| First Author | Ku CJ | Year | 2017 |
| Journal | Mol Cell Biol | Volume | 37 |
| Issue | 12 | PubMed ID | 28320875 |
| Mgi Jnum | J:244976 | Mgi Id | MGI:5913755 |
| Doi | 10.1128/MCB.00052-17 | Citation | Ku CJ, et al. (2017) GATA3 Abundance Is a Critical Determinant of T Cell Receptor beta Allelic Exclusion. Mol Cell Biol 37(12) |
| abstractText | Allelic exclusion describes the essential immunological process by which feedback repression of sequential DNA rearrangements ensures that only one autosome expresses a functional T or B cell receptor. In wild-type mammals, approximately 60% of cells have recombined the DNA of one T cell receptor beta (TCRbeta) V-to-DJ-joined allele in a functional configuration, while the second allele has recombined only the DJ sequences; the other 40% of cells have recombined the V to the DJ segments on both alleles, with only one of the two alleles predicting a functional TCRbeta protein. Here we report that the transgenic overexpression of GATA3 leads predominantly to biallelic TCRbeta gene (Tcrb) recombination. We also found that wild-type immature thymocytes can be separated into distinct populations based on intracellular GATA3 expression and that GATA3LO cells had almost exclusively recombined only one Tcrb locus (that predicted a functional receptor sequence), while GATA3HI cells had uniformly recombined both Tcrb alleles (one predicting a functional and the other predicting a nonfunctional rearrangement). These data show that GATA3 abundance regulates the recombination propensity at the Tcrb locus and provide new mechanistic insight into the historic immunological conundrum for how Tcrb allelic exclusion is mediated. |
