<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<STUDY_SET>
    <STUDY alias="DRP003797" center_name="RIKEN_CSRS" accession="DRP003797">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioProject ID">PRJDB5775</PRIMARY_ID>
        </IDENTIFIERS>
        <DESCRIPTOR>
            <STUDY_TITLE>T cell receptor J alpha repertoire analysis of V alpha2 and V alpha14 in wild type and Traj18-deletion mice.</STUDY_TITLE>
            <STUDY_TYPE existing_study_type="Other"/>
            <STUDY_ABSTRACT>A TCR alpha chain,V alpha14-J alpha18 (Trav11-Traj18), is selectively used in invariant natural killer T (iNKT) cells among alpha beta T cells. We have generated four lines, 1-1L, 1-1S, 1-2, and 2-1, of Traj18-deletion C57BL/6 mice by CRISPR/Cas9 and analyzed usage of Traj in CD4+ CD8+ CD69+ thymocytes by comparing the cells from wild type mice. We chose V alpha2-C alpha (Trav14-Trac) as a representative TCR alpha in alpha beta T cells and V alpha14-C alpha (Trav11-Trac) which contains iNKT-TCR alpha. Traj usage of V alpha2-C alpha in Traj18-deletion mice was same as wild type while V alpha14-C alpha has selective loss of Traj18, suggesting Traj18-deletion mice specifically lack iNKT cells but no influences in the development of alpha beta T cells.</STUDY_ABSTRACT>
            <CENTER_PROJECT_NAME>T cell receptor J alpha repertoire analysis of V alpha2 and V alpha14 in wild type and Traj18-deletion mice.</CENTER_PROJECT_NAME>
            <RELATED_STUDIES>
                <RELATED_STUDY>
                    <RELATED_LINK>
                        <DB>bioproject</DB>
                        <ID>PRJDB5775</ID>
                        <LABEL>PRJDB5775</LABEL>
                    </RELATED_LINK>
                    <IS_PRIMARY>true</IS_PRIMARY>
                </RELATED_STUDY>
            </RELATED_STUDIES>
            <STUDY_DESCRIPTION>A TCR alpha chain,V alpha14-J alpha18 (Trav11-Traj18), is selectively used in invariant natural killer T (iNKT) cells among alpha beta T cells. We have generated four lines, 1-1L, 1-1S, 1-2, and 2-1, of Traj18-deletion C57BL/6 mice by CRISPR/Cas9 and analyzed usage of Traj in CD4+ CD8+ CD69+ thymocytes by comparing the cells from wild type mice. We chose V alpha2-C alpha (Trav14-Trac) as a representative TCR alpha in alpha beta T cells and V alpha14-C alpha (Trav11-Trac) which contains iNKT-TCR alpha. Traj usage of V alpha2-C alpha in Traj18-deletion mice was same as wild type while V alpha14-C alpha has selective loss of Traj18, suggesting Traj18-deletion mice specifically lack iNKT cells but no influences in the development of alpha beta T cells.</STUDY_DESCRIPTION>
        </DESCRIPTOR>
    </STUDY>
</STUDY_SET>
