摘要
To become accessible for rearrangement, the immunoglobulin κ locus must undergo a series of epigenetic changes. This begins in pro-B cells with the relocation of both immunoglobulin κ alleles from the periphery to the center of the nucleus. In pre-B cells, one allele became preferentially packaged into an active chromatin structure characterized by histone acetylation and methylation of histone H3 lysine 4, while the other allele was recruited to heterochromatin, where it was associated with heterochromatin protein-γ and Ikaros. These events in cis made only one allele accessible to trans-acting factors, such as RelB, which mediated DNA demethylation, to facilitate rearrangement. These results suggest that early B lymphoid epigenetic changes generate differential structures that serve as the basis for allelic exclusion.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 198-203 |
| 页数 | 6 |
| 期刊 | Nature Immunology |
| 卷 | 6 |
| 期 | 2 |
| DOI | |
| 出版状态 | 已出版 - 2月 2005 |
| 已对外发布 | 是 |
学术指纹
探究 'Epigenetic ontogeny of the Igk locus during B cell development' 的科研主题。它们共同构成独一无二的指纹。引用此
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