Nyholm Spencer V, Passegue Emmanuelle, Ludington William B, Voskoboynik Ayelet, Mitchel Katrina, Weissman Irving L, De Tomaso Anthony W
Department of Pathology, Stanford University School of Medicine, California 94305, USA.
Immunity. 2006 Jul;25(1):163-73. doi: 10.1016/j.immuni.2006.04.011.
Histocompatibility in the primitive chordate, Botryllus schlosseri, is controlled by a single, highly polymorphic locus, the FuHC. By taking a forward genetic approach, we have identified a locus encoded near the FuHC, called fester, which is polymorphic, polygenic, and inherited in distinct haplotypes. Somatic diversification occurs through extensive alternative splicing, with each individual expressing a unique repertoire of splice forms, both membrane bound and potentially secreted, all expressed in tissues intimately associated with histocompatibility. Functional studies, via both siRNA-mediated knockdown and direct blocking by monoclonal antibodies raised against fester, were able to disrupt predicted histocompatibility outcomes. The genetic and somatic diversity, coupled to the expression and functional data, suggests that fester is a receptor involved in histocompatibility.
原始脊索动物Botryllus schlosseri的组织相容性由一个高度多态性的单一基因座FuHC控制。通过正向遗传学方法,我们在FuHC附近鉴定出一个编码的基因座,称为fester,它具有多态性、多基因性,并以不同的单倍型遗传。体细胞多样化通过广泛的可变剪接发生,每个个体表达独特的剪接形式库,包括膜结合型和潜在分泌型,所有这些都在与组织相容性密切相关的组织中表达。通过siRNA介导的敲低和针对fester产生的单克隆抗体的直接阻断进行的功能研究,能够破坏预测的组织相容性结果。遗传和体细胞多样性,加上表达和功能数据,表明fester是一种参与组织相容性的受体。