Instituto de Genética, Universidad Nacional de Colombia, Bogotá, Colombia.
Department of Molecular, Cellular and Developmental Biology, University of California Santa Barbara, Santa Barbara, CA, USA.
Immunogenetics. 2022 Dec;74(6):559-581. doi: 10.1007/s00251-022-01268-3. Epub 2022 Jun 27.
The genetics of allorecognition has been studied extensively in inbred lines of Hydractinia symbiolongicarpus, in which genetic control is attributed mainly to the highly polymorphic loci allorecognition 1 (Alr1) and allorecognition 2 (Alr2), located within the Allorecognition Complex (ARC). While allelic variation at Alr1 and Alr2 can predict the phenotypes in inbred lines, these two loci do not entirely predict the allorecognition phenotypes in wild-type colonies and their progeny, suggesting the presence of additional uncharacterized genes that are involved in the regulation of allorecognition in this species. Comparative genomics analyses were used to identify coding sequence differences from assembled chromosomal intervals of the ARC and from genomic scaffold sequences between two incompatible H. symbiolongicarpus siblings from a backcross population. New immunoglobulin superfamily (Igsf) genes are reported for the ARC, where five of these genes are closely related to the Alr1 and Alr2 genes, suggesting the presence of multiple Alr-like genes within this complex. Complementary DNA sequence evidence revealed that the allelic polymorphism of eight Igsf genes is associated with allorecognition phenotypes in a backcross population of H. symbiolongicarpus, yet that association was not found between parental colonies and their offspring. Alternative splicing was found as a mechanism that contributes to the variability of these genes by changing putative activating receptors to inhibitory receptors or generating secreted isoforms of allorecognition proteins. Our findings demonstrate that allorecognition in H. symbiolongicarpus is a multigenic phenomenon controlled by genetic variation in at least eight genes in the ARC complex.
同种异体识别的遗传学在 Hydractinia symbiolongicarpus 的近交系中得到了广泛研究,其中遗传控制主要归因于高度多态的同种异体识别 1 (Alr1) 和同种异体识别 2 (Alr2) 基因座,这些基因座位于同种异体识别复合物 (ARC) 内。虽然 Alr1 和 Alr2 的等位基因变异可以预测近交系的表型,但这两个基因座并不能完全预测野生型群体及其后代的同种异体识别表型,这表明存在其他未被描述的基因,它们参与了该物种的同种异体识别的调控。比较基因组学分析用于鉴定来自 ARC 组装染色体间隔区和来自来自回交群体的两个不相容 H. symbiolongicarpus 兄弟姐妹的基因组支架序列的编码序列差异。报道了 ARC 的新免疫球蛋白超家族 (Igsf) 基因,其中 5 个基因与 Alr1 和 Alr2 基因密切相关,表明该复合物内存在多个 Alr 样基因。cDNA 序列证据表明,在 H. symbiolongicarpus 的回交群体中,八个 Igsf 基因的等位基因多态性与同种异体识别表型相关,但在亲代群体与其后代之间未发现这种关联。发现了选择性剪接作为一种机制,通过将潜在的激活受体改变为抑制受体或产生同种异体识别蛋白的分泌同工型,从而导致这些基因的变异性。我们的研究结果表明,H. symbiolongicarpus 的同种异体识别是一种多基因现象,由 ARC 复合物中至少八个基因的遗传变异控制。