完整 MHC 基因座序列的 DNA 结构特征和变异性。

IF 2.8 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY Frontiers in bioinformatics Pub Date : 2024-07-03 eCollection Date: 2024-01-01 DOI:10.3389/fbinf.2024.1392613
Trudy M Wassenaar, Terry Harville, Jonathan Chastain, Visanu Wanchai, David W Ussery
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引用次数: 0

摘要

主要组织相容性(MHC)基因座又称人类白细胞抗原(HLA)基因,位于第 6 号染色体的短臂上,包含三个区域(I 类、II 类和 III 类)。这个 5 Mbp 的基因座是人类基因组中变异最大的区域之一,但它也编码了一组与免疫反应有关的高度保守的重要蛋白质。该区域的基因变异导致的疾病比整个人类基因组的其他区域还要多。然而,有关 DNA 局部结构特征的信息在很大程度上被忽视了。随着长线程测序技术的不断进步,现在可以对整个 5 Mbp MHC 基因座进行测序,从而得到整个区域的完整二倍体单倍型。在此,我们描述了基于六个不同同源 HLA 细胞系完整序列的结构图。我们发现不同序列在 DNA 堆叠能、位置偏好和曲率、重复序列的变化等方面存在长程结构变异,而在形成开放染色质结构的区域则存在更多局部变化,这些变化可能会影响基因表达水平。这些结构图有助于直观显示不同 HLA 类型的大规模结构变异,特别是在有表观遗传学信号补充的情况下。
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DNA structural features and variability of complete MHC locus sequences.

The major histocompatibility (MHC) locus, also known as the Human Leukocyte Antigen (HLA) genes, is located on the short arm of chromosome 6, and contains three regions (Class I, Class II and Class III). This 5 Mbp locus is one of the most variable regions of the human genome, yet it also encodes a set of highly conserved and important proteins related to immunological response. Genetic variations in this region are responsible for more diseases than in the entire rest of the human genome. However, information on local structural features of the DNA is largely ignored. With recent advances in long-read sequencing technology, it is now becoming possible to sequence the entire 5 Mbp MHC locus, producing complete diploid haplotypes of the whole region. Here, we describe structural maps based on the complete sequences from six different homozygous HLA cell lines. We find long-range structural variability in the different sequences for DNA stacking energy, position preference and curvature, variation in repeats, as well as more local changes in regions forming open chromatin structures, likely to influence gene expression levels. These structural maps can be useful in visualizing large scale structural variation across HLA types, in particular when this can be complemented with epigenetic signals.

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