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Killer Immunoglobulin-Like Receptor Transcriptional Regulation: A Fascinating Dance of Multiple Promoters

机译:杀手免疫球蛋白样受体转录调控:多个启动子的迷人舞蹈

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摘要

Killer immunoglobulin-like receptors (KIRs) recognize class I major histocompatibility complex molecules and participate in the calibration of activation thresholds during human natural killer (NK) cell development. The stochastic expression pattern of the KIR repertoire follows the product rule, meaning that the probability of the coexpression of two or more different KIRs equals the product of the individual expression frequencies for those KIRs. The expression frequencies of individual KIRs are independent of major histocompatibility complex class I and are instead established and maintained by a dynamic, yet ill-defined, transcriptional program. Here, we review recent advances in our understanding of the architecture of the regulatory regions within KIR genes and discuss a potential role for non-coding RNA in KIR transcriptional regulation during NK cell development. Understanding the molecular mechanisms that underlie KIR expression may help guide us in the design of novel, rational strategies for the use of NK cells in transplantation and immunotherapy.
机译:杀伤免疫球蛋白样受体(KIR)识别I类主要组织相容性复合物分子,并参与人类自然杀伤(NK)细胞发育过程中的激活阈值校准。 KIR曲目的随机表达模式遵循乘积规则,这意味着两个或多个不同KIR共同表达的概率等于这些KIR的单个表达频率的乘积。各个KIR的表达频率独立于主要的组织相容性复合体I类,而是由动态但不确定的转录程序建立和维持。在这里,我们回顾了我们对KIR基因内调控区结构的了解的最新进展,并讨论了在NK细胞发育过程中非编码RNA在KIR转录调控中的潜在作用。了解构成KIR表达基础的分子机制可能有助于指导我们设计新颖,合理的NK细胞在移植和免疫疗法中的应用策略。

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