Krangel Michael S
Department of Immunology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Nat Immunol. 2003 Jul;4(7):624-30. doi: 10.1038/ni0703-624.
V(D)J recombination assembles genes encoding antigen receptors according to defined developmental programs in immature B and T lymphocytes. The 'accessibility hypothesis' was initially invoked to explain how a single recombinase complex could control the locus and allele specificity of V(D)J recombination. It has been since shown that recombination signal sequences themselves influence recombination efficiency and specificity in ways that had not been previously appreciated. Recent developments have increased our understanding of how the chromatin barrier to V(D)J recombination is regulated, and how chromatin control and the properties of the underlying recombination signal sequences may cooperate to create diverse, lineage-restricted and allelically excluded repertoires of antigen receptors.
V(D)J重组根据未成熟B淋巴细胞和T淋巴细胞中确定的发育程序组装编码抗原受体的基因。“可及性假说”最初被用来解释单个重组酶复合物如何控制V(D)J重组的基因座和等位基因特异性。此后已表明,重组信号序列本身以先前未被认识到的方式影响重组效率和特异性。最近的进展增进了我们对V(D)J重组染色质屏障如何受到调控,以及染色质控制与潜在重组信号序列的特性如何协同作用以产生多样的、谱系受限且等位基因排斥的抗原受体库的理解。