Huang J, Muegge K
Laboratory of Molecular Immuneregulation, SAIC-FCRDC, National Cancer Institute, Frederick, Maryland, USA.
J Leukoc Biol. 2001 Jun;69(6):907-11.
IL-7 is a key factor for lymphoid development, and it contributes to V(D)J recombination at multiple loci in immune-receptor genes. IL-7 signal transduction, involving gamma(c) and Jak3, is required for successful recombination at the TCR-gamma locus. IL-7 signaling controls the initiation phase of V(D)J recombination by controlling access of the V(D)J recombinase to the locus. In the absence of IL-7, the TCR-gamma locus is methylated and packaged in a repressed form of chromatin consisting of hypoacetylated histones. IL-7 signaling likely increases the acetylation state of the nucleosomal core histones resulting in an "open" form of chromatin. This opening leads to a higher accessibility for the transcription machinery and increased accessibility of the Rag heterodimer that performs the cleavage of DNA.
白细胞介素-7是淋巴细胞发育的关键因子,它有助于免疫受体基因多个位点的V(D)J重组。TCR-γ位点成功重组需要涉及γ(c)和Jak3的白细胞介素-7信号转导。白细胞介素-7信号传导通过控制V(D)J重组酶与该位点的结合来控制V(D)J重组的起始阶段。在没有白细胞介素-7的情况下,TCR-γ位点被甲基化,并以由低乙酰化组蛋白组成的染色质抑制形式包装。白细胞介素-7信号传导可能会增加核小体核心组蛋白的乙酰化状态,从而导致染色质呈“开放”形式。这种开放导致转录机制具有更高的可及性,并增加了执行DNA切割的Rag异二聚体的可及性。