Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
J Immunol. 2011 May 1;186(9):5356-66. doi: 10.4049/jimmunol.1003794. Epub 2011 Mar 25.
Nonbiased V gene usage for V(D)J joining is essential for providing an optimal immune system, but no cis-acting sequence with this function has been uncovered. We previously identified a recombination silencer and heterochromatin targeting element in the Vκ-Jκ intervening sequence of germline Igκ transgenes, which we termed Sis. We now have generated Sis knockout mice in the endogenous locus. Intriguingly, Sis(-/-) mice exhibit a skewed Igκ repertoire with markedly decreased distal and enhanced proximal Vκ gene usage for primary rearrangement, which is associated with reduced occupancy of Ikaros and CCCTC-binding factor in the Vκ-Jκ intervening sequence in pre-B cells, proteins believed to be responsible for dampening the recombination of nearby Vκ genes and altering higher-order chromatin looping. Furthermore, monoallelic heterochromatin localization is significantly reduced in Sis(-/-) mice for Igκ in cis and IgH loci in trans in pre-B cells. Because Sis(-/-) mice still allelically excluded Igκ and IgH loci and still exhibited IgL isotype exclusion, we concluded that stable localization at pericentromeric heterochromatin is neither necessary nor sufficient for the establishment or maintenance of allelic exclusion. Hence, Sis is a novel multifunctional element that specifies repertoire and heterochromatin localization to Ig genes.
非偏向性 V 基因的使用对于 V(D)J 连接对于提供最佳的免疫系统是必不可少的,但尚未发现具有此功能的顺式作用序列。我们之前在生殖系 Igκ 转基因的 Vκ-Jκ 间隔序列中鉴定了一个重组沉默子和异染色质靶向元件,我们将其命名为 Sis。我们现在已经在内源性基因座中生成了 Sis 敲除小鼠。有趣的是,Sis(-/-) 小鼠表现出 Igκ 库的偏倚,初级重排时明显减少远端和增强近端 Vκ 基因的使用,这与 Ikaros 和 CCCTC 结合因子在 pre-B 细胞中 Vκ-Jκ 间隔序列中的占据减少有关,这些蛋白被认为负责抑制附近 Vκ 基因的重组并改变高级染色质环。此外,Sis(-/-) 小鼠中 Igκ 顺式和 IgH 基因座反式的单等位基因异染色质定位显著减少。因为 Sis(-/-) 小鼠仍然等位基因排除 Igκ 和 IgH 基因座,并且仍然表现出 IgL 同种型排斥,所以我们得出结论,稳定定位于着丝粒异染色质对于建立或维持等位基因排斥既不是必需的也不是充分的。因此,Sis 是一种新型多功能元件,可指定 Ig 基因的库和异染色质定位。