Taketa Daryl A, Cengher Liviu, Rodriguez Delany, Langenbacher Adam D, De Tomaso Anthony W
Department of Molecular, Cellular and Developmental Biology, University of California - Santa Barbara, Santa Barbara, CA 93106, USA.
bioRxiv. 2024 Feb 15:2024.02.13.580188. doi: 10.1101/2024.02.13.580188.
Histocompatibility is the ability to discriminate between self and non-self tissues, and has been described in species throughout the metazoa. Despite its universal presence, histocompatibility genes utilized by different phyla are unique- those found in sponges, cnidarians, ascidians and vertebrates are not orthologous. Thus, the origins of these sophisticated recognition systems, and any potential functional commonalities between them are not understood. A well-studied histocompatibility system exists in the botryllid ascidians, members of the chordate subphylum, Tunicata, and provides an opportunity to do so. Histocompatibility in the botryllids occurs at the tips of an extracorporeal vasculature that come into contact when two individuals grow into proximity. If compatible, the vessels will , forming a parabiosis between the two individuals. If incompatible, the two vessels will - an inflammatory reaction that results in melanin scar formation at the point of contact, blocking anastomosis. Compatibility is determined by a single, highly polymorphic locus called the with the following rules: individuals that share one or both alleles will fuse, while those who share neither will reject. The locus encodes multiple proteins with roles in allorecognition, including one called which is necessary and sufficient to initiate the rejection response. Here we report the existence of genotype-specific expression levels of , differing by up to 8-fold at the mRNA-level, and that these expression levels are constant and maintained for the lifetime of an individual. We also found that these differences had functional consequences: the expression level of correlated with the speed and severity of the rejection response. These findings support previous conclusions that levels modulate the rejection response, and may be responsible for controlling the variation observed in the timing and intensity of the reaction. The maintenance of genotype specific expression of uncle fester is also evidence of an education process reminiscent of that which occurs in mammalian Natural Killer (NK) cells. In turn, this suggests that while histocompatibility receptors and ligands evolve via convergent evolution, they may utilize conserved intracellular machinery to interpret binding events at the cell surface.
组织相容性是区分自身组织和非自身组织的能力,后生动物中的所有物种都有这种能力。尽管普遍存在,但不同门所利用的组织相容性基因是独特的——海绵动物、刺胞动物、海鞘和脊椎动物中的组织相容性基因并非直系同源。因此,这些复杂识别系统的起源以及它们之间任何潜在的功能共性尚不清楚。被囊动物亚门尾索动物纲的柄海鞘中存在一个经过充分研究的组织相容性系统,这为研究提供了一个契机。柄海鞘的组织相容性发生在体外脉管系统的末端,当两个个体靠近生长时,这些末端会相互接触。如果相容,血管就会融合,在两个个体之间形成联体共生。如果不相容,两条血管就会排斥——引发炎症反应,在接触点形成黑色素瘢痕,阻止吻合。相容性由一个单一的、高度多态的基因座决定,称为“uncle fester”,遵循以下规则:共享一个或两个“uncle fester”等位基因的个体会融合,而那些都不共享的个体则会排斥。“uncle fester”基因座编码多种在异体识别中起作用的蛋白质,包括一种名为“”的蛋白质,它是启动排斥反应所必需且足够的。在这里,我们报告了“”基因存在基因型特异性表达水平,在mRNA水平上差异高达8倍,并且这些表达水平在个体的一生中是恒定且维持不变的。我们还发现这些差异具有功能后果:“”的表达水平与排斥反应的速度和严重程度相关。这些发现支持了之前的结论,即“”水平调节排斥反应,并且可能负责控制观察到的反应时间和强度的变化。“uncle fester”基因型特异性表达的维持也是一个类似于哺乳动物自然杀伤(NK)细胞中发生的教育过程的证据。反过来,这表明虽然组织相容性受体和配体通过趋同进化而进化,但它们可能利用保守的细胞内机制来解释细胞表面的结合事件。