University of Illinois at Urbana-Champaign
Mechanisms of generating T cell receptor diversity
Abstract
dc:descriptionT cells are able to respond to foreign antigens by means of a diverse repertoire of antigen-specific receptors (T cell receptors or TCRs). There are two classes of TCRs (αβ and γδ) that are found on mutually exclusive populations of T cells. Diversity in each receptor subunit (α, β, γ, or δ) is generated by several mechanisms with the key process being gene rearrangement. Sequence analysis of TCR subunits has revealed a region that is variable in amino acid composition and is equivalent to the third complementary determining region (CDR3) found in immunoglobulins (Igs). This region is encoded at the position where gene segments join and it has been shown to be important in defining specificity of an Ig or TCR for antigen. The mechanisms of generating diversity at this junction include the deletion of nucleotides from the ends of the genes and/or addition of nucleotides in this region. It has not been determined if both αβ and γδ T cells use the same recombinational machinery in these processes.
Degree
thesis:*- Name thesis:degree_name
- Ph.D.
- Level thesis:degree_level
- Dissertation
- Discipline thesis:degree_discipline
- Biochemistry
- Grantor
- University of Illinois at Urbana-Champaign
- Year dc:date
- 2011
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Holman, Philmore Omar
- Contributors dc:contributor
-
- Kranz, David M.
Subjects
dc:subject × 2Rights
dc:rights- Statement dc:rights
-
- Copyright 1995 Holman, Philmore Omar
- Language dc:language
- eng
Identifiers
dc:identifier.*- Identifier
-
AAI9543607
(UMI)AAI9543607 - OAI identifier oai:identifier
- oai:www.ideals.illinois.edu:2142/21379