray et al. 2006. /. Immunol. 177: 5393-5404). In this study, we investigated developmentally specific V(D)J recombinase TCRß immune gene rearrangements and coding joint processing at RSS in peripheral T cells in the same pediatric population. This approach provided a unique opportunity to investigate site-specific V(D)J recombinase rearrangements and coding joint processing at immune and nonimmune genes from the same individual T cell population. We determined the genomic sequence of 244 TCRß coding junctions from 112 (63 male, 49 female) subjects from the late stages of fetal development through 9 y of age. We observed both age- and gender-specific V(D)J recombinase-mediated TCRß gene usage and coding joint processing at immune RSS. To the best of our knowledge, these data represent the first description of age- and gender-specific developmental differences in TCR gene usage and coding joint processing that could directly influence TCR diversity and immune specificity. It will be important for future studies to ascertain the mechanistic etiology of these developmental and gender differences in TCR diversity and specificity, as well as their importance with respect to the age and gender risks for infectious and autoimmune diseases in humans. [ABSTRACT FROM AUTHOR] |
| قاعدة البيانات: |
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