NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE105129 Query DataSets for GSE105129
Status Public on Nov 24, 2017
Title The somatically generated T cell receptor CDR3a contributes to the MHC allele specificity of the T cell receptor
Organism Mus musculus
Experiment type Other
Summary Mature T cells bearing ab T cell receptors react with foreign antigens bound to alleles of major histocompatibility complex proteins (MHC) that they were exposed to during their development in the thymus, a phenomenon known as positive selection. The structural basis for positive selection has long been debated. Here, using mice expressing one of two different T cell receptor b chains and various MHC alleles, we show that positive selection-induced MHC bias of T cell receptors is affected both by the germline encoded elements of the T cell receptor a and b chain and, surprisingly, dramatically affected by the non germ line encoded CDR3 of the T cell receptor a chain. Thus, in addition to determining specificity for antigen, the non germline encoded elements of T cell receptors may help the proteins cope with the extremely polymorphic nature of major histocompatibility complex products within the species.
 
Overall design Naïve CD4 T cells were isolated from mice expressing a single T cell receptor b chain and one of 3 different alleles of MHCII. The T cell receptor a chains on these cells were sequenced and their sequences compared. Comparisons were also made in the use of different elements, the TRAVs, TRAJs and non germ line encoded CDR3 of the T cell receptor alpha chains.
 
Contributor(s) Marrack P, Krovi SH, Silberman D, White J, Kushnir E, Nakayama M, Crook J, Danhorn T, Leach SM, Anselment R, Scott-Browne J, Gapin L, Kappler JW
Citation(s) 29148973
NIH grant(s)
Grant ID Grant title Affiliation Name
R01 AI018785 Characteristics of T Cell Receptors NATIONAL JEWISH HEALTH Philippa C. Marrack
R01 DK099317 Molecular Dissection of Insulin Targeting in Anti-Islet Autoimmunity UNIVERSITY OF COLORADO DENVER Maki Nakayama
R01 AI092108 iNKT Cell Recognition of Endogenous Lipid Antigens UNIVERSITY OF COLORADO DENVER Laurent Gapin
T32 AI007405 Training Program in Immunology UNIVERSITY OF COLORADO DENVER Raul M Torres
Submission date Oct 18, 2017
Last update date Jul 25, 2021
Contact name Philippa Marrack
E-mail(s) marrackp@njhealth.org
Phone 303 398 1324
Organization name National Jewish Health
Department Biomedical Research
Lab Marrack
Street address 1400 Jackson St
City Denver
State/province CO
ZIP/Postal code 80206
Country USA
 
Platforms (3)
GPL16331 Ion Torrent PGM (Mus musculus)
GPL16815 454 GS FLX Titanium (Mus musculus)
GPL21744 454 GS Junior (Mus musculus)
Samples (27)
GSM2819740 B6.AKR
GSM2819741 B6.NOD
GSM2819742 b DOb48A m2
Relations
BioProject PRJNA414890
SRA SRP120370

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE105129_RAW.tar 152.5 Mb (http)(custom) TAR (of TXT)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap