T cells play an important role in adaptive immunity. An enormous clonal diversity of T-cells with a different specificity, encoded by the T-cell receptor (TCR), protect the body against infection. Most TCR{beta} chains are generated from a V-, D-, and J-segment during recombination in the thymus. Although complete absence of the D-segment is not easily detectable from sequencing data, we find convincing evidence for a substantial proportion of TCR{beta} rearrangements lacking a D-segment. Additionally, sequences without a D-segment are more likely to be abundant within individuals and/or shared between individuals. We find that such sequences are preferentially generated during fetal development and persist within the elderly. Summarizing, TCR{beta} rearrangements without a D-segment are not uncommon, and tend to allow for TCR{beta} chains with a high abundance in the naive repertoire.
TCRβ rearrangements without D-segment are common, abundant and public
Published 2021 in bioRxiv
ABSTRACT
PUBLICATION RECORD
- Publication year
2021
- Venue
bioRxiv
- Publication date
2021-03-07
- Fields of study
Biology
- Identifiers
- External record
- Source metadata
Semantic Scholar
CITATION MAP
EXTRACTION MAP
CLAIMS
- No claims are published for this paper.
CONCEPTS
- No concepts are published for this paper.
REFERENCES
Showing 1-28 of 28 references · Page 1 of 1
CITED BY
- No citing papers are available for this paper.
Showing 0-0 of 0 citing papers · Page 1 of 1