Department of Clinical Sciences, North Carolina State University College of Veterinary Medicine, William Moore Drive, Raleigh, NC, 27607, USA.
Bioinformatics Research Center, North Carolina State University, Raleigh, NC, USA.
Immunogenetics. 2021 Oct;73(5):381-393. doi: 10.1007/s00251-021-01221-w. Epub 2021 Jun 27.
Of the 12 full-length feline leukocyte antigen class I (FLAI) loci, 3 are presumed to be classical: FLAI-E, FLAI-H, and FLAI-K. As diversity is a class Ia hallmark, multi-allelism is an important surrogate supporting a classical designation, in the absence of direct demonstration of T-cell restriction. Conversely, limited polymorphism at an expressed locus suggests regulation of immune effectors with invariant receptors, and non-classical status. FLAI-A, FLAI-J, FLAI-L, and FLAI-O are putative class Ib genes in cats. For both classes, identifying prevalent variants across outbred populations can illuminate specific genotypes to be prioritized for immune studies, as shared alleles direct shared responses. Since variation is concentrated in exons 2 and 3, which encode the antigen-binding domains, partial-length cloning/sequencing can be used for allele discovery, but is laborious and occasionally ambiguous. Here we develop a targeted approach to FLAI genotyping, using the single-molecule real-time (SMRT) platform, which allows full-length (3.4-kb) reads without assembly. Consensus sequences matched full-length Sanger references. Thirty-one new class Ia genes were found in 17 cats. Alleles segregated strongly by loci, and the origins of formerly difficult-to-assign sequences were resolved. Although not targeted, FLAI-L and FLAI-J, and the pseudogene FLAI-F, were also returned. Eighteen class Ib alleles were identified. Diversity was restricted and outside hypervariable regions. Both class Ib genes were transcriptionally active. Novel alternative splicing of FLAI-L was observed. SMRT sequencing of FLAI amplicons is useful for full-length genotyping at feline class Ia loci. High-throughput sequencing could allow highly accurate allele surveys in large cat cohorts.
在 12 个全长猫白细胞抗原 I 类(FLAI)基因座中,有 3 个被认为是经典的:FLAI-E、FLAI-H 和 FLAI-K。由于多样性是 Ia 类的一个标志,多等位基因是支持经典指定的一个重要替代物,在缺乏 T 细胞限制的直接证明的情况下。相反,在一个表达基因座上的有限多态性表明存在受不变受体调节的免疫效应物,且为非经典状态。FLAI-A、FLAI-J、FLAI-L 和 FLAI-O 是猫的假定的 Ib 类基因。对于这两类,确定在杂交群体中普遍存在的变体可以阐明要优先用于免疫研究的特定基因型,因为共享等位基因指导共享反应。由于变异集中在编码抗原结合域的外显子 2 和 3 中,因此部分长度的克隆/测序可用于等位基因发现,但劳动强度大且偶尔存在歧义。在这里,我们使用单分子实时(SMRT)平台开发了一种针对 FLAI 基因分型的靶向方法,该平台无需组装即可提供全长(3.4kb)读数。一致序列与全长 Sanger 参考序列匹配。在 17 只猫中发现了 31 个新的 Ia 类基因。等位基因按基因座强烈分离,以前难以分配的序列的来源得到解决。尽管不是靶向的,但也返回了 FLAI-L 和 FLAI-J 以及假基因 FLAI-F。鉴定出 18 个 Ib 等位基因。多样性受到限制,不在高变区之外。这两个 Ib 类基因均具有转录活性。观察到 FLAI-L 的新的选择性剪接。对 FLAI 扩增子的 SMRT 测序可用于猫类 Ia 基因座的全长基因分型。高通量测序可以在大型猫科动物队列中进行高度准确的等位基因调查。