Grenache D G, Caldicott I, Albert P S, Riddle D L, Politz S M
Department of Biology and Biotechnology, Worcester Polytechnic Institute, MA 01609, USA.
Proc Natl Acad Sci U S A. 1996 Oct 29;93(22):12388-93. doi: 10.1073/pnas.93.22.12388.
Nematodes can alter their surface coat protein compositions at the molts between developmental stages or in response to environmental changes; such surface alterations may enable parasitic nematodes to evade host immune defenses during the course of infection. Surface antigen switching mechanisms are presently unknown. In a genetic study of surface antigen switching, we have used a monoclonal antibody, M37, that recognizes a surface antigen on the first larval stage of the free-living nematode Caenorhabditis elegans. We demonstrate that wild-type C. elegans can be induced to display the M37 antigen on a later larval stage by altering the growth conditions. Mutations that result in nonconditional display of this antigen on all four larval stages fall into two classes. One class defines the new gene srf-6 II. The other mutations are in previously identified dauer-constitutive genes involved in transducing environmental signals that modulate formation of the dauer larva, a developmentally arrested dispersal stage. Although surface antigen switching is affected by some of the genes that control dauer formation, these two process can be blocked separately by specific mutations or induced separately by environmental factors. Based on these results, the mechanisms of nematode surface antigen switching can now be investigated directly.
线虫在发育阶段之间的蜕皮过程中或对环境变化做出反应时,可以改变其表面 coat 蛋白的组成;这种表面变化可能使寄生线虫在感染过程中逃避宿主的免疫防御。目前尚不清楚表面抗原转换机制。在一项关于表面抗原转换的遗传学研究中,我们使用了一种单克隆抗体 M37,它识别自由生活线虫秀丽隐杆线虫第一幼虫阶段的一种表面抗原。我们证明,通过改变生长条件,可以诱导野生型秀丽隐杆线虫在后期幼虫阶段展示 M37 抗原。导致该抗原在所有四个幼虫阶段无条件展示的突变分为两类。一类定义了新基因 srf-6 II。其他突变存在于先前确定的 dauer 组成型基因中,这些基因参与转导调节 dauer 幼虫形成的环境信号,dauer 幼虫是一个发育停滞的扩散阶段。尽管表面抗原转换受到一些控制 dauer 形成的基因的影响,但这两个过程可以通过特定突变分别阻断,或由环境因素分别诱导。基于这些结果,现在可以直接研究线虫表面抗原转换的机制。