Hawwari Abbas, Bock Cheryl, Krangel Michael S
The Department of Immunology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Nat Immunol. 2005 May;6(5):481-9. doi: 10.1038/ni1189. Epub 2005 Apr 3.
Assembly of the gene encoding T cell receptor alpha (Tcra) is characterized by an orderly progression of primary and secondary V(alpha)-to-J(alpha) recombination events across the J(alpha) array, but the targeting mechanisms responsible for this progression are mostly unknown. Studies have shown that the T early-alpha promoter is important in targeting primary Tcra rearrangements. We found that T early-alpha and a previously unknown promoter associated with J(alpha)49 targeted primary recombination to discrete sets of constant alpha region (C(alpha))-distal J(alpha) segments and together directed nearly all normal primary recombination events. Furthermore, deletion of the T early-alpha promoter activated previously suppressed downstream promoters and stimulated primary rearrangement to centrally located J(alpha) segments. Central promoter derepression also occurred after primary rearrangement, thereby providing a mechanism to target secondary recombination events.
编码T细胞受体α(Tcra)的基因组装的特征是,初级和次级V(α)到J(α)重组事件在J(α)阵列上有序进行,但负责这种进展的靶向机制大多未知。研究表明,T早期α启动子在靶向初级Tcra重排中很重要。我们发现,T早期α和一个与J(α)49相关的先前未知的启动子将初级重组靶向到离散的恒定α区域(C(α))-远端J(α)片段组,并共同指导了几乎所有正常的初级重组事件。此外,T早期α启动子的缺失激活了先前被抑制的下游启动子,并刺激初级重排至位于中央的J(α)片段。初级重排后也发生了中央启动子去抑制,从而提供了一种靶向次级重组事件的机制。